The conserved WW-domain binding sites in Dystroglycan C-terminus are essential but partially redundant for Dystroglycan function
- AS Yatsenko†1, 2, 3,
- MM Kucherenko†1, 2, 3,
- M Pantoja1,
- KA Fischer1,
- J Madeoy4,
- W-M Deng5,
- M Schneider6,
- S Baumgartner7,
- J Akey4,
- HR Shcherbata1, 3Email author and
- H Ruohola-Baker1, 4Email author
© Yatsenko et al; licensee BioMed Central Ltd. 2009
Received: 19 September 2008
Accepted: 27 February 2009
Published: 27 February 2009
Dystroglycan (Dg) is a transmembrane protein that is a part of the Dystrophin Glycoprotein Complex (DGC) which connects the extracellular matrix to the actin cytoskeleton. The C-terminal end of Dg contains a number of putative SH3, SH2 and WW domain binding sites. The most C-terminal PPXY motif has been established as a binding site for Dystrophin (Dys) WW-domain. However, our previous studies indicate that both Dystroglycan PPXY motives, WWbsI and WWbsII can bind Dystrophin protein in vitro.
We now find that both WW binding sites are important for maintaining full Dg function in the establishment of oocyte polarity in Drosophila. If either WW binding site is mutated, the Dg protein can still be active. However, simultaneous mutations in both WW binding sites abolish the Dg activities in both overexpression and loss-of-function oocyte polarity assays in vivo. Additionally, sequence comparisons of WW binding sites in 12 species of Drosophila, as well as in humans, reveal a high level of conservation. This preservation throughout evolution supports the idea that both WW binding sites are functionally required.
Based on the obtained results we propose that the presence of the two WW binding sites in Dystroglycan secures the essential interaction between Dg and Dys and might further provide additional regulation for the cytoskeletal interactions of this complex.
The Dystroglycan-Dystrophin (Dg-Dys) complex has been shown to provide cells with structural integrity by forming a conduit between the extracellular matrix and the cytoskeletal network and there are lines of evidence that implicate an additional signaling role for the complex [1, 2] Dystroglycan binds to extracellular matrix components, including Laminin at its N-terminus and the actin cytoskeleton via Dystrophin at its C-terminus [3, 4] Defects in these interactions can result in muscular dystrophies (MD) and various epithelial cancers 
The characterization of the Dystrophin Glycoprotein Complex (DGC) in Drosophila has revealed that it possesses similar roles in muscle integrity and neuronal migration in flies as it does in humans  These abnormalities include age dependent muscle degeneration, reduced mobility, defects in eye development as manifested by altered photoreceptor axon path finding and photoreceptor morphology. Additionally, mutations in Dys and Dg affect cell polarity in Drosophila [6–8] Interestingly, some of these phenotypes are affected by the nutrition or energy metabolism in the animals  Recently, a reduced lifespan, as well as heart and muscle abnormalities, have been reported in Drosophila mutants of another component of the DGC, δ-sarcoglycan  and heart and further eye phenotypes have been observed in Drosophila Dys and Dg mutants [11, 12]
Analogous defects observed when the Dg-Dys complex is disturbed in both flies and humans make Drosophila an attractive model for further studies on clarifying the cellular function of the DGC. Recent biochemical and in vivo structure-function analyses have revealed that a specific set of C-terminal domains are critical for the function of Dystroglycan. We have found that a putative SH3 domain binding motif but, surprisingly, not the most C-terminal Dystrophin WW domain binding motif is required for Dg function in cellular polarity in Drosophila . However, since two potential WW binding sites exist near the Dg C-terminus it is possible that the second WW binding site can also bind Dystrophin in vivo, as has been shown in vitro . In this study we dissect the roles of the two WW binding sites in the Drosophila Dystroglycan C-terminus in vivo and, interestingly, find that the sites are essential and their functions are partially overlapping.
