asunderIs a Critical Regulator of Dynein–Dynactin Localization duringDrosophilaSpermatogenesis
asunderIs a Critical Regulator of Dynein–Dynactin Localization duringDrosophilaSpermatogenesis
Spermatogenesis uses mitotic and meiotic cell cycles coordinated with growth and differentiation programs to generate functional sperm. Our analysis of a Drosophila mutant has revealed that asunder (asun), which encodes a conserved protein, is an essential regulator of spermatogenesis. asun spermatocytes arrest during prophase of meiosis I. Strikingly, arrested spermatocytes contain free centrosomes that fail to stably associate with the nucleus. Spermatocytes that overcome arrest exhibit severe defects in meiotic spindle assembly, chromosome segregation, and cytokinesis. Furthermore, the centriole-derived basal body is detached from the nucleus in asun postmeiotic spermatids, resulting in abnormalities later in spermatogenesis. We find that asun spermatocytes and spermatids exhibit drastic reduction of perinuclear dynein–dynactin, a microtubule motor complex. We propose a model in which asun coordinates spermatogenesis by promoting dynein–dynactin recruitment to the nuclear surface, a poorly understood process required for nucleus–centrosome coupling at M phase entry and fidelity of meiotic divisions.
- Davidson College United States
- University of Minnesota Morris United States
- Vanderbilt University Medical Center United States
- Vanderbilt University United States
- University of Minnesota System United States
Cell Nucleus, Male, Green Fluorescent Proteins, Immunoblotting, Dyneins, Cell Cycle Proteins, Dynactin Complex, Animals, Genetically Modified, Meiosis, Drosophila melanogaster, Fertility, Microscopy, Fluorescence, Chromosome Segregation, Mutation, Animals, Drosophila Proteins, Humans, Microtubule-Associated Proteins, Infertility, Male, HeLa Cells
Cell Nucleus, Male, Green Fluorescent Proteins, Immunoblotting, Dyneins, Cell Cycle Proteins, Dynactin Complex, Animals, Genetically Modified, Meiosis, Drosophila melanogaster, Fertility, Microscopy, Fluorescence, Chromosome Segregation, Mutation, Animals, Drosophila Proteins, Humans, Microtubule-Associated Proteins, Infertility, Male, HeLa Cells
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