Title

Biogenesis and function of tRNA fragments during sperm maturation and fertilization in mammals

UMMS Affiliation

Department of Biochemistry and Molecular Pharmacology; Program in Molecular Medicine; Program in Bioinformatics and Integrative Biology; RNAi Therapeutics Institute; UMass Metabolic Network

Date

1-22-2016

Document Type

Article

Medical Subject Headings

Animals; Blastocyst; Diet, Protein-Restricted; Epididymis; *Fertilization; *Gene Expression Regulation; Male; Mice; MicroRNAs; RNA, Transfer, Gly; Retroelements; *Sperm Maturation; Spermatozoa; Testis

Disciplines

Biochemistry | Cell Biology | Cellular and Molecular Physiology | Developmental Biology | Molecular Biology | Molecular Genetics | Translational Medical Research

Abstract

Several recent studies link parental environments to phenotypes in subsequent generations. In this work, we investigate the mechanism by which paternal diet affects offspring metabolism. Protein restriction in mice affects small RNA (sRNA) levels in mature sperm, with decreased let-7 levels and increased amounts of 5' fragments of glycine transfer RNAs (tRNAs). In testicular sperm, tRNA fragments are scarce but increase in abundance as sperm mature in the epididymis. Epididymosomes (vesicles that fuse with sperm during epididymal transit) carry RNA payloads matching those of mature sperm and can deliver RNAs to immature sperm in vitro. Functionally, tRNA-glycine-GCC fragments repress genes associated with the endogenous retroelement MERVL, in both embryonic stem cells and embryos. Our results shed light on sRNA biogenesis and its dietary regulation during posttesticular sperm maturation, and they also link tRNA fragments to regulation of endogenous retroelements active in the preimplantation embryo.

Rights and Permissions

Citation: Science. 2016 Jan 22;351(6271):391-6. doi: 10.1126/science.aad6780. Epub 2015 Dec 31. Link to article on publisher's site

Related Resources

Link to Article in PubMed

Keywords

UMCCTS funding

PubMed ID

26721685