In order to understand the regulation of Dg and its role in signaling, we have analyzed the binding motifs that are required for the function of the Dg-Dys complex in cellular polarity in Drosophila. The proline-rich C-terminus of Dg has several potential protein binding motifs, which suggests that it may be involved in regulating the complex and potentially may have signaling role(s). Proline-rich sequences have been shown to be the targets of several protein interaction domains involved in signal transduction. The most C-terminal PPxY motif has been established as a binding site for the WW domain of Dystrophin in humans [14–16] and in Drosophila by in vitro binding studies . However, this WW domain binding site at the very C-terminus of Dystroglycan, is not essential for the function of the Dg-Dys complex in cellular polarity in Drosophila. An internal region of the Dystroglycan C-terminus containing a second WW domain binding site and a putative SH3 domain binding site appear to be sufficient for function in this context. We have also shown that Dystrophin can bind both the C-terminal and the internal WW domain binding sites in vitro . We now test whether the internal WW domain binding site is essential, whether the two WW domain binding sites are redundant or whether neither is required for Dg function in Drosophila. To distinguish between these possibilities we used both overexpression and loss-of-function rescue analyses.
Generation of transgenic lines expressing biochemically verified WWbs mutations
WW binding site function as assayed by oocyte polarity
We have previously shown that overexpression of the wild type form of Drosophila Dystroglycan (FL = full length) is sufficient to generate oocyte polarity defects  (Figure 3B). When FL is overexpressed in the germline, Orb becomes mislocalized, surrounds the entire oocyte nucleus, or accumulates in a clump to one side of the oocyte instead of localizing to the posterior. Therefore, Dystroglycan, when expressed at elevated levels in germline cells, is sufficient to disrupt oocyte polarity. Overexpression of the full length form of Dg with the tubGal4 driver causes semi-lethality (data not shown). Similarly, in vertebrates overexpression of Dg has been shown to cause defects in neuromuscular junctions [18, 19]. We used the overexpression oocyte polarity assays to test whether either of the WW domain binding sites is essential for Dystroglycan function.
To test the function of WWbsI in vivo we overexpressed the PPSG mutant protein in germline cells using the MatTubGal4 driver and determined the localization of the early oocyte polarity marker Orb. As discussed, in wild type cells Orb marks the localization of the microtubule organizing center and is localized to the posterior side of the oocyte during stages 3–6 (Figure 3A). Overproduction of the PPSG protein results in the mislocalization of the usually posterior Orb marker. In mutants Orb surrounds the oocyte nucleus or localizes to the sides of the oocyte nucleus in 44 ± 2% of 3–6 stage oocytes (n = 147, Figure 3E–F). The level of this defect is similar to the one observed with the FL construct [6, 13], which contains both WW binding sites (Figure 1; Figure 3B, D; 49 ± 2%, n = 80). These data suggest that disturbing the second WW binding site at the Dg C-terminus does not dramatically affect the functionality of the protein; similar to FL construct, when overexpressed it still is sufficient to disturb the oocyte polarity.
In contrast to the FL and PPSG constructs, overexpression of a 2WW mutant construct did not result in a high percentage of Orb mislocalization (Figure 3C, F, 19 ± 3%, n = 123). With 2WW overexpression, Orb, in most cases, was localized to the posterior of the oocyte (Figure 3C). The frequency of mislocalization with the 2WW construct, in which both WW binding sites were mutated was similar to that of the C1 construct which lacked all the C-terminal binding sites (Figure 1, Figure 3D, F, 16 ± 2%, n = 86).
These data, in combination with our previous data  show that a single mutation in WWbsII or the lack of WWbsI does not result in dramatic defects in Dg activity in this sufficiency assay measuring the oocyte polarity. However, simultaneous mutations in both WW binding sites dramatically reduce the function of Dystroglycan in this assay.
