生物
拟南芥
组蛋白
H3K4me3
分生组织
转录因子
染色质免疫沉淀
细胞生物学
染色质
开花位点C
博士手指
DNA甲基化
组蛋白H3
遗传学
恶毒的
组蛋白甲基化
多组蛋白
表观遗传学
基因
基因表达
发起人
锌指
抑制因子
突变体
作者
Can Huang,Diao Wang,Yongqiang Yang,Hong Yang,Biaoming Zhang,Haitao Li,Haitao Zhang,Yan Li,Wenya Yuan
标识
DOI:10.1093/plphys/kiae321
摘要
Abstract Maintenance and homeostasis of the quiescent center (QC) in Arabidopsis (Arabidopsis thaliana) root apical meristems are critical for stem cell organization and root development. Despite great progress in relevant research, the molecular mechanisms that determine the root stem cell fate and QC still need further exploration. In Arabidopsis, SUPPRESSOR OF FRIGIDA 4 (SUF4) encodes a C2H2-type zinc finger protein that represses flowering by transcriptional activation of FLOWERING LOCUS C (FLC) through the FRIGIDA (FRI) pathway, and EARLY BOLTING IN SHORT DAYS (EBS) is a bivalent histone reader that prevents premature flowering. Here, we found that SUF4 directly interacts with EBS in vivo and in vitro. Loss of function of SUF4 and/or EBS resulted in disorganization of the QC, aberrant cell division, and stunted root growth. RNA-seq and reverse transcription quantitative real-time polymerase chain reaction analysis revealed that SUF4 and EBS coregulate many root development-related genes. A series of biochemical analyses demonstrated that SUF4 directly binds to the promoter of SCARECROW (SCR), which encodes a key regulator of root development. Chromatin immunoprecipitation assay indicated that both SUF4 and EBS are recruited to the SCR locus in an interdependent manner to promote H3K4me3 levels and suppress H3K27me3 levels, thereby activating the expression of SCR. These findings improve our understanding of the function of SUF4 and EBS and provide insights into the molecular mechanism that couples a transcription factor and a histone methylation reader to modulate QC specification and root development in Arabidopsis.
科研通智能强力驱动
Strongly Powered by AbleSci AI