PRC2
染色质
生物
转录因子
心理压抑
拟南芥
恶毒的
组蛋白H3
细胞生物学
抄写(语言学)
增强子
遗传学
组蛋白
拟南芥
染色质免疫沉淀
突变体
基因
核小体
染色质重塑
计算生物学
转录调控
基因表达
同源异型基因
哲学
语言学
作者
Fernando Baile,Wiam Merini,Inés Hidalgo,Myriam Calonje
出处
期刊:The Plant Cell
[Oxford University Press]
日期:2021-05-18
卷期号:33 (8): 2701-2715
被引量:23
标识
DOI:10.1093/plcell/koab139
摘要
Abstract Polycomb group (PcG) complexes ensure that every cell in an organism expresses the genes needed at a particular stage, time, or condition. However, it is still not fully understood how PcG complexes PcG-repressive complex 1 (PRC1) and PRC2 are recruited to target genes in plants. Recent findings in Arabidopsis thaliana support the notion that PRC2 recruitment is mediated by different transcription factors (TFs). However, it is unclear how all these TFs interact with PRC2 and whether they also recruit PRC1 activity. Here, by using a system to bind selected TFs to a synthetic promoter lacking the complexity of PcG target promoters in vivo, we show that while binding of the TF VIVIPAROUS1/ABSCISIC ACID-INSENSITIVE3-LIKE1 recapitulates PRC1 and PRC2 marking, the binding of other TFs only renders PRC2 marking. Interestingly, all these TFs contain an Ethylene-responsive element binding factor-associated Amphiphilic Repression (EAR) domain that triggers both HISTONE DEACETYLASE COMPLEX and PRC2 activities, connecting two different repressive mechanisms. Furthermore, we show that different TFs can have an additive effect on PRC2 activity, which may be required to maintain long-term repression of gene expression.
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