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利用人类固醇硫酸酯酶的cDNA揭示类固醇硫酸酯酶缺乏症的遗传异质性。

Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase.

作者信息

Conary J T, Lorkowski G, Schmidt B, Pohlmann R, Nagel G, Meyer H E, Krentler C, Cully J, Hasilik A, von Figura K

出版信息

Biochem Biophys Res Commun. 1987 Apr 29;144(2):1010-7. doi: 10.1016/s0006-291x(87)80064-5.

Abstract

Three cDNA clones with inserts of 1.2-1.6 kb that reacted both with antibodies and oligonucleotides specific for steroid sulfatase were isolated from a human placental library in lambda gt11. The 5'-end of one of the inserts, STS-3, was sequenced and colinearity with the amino acid sequence of 3 peptides of steroid sulfatase encompassing 64 amino acids was demonstrated. STS-3 hybridized with 2.5, 4.6 and 6.3 kb species in poly(A)+RNA and with 2.5, 4 and 9 kb fragments of EcoRI digested human DNA. The frequency of the EcoRI fragments in DNA from females was approximately twice that in DNA from males. DNA from two patients with steroid sulfatase deficiency and X-linked ichthyosis did not hybridize with STS-3. DNA from a third patient showed a normal hybridization pattern. It is concluded that steroid sulfatase deficiency is a genetically heterogenous disorder.

摘要

从λgt11载体的人胎盘文库中分离出三个cDNA克隆,其插入片段为1.2 - 1.6 kb,它们既能与针对类固醇硫酸酯酶的抗体反应,也能与寡核苷酸反应。对其中一个插入片段STS - 3的5′端进行测序,结果表明它与类固醇硫酸酯酶的3个包含64个氨基酸的肽段的氨基酸序列具有共线性。STS - 3与poly(A)+RNA中的2.5、4.6和6.3 kb片段杂交,也与经EcoRI酶切的人DNA的2.5、4和9 kb片段杂交。女性DNA中EcoRI片段的频率约为男性DNA中的两倍。两名患有类固醇硫酸酯酶缺乏症和X连锁鱼鳞病的患者的DNA不与STS - 3杂交。第三名患者的DNA显示出正常的杂交模式。由此得出结论,类固醇硫酸酯酶缺乏症是一种遗传异质性疾病。

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