Troponin T isoform expression is modulated during Atlantic Halibut metamorphosis
BMC Developmental Biology volume 7, Article number: 71 (2007)
Flatfish metamorphosis is a thyroid hormone (TH) driven process which leads to a dramatic change from a symmetrical larva to an asymmetrical juvenile. The effect of THs on muscle and in particular muscle sarcomer protein genes is largely unexplored in fish. The change in Troponin T (TnT), a pivotal protein in the assembly of skeletal muscles sarcomeres and a modulator of calcium driven muscle contraction, during flatfish metamophosis is studied.
In the present study five cDNAs for halibut TnT genes were cloned; three were splice variants arising from a single fast TnT (fTnT) gene; a fourth encoded a novel teleost specific fTnT-like cDNA (AfTnT) expressed exclusively in slow muscle and the fifth encoded the teleost specific sTnT2. THs modified the expression of halibut fTnT isoforms which changed from predominantly basic to acidic isoforms during natural and T4 induced metamorphosis. In contrast, expression of red muscle specific genes, AfTnT and sTnT2, did not change during natural metamorphosis or after T4 treatment. Prior to and after metamorphosis no change in the dorso-ventral symmetry or temporal-spatial expression pattern of TnT genes and muscle fibre organization occurred in halibut musculature.
Muscle organisation in halibut remains symmetrical even after metamorphosis suggesting TH driven changes are associated with molecular adaptations. We hypothesize that species specific differences in TnT gene expression in teleosts underlies different larval muscle developmental programs which better adapts them to the specific ecological constraints.
Troponin T (TnT) is a class of skeletal muscle specific proteins that are an important component of the thin-filament. TnT proteins are essential for correct assembly of the sarcomeres [1, 2] and are responsible for anchoring of the Troponin complex to tropomyosin (Tm) and correct assembly and function of Troponin I and C [3, 4]. In tetrapods, three TnT genes exist, fast, slow and cardiac, expressed respectively in white (fast-twitch and glycolytic), red (slow-twitch and oxidative) and cardiac muscle. However, recent studies indicate that in teleosts a greater number of genes exist and at least two fast TnT (fTnT) and two slow TnT (sTnT) genes exist as well as an apparently teleost specific intronless TnT (iTnT) gene [5–7].
In terrestrial vertebrates, TnT genes are known to produce multiple protein isoforms by alternative splicing mechanisms [3, 4, 6, 8–20]. A number of factors, such as contractile properties , intracellular pH  in myofibres, calcium dependence modulation during cross-bridge cycling  and innervation patterns during development , are proposed to be associated with TnT isoform switching in cardiac and fast muscle of foetal and adult terrestrial vertebrates. In contrast, in terrestrial vertebrates, no developmental specific sTnT protein isoform changes occur [4, 9, 13, 18–20], although in adults red-muscle-specific isoforms are detected .
We recently reported the existence of three stage specific fTnT transcripts in a teleost, the sea bream, namely embryonic, larval and adult which are splice variants of a single gene . Moreover, in contrast to tetrapods, two paralogue sTnT genes (sTnT1 and sTnT2) that exhibit developmental specific expression were also identified in sea bream . The teleost specific gene, sTnT2, is first detected in sea bream in late epiboly stages and is the only sTnT gene expressed up until 4 days post-hatch (dph) the time at which sTnT1 expression starts . Throughout larval development and in early juvenile stages, sTnT1 is the predominant sTnT gene expressed in sea bream red muscle, although in adult red muscle sTnT2 is the predominant isoform and sTnT1 is virtually undetectable .
Studies in flatfish indicate that changes occur in muscle during the thyroid hormone driven metamorphosis in which a bilaterally symmetrical larvae changes to an asymmetric juvenile. In pre-metamorphic pelagic larvae of the flatfish Paralichthys olivaceus (flounder) two fTnT immunoreactive proteins of 41.5 and 34 kDa were reported . However, when the larvae enter metamorphosis to become a benthic flatfish, the 41.5 kDa protein is substituted by a new 33.5 kDa isoform. In post-metamorphosis juvenile fish only the 34 and 33.5 kDa isoforms of TnT are present . Similarly, during spontaneous metamorphosis larval 5,5'-dithio-bis-nitrobenzoic acid (DTNB) light chain (myosin light chain 2, MLC2) is replaced by an adult specific isoform . Although it is evident that changes which occur in muscle during metamorphosis are probably associated with changing functional requirements, surprisingly few molecular studies exist of this process. In the present study in order to analyse changes in skeletal muscle and in particular TnT gene expression during halibut (Hippoglossus hippoglossus) natural and T4 induced metamorphosis, cDNAs for slow and fast TnT were cloned and their expression and tissue distribution was studied in relation to changing thyroid hormone concentrations and muscle development.
Halibut TnT genes
Five cDNAs corresponding to different skeletal muscle TnT genes (Fig. 1) were isolated from a cDNA library of metamorphosing halibut larvae. In tBLASTx analysis  against the GeneBank database, three cDNAs gave a highly significant match with teleost, fTnT genes. From the analysis it was determined that the fTnThh cDNAs isolated correspond to a putative embryonic/larval halibut fTnT (denominated efTnThh; DQ680173) and two different adult isoforms (denominated fTnThh-1, DQ680174, and fTnThh-2, DQ680175). The efTnThh cDNA is a full-length clone with 965 nucleotides (nt) and encodes a 286 amino acids (aa) protein from nt 62 to 919. The size of the deduced protein is 34.6 kDa and the predicted pI is 5.27 (Fig. 1). The fTnThh-1 isoform is a 752 bp cDNA which encodes a protein of 232 aa from nt 22 to 717 (Fig. 1). The deduced fTnThh-1 protein has a predicted molecular weight of 27.89 kDa and a pI of 9.42 . The cDNA of the third isoform, denominated fTnThh-2, is 1,020 bp long and encodes a putative protein of 229 aa from nt 70 to 756 (Fig. 1). The predicted molecular weight and pI for the fTnThh-2 protein isoform is respectively 27.5 kDa and 9.55 .
In silico characterisation of the deduced halibut fTnT proteins using ProDom  and PRINTS  software confirmed that they possess all the characteristics of fully functional fTnT proteins. ClustalX  multiple alignment analysis of these putative halibut fTnT cDNAs and their deduced protein sequence indicates that they are the products of alternative splicing of the halibut fTnT gene (Fig. 1). Isoform efTnThh shares 80% sequence identity with fTnThh-1 and -2 isoforms, whereas isoforms fTnThh-1 and -2 are 99% similar. The differences between the halibut TnT cDNA isolated are due to the presence of an insert in efTnThh (aa 12 to 68) and fTnThh-1 (aa 12 to 14) which is lacking in the fThThh-2 isoform (Fig. 1).
