Vyse Kora, Faivre Léa, Romich Melissa, Pagter Majken, Schubert Daniel, Hincha Dirk K, Zuther Ellen
Central Infrastructure Group Genomics and Transcript Profiling, Max-Planck-Institute of Molecular Plant Physiology, Potsdam, Germany.
Institute of Biology, Freie Universität Berlin, Berlin, Germany.
Front Plant Sci. 2020 Feb 7;11:39. doi: 10.3389/fpls.2020.00039. eCollection 2020.
Chromatin regulation ensures stable repression of stress-inducible genes under non-stress conditions and transcriptional activation and memory of stress-related genes after stress exposure. However, there is only limited knowledge on how chromatin genes are regulated at the transcriptional and post-transcriptional level upon stress exposure and relief from stress. We reveal that the repressive modification histone H3 lysine 27 trimethylation (H3K27me3) targets genes which are quickly activated upon cold exposure, however, H3K27me3 is not necessarily lost during a longer time in the cold. In addition, we have set-up a quantitative reverse transcription polymerase chain reaction-based platform for high-throughput transcriptional profiling of a large set of chromatin genes. We find that the expression of many of these genes is regulated by cold. In addition, we reveal an induction of several DNA and histone demethylase genes and certain histone variants after plants have been shifted back to ambient temperature (deacclimation), suggesting a role in the memory of cold acclimation. We also re-analyze large scale transcriptomic datasets for transcriptional regulation and alternative splicing (AS) of chromatin genes, uncovering an unexpected level of regulation of these genes, particularly at the splicing level. This includes several vernalization regulating genes whose AS may result in cold-regulated protein diversity. Overall, we provide a profiling platform for the analysis of chromatin regulatory genes and integrative analyses of their regulation, suggesting a dynamic regulation of key chromatin genes in response to low temperature stress.
染色质调控确保在非应激条件下应激诱导基因的稳定抑制,以及应激暴露后应激相关基因的转录激活和记忆。然而,关于应激暴露和应激缓解时染色质基因在转录和转录后水平如何被调控,我们了解的还很有限。我们发现,抑制性修饰组蛋白H3赖氨酸27三甲基化(H3K27me3)靶向冷暴露时迅速激活的基因,然而,H3K27me3在较长时间的低温过程中不一定会丢失。此外,我们建立了一个基于定量逆转录聚合酶链反应的平台,用于对大量染色质基因进行高通量转录谱分析。我们发现其中许多基因的表达受低温调控。此外,我们还揭示了植物转移回环境温度(去驯化)后,几个DNA和组蛋白去甲基化酶基因以及某些组蛋白变体的诱导,这表明它们在冷驯化记忆中发挥作用。我们还重新分析了大规模转录组数据集,以研究染色质基因的转录调控和可变剪接(AS),发现这些基因存在意想不到的调控水平,特别是在剪接水平。这包括几个春化调控基因,其可变剪接可能导致冷调控的蛋白质多样性。总体而言,我们提供了一个用于分析染色质调控基因及其调控综合分析的谱分析平台,表明关键染色质基因对低温胁迫有动态调控。