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Characterizing ZC3H18, a Multi-domain Protein at the Interface of RNA Production and Destruction Decisions.
- Source :
-
Cell reports [Cell Rep] 2018 Jan 02; Vol. 22 (1), pp. 44-58. - Publication Year :
- 2018
-
Abstract
- Nuclear RNA metabolism is influenced by protein complexes connecting to both RNA-productive and -destructive pathways. The ZC3H18 protein binds the cap-binding complex (CBC), universally present on capped RNAs, while also associating with the nuclear exosome targeting (NEXT) complex, linking to RNA decay. To dissect ZC3H18 function, we conducted interaction screening and mutagenesis of the protein, which revealed a phosphorylation-dependent isoform. Surprisingly, the modified region of ZC3H18 associates with core histone proteins. Further examination of ZC3H18 function, by genome-wide analyses, demonstrated its impact on transcription of a subset of protein-coding genes. This activity requires the CBC-interacting domain of the protein, with some genes being also dependent on the NEXT- and/or histone-interacting domains. Our data shed light on the domain requirements of a protein positioned centrally in nuclear RNA metabolism, and they suggest that post-translational modification may modulate its function.<br /> (Copyright © 2017 The Author(s). Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Cell Nucleus chemistry
Cell Nucleus genetics
Genome-Wide Association Study
HEK293 Cells
HeLa Cells
Humans
Mutagenesis
Nuclear Cap-Binding Protein Complex chemistry
Nuclear Cap-Binding Protein Complex genetics
Protein Domains
RNA genetics
RNA-Binding Proteins chemistry
RNA-Binding Proteins genetics
Cell Nucleus metabolism
Nuclear Cap-Binding Protein Complex metabolism
RNA biosynthesis
RNA Stability physiology
RNA-Binding Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2211-1247
- Volume :
- 22
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 29298432
- Full Text :
- https://doi.org/10.1016/j.celrep.2017.12.037