One WW binding site is required for Dystroglycan function
We also tested the function of the WW binding site mutants in rescue experiments by expressing the transgenes in a Dg loss-of-function background. Dg323 germline mutant clones are arrested prior to stage 3–4 and have mislocalized or missing Orb protein (Figure 4A). We have previously shown that these defects are partially rescued by wild type (full-length) Dg expression  (Figure 4, 36–40% rescue). Full rescue is not expected since the Dg323 deletion also affects a newly described neighboring gene mRpl34 (Additional Figure 3) and recent data implies that the level of nutrients and energy metabolism in the animal may affect cellular polarity . To test if our mutant constructs were capable of rescuing the developmental arrest and the defects in oocyte polarity on the same level as the Dg full-length construct, we expressed them using the germline driver nanosGal4 and calculated the percentage of loss-of-function clones with rescued growth and polarity. Using this assay we tested whether the Dg WWbs mutations were capable of a similar level of rescue as full-length Dg. If the Dg mutant with both WW binding sites mutated (2WW, Figure 1) could rescue the Dg323 phenotype in oocyte polarity at the same level as wild type Dg, we conclude that neither of the WW binding sites in Drosophila is required for Dg activity. On the other hand, if Dg with two WWbs mutations cannot rescue, we conclude that both or just the internal WW binding site is essential for Dg activity (we have already shown that the C-terminal WWbs is not essential ). As discussed above, to distinguish between these possibilities, we have generated a single mutation in WWbsII (PPSG, Figure 1) and will test whether this mutant still has the full length Dg activity in the loss-of-function rescue assays.
Similar to the full length Dg (FL, Figure 4B), the PPSG mutant constructs were capable of partially rescuing the Dg mutant phenotype (Figure 4D). Loss-of-function clones with expression of FL (Figure 4B-B") and PPSG (Figure 4D-D") had similar levels of posterior localization of the polarity marker, Orb (Figure 4F, FL: 36 ± 0.5% n = 52; PPSG: 41% n = 22). These mutants were also capable of restoring the developmental arrest phenotype by showing a higher percentage of loss-of-function clones that were older than stage 4–6 (Figure 4F, FL: 47 ± 8% n = 55; PPSG 38% n = 21). In contrast, 2WW was unable to rescue (2WW rescued at the level of the C1 mutant that lacks most of the Dg C-terminus; ; Figure 1.). Dg loss-of-function clones with expression of 2WW and C1 showed lower percentages of normal polarity (Figure 4F; 2WW: 12 ± 0.6% n = 66; C1: 9% n = 22) and growth rescue (Figure 4F; 2WW: 19 ± 2% n = 66; C1: 13%) than FL or PPSG constructs (Figure 4F). This result indicates that at least one WW binding site is required for normal function of Dg but a mutation in only one of the sites does not alter the functionality of Dg protein dramatically.
Since a single WWbsII mutation or a WWbsI deletion does not cause a severe loss of Dg activity but the double mutant does, we conclude that the two binding sites act, at least partially in a redundant manner in oocyte polarity and growth assays.
WW binding sites are highly conserved
Summary statistics of sequencing data.
5.26 × 10-3
2.73 × 10-4
South East Asia
6.49 × 10-5
3.24 × 10-5
The functional redundancy of the WW binding sites poses interesting questions: have both binding sites survived through evolution to protect organisms from the mutations in an essential complex or does each binding site have a specific function in different tissues and/or developmental stages. Mutations in the DGC cause muscular dystrophies; however only mutations in Dystrophin, but not Dystroglycan per se, are associated with known types of muscular dystrophies in vertebrates. In mice, mutations in Dystroglycan are embryonic lethal, which suggests that Dg is an essential gene and, perhaps the redundant Dystrophin binding sites in Dystroglycan provide an additional means for DGC regulation.
The comparative sequence analysis of Drosophila and human WW binding motifs revealed very high conservation. However, each WWbs resides in a specific protein micro-environment, which may suggest that each site has specific binding partners. The previously performed genetic screens for modifiers  of Dg and Dys showed that the Dg-Dys complex interacts with components of different signaling pathways and components involved in cell/neuronal migration, cytoskeletal rearrangement and muscle development. This suggests that the Dg-Dys complex might be a major hub that regulates transfer of extracellular information to the cytoskeleton. Therefore it will be important in the future to test if WW binding sites have specific and independent biological functions in different tissues. This kind of analysis is likely to provide insights into the specific functions of the Dg-Dys complex and serve as a basis for the development of novel therapeutic approaches for the treatment of muscular dystrophy.
