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XPB和XPD DNA解旋酶是p53介导的凋亡途径的组成部分。

The XPB and XPD DNA helicases are components of the p53-mediated apoptosis pathway.

作者信息

Wang X W, Vermeulen W, Coursen J D, Gibson M, Lupold S E, Forrester K, Xu G, Elmore L, Yeh H, Hoeijmakers J H, Harris C C

机构信息

Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-4255, USA.

出版信息

Genes Dev. 1996 May 15;10(10):1219-32. doi: 10.1101/gad.10.10.1219.

Abstract

The molecular pathway of p53-dependent apoptosis (programmed cell death) is poorly understood. Because p53 binds to the basal transcription-repair complex TFIIH and modulates its DNA helicase activities, we hypothesized that TFIIH DNA helicases XPB and XPD are members of the p53-mediated apoptotic pathway. Whereas transfer of a wild-type p53 expression vector by microinjection or retroviral infection into primary normal human fibroblasts resulted in apoptosis, primary fibroblasts from individuals with xeroderma pigmentosum (XP), who are deficient in DNA repair and have germ-line mutations in the XPB or XPD gene, but not in the XPA or XPC gene, have a deficiency in the apoptotic response. This deficiency can be rescued by transferring the wild-type XPB or XPD gene into the corresponding mutant cells. XP-D lymphocytes also have a decreased apoptotic response to DNA damage by adriamycin, indicating a physiologically relevant deficiency. The XP-B or XP-D mutant cells undergo a normal apoptotic response when microinjected with the Ich-L, and ICE genes. Analyses of p53 mutants and the effects of microinjected anti-p53 antibody, Pab421, indicate that the carboxyl terminus of p53 may be required for apoptosis. Direct microinjection of the p53 carboxy-terminal-derived peptide (amino acid residues 319-393) resulted in apoptosis of primary normal human fibroblasts. These results disclose a novel pathway of p53-induced apoptosis.

摘要

p53依赖的细胞凋亡(程序性细胞死亡)的分子途径目前还了解甚少。由于p53与基础转录修复复合物TFIIH结合并调节其DNA解旋酶活性,我们推测TFIIH DNA解旋酶XPB和XPD是p53介导的细胞凋亡途径的成员。通过显微注射或逆转录病毒感染将野生型p53表达载体导入原代正常人成纤维细胞会导致细胞凋亡,而来自着色性干皮病(XP)患者的原代成纤维细胞,这些患者存在DNA修复缺陷且在XPB或XPD基因中有种系突变,但在XPA或XPC基因中没有,它们在细胞凋亡反应方面存在缺陷。通过将野生型XPB或XPD基因导入相应的突变细胞可以挽救这种缺陷。XP-D淋巴细胞对阿霉素引起的DNA损伤的细胞凋亡反应也降低,表明存在生理相关的缺陷。当用Ich-L和ICE基因进行显微注射时,XP-B或XP-D突变细胞会经历正常的细胞凋亡反应。对p53突变体以及显微注射抗p53抗体Pab421的效果分析表明,p53的羧基末端可能是细胞凋亡所必需的。直接显微注射p53羧基末端衍生肽(氨基酸残基319 - 393)会导致原代正常人成纤维细胞凋亡。这些结果揭示了一种p53诱导细胞凋亡的新途径。

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