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Microhomology 选择用于. 中的 Microhomology 介导末端连接

Microhomology Selection for Microhomology Mediated End Joining in .

机构信息

Department of Molecular Medicine, Institute of Biotechnology, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900, USA.

Genomic Instability Research Center, Ajou University School of Medicine. 164, World Cup-ro, Yeongtong-gu, Suwon 16499, Korea.

出版信息

Genes (Basel). 2019 Apr 8;10(4):284. doi: 10.3390/genes10040284.

Abstract

Microhomology-mediated end joining (MMEJ) anneals short, imperfect microhomologies flanking DNA breaks, producing repair products with deletions in a Ku- and -independent fashion. Puzzlingly, MMEJ preferentially selects certain microhomologies over others, even when multiple microhomologies are available. To define rules and parameters for microhomology selection, we altered the length, the position, and the level of mismatches to the microhomologies flanking homothallic switching (HO) endonuclease-induced breaks and assessed their effect on MMEJ frequency and the types of repair product formation. We found that microhomology of eight to 20 base pairs carrying no more than 20% mismatches efficiently induced MMEJ. Deletion of did not impact MMEJ frequency. MMEJ preferentially chose a microhomology pair that was more proximal from the break. Interestingly, MMEJ events preferentially retained the centromere proximal side of the HO break, while the sequences proximal to the telomere were frequently deleted. The asymmetry in the deletional profile among MMEJ products was reduced when HO was induced on the circular chromosome. The results provide insight into how cells search and select microhomologies for MMEJ in budding yeast.

摘要

微同源介导的末端连接 (MMEJ) 退火短的、不完美的微同源侧翼 DNA 断裂,产生 Ku 独立的缺失修复产物。令人费解的是,即使有多个微同源物可用,MMEJ 也会优先选择某些微同源物而不是其他微同源物。为了定义微同源选择的规则和参数,我们改变了侧翼同源性转换 (HO) 内切酶诱导断裂的微同源物的长度、位置和错配水平,并评估了它们对 MMEJ 频率和修复产物形成类型的影响。我们发现,携带不超过 20%错配的 8 到 20 个碱基的微同源物有效地诱导了 MMEJ。缺失 并不影响 MMEJ 频率。MMEJ 优先选择离断裂更近的微同源物对。有趣的是,MMEJ 事件优先保留了 HO 断裂的着丝粒近端侧,而靠近端粒的序列则经常缺失。当 HO 在线性染色体上诱导时,MMEJ 产物中缺失图谱的不对称性降低。这些结果提供了对细胞如何在芽殖酵母中搜索和选择 MMEJ 微同源物的深入了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3fd/6523938/397cf7f31835/genes-10-00284-g001.jpg

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