4.7 Article

Gemin5-dependent RNA association with polysomes enables selective translation of ribosomal and histone mRNAs

Journal

CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 79, Issue 9, Pages -

Publisher

SPRINGER BASEL AG
DOI: 10.1007/s00018-022-04519-4

Keywords

RNA-binding proteins; Polysome enrichment; Protein synthesis; TOP mRNAs; Histone mRNAs

Funding

  1. Ministerio de Ciencia e Innovacion (MICIN)
  2. Fondo Europeo de Desarrollo Regional (AEI/FEDER UE) [PID2020-115096RB-I00]
  3. Comunidad de Madrid [B2017/BMD-3770]
  4. Fundacion Ramon Areces
  5. CRUE-CSIC
  6. Springer Nature

Ask authors/readers for more resources

Selective translation is regulated by Gemin5, an RNA-binding protein involved in snRNP assembly. Gemin5 stimulates translation of specific mRNAs through interaction with unique cis-acting elements. Ribosomal and histone mRNAs, which contain specific regulatory elements, are enriched in polysomes and coprecipitate with Gemin5. Disruption of these regulatory elements impairs Gemin5-RNA interaction and translation. Therefore, Gemin5 plays a role in the translation of specific mRNA subsets encoding proteins involved in cellular processes.
Selective translation allows to orchestrate the expression of specific proteins in response to different signals through the concerted action of cis-acting elements and RNA-binding proteins (RBPs). Gemin5 is a ubiquitous RBP involved in snRNP assembly. In addition, Gemin5 regulates translation of different mRNAs through apparently opposite mechanisms of action. Here, we investigated the differential function of Gemin5 in translation by identifying at a genome-wide scale the mRNAs associated with polysomes. Among the mRNAs showing Gemin5-dependent enrichment in polysomal fractions, we identified a selective enhancement of specific transcripts. Comparison of the targets previously identified by CLIP methodologies with the polysome-associated transcripts revealed that only a fraction of the targets was enriched in polysomes. Two different subsets of these mRNAs carry unique cis-acting regulatory elements, the 5' terminal oligopyrimidine tracts (5'TOP) and the histone stem-loop (hSL) structure at the 3' end, respectively, encoding ribosomal proteins and histones. RNA-immunoprecipitation (RIP) showed that ribosomal and histone mRNAs coprecipitate with Gemin5. Furthermore, disruption of the TOP motif impaired Gemin5-RNA interaction, and functional analysis showed that Gemin5 stimulates translation of mRNA reporters bearing an intact TOP motif. Likewise, Gemin5 enhanced hSL-dependent mRNA translation. Thus, Gemin5 promotes polysome association of only a subset of its targets, and as a consequence, it favors translation of the ribosomal and the histone mRNAs. Together, the results presented here unveil Gemin5 as a novel translation regulator of mRNA subsets encoding proteins involved in fundamental cellular processes.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available