厦门大学生命科学学院细胞应急生物学国家重点实验室,厦门大学生命科学学院细胞应急生物学国家重点实验室,厦门大学生命科学学院细胞应急生物学国家重点实验室或国家海洋局第三海洋研究所海洋生物遗传资源重点实验室
细胞应激生物学国家重点实验室开放课题(SKLCSB2016KF003)
The State Key Laboratory of the Cellular Stress Biology, School of Life Sciences, Xiamen University,The State Key Laboratory of the Cellular Stress Biology, School of Life Sciences, Xiamen University,The State Key Laboratory of the Cellular Stress Biology, School of Life Sciences, Xiamen University or The Key Laboratory of Marine Biogenetic Resources, Third Institute of Oceanography, State Oceanic
This work was supported by a grant from Open Research Fund of State Key Laboratory of Cellular Stress Biology, Xiamen University (SKLCSB2016KF003)
同源重组是细胞非常重要的生命活动,参与维持基因组的完整性与稳定性,且与人类健康密切相关.同源重组的研究不断取得进步.本文讨论了同源重组的模式,重组酶RecA/Rad51的作用机制以及Rad51调节蛋白对Rad51入核及Rad51参与重组过程中的单链结合、同源配对、入侵及链交换阶段的调控,将有利于我们对同源重组的深入了解.
Homologous recombination (HR) is an important biological activity in the cells, indispensable for the maintenance of genome integrity and stability and closely relative to the human health. In recent years, there is a great progress in this field. Here, we recapitulated four models of HR repair for DNA double-strand break, the mechanism for recombinase RacA/Rad51 action, and the regulation of Rad51 by Rad51 mediators involved in the process of Rad51 nuclear localization, Rad51 binding to ssDNA, homologous DNA pairing, strand invasion and exchange. It is helpful to profoundly understand the HR.
周化民,孙旭利,陈建明.同源重组和重组酶Rad51的调控[J].生物化学与生物物理进展,2016,43(12):1154-1162
复制生物化学与生物物理进展 ® 2025 版权所有 ICP:京ICP备05023138号-1 京公网安备 11010502031771号