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哺乳动物DNA连接酶III:分子克隆、染色体定位及在减数分裂重组的精母细胞中的表达。

Mammalian DNA ligase III: molecular cloning, chromosomal localization, and expression in spermatocytes undergoing meiotic recombination.

作者信息

Chen J, Tomkinson A E, Ramos W, Mackey Z B, Danehower S, Walter C A, Schultz R A, Besterman J M, Husain I

机构信息

Department of Cell Biology, Glaxo Research Institute, Research Triangle Park, North Carolina 27709, USA.

出版信息

Mol Cell Biol. 1995 Oct;15(10):5412-22. doi: 10.1128/MCB.15.10.5412.

Abstract

Three biochemically distinct DNA ligase activities have been identified in mammalian cell extracts. We have recently purified DNA ligase II and DNA ligase III to near homogeneity from bovine liver and testis tissue, respectively. Amino acid sequencing studies indicated that these enzymes are encoded by the same gene. In the present study, human and murine cDNA clones encoding DNA ligase III were isolated with probes based on the peptide sequences. The human DNA ligase III cDNA encodes a polypeptide of 862 amino acids, whose sequence is more closely related to those of the DNA ligases encoded by poxviruses than to replicative DNA ligases, such as human DNA ligase I. In vitro transcription and translation of the cDNA produced a catalytically active DNA ligase similar in size and substrate specificity to the purified bovine enzyme. The DNA ligase III gene was localized to human chromosome 17, which eliminated this gene as a candidate for the cancer-prone disease Bloom syndrome that is associated with DNA joining abnormalities. DNA ligase III is ubiquitously expressed at low levels, except in the testes, in which the steady-state levels of DNA ligase III mRNA are at least 10-fold higher than those detected in other tissues and cells. Since DNA ligase I mRNA is also present at high levels in the testes, we examined the expression of the DNA ligase genes during spermatogenesis. DNA ligase I mRNA expression correlated with the contribution of proliferating spermatogonia cells to the testes, in agreement with the previously defined role of this enzyme in DNA replication. In contrast, elevated levels of DNA ligase III mRNA were observed in primary spermatocytes undergoing recombination prior to the first meiotic division. Therefore, we suggest that DNA ligase III seals DNA strand breaks that arise during the process of meiotic recombination in germ cells and as a consequence of DNA damage in somatic cells.

摘要

在哺乳动物细胞提取物中已鉴定出三种生化性质不同的DNA连接酶活性。我们最近分别从牛肝和睾丸组织中纯化出了近乎纯品的DNA连接酶II和DNA连接酶III。氨基酸测序研究表明,这些酶由同一基因编码。在本研究中,基于肽序列的探针分离出了编码DNA连接酶III的人和小鼠cDNA克隆。人DNA连接酶III cDNA编码一个862个氨基酸的多肽,其序列与痘病毒编码的DNA连接酶的序列比与复制性DNA连接酶(如人DNA连接酶I)的序列更为密切相关。该cDNA的体外转录和翻译产生了一种催化活性的DNA连接酶,其大小和底物特异性与纯化的牛酶相似。DNA连接酶III基因定位于人类染色体17,这排除了该基因作为与DNA连接异常相关的易患癌症疾病布卢姆综合征的候选基因。DNA连接酶III在除睾丸外的其他组织中均以低水平普遍表达,在睾丸中,DNA连接酶III mRNA的稳态水平比在其他组织和细胞中检测到的水平至少高10倍。由于DNA连接酶I mRNA在睾丸中也高水平存在,我们研究了精子发生过程中DNA连接酶基因的表达。DNA连接酶I mRNA的表达与增殖性精原细胞对睾丸的贡献相关,这与该酶先前确定的在DNA复制中的作用一致。相反,在第一次减数分裂前进行重组的初级精母细胞中观察到DNA连接酶III mRNA水平升高。因此,我们认为DNA连接酶III封闭了生殖细胞减数分裂重组过程中以及体细胞DNA损伤时产生的DNA链断裂。

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