Morton M R, Bayney R M, Pickett C B
Merck Frosst Centre for Therapeutic Research, Kirkland, Quebec, Canada.
Arch Biochem Biophys. 1990 Feb 15;277(1):56-60. doi: 10.1016/0003-9861(90)90549-e.
We have isolated and characterized a rat liver glutathione S-transferase Yb1 subunit gene. DNA sequence analysis of the Yb1 subunit gene indicates that it comprises eight exons separated by seven introns and spans approximately 5.0 kb. The transcription initiation site has been mapped by primer extension experiments. Transcription begins at a guanine residue 29 nucleotides downstream from a "TATA" sequence. The DNA sequences of all exons and some introns share significant sequence identity with the corresponding exons and introns in the Yb2 subunit gene characterized by Tu and co-workers [J. Biol. Chem. 263, 11389-11395 (1988)]. The isolation and characterization of the glutathione S-transferase Yb1 gene will allow for a detailed analysis of regulatory elements required for transcriptional regulation of this gene.
我们已经分离并鉴定了大鼠肝脏谷胱甘肽S-转移酶Yb1亚基基因。对Yb1亚基基因的DNA序列分析表明,它由八个外显子和七个内含子分隔,跨度约为5.0 kb。转录起始位点已通过引物延伸实验确定。转录起始于“TATA”序列下游29个核苷酸处的鸟嘌呤残基。所有外显子和一些内含子的DNA序列与Tu及其同事鉴定的Yb2亚基基因中的相应外显子和内含子具有显著的序列同一性[《生物化学杂志》263, 11389 - 11395 (1988)]。谷胱甘肽S-转移酶Yb1基因的分离和鉴定将有助于详细分析该基因转录调控所需的调控元件。