A maternally programmed intergenerational mechanism enables male offspring to make piRNAs from Y-linked precursor RNAs in Drosophila

Author:

Venkei Zsolt G.,Gainetdinov IldarORCID,Bagci Ayca,Starostik Margaret R.ORCID,Choi Charlotte P.,Fingerhut Jaclyn M.ORCID,Chen PeiweiORCID,Balsara Chiraag,Whitfield Troy W.ORCID,Bell George W.,Feng Suhua,Jacobsen Steven E.ORCID,Aravin Alexei A.ORCID,Kim John K.,Zamore Phillip D.ORCID,Yamashita Yukiko M.ORCID

Abstract

AbstractIn animals, PIWI-interacting RNAs (piRNAs) direct PIWI proteins to silence complementary targets such as transposons. In Drosophila and other species with a maternally specified germline, piRNAs deposited in the egg initiate piRNA biogenesis in the progeny. However, Y chromosome loci cannot participate in such a chain of intergenerational inheritance. How then can the biogenesis of Y-linked piRNAs be initiated? Here, using Suppressor of Stellate (Su(Ste)), a Y-linked Drosophila melanogaster piRNA locus as a model, we show that Su(Ste) piRNAs are made in the early male germline via 5′-to-3′ phased piRNA biogenesis initiated by maternally deposited 1360/Hoppel transposon piRNAs. Notably, deposition of Su(Ste) piRNAs from XXY mothers obviates the need for phased piRNA biogenesis in sons. Together, our study uncovers a developmentally programmed, intergenerational mechanism that allows fly mothers to protect their sons using a Y-linked piRNA locus.

Funder

Howard Hughes Medical Institute

U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences

U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology

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