RNA degradation is required for the germ-cell to maternal transition in Drosophila
In sexually reproducing animals, the oocyte contributes a large supply of RNAs that are essential to launch development upon fertilization. The mechanisms that regulate the composition of the maternal RNA contribution during oogenesis are unclear. Here, we show that a subset of RNAs expressed during...
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Published in | Current biology Vol. 31; no. 14; pp. 2984 - 2994.e7 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Inc
26.07.2021
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Subjects | |
Online Access | Get full text |
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Summary: | In sexually reproducing animals, the oocyte contributes a large supply of RNAs that are essential to launch development upon fertilization. The mechanisms that regulate the composition of the maternal RNA contribution during oogenesis are unclear. Here, we show that a subset of RNAs expressed during the early stages of oogenesis is subjected to regulated degradation during oocyte specification. Failure to remove these RNAs results in oocyte dysfunction and death. We identify the RNA-degrading Super Killer complex and No-Go Decay factor Pelota as key regulators of oogenesis via targeted degradation of specific RNAs expressed in undifferentiated germ cells. These regulators target RNAs enriched for cytidine sequences that are bound by the polypyrimidine tract binding protein Half pint. Thus, RNA degradation helps orchestrate a germ cell-to-maternal transition that gives rise to the maternal contribution to the zygote.
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•Ski complex mediated RNA degradation is required in the germline for fertility.•A subset of early oogenic RNAs are degraded concurrent with oocyte specification.•Early oogenic RNAs are degraded utilizing components of the No Go Decay pathway.•Degradation of early oogenic RNAs is required for maintenance of oocyte fate.
Blatt et al. find that a cohort of RNAs expressed in germ cells are targeted for regulated degradation mediated by components of the No Go Decay pathway when oocytes are specified. They find that this regulated RNA degradation is essential for proper oocyte development and fertility. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Conceptualization, P.R., P.B., and M.T.L.; Methodology, P.R. and P.B.; Software, M.T.L. and M.D.H.; Formal Analysis, M.T.L., P.B. and M.D.H.; Investigation, P.B., S.W.-D., A.M., S.B., J.C., B.B., M.U.; Resources, P.B., S.W-D., and P.R.; Data Curation, P.B., and M.T.L.; Writing – Original Draft, P.R. and P.B.; Writing – Review & Editing, P.R., M.T.L. and P.B.; Visualization, P.B., and M.T.L.; Supervision, P.R.; Project Administration, P.R.; Funding Acquisition, P.R., P.B., and M.T.L. Lead contact Author contributions |
ISSN: | 0960-9822 1879-0445 |
DOI: | 10.1016/j.cub.2021.04.052 |