A further 1,107 bp cDNA was also cloned and tBLASTx analysis  suggests that it most closely resembles an fTnT gene and gave the most significant hit to D. rerio fTnTa gene and it was tentatively designated an atypical fast TnT cDNA (AfTnThh-1; DQ680176) as a consequence of its tissue distribution. The predicted protein product encoded by AfTnThh-1 cDNA was 289 aa with a pI of 5.07 and molecular weight of 34.21 kDa (Fig. 1).
A halibut cDNA homologous to a previously reported teleost specific sTnT2 gene was also cloned. This cDNA, designated sTnT2hh (DQ680172), is 980 bp long and encodes a deduced protein of 246 aa (Fig. 1) with a predicted molecular weight of 29 kDa and a pI of 9.24 . It was not possible, despite extensive cDNA library screening to isolate a cDNA that was the product of a putative halibut sTnT1 gene.
ClustalX multiple sequence alignment  of the deduced amino acid sequence of halibut TnT genes show that efTnThh shares 69% and 52% sequence identity, respectively, with AfTnThh and sTnT2hh. Comparison of the other halibut fTnT-1 and -2 isoforms with AfTnThh and sTnT2hh reveal they share ~59% sequence identity while, AfTnThh and sTnT2hh share 50% identity.
Putative genomic organization of halibut skeletal TnT genes
In silico tBLASTx analysis  using halibut fTnT cDNA sequences gave a highly significant hit to Tetraodon nigroviridis genomic scaffold 7217 (SCAF7217). The putative Tetraodon and deduced halibut fTnT gene is composed of 14 exons (Fig. 2A) as previously described for the sea bream . The efTnThh isoform is composed of exons I to III and V to XIV (Fig. 2A). Isoform fTnThh-1 contains all exons except exon V, which codes for the highly acidic peptide containing a glutamic acid (E), proline (P) repeat (Fig. 1 and 2A). In the isoform fTnThh-2 mRNA, exons IV and V are spliced out (Fig. 2A) which results in the loss of 9 nt in relation to fTnThh-1 (Fig. 1). The ATG transcription start signal is located in exon II and exon I bears the beginning of the 5'UTR (Fig. 2A). The 3'UTR and the end of the protein coding region are located in exon XIV. Overall coverage of the fTnThh cDNA sequences was 97% and overall identity between it and the Tetraodon fTnT gene sequence was 82%.
The halibut AfTnThh gene used in tBLASTx analysis led to the identification of the putative Tetraodon AfTnT locus in scaffold 15099 (SCAF15099) as well as five different Tetraodon AfTnT cDNA isoforms (numbered 1 to 5) which seem to be the product of alternative splicing (AfTnTtn-1, CR696067; AfTnTtn-2, CR675364; AfTnTtn-3, CR662746; AfTnTtn-4, CR727722; AfTnTtn-5, CR673164). The Tetraodon AfTnT cDNA and the AfTnThh cDNA were used to deduce the putative genomic organization of the AfTnT gene in Tetraodon scaffold 15099 by aligning the cDNAs and genomic sequences in Spidey . The analysis revealed that the Tetraodon AfTnT gene (AfTnTtn) is composed of 16 exons with conserved intron/exon boundaries spanning 8946 bp in Tetraodon scaffold 15099 (Fig. 2B). Tetraodon AfTnTtn cDNAs had 100% coverage in the Tetraodon genomic sequence of scaffold 15099 and the majority of exons shared 100% nucleotide sequence conservation. The halibut AfTnThh cDNA had 100% coverage in the Tetraodon genomic sequence of scaffold 15099 and shared 79% overall sequence identity. Exon I bears part of the 5'UTR while exon II contains the remainder and the ATG translation start site. Exon III is composed of 13 nt and constitutes together with exons I and II the N-terminal constitutive exons present in all Tetraodon AfTnT cDNAs identified. Exon II and III share 77% sequence identity between the Tetraodon genomic sequence and halibut AfTnThh cDNA, while exon I shares only 58% identity. Exon IV which codes for 3 acidic residues both in Tetraodon and halibut is the first N-terminal alternatively spliced exon in Tetraodon cDNAs, and shares 75% sequence identity between Tetraodon genomic and halibut AfTnThh cDNA sequence. Exon V is the largest alternatively spliced N-terminal exon in Tetraodon and is the most divergent between the Tetraodon genomic sequence and halibut AfTnT cDNA. In this exon the sequence identity is only 52% and a 41 nt insertion in the third quarter of the Tetraodon genomic sequence renders this exon bigger in Tetraodon than in halibut. However, the 5' and 3' regions of the Tetraodon sequence are well conserved with the corresponding halibut AfTnT sequence. Exons VI and VII are highly conserved (94%) between the Tetraodon genomic sequence and halibut AfTnT cDNA sequence and are alternatively spliced in Tetraodon. Exons VIII to XVI encode the C-terminal constitutive region present in all vertebrate TnT genes and sequence conservation between the Tetraodon and halibut was always greater than 85% and no splice variants of this region were observed in Tetraodon. Exon XVI codes for the last 11 amino acid residues of the protein and the entire 3'UTR. Although exon XVI shares only 47% sequence identity between Tetraodon and halibut the sequence divergence is in the 3'UTR rather than the coding region (86% sequence identity).
The genomic organization of halibut sTnT2 gene in Tetraodon was also determined (Fig. 2C). Using the sTnT2hh sequence in tBLASTx analysis  of the Tetraodon genome database  a single hit with Tetraodon scaffold 15000 (SCF15000) was found. A single cDNA transcript (CR734482) arising from Tetraodon sTnT2 gene (SCF15000) was isolated and introduced in Spidey aligning software  along with the halibut sTnT2 cDNA sequence to determine the putative genomic organization of sTnT2. The putative Tetraodon sTnT locus is composed of 12 exons and spans 2567 nt in the Tetraodon genomic sequence (Fig. 2C). Exon I bears the first three-quarters of the 5'UTR and the beginning of the coding region is located in exon II. Exon XII contains the 3'-end of the coding region as well as the 3'UTR (Fig. 2C). The halibut sTnT2hh cDNA sequence had 86% coverage in the Tetraodon genomic sequence and shared 82% sequence identity.
Tissue specificity of halibut TnT genes
Northern blot and RT-PCR analysis were carried out in order to determine tissue specificity of the halibut TnT genes isolated. The northern blot results (Fig. 3A) show that fTnThh, as expected, is expressed in adult halibut white (fast) muscle and is absent from red muscle, cardiac muscle and liver. However, the more sensitive RT-PCR technique revealed that fTnThh is also expressed in halibut adult red muscle (Fig. 3B). The tBLASTx and phylogenetic analysis of AfTnThh classified this cDNA as the product of a fast TnT gene, although its expression is red (slow) muscle specific (Fig. 3A) and it is not detected in adult white (fast) muscle, cardiac muscle or liver. The halibut sTnT2 gene is exclusively expressed in halibut adult red muscle (Fig. 3A). The red muscle tissue specificity of AfTnThh and sTnT2hh was further confirmed by RT-PCR (Fig. 3B).