We have investigated the role of the WW binding sites at the C-terminus of Dystroglycan protein and found that both sites may bind to the WW+EF hand domain of Dystrophin. Our previous studies [6, 13], indicate that WWbsI and WWbsII both can bind Dystrophin protein in vitro. To test whether both WW binding sites can function and are required in vivo we generated two transgenic mutants: 2WW, which has mutations in both WW binding sites (WWbsI, PPPY → WAPY and WWbsII, PPSY → PPSG), and PPSG, which has a mismatch in WWbsII (PPSY → PPSG). We used the establishment of early oocyte polarity as an assay to verify the functionality of WWbsI and WWbsII. Importantly, the data show that while each WW binding site mutation yields to close to normal Dg function, the double WWbs mutation has lost Dg C-terminal activity. These data suggest that at least one WWbs is required for full Dg function in vivo and that the two sites may be partially redundant.
Drosophila melanogaster stocks were raised on standard cornmeal/yeast/agar medium at 25°C. For overproduction of pUASp-Dg in the germline, we used the following: NGT40; P(w+:nanosGal4:VP-16)Ab-2 [21, 22] and Mat-α4-TubGal4-VP16/CyO . For overproduction of pUASp-Dg in the follicle cells, we used hsFlp; act < FRT-CD2-FRT < Gal4; UAS-GFP. For generation of Dystroglycan clones, we used FRT42D-Dg323/CyO (Dg323 is a Dystroglycan loss-of-function mutant with a 3324 bp deletion between bp 32,345 and 35,669 of DS03910  disrupting the Dg 5' region and the adjacent mRPL34 gene; Additional Figure 3) and hsFLP;FRT42D Ubi-GFP/CyO. For overproduction of pUASp-Dg in a Dystroglycan mutant background, we used FRT42D-Dg323/CyO; P(w nos-Gal4:VP16)A4-2 III, and hsFLP; FRT42D Ubi-GFP/CyO; pUASp-Dg/TM3 (pUASp-Dg refers to all Dystroglycan constructs: FL, C1, 2WW, PPSG). Two deletions in the Dystroglycan region exist; Dg248 (11985709:11986494) whose breakpoints are 333 bp downstream of the Dg transcription start site (11986042) and 3 bp upstream of the mRpL34 start codon (11986498) and Dg323 (11983340:11986664) whose breakpoints are 2.7 kb downstream of the Dg transcription start site and 166 bp downstream of the mRpL34 start codon (Additional Figure 3). We also used: dg043 .
Generation of pUASp-Dg Transgenic Animal
Full length and modified Dystroglycan PCR products that can be expressed in the germline were synthesized from the template LD11619. pUASp-FL and pUASp-C1 constructs used in this work have been described previously . To generate a construct with mutated WWbsII (pUASp-PPSG) LD11619 was used as a template with the following primers: 5'-GGGGTACCAACATGAGATTCCAGTGGTTCT-3' 5'-GCTCTAGATTATGGCGACACACATA-TGGCGGT-3'. The PCR products were digested with KpnI and XbaI and cloned into the pUASp vector . The constructs were injected into embryos to obtain at least two independent stable transformant lines. Injections were done by Rainbow Transgenic Flies, Inc. (California, USA).
Overproduction of Dystroglycan in the Germline and Follicle Cell
For overproduction in germline cells, balanced pUASp-Dg/Mat-α4-TubGal4-UP16/CyO or P(w-: nanosGal4:VP-16)Ab-2 animals were raised in yeasted vials at 25°C for 3 days before dissection and analysis. For overproduction in the follicle cells, hsFlp; UAS-GFP act <FRTCD2FRT <Gal4/pUASp-Dg animals were heat-shocked at 37°C for 1 h, raised in yeasted vials at 25°C for 3 days before dissection and analysis. All pUASp-Dg constructs used were crossed to these three Gal4 drivers to test for proper overproduction of protein and correct localization of protein to the membrane in the germline and somatic cells. The following pUASp-Dg lines were used for germline analysis: FL-1, 5; C1-1, -2; 2WW-10.2, -5.6, -13, 15.4; PPSG-11.1, -12.5, -6.3, -13.4. For the rescue experiments the following lines were used: FL-1, -2, -5; C1-1, -2; 2WW-10.4, -13, -15.6; PPSG-11.4, 11.1.
