Zhou Yue, Tergemina Emmanuel, Cui Haitao, Förderer Alexander, Hartwig Benjamin, Velikkakam James Geo, Schneeberger Korbinian, Turck Franziska
Department of Plant Developmental Biology, Max Planck Institute for Plant Breeding Research, 50829 Cologne, Germany.
Department of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829 Cologne, Germany.
Proc Natl Acad Sci U S A. 2017 May 2;114(18):4833-4838. doi: 10.1073/pnas.1620955114. Epub 2017 Apr 20.
Polycomb Repressive Complex (PRC) 2 catalyzes the H3K27me3 modification that warrants inheritance of a repressive chromatin structure during cell division, thereby assuring stable target gene repression in differentiated cells. It is still under investigation how H3K27me3 is passed on from maternal to filial strands during DNA replication; however, cell division can reinforce H3K27me3 coverage at target regions. To identify novel factors involved in the Polycomb pathway in plants, we performed a forward genetic screen for enhancers of the () mutant, which shows relatively mild phenotypic alterations compared with other plant PRC mutants. We mapped ( to a gene related to yeast () based on phylogenetic analysis, structural similarities, physical interaction with the CMG helicase component SLD5, and an expression pattern confined to actively dividing cells. A combination of with the () allele, carrying a mutation in the catalytic core of PRC2, strongly enhanced the phenotype; furthermore, H3K27me3 coverage at target genes was strongly reduced in double mutants compared with single mutants. EOL1 physically interacted with CLF, its partially redundant paralog SWINGER (SWN), and LHP1. We propose that EOL1 interacts with LHP1-PRC2 complexes during replication and thereby participates in maintaining the H3K27me3 mark at target genes.
多梳抑制复合体(PRC)2催化H3K27me3修饰,该修饰保证了细胞分裂过程中抑制性染色质结构的遗传,从而确保分化细胞中靶基因的稳定抑制。目前仍在研究DNA复制过程中H3K27me3是如何从母链传递到子链的;然而,细胞分裂可以增强靶区域的H3K27me3覆盖。为了鉴定植物多梳途径中涉及的新因子,我们对()突变体的增强子进行了正向遗传筛选,与其他植物PRC突变体相比,该突变体表现出相对温和的表型改变。基于系统发育分析、结构相似性、与CMG解旋酶组分SLD5的物理相互作用以及局限于活跃分裂细胞的表达模式,我们将()定位到一个与酵母()相关的基因。()与携带PRC2催化核心突变的()等位基因的组合强烈增强了()表型;此外,与()单突变体相比,()双突变体中靶基因的H3K27me3覆盖显著降低。EOL1与CLF、其部分冗余的旁系同源物SWINGER(SWN)和LHP1发生物理相互作用。我们提出,EOL1在复制过程中与LHP1-PRC2复合体相互作用,从而参与维持靶基因上的H3K27me3标记。