Phylogenetic analysis of Halibut TnT genes
ClustalX multiple sequence alignment  of the deduced protein of halibut TnT and other vertebrate TnT protein sequences and striated muscle TnT from C. elegans was performed and the resulting phylogenetic relationships were determined in PAUP* version 4.0b software  using the maximum-parsimony method with 1000 bootstraps  and C. elegans TnT as an outgroup.
The phylogenetic tree shows that the vertebrate fTnTs form a single clade and that within it the tetrapod fTnTs cluster apart from the fish fTnTs (Figure 4). Moreover, efTnThh, fTnThh-1 and fTnThh-2 cluster with highly significant bootstrap values with other teleost fTnT genes. Within the main fTnT clade, AfTnThh and Tetraodon AfTnTtn isoforms clustered together and formed a separate group and this topology was supported by highly significant bootstrap values (Fig. 4).
Two principal clades were found for sTnT which corresponded to sTnT1 and sTnT2 (Fig. 4). The halibut sTnT2hh clusters with other teleost specific sTnT2 genes (Fig. 4) and forms a group apart from tetrapod sTnT and sTnT1, which clustered together.
TnTexpression during halibut metamorphosis
The expression of the isolated halibut fTnT, AfTnT and sTnT2 genes was analysed by RT-PCR during halibut metamorphosis (Fig. 5, 6 and 7, respectively). The primers used in this analysis encompass the entire N-terminal hypervariable region which is known in vertebrates to generate alternative spliced isoforms [3, 4, 6, 8–20]. Three fTnThh isoforms were amplified by RT-PCR during halibut metamorphosis, the largest product corresponded to efTnThh (423 bp) while the smaller products correspond to, fTnThh-1 (261 bp) and fTnThh-2 (252 bp; Fig. 5A). A further reaction product is observed between the efTnThh and the other two isoforms that does not represent an authentic isoform but a heteroduplex of efTnThh and the other two isoforms since isolation followed by PCR, subcloning and sequencing always yield either efTnThh or one of the other two isoforms.
The three halibut fTnT isoforms are all present in pre-metamorphic halibut larvae (stg 5–7) and efTnThh is the predominant isoform expressed up until the beginning of climax and has approximately 2-fold higher expression than fTnThh-1 and -2 (stg 8; HSD, p < 0.001; Fig. 5A and 5B). At the beginning of climax fTnThh-2 expression starts to increase and at the climax of metamorphosis (stg 9) the efTnThh isoform is downregulated and is almost undetectable in fully metamorphosed juveniles (stg 10, Fig. 5A and 5B). In parallel fTnThh-2 becomes the most highly expressed fTnThh isoform and increases ~3-fold in juveniles (Fig. 5A and 5B). Prior to, and after metamorphosis fTnThh-1 expression does not change significantly (Fig. 5A and 5B). Analysis of fTnT isoform expression in adult halibut muscle by RT-PCR confirmed the general pattern encountered by Northern blot (Fig. 3A). However, the more sensitive RT-PCR technique permitted detection of fTnThh isoforms in halibut adult red -muscle (Fig. 3B and 3C). In halibut adult white muscle low expression of efTnThh (~14-fold lower than fTnThh-2) is observed, fTnThh-2 continues to be the predominant isoform although fTnThh-1 expression has increased and is about half that of fTnThh-2 (Fig. 3B and 3C). The ratio of the different fTnThh mRNA in red muscle differs from white muscle since fTnThh-2 is ~10-fold more expressed than efTnThh and fTnThh-1 which are almost undetectable (Fig. 3B and 3C).
In contrast to fTnThh, expression of halibut AfTnThh (Fig. 6A) and sTnT2hh (Fig. 7A) detected by RT-PCR does not change during metamorphosis (Fig. 7). However, 4 alternatively spliced isoforms of AfTnThh are detected (Fig. 8A and 8D). Sequence analysis reveals that the AfTnThh isoforms are a result of alternative splicing of exons IV, V and VII (Fig. 2) and are designated AfTnThh-1 to -4. The largest product, AfTnThh-1 (439 bp) is identical to the AfTnThh cDNA isolated by library screening and includes all alternatively spliced exons (Fig. 6A and 6D); AfTnThh-2 (412 bp; DQ680177) lacks exons IV and VII but exon V is maintained (Fig. 6A and 6D); AfTnThh-3 (301 bp; DQ680178) is composed of exon IV and VII but exon V is spliced out (Fig. 6A and 6D); and in AfTnThh-4 (283 bp; DQ680179) only exon IV is spliced in and all other alternatively spliced exons (exons V and VII) are spliced out (Fig. 6A and 6D). All the halibut AfTnThh isoforms detected contain exon VI (Fig. 6D) and neither the isoform expression pattern nor the ratio between these AfTnThh isoforms is altered during metamorphosis (Fig. 6A–C). A small but statistically significant (HSD, p ≤ 0.005; Fig. 6A and 6B) decrease in expression of all the isoforms is observed in stg 10 juveniles; AfTnThh-1 is the predominant isoform throughout the halibut's life. In turn, AfTnThh-2 is the second most abundant isoform and its expression increases after climax (HSD, p ≤ 0.006; Fig. 6A and 6B). However, in adult red muscle the ratio of the two isoforms is identical to pre-metamorphic stg 5 animals (Fig. 6A and 6C). The AfTnThh-3 and -4 isoforms have identical (HSD, p > 0.05), very low expression (Fig. 6A–C) and their expression and ratio in relation to other isoforms does not change during metamorphosis (HSD, p > 0.05; Fig. 6A–C). Moreover, in adult red muscle these low molecular weight isoforms are not expressed (Fig. 6A and 6B).
Spatial-temporal expression pattern of halibut TnTgenes during metamorphosis
The spatial-temporal expression pattern of TnT mRNA was determined in free- swimming halibut larvae which feed exogenously. In such larvae two distinct muscle layers are evident, an inner white and superficial red muscle layer (Fig. 8). In stage 5 halibut the anatomical organisation of the white muscle is very simple with a "V" shaped myomere and it is composed of several block-like bilaterally symmetrical myotomes bounded by a septum. The extreme dorsal and ventral myotomes and the lateral region of the myotomes close to the red muscle is characterized by the presence of numerous small rounded fibres, characteristic of germinal zones, while in the deeper region of the larger myotomes, fibres are much larger, more block-like and are closely packed. In subsequent stages myotome number increases and in stage 6 halibut larvae they take on the typical "W" shaped myomer organisation.
