MUTATIONS THAT INCREASE THE AFFINITY OF A TRANSLATIONAL REPRESSOR FOR RNA

被引:63
作者
LIM, F
PEABODY, DS
机构
[1] UNIV NEW MEXICO, SCH MED, DEPT CELL BIOL, ALBUQUERQUE, NM 87131 USA
[2] CANC RES & TREATMENT CTR, ALBUQUERQUE, NM 87131 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1093/nar/22.18.3748
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
The coat protein of the RNA bacteriophage MS2 is a specific RNA binding protein that represses translation of the viral replicase gene during the infection cycle. As an approach to characterizing the RNA-binding site of coat protein we have isolated a series of coat mutants that suppress the effects of a mutation in the translational operator. Each of the mutants exhibits a super-repressor phenotype, more tightly repressing both the mutant and wild-type operators than does the wild-type protein. The variant coat proteins were purified and subjected to filter binding assays to determine their affinities for the mutant and wild-type operators. Each protein binds the operators from 3 to 7.5-fold more tightly than normal coat protein. The amino acid substitutions seem to extend the normal binding site by introducing new interactions with RNA.
引用
收藏
页码:3748 / 3752
页数:5
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