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多聚(ADP-核糖)聚合酶参与拟南芥微同源介导的备份非同源末端连接。

Poly(ADP-ribose)polymerases are involved in microhomology mediated back-up non-homologous end joining in Arabidopsis thaliana.

机构信息

Department of Molecular and Developmental Genetics, Institute of Biology, Leiden University, Leiden, The Netherlands.

出版信息

Plant Mol Biol. 2013 Jul;82(4-5):339-51. doi: 10.1007/s11103-013-0065-9. Epub 2013 Apr 28.

Abstract

Besides the KU-dependent classical non-homologous end-joining (C-NHEJ) pathway, an alternative NHEJ pathway first identified in mammalian systems, which is often called the back-up NHEJ (B-NHEJ) pathway, was also found in plants. In mammalian systems PARP was found to be one of the essential components in B-NHEJ. Here we investigated whether PARP1 and PARP2 were also involved in B-NHEJ in Arabidopsis. To this end Arabidopsis parp1, parp2 and parp1parp2 (p1p2) mutants were isolated and functionally characterized. The p1p2 double mutant was crossed with the C-NHEJ ku80 mutant resulting in the parp1parp2ku80 (p1p2k80) triple mutant. As expected, because of their role in single strand break repair (SSBR) and base excision repair (BER), the p1p2 and p1p2k80 mutants were shown to be sensitive to treatment with the DNA damaging agent MMS. End-joining assays in cell-free leaf protein extracts of the different mutants using linear DNA substrates with different ends reflecting a variety of double strand breaks were performed. The results showed that compatible 5'-overhangs were accurately joined in all mutants, that KU80 protected the ends preventing the formation of large deletions and that PARP proteins were involved in microhomology mediated end joining (MMEJ), one of the characteristics of B-NHEJ.

摘要

除了 KU 依赖性经典非同源末端连接(C-NHEJ)途径外,哺乳动物系统中首次鉴定的替代 NHEJ 途径,通常称为备用 NHEJ(B-NHEJ)途径,也在植物中发现。在哺乳动物系统中,PARP 被发现是 B-NHEJ 的必需组成部分之一。在这里,我们研究了 PARP1 和 PARP2 是否也参与了拟南芥中的 B-NHEJ。为此,分离并功能表征了拟南芥 parp1、parp2 和 parp1parp2(p1p2)突变体。将 p1p2 双突变体与 C-NHEJ ku80 突变体杂交,得到 parp1parp2ku80(p1p2k80)三突变体。正如预期的那样,由于它们在单链断裂修复(SSBR)和碱基切除修复(BER)中的作用,p1p2 和 p1p2k80 突变体对 DNA 损伤剂 MMS 的处理表现出敏感性。使用具有不同末端的线性 DNA 底物在不同突变体的无细胞叶蛋白提取物中进行末端连接测定,这些末端反映了各种双链断裂。结果表明,在所有突变体中都准确地连接了兼容的 5'-突出端,KU80 保护末端防止形成大的缺失,并且 PARP 蛋白参与微同源介导的末端连接(MMEJ),这是 B-NHEJ 的特征之一。

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