首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >Karyomegalic interstitial nephritis and DNA damage-induced polyploidy in Fan1 nuclease-defective knock-in mice
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Karyomegalic interstitial nephritis and DNA damage-induced polyploidy in Fan1 nuclease-defective knock-in mice

机译:Fan1核酸酶缺陷敲入小鼠的核糖体间质性肾炎和DNA损伤诱导的多倍体。

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摘要

The Fan1 endonuclease is required for repair of DNA interstrand cross-links (ICLs). Mutations in human Fan1 cause karyomegalic interstitial nephritis (KIN), but it is unclear whether defective ICL repair is responsible or whether Fan1 nuclease activity is relevant. We show that Fan1 nuclease-defective (Fan1(ndd)) mice develop a mild form of KIN. The karyomegalic nuclei from Fan1(ndd) kidneys are polyploid, and fibroblasts fromFan1(ndd) mice become polyploid upon ICL induction, suggesting that defective ICL repair causes karyomegaly. Thus, Fan1 nuclease activity promotes ICL repair in a manner that controls ploidy, a role that we show is not shared by the Fanconi anemia pathway or the Slx4-Slx1 nuclease also involved in ICL repair.
机译:Fan1内切核酸酶是修复DNA链间交联(ICL)所必需的。人类Fan1的突变会引起核仁性间质性肾炎(KIN),但尚不清楚ICL修复缺陷是负责任的还是Fan1核酸酶活性是否相关。我们显示,Fan1核酸酶缺陷(Fan1(nd / nd))小鼠发展的皮肤的轻度形式。 Fan1(nd / nd)肾脏的核巨细胞核是多倍体,Fan1(nd / nd)小鼠的成纤维细胞在ICL诱导后变成多倍体,这表明ICL修复缺陷会导致核仁肿大。因此,Fan1核酸酶活性以控制倍性的方式促进ICL修复,我们显示的作用与Fanconi贫血途径或也参与ICL修复的Slx4-Slx1核酸酶不共有。

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