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A Family of Argonaute-Interacting Proteins Gates Nuclear RNAi.
- Source :
-
Molecular cell [Mol Cell] 2020 Jun 04; Vol. 78 (5), pp. 862-875.e8. Date of Electronic Publication: 2020 Apr 28. - Publication Year :
- 2020
-
Abstract
- Nuclear RNA interference (RNAi) pathways work together with histone modifications to regulate gene expression and enact an adaptive response to transposable RNA elements. In the germline, nuclear RNAi can lead to trans-generational epigenetic inheritance (TEI) of gene silencing. We identified and characterized a family of nuclear Argonaute-interacting proteins (ENRIs) that control the strength and target specificity of nuclear RNAi in C. elegans, ensuring faithful inheritance of epigenetic memories. ENRI-1/2 prevent misloading of the nuclear Argonaute NRDE-3 with small RNAs that normally effect maternal piRNAs, which prevents precocious nuclear translocation of NRDE-3 in the early embryo. Additionally, they are negative regulators of nuclear RNAi triggered from exogenous sources. Loss of ENRI-3, an unstable protein expressed mostly in the male germline, misdirects the RNAi response to transposable elements and impairs TEI. The ENRIs determine the potency and specificity of nuclear RNAi responses by gating small RNAs into specific nuclear Argonautes.<br />Competing Interests: Declaration of Interests E.A.M. is a founder and director of STORM Therapeutics. This company has not contributed to this research in any way. The authors declare no competing interests.<br /> (Copyright © 2020. Published by Elsevier Inc.)
- Subjects :
- Animals
Argonaute Proteins genetics
Argonaute Proteins metabolism
Caenorhabditis elegans genetics
Caenorhabditis elegans metabolism
Cell Nucleus metabolism
Germ Cells metabolism
Nuclear Proteins metabolism
RNA Interference physiology
RNA, Double-Stranded metabolism
RNA, Nuclear metabolism
RNA, Small Interfering genetics
RNA-Binding Proteins genetics
Caenorhabditis elegans Proteins genetics
Caenorhabditis elegans Proteins metabolism
Gene Silencing physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4164
- Volume :
- 78
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Molecular cell
- Publication Type :
- Academic Journal
- Accession number :
- 32348780
- Full Text :
- https://doi.org/10.1016/j.molcel.2020.04.007