Multiple upstream modules regulate zebrafish myf5expression
© Chen et al; licensee BioMed Central Ltd. 2007
Received: 24 July 2006
Accepted: 03 January 2007
Published: 03 January 2007
Myf5 is one member of the basic helix-loop-helix family of transcription factors, and it functions as a myogenic factor that is important for the specification and differentiation of muscle cells. The expression of myf5 is somite- and stage-dependent during embryogenesis through a delicate regulation. However, this complex regulatory mechanism of myf5 is not clearly understood.
We isolated a 156-kb bacterial artificial chromosome clone that includes an upstream 80-kb region and a downstream 70-kb region of zebrafish myf5 and generated a transgenic line carrying this 156-kb segment fused to a green fluorescent protein (GFP) reporter gene. We find strong GFP expression in the most rostral somite and in the presomitic mesoderm during segmentation stages, similar to endogenous myf5 expression. Later, the GFP signals persist in caudal somites near the tail bud but are down-regulated in the older, rostral somites. During the pharyngula period, we detect GFP signals in pectoral fin buds, dorsal rostral myotomes, hypaxial myotomes, and inferior oblique and superior oblique muscles, a pattern that also corresponds well with endogenous myf5 transcripts. To characterize the specific upstream cis-elements that regulate this complex and dynamic expression pattern, we also generated several transgenic lines that harbor various lengths within the upstream 80-kb segment. We find that (1) the -80 kb/-9977 segment contains a fin and cranial muscle element and a notochord repressor; (2) the -9977/-6213 segment contains a strong repressive element that does not include the notochord-specific repressor; (3) the -6212/-2938 segment contains tissue-specific elements for bone and spinal cord; (4) the -2937/-291 segment contains an eye enhancer, and the -2937/-2457 segment is required for notochord and myocyte expression; and (5) the -290/-1 segment is responsible for basal transcription in somites and the presomitic mesoderm.
We suggest that the cell lineage-specific expression of myf5 is delicately orchestrated by multiple modules within the distal upstream region. This study provides an insight to understand the molecular control of myf5 and myogenesis in the zebrafish.
Members of the basic helix-loop-helix (bHLH) family of transcription factors, such as Myf5, MyoD, Myogenin, and MRF4, are crucially important in the specification and differentiation of skeletal muscle progenitors . These myogenic regulatory factors (MRFs) activate muscle-specific transcription by binding to an E-box in the promoter of numerous muscle-specific genes [2, 3]. MRF genes are expressed in zebrafish somites in a characteristic temporal sequence, with myf5 at 7.5 hours postfertilization (hpf) , myod at 8 hpf , and myogenin at 10.5 hpf . The same temporal sequence occurs in mice . These observations indicate that myf5 is the first MRF expressed during vertebrate myogenesis.
Mechanisms that lead to Myf5 activation at multiple sites in mouse embryos have been described [6, 7]. Yeast artificial chromosomes (YAC)  and bacterial artificial chromosomes (BAC)  have been used to map the promoter of mouse myf5, suggesting that several different cis-regulatory elements are required to activate myf5 expression in different cells at different developmental times. An enhancer at -6.6 kb is required for myf5 expression in the epaxial domain . A 270-bp core enhancer at -57 kb directs myf5 expression in limbs and maintains myf5 expression in somites . In Xenopus, two negative regulatory elements have been identified: an interferon regulatory factor-like DNA binding element that down-regulates Xmyf5 expression in differentiating myocytes , and a distal TCF-3 binding site by which Wnt/β-catenin signaling restricts Xmyf5 expression to the midline mesoderm . A T-box binding site mediates dorsal activation of Xmyf5 transcription and is involved in the regulation of muscle development . Using transient expression of transgenes, we previously identified some cis-elements that regulate zebrafish myf5 [4, 13, 14]. Recently, Lee et al.  demonstrated that Foxd3 binds to the -82/-62 regulatory module and regulates zebrafish myf5 expression during early somitogenesis. These observations highlight the complicated and dispersed nature of the upstream elements that control somite- and stage-specific expression of myf5.
