MINA-1 and WAGO-4 are part of regulatory network coordinating germ cell death and RNAi in C. elegans
Post-transcriptional control of mRNAs by RNA-binding proteins (RBPs) has a prominent role in the regulation of gene expression. RBPs interact with mRNAs to control their biogenesis, splicing, transport, localization, translation, and stability. Defects in such regulation can lead to a wide range of...
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Veröffentlicht in: | Cell death and differentiation 2019-10, Vol.26 (10), p.2157-2178 |
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Zusammenfassung: | Post-transcriptional control of mRNAs by RNA-binding proteins (RBPs) has a prominent role in the regulation of gene expression. RBPs interact with mRNAs to control their biogenesis, splicing, transport, localization, translation, and stability. Defects in such regulation can lead to a wide range of human diseases from neurological disorders to cancer. Many RBPs are conserved between
Caenorhabditis elegans
and humans, and several are known to regulate apoptosis in the adult
C. elegans
germ line. How these RBPs control apoptosis is, however, largely unknown. Here, we identify
mina-1(C41G7.3)
in a RNA interference-based screen as a novel regulator of apoptosis, which is exclusively expressed in the adult germ line. The absence of MINA-1 causes a dramatic increase in germ cell apoptosis, a reduction in brood size, and an impaired P granules organization and structure. In vivo crosslinking immunoprecipitation experiments revealed that MINA-1 binds a set of mRNAs coding for RBPs associated with germ cell development. Additionally, a system-wide analysis of a
mina-1
deletion mutant compared with wild type, including quantitative proteome and transcriptome data, hints to a post-transcriptional regulatory RBP network driven by MINA-1 during germ cell development in
C. elegans
. In particular, we found that the germline-specific Argonaute WAGO-4 protein levels are increased in
mina-1
mutant background. Phenotypic analysis of double mutant
mina-1;wago-4
revealed that contemporary loss of MINA-1 and WAGO-4 strongly rescues the phenotypes observed in
mina-1
mutant background. To strengthen this functional interaction, we found that upregulation of WAGO-4 in
mina-1
mutant animals causes hypersensitivity to exogenous RNAi. Our comprehensive experimental approach allowed us to describe a phenocritical interaction between two RBPs controlling germ cell apoptosis and exogenous RNAi. These findings broaden our understanding of how RBPs can orchestrate different cellular events such as differentiation and death in
C. elegans
. |
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ISSN: | 1350-9047 1476-5403 |
DOI: | 10.1038/s41418-019-0291-z |