RNA-protein coevolution study of Gemin5 uncovers the role of the PXSS motif of RBS1 domain for RNA binding.
Amino Acid Sequence
Binding Sites
Biological Evolution
Conserved Sequence
Nucleic Acid Conformation
Protein Binding
Protein Conformation
Protein Interaction Domains and Motifs
RNA
/ chemistry
RNA, Messenger
/ chemistry
RNA-Binding Motifs
RNA-Binding Proteins
/ chemistry
SMN Complex Proteins
/ chemistry
Gemin5
RNA SHAPE reactivity
RNA-binding
RNA-protein interaction
coevolving pairs
translation control
Journal
RNA biology
ISSN: 1555-8584
Titre abrégé: RNA Biol
Pays: United States
ID NLM: 101235328
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
pubmed:
2
6
2020
medline:
8
7
2021
entrez:
2
6
2020
Statut:
ppublish
Résumé
Regulation of protein synthesis is an essential step of gene expression. This process is under the control of cis-acting RNA elements and trans-acting factors. Gemin5 is a multifunctional RNA-binding protein organized in distinct domains. The protein bears a non-canonical RNA-binding site, designated RBS1, at the C-terminal end. Among other cellular RNAs, the RBS1 region recognizes a sequence located within the coding region of Gemin5 mRNA, termed H12. Expression of RBS1 stimulates translation of RNA reporters carrying the H12 sequence, counteracting the negative effect of Gemin5 on global protein synthesis. A computational analysis of RBS1 protein and H12 RNA variability across the evolutionary scale predicts coevolving pairs of amino acids and nucleotides. RBS1 footprint and gel-shift assays indicated a positive correlation between the identified coevolving pairs and RNA-protein interaction. The coevolving residues of RBS1 contribute to the recognition of stem-loop SL1, an RNA structural element of H12 that contains the coevolving nucleotides. Indeed, RBS1 proteins carrying substitutions on the coevolving residues P
Identifiants
pubmed: 32476560
doi: 10.1080/15476286.2020.1762054
pmc: PMC7549667
doi:
Substances chimiques
GEMIN5 protein, human
0
RNA, Messenger
0
RNA-Binding Proteins
0
SMN Complex Proteins
0
RNA
63231-63-0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1331-1341Références
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