Zgombić-Knight M, Deltour L, Haselbeck R J, Foglio M H, Duester G
Burnham Institute, La Jolla, California 92037, USA.
Genomics. 1997 Apr 1;41(1):105-9. doi: 10.1006/geno.1997.4637.
Class IV alcohol dehydrogenase (ADH) has been shown to function in vitro as a retinol dehydrogenase catalyzing the synthesis of retinoic acid, a pleiotropic gene regulator. To enable genetic studies on the function of this enzyme and regulation of its gene, we have screened a genomic library and isolated the mouse class IV ADH gene (Adh3). The complete mouse class IV ADH coding region was found in nine exons spanning a 14-kb region. Primer extension analysis was used to map the transcription initiation site to a position lying 30 bp upstream of the ATG translation start codon. Nucleotide sequence analysis of the promoter region indicated an absence of both TATA-box and GC-box sequences; this distinguishes it from the promoters for class I, II, and III ADH genes. Sequence comparison of the mouse and human class IV ADH promoters indicated that they share a conserved region located 125-145 bp upstream of the coding region containing adjacent sequences matching the consensus binding sites for transcription factors AP-1 and C/EBP.
IV类乙醇脱氢酶(ADH)已被证明在体外作为视黄醇脱氢酶发挥作用,催化视黄酸的合成,视黄酸是一种多效性基因调节剂。为了对该酶的功能及其基因调控进行遗传学研究,我们筛选了一个基因组文库并分离出小鼠IV类ADH基因(Adh3)。完整的小鼠IV类ADH编码区位于9个外显子中,跨度为14 kb区域。引物延伸分析用于将转录起始位点定位到ATG翻译起始密码子上游30 bp处的位置。启动子区域的核苷酸序列分析表明,既没有TATA盒也没有GC盒序列;这使其与I类、II类和III类ADH基因的启动子区分开来。小鼠和人类IV类ADH启动子的序列比较表明,它们在编码区上游125 - 145 bp处共享一个保守区域,该区域包含与转录因子AP - 1和C/EBP的共有结合位点匹配的相邻序列。