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拟南芥DNA连接酶I同源物的分子克隆与功能分析。

Molecular cloning and functional analysis of the Arabidopsis thaliana DNA ligase I homologue.

作者信息

Taylor R M, Hamer M J, Rosamond J, Bray C M

机构信息

School of Biological Sciences, University of Manchester, UK.

出版信息

Plant J. 1998 Apr;14(1):75-81. doi: 10.1046/j.1365-313x.1998.00094.x.

Abstract

A cDNA encoding the DNA ligase I homologue has been isolated from Arabidopsis thaliana using a degenerate PCR approach. The ORF of this cDNA encodes an amino acid sequence of 790 residues, representing a protein with a theoretical molecular mass of 87.8 kDa and an isoelectric point (pi) of 8.20. Alignment of the A. thaliana DNA ligase protein sequence with the sequence of DNA ligases from human (Homo sapiens), murine (Mus musculus), clawed toad (Xenopus laevis) and the yeasts Schizosaccharomyces pombe and Saccharomyces cerevisiae showed good sequence homology (42-45% identity, 61-66% similarity), particularly around the active site. Sequence data indicate that the Arabidopsis DNA ligase is the homologue of the animal DNA ligase I species. Functional analysis of the cDNA clone demonstrated its ability to complement the conditional lethal phenotype of an S. cerevisiae cdc9 mutant defective in DNA ligase activity, confirming that the cloned sequence encodes an active DNA ligase. The level of the DNA ligase transcript was not increased in A. thaliana seedlings in response to DNA damage induced by a period of enhanced UV-B irradiation. However, the cellular level of the DNA ligase mRNA transcript does correlate with the replicative state of plant cells.

摘要

利用简并PCR方法从拟南芥中分离出一个编码DNA连接酶I同源物的cDNA。该cDNA的开放阅读框编码一个由790个氨基酸残基组成的氨基酸序列,代表一种理论分子量为87.8 kDa、等电点(pi)为8.20的蛋白质。将拟南芥DNA连接酶蛋白序列与人(智人)、小鼠(小家鼠)、爪蟾(非洲爪蟾)以及裂殖酵母和酿酒酵母的DNA连接酶序列进行比对,结果显示出良好的序列同源性(同一性为42 - 45%,相似性为61 - 66%),尤其是在活性位点周围。序列数据表明,拟南芥DNA连接酶是动物DNA连接酶I类的同源物。对该cDNA克隆的功能分析表明,它能够弥补DNA连接酶活性缺陷的酿酒酵母cdc9突变体的条件致死表型,证实克隆的序列编码一种活性DNA连接酶。在经一段时间增强UV - B辐射诱导DNA损伤后,拟南芥幼苗中DNA连接酶转录本的水平并未升高。然而,DNA连接酶mRNA转录本的细胞水平确实与植物细胞的复制状态相关。

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