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A human poly(ADP-ribose) polymerase gene family (ADPRTL): cDNA cloning of two novel poly(ADP-ribose) polymerase homologues.

机译:人类聚(ADP-核糖)聚合酶基因家族(ADPRTL):两种新型聚(ADP-核糖)聚合酶同源物的cDNA克隆。

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摘要

Posttranscriptional modification of nuclear proteins by poly(ADP-ribosyl)ation in response to DNA strand breaks plays an important role in DNA repair, regulation of apoptosis, and maintenance of genomic stability. A 113-kDa human poly(ADP-ribose) polymerase (PARP) has previously been identified and cloned. However, there is evidence that additional enzymes with PARP activity exist in mammalian cells. I have identified and cloned the cDNAs of two novel approximately 60-kDa human proteins that are 40 and 31% identical to the catalytic C-terminal domain of PARP. These proteins, named PARP-2 and PARP-3, lack the DNA-binding and automodification domains. PARP-2 and PARP-3 mRNAs were detected in 16 different human tissues as major bands of 2.0 and 2.2 kb, respectively. Radiation hybrid analysis assigned the PARP-2 gene (HGMW-approved symbol ADPRTL2) to chromosome 14q11.2-q12 and the PARP-3 gene (HGMW-approved symbol ADPRTL3) to 3p21.1-p22.2. This report shows the existence of a human PARP gene family with at least three closely related members. Copyright 1999 Academic Press.
机译:响应于DNA链断裂,通过聚(ADP-核糖基)修饰核蛋白的转录后修饰在DNA修复,凋亡调控和基因组稳定性维持中起着重要作用。先前已确定并克隆了一个113 kDa的人类聚(ADP-核糖)聚合酶(PARP)。但是,有证据表明哺乳动物细胞中还存在其他具有PARP活性的酶。我已经鉴定并克隆了两种新颖的约60kDa人蛋白质的cDNA,它们与PARP的催化C端结构域具有40%和31%的同一性。这些被称为PARP-2和PARP-3的蛋白质缺少DNA结合和自修饰域。在16个不同的人体组织中分别以2.0 kb和2.2 kb的主要条带检测到PARP-2和PARP-3 mRNA。辐射杂交分析将PARP-2基因(HGMW批准的符号ADPRTL2)分配给了14q11.2-q12染色体,并将PARP-3基因(HGMW批准的符号ADPRTL3)分配给了3p21.1-p22.2。该报告显示了具有至少三个密切相关的成员的人类PARP基因家族的存在。版权所有1999 Academic Press。

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