Footitt Steven, Müller Kerstin, Kermode Allison R, Finch-Savage William E
School of Life Sciences, Wellesbourne Campus, University of Warwick, Warwickshire, CV35 9EF, UK.
Plant J. 2015 Feb;81(3):413-25. doi: 10.1111/tpj.12735. Epub 2014 Dec 26.
The involvement of chromatin remodelling in dormancy cycling in the soil seed bank (SSB) is poorly understood. Natural variation between the winter and summer annual Arabidopsis ecotypes Cvi and Bur was exploited to investigate the expression of genes involved in chromatin remodelling via histone 2B (H2B) ubiquitination/de-ubiquitination and histone acetylation/deacetylation, the repressive histone methyl transferases CURLY LEAF (CLF) and SWINGER (SWN), and the gene silencing repressor ROS1 (REPRESSOR OF SILENCING1) and promoter of silencing KYP/SUVH4 (KRYPTONITE), during dormancy cycling in the SSB. ROS1 expression was positively correlated with dormancy while the reverse was observed for CLF and KYP/SUVH4. We propose ROS1 dependent repression of silencing and a sequential requirement of CLF and KYP/SUVH4 dependent gene repression and silencing for the maintenance and suppression of dormancy during dormancy cycling. Seasonal expression of H2B modifying genes was correlated negatively with temperature and positively with DOG1 expression, as were histone acetyltransferase genes, with histone deacetylases positively correlated with temperature. Changes in the histone marks H3K4me3 and H3K27me3 were seen on DOG1 (DELAY OF GERMINATION1) in Cvi during dormancy cycling. H3K4me3 activating marks remained stable along DOG1. During relief of dormancy, H3K27me3 repressive marks slowly accumulated and accelerated on exposure to light completing dormancy loss. We propose that these marks on DOG1 serve as a thermal sensing mechanism during dormancy cycling in preparation for light repression of dormancy. Overall, chromatin remodelling plays a vital role in temporal sensing through regulation of gene expression.
染色质重塑在土壤种子库(SSB)休眠循环中的作用尚不清楚。利用冬性和夏性一年生拟南芥生态型Cvi和Bur之间的自然变异,研究了参与染色质重塑的基因的表达,这些基因通过组蛋白2B(H2B)泛素化/去泛素化、组蛋白乙酰化/去乙酰化、抑制性组蛋白甲基转移酶卷曲叶(CLF)和摆动蛋白(SWN),以及基因沉默抑制因子ROS1(沉默抑制因子1)和沉默启动子KYP/SUVH4(氪石),在SSB的休眠循环过程中。ROS1的表达与休眠呈正相关,而CLF和KYP/SUVH4则相反。我们提出,ROS1依赖的沉默抑制以及CLF和KYP/SUVH4依赖的基因抑制和沉默的顺序要求,对于休眠循环期间休眠的维持和抑制。H2B修饰基因的季节性表达与温度呈负相关,与DOG1表达呈正相关,组蛋白乙酰转移酶基因也是如此,组蛋白去乙酰化酶与温度呈正相关。在Cvi的休眠循环过程中,在DOG1(发芽延迟1)上观察到组蛋白标记H3K4me3和H3K27me3的变化。H3K4me3激活标记在DOG1上保持稳定。在休眠解除期间,H3K27me3抑制标记缓慢积累,并在光照下加速积累,完成休眠丧失。我们提出,DOG1上的这些标记在休眠循环期间作为一种热传感机制,为休眠的光抑制做准备。总体而言,染色质重塑通过基因表达的调控在时间感知中起着至关重要的作用。