No change in the bilateral symmetry of the muscle anatomy accompanies metamorphosis, although a significant increase in the volume of muscle occurs in stages 8, 9 and 10 (Fig. 8). Regions of hyperplastic growth persist in the most ventral and dorsal myotomes in all of the stages analysed. A rapid increase in myotome number is evident from stage 5 through 7 and in subsequent stages hypertrophic growth leads to a considerable increase in myotome and overall muscle volume. In stage 5 the red muscle layer is a monolayer of fibres at the outermost region of the myotomes, although proliferating red muscle fibres at the midline region of the myotome generate a small region with a double layer of fibres. In stage 6 larvae this double layer is much more evident and in successive larval stages all the red muscle layer is proliferating so that in stage 9 halibut it is composed of several layers of fibres of different sizes. Notably during the entire metamorphic process the symmetry of the myotomes is maintained even though the skull becomes asymmetric with the right eye migrating to the left side of the head that at the end of metamorphosis constitutes the dorsal side of halibut body.
Halibut embryonic/larval fTnT exon expression in pre-metamorphic halibut larvae (Stg5 and 6; Fig. 8 and Fig. 9A and 9B) is restricted to white muscle, in the lateral and apical germinal zones of the myotome. As the halibut larvae approach metamorphic climax (Stg8; Fig. 8 and Fig. 9C) the efTnThh expression is significantly downregulated and confined to very small fibres and to presumptive satellite cells (arrows in Fig. 8 and Fig. 9C). From climax of metamorphosis (stg 9; Fig. 8 and 9D) onwards no efTnThh expression is detected. The 3'UTR fTnT probe reveals the general fTnThh expression pattern in stage 5 (Fig. 8 and Fig. 9E) and stage 6 larvae (Fig. 8 and Fig. 9F) which is similar to that observed with the embryonic/larval fTnT exon probe. At stage 8 (Fig. 8 and Fig. 9G) fTnT is uniformly distributed in the white muscle. As the animals reach post-metamorphic juvenile stage 10 (Fig. 8 and Fig. 9H) fTnThh expression looses its uniformity and although still expressed in the entire myotome, the signal is more intense in cells close to the myosepta (Fig. 8).
Halibut AfTnT and sTnT2 gene expression is confined to red muscle fibres in all metamorphic stages analysed. Expression of AfTnT in pre-metamorphic stage 5 larvae (Fig. 8 and Fig. 9I) is highly abundant in the red muscle layer. At the end of larval life, just before the onset of metamorphosis, (stg 6) in the myotome midline region two red muscle cell layers both expressing AfTnT are present (data not shown). In stage 8 (Fig. 9K) the expression of AfTnThh is detected uniformly in all the fibres of the red muscle, while in post-metamorphic juveniles at stage 10 (Fig. 8 and Fig. 9L) it is mostly present in the smaller fibres (arrowheads in Fig. 9L). In the case of sTnT2, expression is restricted to the red muscle layer and is very similar to AfTnT in stage 5 (Fig. 9M), 6 (Fig. 9N), 8 (Fig. 9O), 10 (Fig. 9P) halibut. The spatial-temporal expression pattern of red muscle specific halibut TnT genes is symmetrical and does not change during halibut metamorphosis (Fig. 8 and 9).
TH levels in metamorphosing halibut
At the beginning of metamorphosis and up until the beginning of climax (stg 8), T4 levels remain low with no significant differences observed between stages 5, 6 and 8 (HSM, p > 0.05; Fig. 10). In fact in larvae at the beginning of metamorphosis (stg 7) T4 levels are lower than in pre-metamorphic larvae (stg 5, HSD, p < 0.05). At the climax of metamorphosis (stg 9), whole-body T4 content increases about 3-fold in relation to all the previous stages (HSM, p < 0.005, Fig. 10). In post-metamorphic juveniles (stg 10) T4 levels continue high and, although not significantly different from stage 9, they are significantly higher than all other preceding stages (stg 5 to 8, HSM, p < 0.001; Fig. 10).
Before metamorphosis and up until climax of metamorphosis (stg 9) T3 levels are lower than T4 (HSD, p < 0.001; Fig. 10). In fact, T3 levels decrease from pre-metamorphic larvae (stg 5) until the start of metamorphosis (stg 8) (Fig. 10). However, in halibut at climax (stg 9) T3 levels increase more than 200-fold and are higher than T4 levels (HSD, p < 0.001; Fig. 10). However, after metamorphosis T4 levels are again higher than T3 levels (HSD, p < 0.001; Fig. 10). T3 levels at climax and in fully metamorphosed juveniles are significantly higher than all previous halibut stages (HSD, p < 0.001; Fig. 10).
T4 treatment and halibut TnT expression
Treatment of pre-metamorphic halibut larvae for 10 days with T4 totally repressed efTnThh isoform expression (HSD, p < 0.05, Fig. 11A) without affecting the expression of the other two fTnThh isoforms (HSD, p > 0.05, Fig. 11A). Neither AfTnThh or sTnT2hh expression or isoform profile is altered from that of control larvae by T4 treatment (Fig 11B and 11C).
We have isolated cDNAs from three different striated muscle TnT genes in the halibut one of which is white muscle specific while the other two are red muscle specific. Alternative splicing of the fTnThh gene gives rise to three alternative splice variants which encode three proteins varying only in the N-terminal region (Fig. 1). As observed for the fTnT gene of S. auratus , halibut fTnT is also expressed in adult red muscle. In fact, the expression of teleost fast-specific genes in red muscle seems to be a common feature in teleost species [36, 37]. In relation to fTnThh-1 (predicted MR 27.89 kDa and pI 9.42) and fTnThh-2 (predicted MR 27.5 kDa and pI 9.55), the putative efTnThh protein isoform is bigger (MR 34.6 kDa) and more acidic (pI 5.27) and the difference arises as a consequence of splicing in of exon V (Fig. 2A), in a way similar to that previously reported in S. auratus, a perciform and also in other vertebrates [4, 10–13], [38–50]. In the halibut the number of alternatively spliced fTnT isoforms are the same as found in Tetraodon and S. auratus . In common with Tetraodon efTnT, exon V is spliced in and exon IV is spliced out (Fig. 1 and 2A). This is in contrast to efTnT in S. auratus in which exon IV is also spliced in along with exon V  suggesting that in the halibut and Tetraodon exons IV and V are mutually exclusively expressed (Fig. 2A). Although no data is available about the specific biochemical characteristics of muscle fibres in halibut, S. aurata or Tetraodon larvae, the present study indicates that differences probably exist between teleost species and these differences are probably an adaptation to their differing ecologies and locomotive strategies.
