Tutic M, Lu X A, Schirmer R H, Werner D
Institute of Cell and Tumor Biology, German Cancer Research Center, Heidelberg.
Eur J Biochem. 1990 Mar 30;188(3):523-8. doi: 10.1111/j.1432-1033.1990.tb15431.x.
The molecular cloning of a partial cDNA to mouse glutathione reductase mRNA and of a full-length cDNA to the mRNA of the human enzyme is described. An initial cDNA clone designated lambda GRM-B11 was isolated by plaque-screening of an induced mouse cDNA expression library in the lambda gt11 vector with a rabbit antibody probe to human glutathione reductase. 125Iodine-labelled whole anti-rabbit immunoglobulin was used as second antibody. EcoRI digestion of the lambda GRM-B11 clone released a 720-bp fragment which was identified as a partial mouse glutathione reductase cDNA by the following techniques. (a) Escherichia coli Y1089 lysogenized with lambda GRM-B11 could be induced to synthesize a recombinant polypeptide whose antigenicity to anti-(glutathione reductase) serum was established by SDS/polyacrylamide gel electrophoresis and subsequent immunoblotting. (b) The GRM-B11 sequence, recloned in the Bluescript vector to give the plasmid pGRM-B11, was found to code for a polypeptide consisting of 242 amino acid residues exhibiting 82% identities with the known amino acid sequence of the human glutathione reductase from position 77 to 318. The insert of the pGRM-B11 plasmid was used as a bona fide nucleic acid probe to screen mouse and human cDNA libraries prepared in the lambda gt11 or in the lambda gt10 vector. The first full-length cDNA clone (lambda GRH-Mev10) was identified in a human cDNA library based on RNA of human placental cells. Its insert was composed of three EcoRI fragments of 720, 613 and 336 bp. The three fragments were recloned in the Bluescript vector and sequenced. The largest fragment (pGRH-B) is colinear with the mouse sequence cloned in the pGRM-B11 plasmid. The fragment of intermediate size (pGRH-CT) comprises the 3' end of the mRNA and the poly(A) tail while the short fragment (pGRH-NT) corresponds to the 5' region of the mRNA. The amino acid sequence deduced from the nucleotide sequences of the three subclones is identical with the known sequence of the mature glutathione reductase from human erythrocytes in all 478 positions.
本文描述了小鼠谷胱甘肽还原酶mRNA部分cDNA以及人谷胱甘肽还原酶mRNA全长cDNA的分子克隆。最初的cDNA克隆命名为λGRM - B11,通过用针对人谷胱甘肽还原酶的兔抗体探针筛选λgt11载体中的诱导型小鼠cDNA表达文库获得。用125碘标记的抗兔全免疫球蛋白作为二抗。λGRM - B11克隆经EcoRI酶切后释放出一个720 bp的片段,通过以下技术鉴定该片段为小鼠谷胱甘肽还原酶的部分cDNA。(a) 用λGRM - B11溶源化的大肠杆菌Y1089可被诱导合成一种重组多肽,其对抗(谷胱甘肽还原酶)血清的抗原性通过SDS/聚丙烯酰胺凝胶电泳及随后的免疫印迹得以确定。(b) 在蓝思质粒载体中重新克隆的GRM - B11序列被发现编码一个由242个氨基酸残基组成的多肽,该多肽在第77位至318位氨基酸残基处与已知的人谷胱甘肽还原酶氨基酸序列具有82%的同源性。pGRM - B11质粒的插入片段被用作真正的核酸探针,以筛选在λgt11或λgt10载体中构建的小鼠和人cDNA文库。在基于人胎盘细胞RNA构建的人cDNA文库中鉴定出了第一个全长cDNA克隆(λGRH - Mev10)。其插入片段由三个EcoRI片段组成,分别为720 bp、613 bp和336 bp。这三个片段在蓝思质粒载体中重新克隆并进行测序。最大的片段(pGRH - B)与克隆在pGRM - B11质粒中的小鼠序列共线性。中等大小的片段(pGRH - CT)包含mRNA的3'末端和poly(A)尾,而短片段(pGRH - NT)对应于mRNA的5'区域。从这三个亚克隆的核苷酸序列推导的氨基酸序列在所有478个位置上与已知的人红细胞成熟谷胱甘肽还原酶序列相同。