To elucidate the nature of this finely tuned control mechanism, we needed a transgenic line that recapitulates the specific endogenous expression pattern of myf5. Such a line requires a transgene that contains a very long upstream region of myf5. We modified the techniques used in mice [16, 17] and present here a highly efficient method for engineering zebrafish BAC. The BAC is an Escherichia coli F factor-based vector that is capable of propagating cloned DNA fragments up to 300 kb long . Previously, Jessen et al.  reported a homologous recombination technique for BAC cloning to generate transgenic zebrafish. This technique, however, is rather laborious because it requires a chi-based plasmid with a very large recombination targeting region. With our new method, we efficiently generate transgenic lines containing a 156-kb genomic sequence of myf5 (80-kb upstream and 70-kb downstream segments) replaced with green fluorescent protein (GFP) in the coding region. We find that the 156-kb genomic sequence is long enough to recapitulate the endogenous myf5 transcription pattern during the somitogenesis and pharyngula development stages. To characterize the functions of individual cis-regulatory elements, we also generated several transgenic lines that carry various lengths of the zebrafish myf5 upstream sequence. Comparing the GFP expression patterns of these lines, we identified and characterized the functions of upstream regulatory elements, including a repressive element and tissue-specific enhancers for jaw and fin muscles, bones, eyes, somites, olfactory organs, and the presomitic mesoderm. Whole-mount in situ hybridization reveals that endogenous zebrafish myf5 transcripts are first detectable in the presomitic mesoderm . In contrast, myf5 expression has not been observed by in situ hybridization in the presomitic mesoderm of mouse embryos, although weak signals have been detected by reverse transcriptase-polymerase chain reaction (RT-PCR) [20, 21]. These comparisons illustrate the advantage of our transgenic lines for studying the initiation and regulation of myf5, particularly in the presomitic mesoderm.
Genomic organization of zebrafish myf5is conserved with mammals
We cloned the myf5 genomic locus using a sequential screening method. We screened 10 primary pools of zebrafish BAC library clones using PCR; one (P1) was positive. We then screened 48 secondary pools derived from P1 and found 5 positive pools. Subsequent screening of the positive pools identified a single myf5-positive BAC clone with a 156-kb insert as indicated by PFGE. We searched sequence databases from the Sanger Institute and identified a contig, ctg9418, which contains the entire sequence of the myf5 BAC clone. BLAST analysis using the myf5 coding region and junction sequences flanking the T7 and SP6 sites showed that the BAC clone spans the sequences of ctg9418 from 1460 to 1304 kb, with the coding sequence starting at 1380. Thus, the myf5 5' and 3' regions contained in this BAC clone extend approximately 80 kb and 70 kb, respectively, beyond the coding sequence.
Radiation hybrid mapping of zebrafish myf5 revealed that myf5 is located on linkage group 4 (LG4), between expressed sequence tags (ESTs) fb62d08 and fb78c03, and at 5.87 CR from EST marker z9667 (data not shown). This syntenic relationship indicates that the region of zebrafish LG4 between EST markers fa05f06 and fk68a09 (including myf5) is conserved with human chromosome 12q13–12q21.
DNA fragments of myf5:GFPare inherited
The 156-kb genomic sequence of myf5drives GFP expression in muscle precursors
GFP expression reveals the development of head skeletal muscles
Proximal element regulates myf5expression in the presomitic mesoderm
Summary of GFP expression domains in different myf5:GFP transgenic lines
Repressive element located at -80/-10 kb blocks GFP expression in notochord driven by module -2937/-2457
Multiple modules regulate myf5expression in the spinal cord, bones, eyes, and olfactory pits
Stable transgenic lines provide greater sensitivity for studies of gene regulation and confirm transient transgenesis studies
The regulatory elements for muscle lineage-specific expression, including slow and fast myotomes, are controlled by Hedgehog signaling and myocyte enhancer factor 2 (MEF2) [8, 23–25]. We propose that the somite- and myotomal-restricted enhancer element is located within the -290/-1 segment (Fig. 9). Thus, it is important to look for the putative myotomal enhancers, such as Hedgehog-responsive elements and MEF2-binding sites within this segment. After sequence analysis, we find that there are one MEF2-binding (-277/-268) and two Gli-binding (-252/-243 and -196/-183) sites located within the -290/-1 segment. In addition, our previous studies showed that the -82/-62 cassette that contains a binding site for the cognate trans-acting factor Foxd3  is able to drive transient expression in somites . On the basis of these observations, we propose that -82/-62 motif is a key element for driving somite specificity, and multiple elements within the -290/-1 segment such as MEF2- and Gli-binding sites are responsible for myotomal expression. Together, these results demonstrate that transient analysis is suitable for rapid identification of putative cis-elements, whereas germ-line transmission studies provide great sensitivity and enable confirmation.
