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PMID: 954097 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Kinetics of formation of 5' terminal caps in mRNA.

Cell ·Vol. 8 ·No. 3 ·1976-07-00 ·Pages 433-42

Perry RP, Kelley DE

Abstract

A kinetic analysis of the labeling of the methylated components of messenger RNA and heterogeneous nuclear RNA in mouse L cells indicates that the 5' terminal cap I structures (m7GpppXmpYp) of mRNA are derived from 5' terminal cap structures of hnRNA. Most of the hnRNA caps are conserved during processing, whereas only a portion of the internal m6A residues in hnRNA are conserved. The cap II structures (m7GpppXmpYmpZp), which constitute the 5' termini of some mRNAs, arise by a "secondary" methylation that occurs after the mRNAs have entered the cytoplasm. This secondary methylation is apparently restricted to a particular subclass of mRNAs having a high frequency of pyrimidine nucleotides at position Y, a composition at position X which differs from that of the bulk of the cap I-terminated mRNAs, and a relatively slow rate of turnover.

MeSH Terms
Kinetics L Cells Methionine/metabolism Methylation Poly A Polyribosomes/metabolism RNA/metabolism RNA, Messenger/analysis,metabolism
Chemicals
RNA, Messenger Poly A RNA Methionine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Perry R P
Kelley D E
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1976-07-00
Pages
433-42
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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