POTENTIAL BINDING-SITES OF THE TRANSACTIVATOR FIS ARE PRESENT UPSTREAM OF ALL RIBOSOMAL-RNA OPERONS AND OF MANY BUT NOT ALL TRANSFER-RNA OPERONS

被引:41
作者
VERBEEK, H
NILSSON, L
BALIKO, G
BOSCH, L
机构
[1] LEIDEN STATE UNIV,GORLAEUS LABS,DEPT BIOCHEM,POB 9502,2300 RA LEIDEN,NETHERLANDS
[2] UNIV STOCKHOLM,ARRHENIUS LAB,DEPT CELL BIOL,S-10691 STOCKHOLM,SWEDEN
[3] BIOL RES CTR,INST BIOCHEM,H-6701 SZEGED,HUNGARY
关键词
FIS; Stable RNA synthesis; Upstream activating sequence;
D O I
10.1016/0167-4781(90)90185-5
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
FIS, the Escherichia coli protein that stimulates the inversion of various DNA segments by binding to a recombinational enhancer, trans-activates a number of stable RNA operons and binds to the upstream activator sequence (UAS) of these operons (Nilsson et al. (1990) EMBO J. 9, 727). In a search for potential FIS-binding sites we have compared UASs of other stable RNA operons with a consensus FIS-binding sequence, compiled by comparing recombinational enhancers. Such sites can thus be recognized upstream of all rRNA and 13 tRNA operons. Matching with the consensus sequence varied, suggesting that the affinity of FIS for the sites differed. Accordingly, FIS binding to an upstream sequence of the metY(nusA) operon was found to be weaker than that to the UAS of the thrU(tufB) operon. No FIS binding sites were found upstream three tRNA operons. © 1990.
引用
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页码:302 / 306
页数:5
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