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绵羊6-磷酸葡萄糖酸脱氢酶。基于通过聚合酶链反应获得的cDNA克隆序列修订的蛋白质序列。

Sheep 6-phosphogluconate dehydrogenase. Revised protein sequence based upon the sequences of cDNA clones obtained with the polymerase chain reaction.

作者信息

Somers D O, Medd S M, Walker J E, Adams M J

机构信息

M.R.C. Laboratory of Molecular Biology, Cambridge, U.K.

出版信息

Biochem J. 1992 Dec 15;288 ( Pt 3)(Pt 3):1061-7. doi: 10.1042/bj2881061.

Abstract

Sheep liver 6-phosphogluconate dehydrogenase (6-PGDH) is an enzyme of the pentose phosphate pathway. Evidence has appeared which suggests that the 6-PGDH protein sequence determined previously by direct analysis of the protein isolated from ovine liver is incorrect. Determining the enzyme's DNA sequence was considered to be the best way of solving the problem. In the first instance, a degenerate forward and a degenerate reverse primer were designed on the basis of the known protein sequence, and a partial-length cDNA clone was isolated from total sheep liver cDNA using the polymerase chain reaction. The clone encoded the expected part of the protein sequence. The clone was unsuccessfully used as a prime-cut probe to screen a sheep liver library and a bovine heart library. As a result, the polymerase chain reaction was utilized again to successfully generate a family of overlapping cDNA clones encoding a mature protein of 482 amino acids. The mature protein sequence encoded by the cDNA differs significantly from the sequence derived by direct analysis of the protein, but on closer examination the fundamental difference is caused by the incorrect placement of three enzyme fragments obtained by cyanogen bromide cleavage during the direct sequence analysis of the protein. Placing the fragments in the correct order results in the two sequences being virtually identical except for some minor amino acid changes between the amide and acid forms, and a small number of deletions and insertions.

摘要

绵羊肝脏6-磷酸葡萄糖酸脱氢酶(6-PGDH)是戊糖磷酸途径中的一种酶。已有证据表明,先前通过直接分析从绵羊肝脏分离的蛋白质所确定的6-PGDH蛋白质序列是不正确的。确定该酶的DNA序列被认为是解决该问题的最佳方法。首先,根据已知的蛋白质序列设计了一个简并正向引物和一个简并反向引物,并使用聚合酶链反应从绵羊肝脏总cDNA中分离出一个部分长度的cDNA克隆。该克隆编码了预期的部分蛋白质序列。该克隆作为引物切割探针用于筛选绵羊肝脏文库和牛心脏文库,但未成功。结果,再次利用聚合酶链反应成功产生了一系列重叠的cDNA克隆,这些克隆编码一个由482个氨基酸组成的成熟蛋白质。由cDNA编码的成熟蛋白质序列与通过直接分析蛋白质得出的序列有显著差异,但仔细检查发现,根本差异是由于在蛋白质直接序列分析过程中,溴化氰裂解得到的三个酶片段位置错误所致。将这些片段按正确顺序排列后,除了酰胺形式和酸形式之间的一些小氨基酸变化以及少量缺失和插入外,两个序列几乎相同。

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