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首页> 外文期刊>Cancer biology & therapy >Evidence that hMLH3 functions primarily in meiosis and in hMSH2-hMSH3 mismatch repair
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Evidence that hMLH3 functions primarily in meiosis and in hMSH2-hMSH3 mismatch repair

机译:hMLH3主要在减数分裂和hMSH2-hMSH3错配修复中起作用的证据

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摘要

The MutS (MSH) and MutL (MLH) homologs are conserved proteins that function in mismatch repair (MMR) and meiosis. We examined mRNA and protein expression of hMLH3 compared to other human MSH and MLH in a panel of human tissues and the HeLa cell line. Quantitative PCR suggests that MSH and MLH transcripts are expressed ubiquitously. hMLH3 mRNA is present at low levels in numerous tissues. Protein expression appears to correlate with a threshold of mRNA expression with hMLH3 present at high levels in testis. In addition, we have found and mapped interactions between hMLHl and hMLH3 with hMSH3. These data are consistent with yeast studies and suggest a role for hMLH3 in meiosis as well as hMSH2-hMSH3 repair processes and little if any role in Hereditary Non-Polyposis Colorectal Cancer (HNPCC).
机译:MutS(MSH)和MutL(MLH)同源物是在失配修复(MMR)和减数分裂中起作用的保守蛋白。我们在一组人类组织和HeLa细胞系中检测了与其他人类MSH和MLH相比的hMLH3的mRNA和蛋白质表达。定量PCR表明MSH和MLH转录物无处不在表达。 hMLH3 mRNA在许多组织中含量较低。蛋白表达似乎与睾丸中高水平存在hMLH3的mRNA表达阈值相关。另外,我们已经发现并映射了hMLH1和hMLH3与hMSH3之间的相互作用。这些数据与酵母菌研究一致,表明hMLH3在减数分裂以及hMSH2-hMSH3修复过程中的作用,在遗传性非多发性结肠直肠癌(HNPCC)中几乎没有作用。

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