Peltoketo H, Isomaa V, Mäentausta O, Vihko R
Department of Clinical Chemistry, University of Oulu, Finland.
FEBS Lett. 1988 Oct 24;239(1):73-7. doi: 10.1016/0014-5793(88)80548-9.
cDNA clones for 17 beta-hydroxysteroid dehydrogenase (17-HSD; EC 1.1.1.62) were isolated from a placental lambda gt11 expression library using polyclonal antibodies against placental 17-HSD. The largest cDNA contained 1325 nucleotides, consisting of a short 5'-noncoding segment, a coding segment of 987 nucleotides terminated by a TAA codon, and a 329 nucleotide long 3'-noncoding segment. The open reading frame encoded a polypeptide of 327 amino acid residues with a predicted Mr of 34853. The amino acid sequence of 23 N-terminal amino acids determined from purified 17-HSD agreed with the sequence deduced from cDNA. The deduced amino acid sequence also contained two peptides previously characterized from the proposed catalytic area of placental 17-HSD.
利用针对胎盘17β-羟基类固醇脱氢酶(17-HSD;EC 1.1.1.62)的多克隆抗体,从胎盘λgt11表达文库中分离出17β-羟基类固醇脱氢酶的互补DNA(cDNA)克隆。最大的cDNA包含1325个核苷酸,由一个短的5'非编码区、一个987个核苷酸的编码区(以TAA密码子终止)和一个329个核苷酸长的3'非编码区组成。开放阅读框编码一个由327个氨基酸残基组成的多肽,预测分子量为34853。从纯化的17-HSD中确定的23个N端氨基酸的序列与从cDNA推导的序列一致。推导的氨基酸序列还包含先前从胎盘17-HSD的假定催化区域鉴定出的两个肽段。