Many myf5regulatory modules are similar between mouse and zebrafish
Few reports have proposed using transgenic animals to study the delicate transcriptional regulation of myf5. Only three species (mice, zebrafish, and Xenopus) have been documented so far. With limited information on the interactions between trans-acting factors and their binding sequences upstream of the myf5 gene, the alternative ways to study transcriptional mechanistic conservation are those making comparisons of sequence similarities and genomic organizations of the myf5 gene among these three known species. As in zebrafish, myf5 expression is regulated by multiple upstream sites in mouse embryos [7, 26]. Multiple enhancers are distributed throughout a 90-kb region of the mouse mrf4/myf5 locus, including a limb enhancer at -58/-48 kb, two head muscle enhancers at -88/-63 and -45/-23 kb, a repressive element at -58/-8.8 kb, a central nervous system-specific enhancer at -0.5/-0.1 kb, a hypaxial myotome enhancer at 0.5/3.5 kb, an epaxial myotome enhancer at -5.6/-4.6 kb, and branchial enhancers at -1.5/-0.5 and 0.5/3.5 kb [6, 7, 27]. Gene regulation of Myf5 in frog is apparently quite different, because only a relatively short region of flanking DNA (about 1.2 kb) is sufficient to drive endogenous Xenopus Xmyf5 expression at gastrula stages. Two negative regulatory elements (an interferon-like regulatory factor and a distal TCF-3 binding site) have been identified in the Xmyf5 promoter [10, 11]. It seems likely that each species (i.e., mice, zebrafish and Xenopus) uses distinct mechanisms, given the developmental differences in timing and signaling.
The genomic organizations of myf5 regulatory modules are also conserved between mice and zebrafish. As in mouse, the zebrafish regulatory modules that are responsible for lineage-specific expression of myf5 are distributed throughout a large (80-kb) region of the mrf4/myf5 locus (Fig. 9). The locations and functions of some enhancers are similar to those of mouse myf5. For example, the fin muscle enhancer and the cranial muscle enhancer at -80/-10 kb probably correspond to the mouse limb and head muscle enhancers at -88/-23 kb, a repressive one at -10/-6 kb is similar to the mouse repressor at -58/-8.8 kb, and a spinal cord enhancer at -6/-3 kb is similar to the mouse central nervous system-specific enhancer at -0.5/-0.1 kb (Fig. 9).
On the other hand, however, we also identified enhancers that have not been described in mouse, including a bone enhancer at -6/-3 kb, a notochord enhancer at -3/-2.4 kb, and a presomitic mesoderm enhancer at -290/-1 bp (Fig. 9). Epaxial- and hypaxial-specific enhancers have been identified in mouse myf5 [6, 7, 27], but we have not seen muscle lineage-specific enhancers, especially slow and fast muscle enhancers in zebrafish, with the exception of limb and head muscle enhancers. This finding suggests that more transgenic lines that carry shorter elements should be generated, especially deletions within the -80/-10 kb and -10/-6 kb regions. Taken together, we propose that the regulation of zebrafish myf5 is more similar to mouse myf5 than that of Xenopus.
Excellent experimental materials to study transcriptional regulation on myf5
Myf5 is the first member of the MRF family expressed during somitogenesis in zebrafish. Knockdown of myf5 in zebrafish results in malformation of somites and brain defects, indicating that trunk and head myogenesis is impaired, underscoring the importance of understanding the regulation of myf5. Numerous factors have been implicated as upstream regulators of myf5, including extracellular signals, such as shh, wingless (wnt), and fibroblast growth factor (FGF) [28, 29]. Shh, produced by the notochord and floor plate of the neural tube, and Wnt proteins, produced by the dorsal neural tube and surface ectoderm, have been implicated in the maintenance of mouse myf5 [8, 21, 30, 31], Xenopus Xmyf5 , and zebrafish myf5  expression. Together with our previous identification of the cognate trans-acting factor, Foxd3 , these results demonstrate that the complex spatial and temporal pattern of myf5 gene expression is regulated by multiple upstream regulatory modules.
We generated several transgenic lines of zebrafish that contain various lengths of zebrafish myf5 upstream genomic sequence linked to the GFP reporter gene. We demonstrate that the 156-kb genomic sequence (an upstream 80-kb and a downstream 70-kb segment) is able to recapitulate the pattern of endogenous myf5 expression. By dissecting this upstream region, we further show that tissue-specific regulatory elements are organized as modules in various regions of the 5'-flanking sequence. These transgenic lines not only provide excellent materials for studying the regulatory mechanism of myf5, but they also will facilitate mutant screens to identify novel genes that regulate somitogenesis and more detailed studies to the morphogenesis of somites, presomitic mesoderm, and cranial muscles.
Embryos were produced using standard procedures  and were staged according to standard criteria  or by hpf at 28°C. The wild-type line used in this study was AB. Line and gene names follow the zebrafish nomenclature conventions .
