Nucleotide sequence of γδ resolvase gene and demonstration that its gene product acts as a repressor of transcription
Nucleotide sequence of γδ resolvase gene and demonstration that its gene product acts as a repressor of transcription
复制标题
γδ解离酶基因的核苷酸序列及其基因产物作为转录阻遏蛋白的证明
作者:
R. Reed;G. I. Shibuya;J. Steitz
The related transposons γδ and Tn3 each encode an efficient site-specific recombination system essential for transposition1,2. The recombination occurs at a particular site, res, located within the intercistronic region between the two divergently transcribed genes that are required for transposition2. The product of one of these genes, resolvase, catalyses the recombination at res. Recently, in vitro site-specific recombination has been demonstrated using purified resolvase and a model substrate containing two res sites3. Genetic analysis of mutants in the γδ/Tn3 tnpR gene, which encodes the resolvase protein, suggested that resolvase regulates the frequency of transposition in addition to catalysing recombination4–6. Analysis of element-encoded proteins in minicells indicated a direct effect of resolvase on the levels of the element-encoded transposase, as well as on its own expression7. Here we report the sequence of the gene encoding γδ resolvase and compare the predicted amino acid sequence with that of the functionally interchangeable Tn3 protein6. In addition, we have determined the sites at which transcription of the transposase and resolvase genes initiates in vitro and have demonstrated that purified resolvase protein specifically represses transcription of both transposition related genes in this in vitro transcription system.
DOI:
10.1073/pnas.78.2.752
发表时间:
1981-01-01
期刊:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES
影响因子:
--
作者:
LEE, NL;GIELOW, WO;WALLACE, RG
通讯作者:
WALLACE, RG
DOI:
10.1073/pnas.79.1.46
发表时间:
1982
影响因子:
11.1
作者:
Kitts,P;Symington,L;Burke,M;Reed,R;Sherratt,D
通讯作者:
Sherratt,D
DOI:
10.1073/pnas.78.6.3428
发表时间:
1981
影响因子:
11.1
作者:
Reed,RR
通讯作者:
Reed,RR