In rat, human and mouse it has been reported that some fTnT isoforms predominate over others due to the specific biochemical characteristics of different fibres types . In these mammals acidic, fetal fTnT isoforms predominate in mainly glycolytic fibres whereas more basic isoforms are predominant in mainly oxidative fibres . However, there are clear differences between teleost and tetrapod fTnT genes. In tetrapods alternative splicing of the fTnT gene generates several N-terminal protein isoforms through the use of a greater number of alternatively spliced exons [4, 11] whereas in teleosts it seems that only two exons undergo alternative splicing (Fig. 2A; ). Although the fetal/embryonic exon is bigger in teleosts than in tetrapods they have similar biochemical characteristics as it encodes an acidic peptide containing several glutamic acid residues (present study; [5, 12]). No fTnT cDNA isoforms which give rise to 3' spliced variants and therefore proteins with differing C-terminal sequences are observed in halibut, Tetraodon or S. auratus. Curiously, the deduced C-terminal amino acid sequence of all halibut fTnT isoforms share greatest identity to tetrapod isoforms containing the embryonic specific exon 17 [4, 10, 47, 52]. Together with a previous study in teleosts  the present data in halibut seem to reinforce the idea that the occurrence of alternatively spliced exons in the C-terminal region of the fTnT gene is a characteristic exclusive to terrestrial vertebrates. Nonetheless, the genomic organization of fTnT genes in teleosts is identical to tetrapods  and from an evolutionary perspective, it seems likely that alternative splicing to generate N-terminal protein variants of the fTnT gene in vertebrates already occurred before the divergence of actinoperigii and sarcopterigii vertebrate lineages.
An unexpected observation arising from the present study was the identification of a large (predicted MR 34.21 kDa), highly acidic (predicted pI 5.07) halibut skeletal muscle TnT (AfTnT) gene with high sequence identity to D. rerio fTnTa gene . A homologue of this TnT gene was found in Tetraodon together with five splice variants and despite its unusual characteristics it had a similar organization to other vertebrate TnT genes [4, 7, 10–13, 19, 38–52]. The highly acidic nature of the protein isoforms encoded by this gene is a consequence of splicing in of exon V which encodes a very acidic stretch (~50 aa) of amino acids. Regardless of the fact that both sequence similarity and phylogenetic analysis categorise the putative AfTnThh protein as a fast TnT the tissue expression analysis (Fig. 3) indicates that the AfTnT is a red muscle specific gene in halibut. This is the first time to our knowledge that a gene presumed to be fast muscle specific in vertebrates is exclusively expressed in red muscle. The observations of TnTs in halibut and zebrafish  indicate that despite the apparent anatomical simplicity of striated skeletal muscle in teleosts, at the molecular level they have novel adaptations that probably underline species-specific control mechanisms of muscle development.
Halibut TnTgenes expression during metamorphosis
The expression of AfTnThh and sTnT2hh transcripts does not appear to change at climax of metamorphosis, although changes in the expression of fTnT gene isoforms do coincide with this developmental stage in halibut. The transition in expression of fTnT isoforms is correlated with the increase in whole-body T3 and T4 levels and the downregulation of efTnThh (Fig. 5) In turn, TH levels correlate positively with the increase in expression of fTnThh-2 (Fig. 5, 9 and 10). A similar situation also occurs in other flatfish, Paralichthys olivaceus , Solea solea and Scophthalmus maximus  and at the climax of metamorphosis an acidic efTnT isoform is downregulated and lower molecular weight and more basic isoforms are upregulated, and detected in juvenile and adult white muscle.
The changes in fTnT isoform expression in different teleost (present study, [5, 25, 53]) are reminiscent of what occurs in tetrapods in which fetal acidic fTnT isoforms are downregulated immediately after birth and are substituted by basic adult isoforms [10, 54, 55]. Moreover, a common mechanism of alternative splicing of 5' exons in the fTnT gene in teleosts, birds and mammals, implied by similar codon splitage combinations [5, 11], further reinforces the hypothesis that alternative splicing of the fTnT gene is conserved and occurs in order to cope with similar developmental demands on muscle in all vertebrates. The transition from acidic to a basic isoforms in fTnT genes seems to be a common trend in vertebrates and represents a physiological, mechanistic and functional adaptation of developing striated muscle [3, 10, 22, 23]. This strong conservation suggests that the same factors responsible for fTnT isoform transition during development are common throughout vertebrates and may be a trait acquired long before the divergence of the actinoperigii and sarcopterigii vertebrate lineages. In fact, teleost muscle and tetrapod muscle face similar physiological and biochemical changes during development. Foetal mammalian muscle grows by hyperplasia up until birth and muscle fibres are mainly glycolytic while the mainly oxidative adult muscle fibres, that differentiate after birth, express predominantly basic fTnT isoforms . In teleosts, the muscle fibres also change their biochemical and physiological characteristics during development and up until metamorphosis white muscle is the major respiratory surface of the larvae and fibres are mainly aerobic and rich in mitochondria whereas the adult muscle fibres are mainly anaerobic [56–62].
As shown by others, and in contrast to tetrapod post-embryonic muscle development, in teleost species of large size, like the halibut, post-embryonic muscle development takes place in two steps in which hyperplasia is the main mechanism of muscle growth [36, 56, 58, 60, 61, 63, 64]. The first hyperplasic phase of post-embryonic muscle development in large size teleost larvae is characterised by proliferative epaxial and lateral areas of the myotome and as animals reach the juvenile stage these regions are depleted and a second stage of hyperplasic growth continues in scattered myogenic cells throughout the myotome. Notably, the efTnThh isoform is mainly found at the most epaxial and lateral zones of halibut pre-metamorphic larval white muscle myotome, especially in small diameter white muscle fibres (Fig. 8 and 9A–E and A'-E'). The early differentiated halibut larvae white-muscle myoblasts appear to first express predominantly efTnT and as they mature and are incorporated in the myotome expression is downregulated and other fTnT isoforms take their place. In vertebrates the embryonic to adult fTnT isoforms pattern of change is related to alterations in cellular pH, metabolic and physiological characteristics of maturing muscle fibres [3, 10, 22, 23]. The transition from acid to basic pI fTnT isoforms in developing halibut muscle may be associated with the transition from proliferative small diameter muscle cells to more basic larger white muscle fibres. In fact, in S. auratus it was found that larval small diameter myoblast cells located in the hyperplasic lateral and epaxial region of the larval myotome contain acid mATPase activity whereas mature large diameter muscle fibres have mild alkali mATPase activity . Together with the downregulation of expression of efTnThh at halibut metamorphosis these hyperplasic proliferative areas of the myotome are gradually depleted just as metamorphosis starts and totally absent in animals entering climax (Fig. 8 and 9A–E and A'-E'). This resembles the situation in S. auratus where at the end of larval life the same lateral and apical hyperplasic white muscle germinative areas are depleted . However, and in contrast to what occurs in S. auratus , the treatment of pre-metamorphic halibut larvae with T4 shows that thyroid hormones control the expression profile of fTnT isoforms in the halibut and also in other flatfish .
