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Xpa基因敲除小鼠。

Xpa knockout mice.

作者信息

de Vries A, van Steeg H

机构信息

Department of Carcinogenesis, Mutagenesis and Genetics, National Institute of Public Health and Environment, Bilthoven, The Netherlands.

出版信息

Semin Cancer Biol. 1996 Oct;7(5):229-40. doi: 10.1006/scbi.1996.0031.

Abstract

The xeroderma pigmentosum group A correcting (XPA) gene encodes a DNA binding zinc-finger protein that recognizes DNA damage. As such the XPA protein participates in the initial step of the process of nucleotide excision repair. The multicomponent nucleotide excision repair pathway is one of the most thoroughly studied mechanisms that defends both eukaryotic and prokaryotic cells against the deleterious effects of UV-B and several chemical components. In the absence of nucleotide excision repair common cellular processes like transcription and replication are disturbed by persisting (unrepaired) DNA lesions (adducts), which may lead to the accumulation of gene mutations and ultimately to cancer. Xeroderma pigmentosum patients have a > 2000 fold increased risk to develop skin cancer at sun-exposed areas. Here we describe that XPA-deficient transgenic mice show features that mimic the phenotype found in humans. Furthermore, the possible use of Xpa- and other nucleotide excision repair deficient mice in cancer research will be outlined in more detail.

摘要

着色性干皮病A组修复(XPA)基因编码一种识别DNA损伤的DNA结合锌指蛋白。因此,XPA蛋白参与核苷酸切除修复过程的起始步骤。多组分核苷酸切除修复途径是最深入研究的机制之一,可保护真核细胞和原核细胞免受UV-B和几种化学成分的有害影响。在缺乏核苷酸切除修复的情况下,常见的细胞过程如转录和复制会因持续存在(未修复)的DNA损伤(加合物)而受到干扰,这可能导致基因突变的积累并最终引发癌症。着色性干皮病患者在阳光暴露部位患皮肤癌的风险增加超过2000倍。在此我们描述XPA缺陷转基因小鼠表现出类似于人类中发现的表型特征。此外,将更详细地概述Xpa和其他核苷酸切除修复缺陷小鼠在癌症研究中的可能用途。

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