Wetmore L A, Gerard C, Drazen J M
Department of Medicine, Brigham and Women's Hospital, Boston, MA.
Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7461-5. doi: 10.1073/pnas.90.16.7461.
gamma-Glutamyl transpeptidase (EC 2.3.2.2, gamma GT) is a membrane-bound ectoenzyme that plays an important role in the metabolism of glutathione. It is composed of two subunits, both of which are encoded by a common mRNA. We examined the expression of gamma GT in human lung tissue by Northern blot analysis and screening a cDNA library made from human lung poly(A)+ RNA. Our results show that there are two gamma GT mRNA populations in human lung tissue. We define these as group I (2.4 kb) and group II (approximately 1.2 kb) transcripts. In the present communication, we characterize the unique lung transcript. Sequence analysis of representative clones shows that group I transcripts are virtually identical to those previously isolated from liver and placenta but possess a unique 5' untranslated region. In marked contrast, group II transcripts appear to be human-lung-specific. Group II transcripts appear on Northern blots probed with full-length or 3'-biased gamma GT cDNA. Sequence analysis of group II clones shows them to be homologous with group I clones in the region that encodes the reading frame for the light chain; however, they possess a series of unique 5' untranslated regions, which suggests that they arise from lung-specific message processing. Additionally, approximately 50% of the isolated group II clones contain 34 nt substitutions compared with the "wild-type" gamma GT transcripts. These data indicate that human lung expresses unique gamma GT transcripts of unknown function as well as the classical form. The abundant group II transcripts may encode part of a heterodimer related to gamma GT or represent processed lung-specific pseudogenes.
γ-谷氨酰转肽酶(EC 2.3.2.2,γGT)是一种膜结合的胞外酶,在谷胱甘肽代谢中起重要作用。它由两个亚基组成,这两个亚基均由一个共同的mRNA编码。我们通过Northern印迹分析并筛选由人肺聚腺苷酸加尾RNA构建的cDNA文库,检测了γGT在人肺组织中的表达。我们的结果表明,人肺组织中有两种γGT mRNA群体。我们将其定义为I组(2.4 kb)和II组(约1.2 kb)转录本。在本通讯中,我们对独特的肺转录本进行了表征。代表性克隆的序列分析表明,I组转录本实际上与先前从肝脏和胎盘中分离出的转录本相同,但具有独特的5'非翻译区。与之形成鲜明对比的是,II组转录本似乎是人类肺特异性的。用全长或3'偏向性γGT cDNA探针进行Northern印迹时可出现II组转录本。II组克隆的序列分析表明,它们在编码轻链阅读框的区域与I组克隆同源;然而,它们具有一系列独特的5'非翻译区,这表明它们源自肺特异性的信息加工。此外,与“野生型”γGT转录本相比,约50%的分离出的II组克隆含有34个核苷酸的替换。这些数据表明,人肺不仅表达功能未知的独特γGT转录本,还表达经典形式。丰富的II组转录本可能编码与γGT相关的异二聚体的一部分,或者代表经过加工的肺特异性假基因。