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人类和烟草细胞中不同的基因组维持策略。

Different genome maintenance strategies in human and tobacco cells.

作者信息

Pelczar Pawel, Kalck Véronique, Kovalchuk Igor

机构信息

Friedrich Miescher Institute, PO Box 2543, CH-4002 Basel, Switzerland.

出版信息

J Mol Biol. 2003 Aug 22;331(4):771-9. doi: 10.1016/s0022-2836(03)00839-8.

Abstract

In this work, genome maintenance strategies of organisms belonging to different kingdoms (animals versus plants) but of similar genome size were investigated using a novel, universal double-strand break (DSB) repair assay. Different plasmids linearised with KpnI, Acc65I or EcoRV yielding either 3' or 5' protruding or blunt DNA termini, respectively, were transfected into HeLa cells and Nicotiana plumbaginifolia protoplasts and assayed for the efficiency and fidelity of DSB repair. We show that the mechanism of break sealing is similar but that drastic differences are seen in the fidelity of repair: in HeLa cells, 50-55% DSBs were repaired precisely, compared to as little as 15-30% in tobacco cells. Moreover, the DSB repair in plants resulted in 30-40% longer deletions and significantly shorter insertions. Combined, these led to more than twofold larger net DNA loss in tobacco cells. Our observations point to possible differences in the strategies of DSB repair and genome maintenance in plants and animals.

摘要

在这项工作中,我们使用一种新颖的通用双链断裂(DSB)修复检测方法,研究了不同界(动物与植物)但基因组大小相似的生物体的基因组维持策略。分别用KpnI、Acc65I或EcoRV线性化产生3'或5'突出端或平端DNA末端的不同质粒,转染到HeLa细胞和烟草叶肉原生质体中,并检测DSB修复的效率和保真度。我们发现断裂封闭机制相似,但修复保真度存在显著差异:在HeLa细胞中,50 - 55%的DSB得到精确修复,而在烟草细胞中这一比例低至15 - 30%。此外,植物中的DSB修复导致的缺失长30 - 40%,插入明显更短。综合起来,这导致烟草细胞中的净DNA损失增加了两倍多。我们的观察结果表明,植物和动物在DSB修复和基因组维持策略上可能存在差异。

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