Molecular cloning and characterization of the mouse Kin17 coding for a Zn-finger protein that preferentially recognizes bent DNA

被引:16
作者
Tissier, A
Kannouche, P
Mauffrey, P
Allemand, I
Frelat, G
Devoret, R
Angulo, JF
机构
[1] CEN,CEA,DEPT RADIOBIOL & RADIOPATHOL,LAB GENET RADIOSENSIBIL,DIRECT SCI VIVANT,F-92265 FONTENAY ROSES,FRANCE
[2] UNIV PARIS 11,INST CURIE BIOL,ETUD MUTAGENESE & CANCEROGENESE GRP,F-91405 ORSAY,FRANCE
关键词
D O I
10.1006/geno.1996.0623
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We report the isolation of the mouse Kin17 gene, located on chromosome 2, coding a nuclear Zn-finger protein that has a 39-residue region homologous to Escherichia coli RecA protein and that is recognized by anti-RecA antibodies. Kin17 protein preferentially binds to curved DNA in vitro and in vivo, suggesting a role in illegitimate recombination and in regulation of gene expression. We have shown that the Kin17 gene is about 8 kb in length and displays three exons and two introns. The 5' flanking regions lacks a canonical TATAA box but presents several putative regulatory domains. A major transcription initiation site is located 322 nucleotides upstream of the translation start site. The 1.7-kb transcript of the Kin17 gene is weakly and ubiquitously expressed in murine tissues and cell lines as determined by Northern analysis. The cross-hybridization of Kin17 cDNA with the genomic DNA of other species in Southern analysis indicates the conservation of the gene among mammals and suggests that the Kin17 gene plays a conserved role in DNA metabolism. (C) 1996 Academic Press, Inc.
引用
收藏
页码:238 / 242
页数:5
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