Abstract
Spermatogenesis is a dynamic developmental process requiring precisely timed transitions between discrete stages. Specifically, the germline undergoes three transitions: from mitotic spermatogonia to spermatocytes, from meiotic spermatocytes to spermatids, and from morphogenetic spermatids to spermatozoa. The somatic cells of the testis provide essential support to the germline throughout spermatogenesis, but their precise role during these developmental transitions has not been comprehensively explored. Here, we describe the identification and characterization of genes that are required in the somatic cells of the Drosophila melanogaster testis for progress through spermatogenesis. Phenotypic analysis of candidate genes pinpointed the stage of germline development disrupted. Bioinformatic analysis revealed that particular gene classes were associated with specific developmental transitions. Requirement for genes associated with endocytosis, cell polarity, and microtubule-based transport corresponded with the development of spermatogonia, spermatocytes, and spermatids, respectively. Overall, we identify mechanisms that act specifically in the somatic cells of the testis to regulate spermatogenesis.
MeSH terms
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Animals
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Cell Differentiation
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Computational Biology
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Drosophila Proteins / genetics
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Drosophila Proteins / metabolism
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Drosophila melanogaster / genetics
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Drosophila melanogaster / growth & development
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Female
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Gene Expression Regulation
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Gene Regulatory Networks*
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Male
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Meiosis / genetics
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Mitosis / genetics
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RNA Interference
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Spermatids / growth & development
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Spermatogenesis*
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Spermatozoa / growth & development
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Testis / cytology*
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Tubulin / genetics
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Tubulin / metabolism
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rab5 GTP-Binding Proteins / genetics
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rab5 GTP-Binding Proteins / metabolism
Substances
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Drosophila Proteins
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Tubulin
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Rab5 protein, Drosophila
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rab5 GTP-Binding Proteins
Grants and funding
This work was funded by a grant to GT for “Analysis of Soma-Germline interactions in the fly testes” from the Canadian Institutes of Health Research (
www.cihr-irsc.gc.ca). Additional funding included an Alexander Graham Bell Canada Graduate Scholarship to MJF for “A genome wide screen for cytoskeletal regulators of stem cell differentiation in Drosophila testes” from the Canadian Natural Sciences and Engineering Research Council (
www.nserc-crsng.gc.ca). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.