BAC library screening
The zebrafish BAC library was obtained from the RZPD , and the screening protocols followed the manufacturer's instructions, with minor modifications. The primary BAC library pools were screened by PCR using the zebrafish myf5 intron 1-specific primers 1261F (5'-TGTTCATTCACTCATTTTCTTTTCA-3') and 2582R (5'-GCAGTCTTCCTACAATGACAA-3'). The positive clones isolated from the primary pools were further confirmed by screening the secondary pools to isolate a myf5-containing BAC clone.
Pulsed-field gel electrophoresis
DNA from a myf5-containing BAC clone was extracted; digested with EcoRI, HindIII, and SacI; and analyzed by 0.8% Agarose pulsed-field gel electrophoresis (PFGE; Biometra). The electrophoresis conditions were 200 volts at 10°C for 24 h with electrode angles at 120°, and rotor speed of 2–6 s. After electrophoresis, the BAC DNA size was analyzed with Kodak 1D image software.
We used the zebrafish myf5-specific primers 1261F and 2582R for mapping myf5 against the LN54 radiation hybrid (RH) panel. The RH panel was scored according to Hudson et al.  using the public web site . For screening the myf5-containing BAC clone, the junctions of BAC DNA were sequenced using T7 and SP6 primers. These junction sequences and adjacent coding regions were analyzed by BlastN , and the location of the myf5-containing BAC clone was characterized and named myf5(80K).
Generation of a myf5(80K) clone containing the GFP reporter
Plasmid p(myf5(80K):GFP) contains the approximately 80-kb region around myf5 fused to GFP (Fig. 1A). Basically, we followed the protocols described by Lee et al. , with some modifications. The cassette used for targeting the myf5 locus was amplified from template pZMYP-82E  with primers ZMFP-82F (5'-CTCTTAGCTCTGTCCTGGCCA-3') and Kan-817R (5'-ATTTACAAATGAGCAAGCAGTGTGAATAAAGCGTTGGCCTGAGTCGGTCATTTCGAACCCCAG-3') by using Deep Vent (NEB) to carry out PCR at the following conditions: 94°C, 40 s; 58°C, 30 s; 72°C, 150 s; for 35 cycles. PCR products were digested with DpnI to remove template.
For myf5(80K) transformation, 1 μg of myf5(80K) DNA was used to transform competent cells, E. coli DY380. For myf5(80K) modification with GFP, putative transformants harboring myf5(80K) were isolated and grown in LB medium containing 25 μg/ml of chloramphenicol (CAM) overnight at 32°C with shaking at 150 rpm. Subsequently a 0.1% inoculum was cultured in 50 ml of LB-CAM to an OD600 of 0.8. Then, the bacteria were cultured at 42°C for 15 min, transferred to an ice slurry for 30 min, washed 5 times in ice-cold water, and electroporated immediately. Approximately 2 μg of targeting cassette DNA was mixed with the freshly prepared electrocompetent cells of DY380 carrying myf5(80K). Electroporation was performed at 1.8 kV, 200 Ohms, 25 μF for 3 × 30 s intervals (Gene Pulser Xcell, BioRad). After electroporation, cells were dispersed on the LB plates with 30 μg/ml of kanamycin and incubated at 32°C overnight. Then, recombinants were picked and checked by PCR using primers ZMFP-117F (5'-TTTGGGTGGGGATCTAGATGGTG-3') and GFP-407R (5'-GTTGCCGTCCT-CCTTGAAGT-3'), and Kan-F (5'-ATGATTGAACAAGATGGATTGC-3') and ZMF-1000R (5'-AGCGAGTTAAGTTTAAAGTCTGACCC-3') to check both integration ends.
Plasmid constructs for promoter analysis
Following our previously described procedure , a 3.7-kb SacI-cut fragment from a myf5-positive recombinant bacteriophage was ligated with the SacI-digested plasmid, pZMYP-6212E, in which a -6212/-1 segment of zebrafish myf5 was fused with enhanced GFP (EGFP) cDNA. The resulting plasmid, pZMYP-9977E, contained the -9977/-1 segment of zebrafish myf5 fused with EGFP cDNA (Fig. 1B).