Antibody Staining Procedures
Drosophila ovaries were dissected rapidly in PBS and fixed in 4% paraformaldehyde for 10 minutes. The antibody staining procedure was the same as described previously . The following primary antibodies were used at the following designated dilutions: rabbit anti-Dystroglycan (1:3000 ), mouse anti-Orb (1:20; Developmental Studies Hybridoma Bank), the following secondary antibodies were used at the designated dilutions: Alexa 488 anti-rabbit and Alexa 568 anti-mouse (1:500; Molecular Probes).
Western Blot and densitometry analyses
Sample preparation and SDS-PAGE have been described previously . Bio-Rad ready-made 4–20% polyacrylamide gels were used for protein separation. Proteins were transferred to polyvinylidene difluoride (PDVF) membranes (Immobilon) using a semi-dry transfer apparatus (Bio-Rad). Primary affinity purified anti-Dg antibodies were used at 1:30,000 dilutions. Goat anti-rabbit HRP conjugated antibodies (Bio-Rad) were used as detection reagents at 1:10,000 dilutions. Proteins were visualized via enhanced chemiluminescence (Millipore). Densitometry analysis was performed with the public domain NIH IMAGEJ program (developed at the US National Institutes of Health and available on the Web at http://rsb.info.nih.gov/ij/). Scans of immunoblots determined to be in the linear range (i.e. twice the amount of protein correlated with twice the signal seen on photographic film) were used as sources for analysis.
Sequences of 12 species of Drosophila were obtained from the FlyBase genome database. Sequence alignment was done using software ClustalW designed by the European Bioinformatics Institute http://www.ebi.ac.uk/Tools/clustalw/index.html.
DNA samples used for sequencing
We sequenced a 348 bp fragment of DAG that includes both WW domains in DNA samples from 88 humans representing six populations. Samples were obtained from the Coriell Institute for Medical Research Cell Repositories (Camden, NJ, USA). Coriell repository numbers for these samples are as follows: CEPH European-American (NA06990, NA07019, NA10830, NA10831, NA07348, NA07349, NA10842, NA10843, NA10844, NA10845, NA10848, NA10850, NA10851, NA10852, NA10853, NA10854, NA10857, NA10858, NA10860, NA10861, NA17201) Han Chinese of L.A. (NA17733 – NA17747, NA17749, NA17752 – NA17757, NA17759, and NA17761), Middle East (NA17041 – NA17050), Pygmy (NA10469 – NA10473, NA10492 – NA10496), South Africa (NA17319, NA17341 – NA17348), South America (NA17301 – NA17310) and South East Asia (NA17081 – NA17090). We compared patterns of polymorphism to 322 genes that were sequenced as part of the SeattleSNPs project .
DNA sequencing and statistical analysis
Sequencing primers were designed with primer3 (http://frodo.wi.mit.edu/cgi-bin/primer3/primer3_www.cgi; primer sequences available upon request). We used standard PCR-based sequencing reactions using Applied Biosystem's Big Dye sequencing protocol on an ABI 3130xl. Sequence data was assembled using Phred/Phrap [28, 29] and the alignments were inspected for accuracy with Consed [30, 31]. Polymorphisms were identified with PolyPhred 4.0 . All polymorphic sites were manually verified and confirmed by sequencing the opposite strand. Standard measures of nucleotide diversity, including θW and π were calculated as previously described .
We thank members of the Ruohola-Baker lab for useful discussions and Dr. R. Ray for fly lines. This work was supported by an AHA fellowship for H.R.S., CRDF for A.S.Y., K.M.M., H.R.S. and H.R-B. and by the grants from the National Institute of Health and Muscular Dystrophy Association for H.R-B.
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