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γ-谷氨酰半胱氨酸连接酶调节亚基(GLCLR)基因物理图谱的构建与精细定位,该基因位于人类恶性间皮瘤关键缺失区域的1号染色体1p22.1上。

Structure and refinement of the physical mapping of the gamma- glutamylcysteine ligase regulatory subunit (GLCLR) gene to chromosome 1p22.1 within the critically deleted region of human malignant mesothelioma.

作者信息

Rozet J M, Gerber S, Perrault I, Calvas P, Souied E, Châtelin S, Molina-Gomez D, Munnich A, Kaplan J

机构信息

Unité de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U-393, Paris Cedex 15, France.

出版信息

Cytogenet Cell Genet. 1998;82(1-2):91-4. doi: 10.1159/000015072.

DOI:10.1159/000015072
PMID:9841137
Abstract

Glutathione is a ubiquitous antioxidant in mammalian tissues. The first step of its synthesis is catalyzed by the glutamate-cysteine ligase (GLCL) which consists of a heavy, catalytic subunit and a light, regulatory subunit (GLCLR). Previous genetic analyses have revealed frequent losses of chromosome 1p22-->p21 in human malignant mesothelioma and the shortest region of overlapping deletions has been narrowed between the two loci D1S435 and D1S236. An expressed sequence tag of the GLCLR gene was found within a YAC contig encompassing the same interval aoffwas therefore considered as a good candidate gene for predisposition to human mesothelioma. We report here the characterization of the genomic structure of the GLCLR gene and the refine its physical mapping to chromosome 1p22.1.

摘要

谷胱甘肽是哺乳动物组织中普遍存在的一种抗氧化剂。其合成的第一步由谷氨酸-半胱氨酸连接酶(GLCL)催化,该酶由一个重的催化亚基和一个轻的调节亚基(GLCLR)组成。先前的基因分析显示,人类恶性间皮瘤中常出现1p22→p21染色体缺失,两个位点D1S435和D1S236之间的最短重叠缺失区域已被缩小。在一个包含相同区间的酵母人工染色体(YAC)重叠群中发现了GLCLR基因的一个表达序列标签,因此被认为是人类间皮瘤易感性的一个良好候选基因。我们在此报告GLCLR基因的基因组结构特征,并将其物理定位精确到1p22.1染色体。

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Structure and refinement of the physical mapping of the gamma- glutamylcysteine ligase regulatory subunit (GLCLR) gene to chromosome 1p22.1 within the critically deleted region of human malignant mesothelioma.γ-谷氨酰半胱氨酸连接酶调节亚基(GLCLR)基因物理图谱的构建与精细定位,该基因位于人类恶性间皮瘤关键缺失区域的1号染色体1p22.1上。
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Assignment of the human gene (GLCLR) that encodes the regulatory subunit of gamma-glutamylcysteine synthetase to chromosome 1p21.将编码γ-谷氨酰半胱氨酸合成酶调节亚基的人类基因(GLCLR)定位于染色体1p21。
Cytogenet Cell Genet. 1996;72(2-3):252-4. doi: 10.1159/000134202.
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Loss of heterozygosity analysis defines a critical region in chromosome 1p22 commonly deleted in human malignant mesothelioma.杂合性缺失分析确定了人类恶性间皮瘤中常见缺失的1号染色体1p22区域的一个关键区域。
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Mapping of the glutamate-cysteine ligase catalytic subunit gene (GLCLC) to human chromosome 6p12 and mouse chromosome 9D-E and of the regulatory subunit gene (GLCLR) to human chromosome 1p21-p22 and mouse chromosome 3H1-3.将谷氨酸-半胱氨酸连接酶催化亚基基因(GLCLC)定位于人类染色体6p12和小鼠染色体9D-E,以及将调节亚基基因(GLCLR)定位于人类染色体1p21-p22和小鼠染色体3H1-3。
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Molecular cloning and sequencing of the cDNA encoding mouse glutamate-cysteine ligase regulatory subunit.编码小鼠谷氨酸-半胱氨酸连接酶调节亚基的cDNA的分子克隆与测序
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