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首页> 外文期刊>DNA research: an international journal for rapid publication of reports on genes and genomes >cDNA cloning, tissue expression, and chromosomal assignment of a mouse gene, encoding a 127 kDa UV-damaged DNA binding protein which is defective in XPE cells.
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cDNA cloning, tissue expression, and chromosomal assignment of a mouse gene, encoding a 127 kDa UV-damaged DNA binding protein which is defective in XPE cells.

机译:小鼠基因的cDNA克隆,组织表达和染色体分配,编码在XPE细胞中有缺陷的127kDa紫外损的DNA结合蛋白。

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摘要

A subset of xeroderma pigmentosum (XP) group E cells lack a factor of the UV-damaged DNA binding activity. Both 127 kDa and 48 kDa proteins have been reported to be responsible for the binding activity. A cDNA for the 127 kDa UV-damaged DNA-binding protein (p127-Ddb1) was isolated from a mouse fetal brain full length-enriched cDNA library, and an open reading frame of 1140 amino acids was identified. Reverse transcription-coupled polymerase chain reaction (RT-PCR) showed that mouse Ddb1 messenger is ubiquitously expressed in adult tissues as well as in embryo's. The gene was mapped to near the public locus D19Mit22 region of mouse chromosome 19.
机译:Xeroderma Pigmentosum(XP)组E细胞的子集缺乏UV受损DNA结合活性的因子。 据报道,127kDA和48kDa蛋白均负责结合活性。 从小鼠胎儿脑全长富集的cDNA文库中分离出127kDa紫外损损伤的DNA结合蛋白(P127-DDB1)的cDNA,并鉴定了1140氨基酸的开放阅读框。 逆转录偶联聚合酶链反应(RT-PCR)显示,小鼠DDB1信使在成人组织和胚胎中普遍地表达。 将该基因映射到小鼠染色体19的公共轨迹D19MIT22区域附近。

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