The relationship between THs and change in fTnT isoform expression has yet to be directly demonstrated in teleosts. It is notable that despite the accepted role of THs in driving flatfish metamorphosis and the change from a symmetrical larvae to an asymmetrical juvenile, the way in which muscle symmetry changes has been largely ignored. In the present study muscle development was found to be a bilaterally symmetrical process before, during and after metamorphosis as revealed by histology and in situ gene expression studies. Nonetheless, the changes in TnT isoform expression in halibut, S. solea, S. maximus and P. olivaceus indicate muscle is TH responsive [53, 25] as has been demonstrated in mammals. In rats T3 increased the expression of Ca2+ ATPase specifically in white muscle fibres and the increase in relaxation rate of post-embryonic white muscle was strictly dependent on THs . Moreover, in mammals THs are necessary to complete development of skeletal muscle . The results from experiments in teleosts suggest that various post-embryonic muscle development mechanisms exist. For example, in S. auratus  slow muscle seems to be more sensitive to THs than white muscle, whereas in halibut, expression of the slow-muscle specific genes sTnT2hh and AfTnThh does not alter during metamorphosis (when endogenous T4 levels rise) or in response to exongenous T4 (Fig. 6, 7 and 11).
Together with previous studies in teleost TnT genes [6, 7, 25, 53] the present work shows that teleost muscle, although apparently simpler and having a smaller number of specialized muscles in comparison to tetrapods [3, 4] shows remarkable genetic heterogeneity and species-specific regulation. The diversity of TnT forms in teleost muscle arise from alternative splicing but also from a new teleost specific TnT gene and this heterogeneity probably contributes to better adapt the musculature to the specific functional demands of different teleost species. In common with other flatfish, but in contrast to the round fish, S. auratus , the halibut fTnT gene isoform expression profile is regulated at metamorphosis by THs, although halibut red muscle specific genes seem to be insensitive. Interestingly, the asymmetry arising during flatfish metamorphosis does not extend to the musculature and the temporal and spatial expression patterns of TnT genes and muscle fibre organization remains symmetrical before, during and after metamorphosis (Fig. 8 and 9). Clearly THs regulate muscle development but far more work is required to establish the specific molecular and cellular events during flatfish and round fish muscle development.
TnT cDNA library screening
A lambda phage cDNA library made from metamorphosing larvae of halibut was plated in densities ranging from 1,000–5,000 plaque forming units (pfu). A probe was obtained for skeletal TnT by randomly isolating and sequencing 10 clones. A putative halibut fTnT obtained in this way was used as a probe for cDNA library screening or alternatively a PstI/EcoRI digested cDNA fragment from a sea bream sTnT2 gene (sTnT2sb) was utilised. In each screen using the halibut fTnT or the sTnT2sb probe, nitrocellulose membrane lifts were performed and membranes pre-hybridized for 2 hours, respectively, at 65°C or 60°C in hybridization solution (6×SSC, 0.1%SDS, 100 μg/mL tRNA, 5× Denhardt's). DNA probes were labelled with [32P] by random priming (Megaprime, random labelling kit, Amersham Biosciences, UK) and purified on a sephadex column. Radioactively labelled probes were diluted in new hybridization mix and allowed to hybridize overnight with the membranes. Two post-hybridisation stringency washes were carried out for ~30 minutes at room temperature (1×SSC, 0.1%SDS) followed by two 30 minute washes (1×SSC, 0.1%SDS) at 65°C or 60°C, respectively. Membranes where then exposed overnight at -80°C to Biomax MS film (Kodak, Palo Alto, CA, USA) and several positive plaques were isolated and automatically excised into pBluescript SK+/- (Stratagene), DNA purified and cDNA clones sequenced to give 3-fold coverage using BigDye Version 3 (Perkin-Elmer, UK) chemistry and an ABI 3700 sequencer.
The identity of the halibut TnT cDNA isolated was assigned by tBLASTx analysis  against GenBank and the Medaka (Oryzia latipes) EST database . All tetrapod and teleost TnT cDNA sequences were retrieved and their deduced amino acid sequence compared to that of halibut TnTs using ClustalX software . The phylogenetic relationship of halibut TnT genes with other vertebrate TnT genes was analysed using the maximum-parsimony method option of PAUP* version 4.0b software  with 1000 bootstraps  and TnT sequences available from databases (Table 1). Caenorhabditis elegans striated muscle TnT (GenBank accession no. NP509076.1) was used as outgroup. All the sequences obtained during this study have been submitted to EMBL/GenBank data library under the accession numbers DQ680172 to DQ680179 (corresponding respectively to sTnThh2, efTnThh, fTnThh-1, fTnThh2, AfTnThh-1, AfTnThh-2, AfTnThh-3 and AfTnThh-4).
Putative genomic organisation of halibut TnT genes
The putative genomic organisation of isolated halibut TnT genes was established in silico using the Tetraodon nigroviridis genome database . The Tetraodon scaffolds giving the most significant hit by tBLASTx analysis  with the halibut TnT sequences were recovered. Pairwise alignment of halibut and Tetraodon TnT cDNA sequences with the selected Tetraodon scaffold using Spidey mRNA-to-genome software  permitted identification of the putative exon/intron boundaries of the halibut TnT genes
Atlantic halibut at different developmental stages (Saele et al. 2004) ranging from pre-metamorphic larvae to fully metamorphosed juveniles were obtained from Fiskey (Iceland). Animals (n = 10) were anesthetized in MS-222 (Sigma) and immediately collected for total RNA extraction by preservation in RNAlater (QIAgen, UK) according to the manufacturers instruction. An adult halibut was anesthetised in MS-222 (Sigma-Aldrich, UK) and killed by decapitation and white muscle, red muscle, heart and liver were immediately collected into RNAlater (QIAgen) according to the manufacturers instructions. Alternatively, for in situ hybridization and histology anaesthetized halibut larvae and juveniles were fixed in paraformaldehyde (4% PFA) at 4°C overnight. Samples were subsequently washed twice for 5–10 minutes with PBT and stored in 100% methanol at 4°C. Samples where embedded in paraffin and 5 μm post-anal transverse section were made from each animal.
For radioimmunoassay five individual samples were collected for each stage, anesthetised in MS-222 (100ng/mL, Sigma-Aldrich) and immediately frozen in dry ice.
Total RNA extraction
Total RNA was extracted from whole-body metamorphosing larvae and 100 mg of adult halibut tissue using Tri reagent (Sigma-Aldrich) according to the manufacturer's instructions, quantified in a GeneQuant (Amersham Biosciences) spectrophotometer and stored at -80°C until use.
