首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis.
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Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis.

机译:类固醇硫酸酯酶cDNA的克隆:隐性X染色体连锁鱼鳞病患者频繁发生基因缺失。

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摘要

A human steroid sulfatase (steryl-sulfatase; steryl-sulfate sulfohydrolase, EC 3.1.6.2) cDNA 2.4 kilobases long was isolated from a human placental lambda gt11 cDNA expression library. The library was screened with monospecific rabbit antibodies elicited by injection of steroid sulfatase protein purified from human placentas. Hybridization of the cDNA with EcoRI-digested genomic DNA indicated that patients from 14 of 15 apparently unrelated families have gross deletions of the gene for steroid sulfatase. One patient had genomic DNA fragments that were identical to those from normal individuals, indicating the absence of any major deletions as the cause of his lack of steroid sulfatase enzyme activity.
机译:从人胎盘λgt11cDNA表达文库中分离出一个长2.4千碱基的人类固醇硫酸酯酶(甾基硫酸酯酶;甾醇硫酸酯磺基水解酶,EC 3.1.6.2)cDNA。通过注射从人胎盘中纯化的甾族硫酸酯酶蛋白引发的单特异性兔抗体筛选该文库。 cDNA与EcoRI消化的基因组DNA的杂交表明,来自15个显然无关的家庭中的14个患者的类固醇硫酸酯酶基因完全缺失。一名患者的基因组DNA片段与正常人的基因组DNA片段相同,表明没有任何重大缺失是导致他的类固醇硫酸酯酶活性不足的原因。

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