生物
DNA再复制
复制计时
DNA复制
拟南芥
染色质
细胞生物学
DNA复制因子CDT1
染色质免疫沉淀
DNA损伤
DNA修复
原点识别复合体
许可因素
抄写(语言学)
复制(统计)
复制前复合体
遗传学
转录因子
染色体复制控制
真核细胞DNA复制
突变体
DNA
基因表达
基因
发起人
病毒学
哲学
语言学
作者
Maherun Nisa,Thomas Eekhout,Clara Bergis,José Antonio Pedroza-García,Xiaoning He,Christelle Mazubert,Ilse Vercauteren,Toon Cools,Rim Brik-Chaouche,Jeannine Drouin-Wahbi,Layla Chmaiss,David Latrasse,Catherine Bergounioux,Klaas Vandepoele,Moussa Benhamed,Lieven De Veylder,Cécile Raynaud
标识
DOI:10.1016/j.molp.2023.07.002
摘要
Abstract
Survival of living organisms is fully dependent on their maintenance of genome integrity, being permanently threatened by replication stress in proliferating cells. Although the plant DNA damage response (DDR) regulator SOG1 has been demonstrated to cope with replication defects, accumulating evidence points to other pathways functioning independent of SOG1. Here, we report the roles of the Arabidopsis E2FA and EF2B transcription factors, two well-characterized regulators of DNA replication, in plant response to replication stress. Through a combination of reverse genetics and chromatin immunoprecipitation approaches, we show that E2FA and E2FB share many target genes with SOG1, providing evidence for their involvement in the DDR. Analysis of double- and triple-mutant combinations revealed that E2FB, rather than E2FA, plays the most prominent role in sustaining plant growth in the presence of replication defects, either operating antagonistically or synergistically with SOG1. Conversely, SOG1 aids in overcoming the replication defects of E2FA/E2FB-deficient plants. Collectively, our data reveal a complex transcriptional network controlling the replication stress response in which E2Fs and SOG1 act as key regulatory factors.
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