Three micrograms of total RNA obtained from adult halibut white muscle, red muscle, heart and liver where fractioned on a 1.5% agarose/5.5% formaldehyde gel which was run in 1× MOPS. RNA was transferred to nylon Hybond-N membranes (Amersham Biosciences) with 10× SSC overnight and cross-linked using UV light (Stratalinker, Stratagene). Hybridisations were carried out using 3'UTR probe prepared from each cloned halibut TnT gene (~10 μg) by digestion for 2 hours at 37°C with 10U of appropriate restriction enzyme (Promega) and 1× buffer (Table 2). The resulting DNA for probes was purified by electrophoresis followed by extraction of DNA using the GFX gel band extraction kit (Amersham Biosciences).
Individual membranes were hybridized overnight at high stringency (65°C in 6×SSC, 5× Denharts solution, 100 μg/mL tRNA and 0.1%SDS) with its respective 32P-dCTP-labeled halibut TnT probe. The membranes were then washed twice for 30 minutes at room temperature (1×SSC and 0.1%SDS) followed by two 30 minute high stringency washes (65°C in 1×SSC and 0.1%SDS) and exposed at -80°C to Biomax MS film (Kodac, USA).
Semi-quantitative RT-PCR analysis of TnT expression during halibut metamorphosis
In order to determine expression of halibut TnT genes during metamorphosis a semi-quantitative RT-PCR assay was developed. For that, 0.5 μg of total RNA were DNased with the Ambion DNA Free kit (Ca, USA), according to the manufacturers instruction, and used for first strand cDNA synthesis which was carried out in a 20 μL volume using 0.05 M Tris-HCl, pH8.3, 0.075 M KCl, 3 mM MgCl2, 0.01 M DTT, 1 mM dNTP, 5 pmol/μl random hexamer primers, 4U of RNAse inhibitor (Promega, UK) and 10U of Superscript II reverse transcriptase (Invitrogen, UK). Synthesis reactions were carried out in an iCycler thermocycler (Perkin Elmer) for 10 minutes at 25°C followed by 50 minutes at 42°C and heating for 2 minutes at 70°C terminated synthesis. Five individual cDNA synthesis reactions corresponding to five individual animals per stage were performed.
Initial RT-PCR amplifications with primers specific for each halibut TnT gene were conducted to determine optimal cycle number and ensure that amplification occurred in the logarithmic phase of the reaction. The expression of 18s ribosomal RNA (rRNA) was used as an internal standard for normalisation.
RT-PCR analysis of halibut TnT genes was carried out in a 25 μl reaction volume containing ~20 ng of cDNA for each sample and 1.5 mM MgCl2, 0.1 mM dNTP's, 1 pmol/μl of halibut specific TnT gene forward and reverse primer (Table 3) and 0.6U Taq polymerase (Sigma-Aldrich). Primers for all the halibut TnT genes analysed were selected to amplify the entire N-terminal region, which in terrestrial vertebrates  and sea bream [5, 6] undergoes alternative splicing. The forward primer was located in the 5'UTR region of the isolated halibut TnT cDNAs. The reverse primer was designed in a constitutively expressed region of the halibut TnT cDNAs.
The PCR reactions were performed in an iCycler (Perkin Elmer) thermocycler, using the following cycle; 1 minute at 95°C followed by 27 cycles, for fTnThh and sTnT2hh, or 28 cycles, for AfTnThh of; 30 seconds at 95°C, 1 minute at 56°C and 30 seconds at 72°C, followed by a final step of 1 minute at 72°C. Negative reactions without sample cDNA were also performed.
Amplification of the housekeeping gene 18s rRNA used for normalisation was carried out as described above using 1 pmol/μl of forward and reverse primer (5'-TCAAGAACGAAAGTCGGAGG-3' and 5'-GGACATCTAAGGGCATCACA-3' respectively). The thermocycle utilised was: 1 minute at 95°C followed by 16 cycles of 30 seconds at 95°C, 1 minute at 56°C and 30 seconds at 72°C, followed by a final step of 1 minute at 72°C. All RT-PCR reaction products were fractionated on 2.5% agarose gels and analysed by densitometry using LabWorks software, version 4.5 (Ultra-Violet Products Cambridge, UK). Results are expressed as the mean and standard error of five independent samples.
In situ hybridisation
The developmental ontogeny of halibut muscle was characterised using 5 μm post-anal transverse section from several larvae from each stage. Several sections per fish were dewaxed, rehydrated and stained using haematoxylin and eosin and mounted in DPX reagent (Sigma-Aldrich).
The spatial-temporal expression pattern of halibut fTnT gene, and its efTnT isoform, sTnT2 and AfTnThh in metamorphosing halibut larvae and post-metamorphosed juveniles was investigated by in situ hybridisation using specific digoxygenin riboprobes. For fTnThh gene expression a 582 bp riboprobe for the conserved 3'UTR region in all fTnThh isoforms was generated. The expression of efTnThh isoform was established by generating a riboprobe complementary to the embryonic/larval exon (aa 12 to 68). AfTnThh gene expression was established using a 641 bp riboprobe complementary to the constitutive 3' coding region and the 3'UTR of the AfTnThh cDNA. Riboprobes were generated by linearising AfTnThh cDNA clones with the appropriate restriction enzyme for 1.5 h at 37°C and isolating the linearised vector by phenol (pH 8) extraction and precipitation in 3 M sodium acetate (pH 5) and ethanol overnight at -20°C.
Specific riboprobes were generated by in vitro transcription using the linearized vector as template and was carried out using 20U of T7 RNA polymerase or SP6 RNA polymerase in the case of efTnThh, in transcription buffer (Promega) with 1 μl of digoxigenin-RNA labelling mix (Roche Diagnostics, Mannheim, Germany), for 1.5 h at 37 °C. The reaction was stopped with 2 μl of 0.2 M EDTA. The digoxygenin labelled riboprobes were purified by lithium precipitation and ressuspended in 25 μl of water. Riboprobe purity and concentration were determined by fractionation of reaction products on an agarose gel (1.5%). To assess potential cross hybridization between probes and target sequences dot blots were performed. Each digoxygenin labeled riboprobe was hybridized with all the halibut TnT target sequence, no cross hybridization reactions were detected and each probe was found to be specific for its target template.
For in situ hybridisation experiments adjacent transverse tissue sections of halibut larvae were dewaxed, rehydrated and then prehybridised at 58°C for 2 h in hybridisation solution without probe (50% formamide, 4× SSC, 1 mg ml-1 torula RNA, 0.1 mg ml-1 heparin, 1× Denhardt's, 0.04% CHAPS). Tissues were then hybridised overnight in a humidified box at 58°C in 100 μl per section of hybridisation solution containing approximately 2 ng μl-1 of the riboprobes. Control sections were pretreated with RNase prior to hybridization with riboprobes or the riboprobes were excluded from the hybridizations.
