Functional Interaction between U1snRNP and Sam68 Insures Proper 3′ End Pre-mRNA Processing during Germ Cell Differentiation

Claudio Sette, Eleonora Cesari, Livia Pellegrini, Ariane Jolly, Donatella Farini, Pamela Bielli, Pierre De La Grange

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Male germ cells express the widest repertoire of transcript variants in mammalian tissues. Nevertheless, factors and mechanisms underlying such pronounced diversity are largely unknown. The splicing regulator Sam68 is highly expressed in meiotic cells, and its ablation results in defective spermatogenesis. Herein, we uncover an extensive splicing program operated by Sam68 across meiosis, primarily characterized by alternative last exon (ALE) regulation in genes of functional relevance for spermatogenesis. Lack of Sam68 preferentially causes premature transcript termination at internal polyadenylation sites, a feature observed also upon depletion of the spliceosomal U1snRNP in somatic cells. Notably, Sam68-regulated ALEs are characterized by proximity between U1snRNP and Sam68 binding motifs. We demonstrate a physical association between Sam68 and U1snRNP and show that U1snRNP recruitment to Sam68-regulated ALEs is impaired in Sam68 −/− germ cells. Thus, our study reveals an unexpected cooperation between Sam68 and U1snRNP that insures proper processing of transcripts essential for male fertility.
Original languageEnglish
Pages (from-to)2929-2941.e5
JournalCell Reports
Volume26
DOIs
Publication statusPublished - 2019

Keywords

  • Biochemistry, Genetics and Molecular Biology (all)
  • Sam68
  • U1snRNP
  • alternative polyadenylation
  • alternative splicing
  • germ cell differentiation
  • male fertility
  • spermatogenesis

Fingerprint

Dive into the research topics of 'Functional Interaction between U1snRNP and Sam68 Insures Proper 3′ End Pre-mRNA Processing during Germ Cell Differentiation'. Together they form a unique fingerprint.

Cite this