THE MECHANISM FOR APO-B MESSENGER-RNA EDITING IS DEAMINATION

被引:38
作者
JOHNSON, DF
POKSAY, KS
INNERARITY, TL
机构
[1] The Gladstone Institute of Cardiovascular Disease, Cardiovascular Research Institute, University of California, San Francisco
关键词
D O I
10.1006/bbrc.1993.2172
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apolipoprotein (apo-) B mRNA editing at nucleotide 6666 converts cytidine to uridine, transforming the codon for glutamine-2153 to a termination codon. To investigate this editing mechanism, [α-32P] and [5-3H] CTP were incorporated into synthetic apo-B RNA. After the substrate had been edited extensively in vitro by a partially purified editing extract, the edited base was isolated and analyzed for radioactivity. The uridine-6666 resulting from the editing reaction had the same ratio of 3H to 32P as did the cytidine-6666, demonstrating that deamination rather than base exchange or nucleotide replacement is the mechanism for apo-B mRNA editing. © 1993 Academic Press, Inc.
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收藏
页码:1204 / 1210
页数:7
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