Stringency washes were 3 × 5 min at 58°C with 2× SSC and 5 min at 58°C in 1× SSC. Tissue sections were then washed 2× 5 min with 2× SSC:0.12% CHAPS at RT, followed by a wash for 5 min in 2× SSC:PTW (1:1, v/v) and finally 5 min in PTW. Blocking was performed by incubation in blocking reagent (Boehringer Mannheim, Germany) with 10% heat inactivated sheep serum, detection of hybridised probe was carried out using sheep anti-digoxigenin-alkaline phosphatase (AP) Fab fragments (1/600) (Roche, Lisbon, Portugal). The chromagens for colour detection were NBT (4-nitroblue tetrazolium chloride) and BCIP (5-bromo-4-chloro 3-indolylphosphate) and colour development was carried out over 2 h at 38°C.
Stained sections from in situ hybridisation were rinsed in PBS, fixed for 15 min in 4% formaldehyde at room temperature, rinsed in PBS and mounted in glycerol gelatine. Histological and in situ sections were analysed using a microscope (Olympus BH2) coupled to a digital camera (Olympus DP11) linked to a computer for digital image analysis.
Radioimmunoassay for thyroid hormones
Larval extracts were used to assess T4 and T3 content of whole larvae by radioimmunoassay (RIA) using a double-antibody method under equilibrium conditions.
Frozen larvae (n = 8 per stage) were extracted individually in 50 μl methanol, 200 μl chloroform and 100 μl barbital buffer, centrifuged (3,000 rpm for 30 min at 4°C) and the upper phase removed, lyophilized, reconstituted in assay buffer, heat denatured (75°C for 2 hours) and assayed. Standard curves were prepared with T4 or T3 standards (Sigma-Aldrich) dissolved in 0.1N NaOH and diluted to appropriate concentrations in assay buffer. T3 and T4 assays were conducted in barbital buffer (0.07 M, pH 8.6) and Tris buffer (0.1 M, pH 7.4), respectively, and contained 0.1% BSA and 0.1% sodium azide. In both RIA, either 100 μl of standard or larval extract was added. For both hormones, the total assay volume was 300 μl and included 100 μl of 125I-T3 (Amersham Biosciences, Buckinghamshire, UK) or 125I-T4 and 100 μl T3 antisera (1:15,000, Sigma-Aldrich) or T4 antisera (1:10,000, Sigma-Aldrich). Antisera were added to all tubes apart from those to determine total count (cpm) and non-specific binding. The T3 and the T4 assays were incubated for 16–24 h at 4°C and subsequently, the free hormone was separated from the bound hormone using precipitation with a second antibody .
Two-way analysis of variance (ANOVA) was performed in order to establish if significant differences in the concentration of T4 or T3 were detected between different metamorphic stages. If the two-way ANOVA detected significant differences in T4 or T3 between stages the Holm-Sidak (HSM) multiple comparison analysis was performed to determine which stages have different T4 or T3 levels. Both T4 and T3 concentration values were transformed using the logarithmic function before statistical analysis. Significance was considered if p < 0.05. All statistical analysis was performed using SigmaStat version 3 software (SPSS Corp.)
T4 treatment and halibut TnT expression
Pre-metamorphic halibut larvae (stage 5) were treated for 10 days with T4 (Sigma-Aldrich). The halibut larvae were maintained in 100 L vessels with sea water at 10.5°C. The waterflow was kept at around 0,3 l/min, with the oxygen level at full saturation and disinfected clay dissolved in water was put in the tanks prior to each feeding to shade the environment and ensure maximum feed uptake and the right distribution of light in the tanks.
The hormone (T4) was administered by feeding the larvae T4-enriched artemia and control animals were fed with unenriched artemia. In order to enrich the artemia a solution (1 mg/ml) of sodium-pentahydrate salt of thyroxin (3-(4-(hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl)L-alanine, Sigma T2501) was prepared in distilled water. Artemia was enriched using 1 ml of T4 stock per liter of artemia (each liter containing 300.000 artemia naupli). T4-enriched artemia was fed to the larvae in the afternoon (2/3 of the total feedings) but in the morning the larvae were fed regular artemia (only 1/3 of the total feedings). The experiment lasted for 10 days. Samples of the artemia were taken and RIA for T4 was performed to validate the uptake of T4 by the artemia which contained a T4 concentration of 2 μg T4/g artemia.
At the end of the experiment animals were anesthetized with MS-222 (Sigma-Aldrich) and immediately fixed in RNAlater (Sigma-Aldrich) and kept at -20°C until analysis. Four individual treated and control larvae were used for RNA extraction and first strand synthesis reactions which were carried out as described previously. All experiments and animals collection were performed in accordance with EU legislation for Animal Welfare.
RT-PCR for fTnThh, AfTnThh, sTnT2hh and 18s rRNA was performed with the primers and conditions described previously. Results are presented as the ratio between the gene of interest and 18s. Results are presented as the mean expression of fTnThh, AfTnThh and sTnT2hh of four individual larvae from control and T4 treated groups. One-way ANOVA was performed to determine if statistically significant differences in halibut TnT gene expression occurred between control and T4-treated animals. If one-way ANOVA gave significant differences between the control and the T4-treated group in any of the halibut TnT genes analysed a multiple comparison test was performed using the Holm-Sidak multiple comparison test (HSD). All statistical analysis was performed using SigmaStat version 3 software (SPSS Corp.) and significance was considered at p < 0.05.
Atypical fast TnT
fast muscle TnT
Slow muscle TnT
Myosin heavy chain
Myosin light chain
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This work was carried out within the project Q5RS-2002-01192 with financial support from the Commission of the European Communities. However, it does not necessarily reflect the Commission's views and in no way anticipates its future policy in this area. This project was further co-financed by POCI 2010 and the European social funds attributed by the Portuguese National Science Foundation (FCT) to a Pluriannual project to CCMAR and a PhD fellowship to MAC (SFRH/BD/6133/2001).
MAC contributed to the devise of the experiments and acquisition and analysis of molecular data from the experiments, including all bioinformatics analysis, as well as drafting and revision of the manuscripts. NS carried out histological and microscopical data acquisition and drafting of the manuscript. MAN was responsible for the cDNA library construction, isolation and preliminary characterisation of the halibut incomplete TnT clone described in the methods and material section that was subsequently used as a probe in the isolation of further fTnT and sTnT isoforms. LL was also involved in the cDNA library construction, preliminary characterisation of the halibut TnT clone described in the methods and material section that was subsequently used as a probe in the isolation of further fTnT and sTnT isoforms. GES was responsible for the elaboration of the experiments, data analysis and drafting and revision of the manuscript. DMP was responsible for the elaboration of the experiments, data analysis and drafting and revision of the manuscript. All authors read and approved the final manuscript.
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Campinho, M.A., Silva, N., Nowell, M.A. et al. Troponin T isoform expression is modulated during Atlantic Halibut metamorphosis. BMC Dev Biol 7, 71 (2007). https://doi.org/10.1186/1471-213X-7-71
- White Muscle
- White Muscle Fibre
- Exon Versus
- Halibut Larva
- tBLASTx Analysis