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不同的γ-谷氨酰转肽酶信使核糖核酸在人类肝脏和肾脏中表达。

Different gamma-glutamyl transpeptidase mRNAs are expressed in human liver and kidney.

作者信息

Pawlak A, Wu S J, Bulle F, Suzuki A, Chikhi N, Ferry N, Baik J H, Siegrist S, Guellaën G

机构信息

Unité INSERM 99, Hôpital Henri Mondor, Creteil, France.

出版信息

Biochem Biophys Res Commun. 1989 Oct 31;164(2):912-8. doi: 10.1016/0006-291x(89)91545-3.

Abstract

In human, the two subunits of gamma-glutamyl transpeptidase (GGT) arise from a common precursor encoded by a multigene family. Until now, a single specific coding sequence for this precursor (type I) has been identified in human placenta and liver. In the present study, we have isolated from a human kidney cDNA library, a GGT specific clone (0.8 Kb). The sequence of which (type II) i) covers the carboxy terminal part of the GGT precursor, ii) exhibits 22 point mutations and a 30 bp deletion as compared to the type I GGT sequence. The sequencing of a human genomic clone reveals that this type II GGT mRNA is encoded by a different gene than the type I GGT mRNA. Both type I and type II GGT mRNAs are expressed in human liver, while almost exclusively type II GGT mRNA is detected in human kidney.

摘要

在人类中,γ-谷氨酰转肽酶(GGT)的两个亚基源自一个多基因家族编码的共同前体。到目前为止,已在人胎盘和肝脏中鉴定出该前体(I型)的单一特定编码序列。在本研究中,我们从人肾cDNA文库中分离出一个GGT特异性克隆(0.8 Kb)。其序列(II型):i)覆盖GGT前体的羧基末端部分;ii)与I型GGT序列相比,有22个点突变和一个30 bp的缺失。对一个人类基因组克隆的测序表明,这种II型GGT mRNA由一个与I型GGT mRNA不同的基因编码。I型和II型GGT mRNA均在人肝脏中表达,而在人肾中几乎只检测到II型GGT mRNA。

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