A SalI/EcoRV fragment from pZMYP-6212E  was ligated with a Klenow-filled pGEMT-easy vector (Promega), in which the EcoRV site but not the SalI site was retained, to produce an intermediate plasmid, p(6212/1984). Then, a 3.8-kb SacI fragment from a myf5-positive phage clone  was ligated with SacI-treated p(6212/1984) to produce another intermediate plasmid, p(9977/1984). Finally, a SacI/EcoRV fragment cut from p(9977/1984) was ligated with SacI/EcoRV-treated pZMYP-6212E-ITR (Fig. 1B). The resulting plasmid, pZMYP-9977E-ITR, contained the -9977/-1 segment of myf5 and was flanked with inverted terminal repeats of adeno-associated virus (AAV-ITR) (Fig. 1B).
(C) pZMYP-6212E-ITR and pZMYP-2937E-ITR
A SalI/AgeI fragment from either pZMYP-6212E or -2937E  was ligated with a 4.2-kb SalI/AgeI fragment obtained from pCMV-EGFP-ITR . The resulting plasmids, pZMYP-6212E-ITR and pZMYP-2937E-ITR, contained the -6212/-1 and -2937/-1 segments of zebrafish myf5, respectively. Each plasmid was also flanked with AAV-ITR at both ends (Fig. 1B).
Plasmid pZMYP-290E  was cut with HindIII, blunted and then cut with AgeI. The resulting 0.3-kb fragment was ligated with a 4.2-kb fragment produced by cutting pCMV-EGFP-ITR  with SalI, blunting and then cutting with AgeI. The resulting plasmid, pZMYP-290E-ITR, contained a zebrafish myf5 -290/-1 segment and was flanked with AAV-ITR at both ends (Fig. 1B).
(E) pEGFPm(2937/2457) and pEGFPm(2457/2937)
For functional identification of the notochord-specific cis-element, we used a forward primer (5'-TCTAGAACAGATTCTCATCCAA-3') and a reverse primer (5'-AACTGCACACTGGAGATTCATAAG-3') to generate module -2937/-2457. This module was ligated with pGEM T-Easy vector and then treated with EcoRI to produce the insert. EcoRI-cut pEGFPmTATA, which contained a minimal TATA-box of cytomegalovirus (CMV) promoter for the EGFP gene , was ligated with one copy of the EcoRI-cut module -2937/-2457 to generate pEGFPm(2937/2457). Plasmid pEGFPm(2457/2937), containing one copy of module -2457/-2937, was also constructed.
DNA preparation for microinjection and transient GFP expression
The procedures of microinjection and transient GFP detection were described by Chen et al. , except that we observed the GFP expression of transgenic embryos hourly, especially from 6 to 36 h.
Identification of germ-line transmission
All GFP-positive embryos at 24 h were raised to adulthood. Transgenic founders (F0) were mated with wild-types individually to confirm that they could transmit the BAC through the germ line. At least 200 embryos from each pair were examined for GFP fluorescence. After screening, GFP-positive F1 embryos were raised to adulthood and crossed with wild-type adults to generate the heterozygous F2 generation. GFP-positive F2 individuals were then crossed to each other to generate homozygous F3 fish that produced 100% GFP-positive F4 offspring.
Antibody labeling was performed as previously described, with minor modifications . Embryos were fixed in 4% paraformaldehyde in phosphate buffered saline (PBS, pH 7.0) for 4 h at room temperature, or overnight at 4°C. Then, embryos were washed in 0.1 M PBS twice for 15 min each, soaked in 100% acetone at -20°C for at least 10 min, and rehydrated with 0.1% (v/v) Tween 20 in PBS 3 times for 15 min each. After rehydration, the embryos were treated with PBS containing 5% goat serum albumin and subjected to immunofluorescence labeling. To detect zebrafish slow muscle fibers, the F59 monoclonal antibody (1:10; Hybridoma Bank) was used with Alexa Fluor 568 rabbit anti-mouse IgG (1:200; Molecular Probes) as the secondary antibody.
Whole-mount in situhybridization, cryosection and fluorescence observation
The procedures of cryosectioning and whole-mount in situ hybridization were described by Chen and Tsai , except that embryos from 7.5 to 60 h were used. Transgenic embryos were observed hourly, especially from 1 to 14 hpf, under a stereo fluorescence dissecting microscope (MZ12, Leica) equipped with GFP and DsRed filter cubes (Kramer Scientific). Photographs were taken with an S2 Pro digital camera (Fuji).
We are grateful to Dr. Marc Ekker for providing the LN54 mapping panel in this study. We are also grateful to Dr. Copeland, National Cancer Institute, for providing the E. coli strain DY380. This project was supported by the National Science Council, Republic of China [NSC 92-2321-B-002-018 (Y.H.C.) and NSC 92-2313-B-002-056 (H.J.T.)] and National Institutes of Health, USA [NIH HD22486 and AR45575 (M.W.)].
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