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粟酒裂殖酵母POL3基因产物的特性表明DNA聚合酶δ催化亚基存在种间保守性。

Characterization of the POL3 gene product from Schizosaccharomyces pombe indicates inter-species conservation of the catalytic subunit of DNA polymerase delta.

作者信息

Pignède G, Bouvier D, de Recondo A M, Baldacci G

机构信息

Laboratoire de Biologie Moléculaire de la Réplication UPR 272 IRSC-CNRS, Villejuif, France.

出版信息

J Mol Biol. 1991 Nov 20;222(2):209-18. doi: 10.1016/0022-2836(91)90207-m.

Abstract

The Schizosaccharomyces pombe POL3 gene was isolated by sequence homology with a region of the Saccharomyces cerevisiae POL3 gene, the only gene sequenced to date encoding the catalytic subunit of eukaryotic DNA polymerase delta. The fission yeast POL3 gene contains a 52 base-pair (bp) intron and encodes a 3600 bp transcript the 5'-end of which is located 32 bp upstream from the initiation codon. The polypeptides predicted from budding and fission yeast POL3 genes share 52% of conserved amino acid residues and have a 60% identical central region. This structural conservation of the catalytic subunit of DNA polymerases delta is probably related to functional constraints. A portion of the most conserved region was used to raise antibodies against an S. pombe polymerase delta/beta-galactosidase fusion protein expressed in Escherichia coli. The purified antibodies recognized a 123,000 Da protein in S. pombe wild-type cell extracts and inhibited an aphidicolin-sensitive DNA polymerase activity that was distinct from DNA polymerase alpha. The antibodies also detected a 140,000 Da protein in extracts from different proliferating mammalian cells, indicating that the catalytic subunits of DNA polymerase delta are highly conserved between yeast and higher eukaryotes.

摘要

粟酒裂殖酵母POL3基因是通过与酿酒酵母POL3基因的一个区域进行序列同源性分析而分离得到的,酿酒酵母POL3基因是迄今为止唯一测序的编码真核DNA聚合酶δ催化亚基的基因。裂殖酵母POL3基因含有一个52个碱基对(bp)的内含子,编码一个3600 bp的转录本,其5'端位于起始密码子上游32 bp处。从芽殖酵母和裂殖酵母POL3基因预测的多肽共有52%的保守氨基酸残基,且中央区域有60%的同一性。DNA聚合酶δ催化亚基的这种结构保守性可能与功能限制有关。利用最保守区域的一部分制备了针对在大肠杆菌中表达的粟酒裂殖酵母聚合酶δ/β-半乳糖苷酶融合蛋白的抗体。纯化的抗体在粟酒裂殖酵母野生型细胞提取物中识别出一种123,000 Da的蛋白质,并抑制了一种对阿非科林敏感的DNA聚合酶活性,该活性不同于DNA聚合酶α。这些抗体还在来自不同增殖哺乳动物细胞的提取物中检测到一种140,000 Da的蛋白质,表明DNA聚合酶δ的催化亚基在酵母和高等真核生物之间高度保守。

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