State Key Laboratory of Plant Cell and Chromosome Engineering, Center for Agricultural Resources Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Shijiazhuang, China.
Hebei Collaboration Innovation Center for Cell Signaling, Shijiazhuang, 050021, China.
Plant J. 2018 Jun;94(6):1083-1097. doi: 10.1111/tpj.13921. Epub 2018 May 10.
WUSCHEL (WUS) is critical for plant meristem maintenance and determinacy in Arabidopsis, and the regulation of its spatiotemporal expression patterns is complex. We previously found that AGAMOUS (AG), a key MADS-domain transcription factor in floral organ identity and floral meristem determinacy, can directly suppress WUS expression through the recruitment of the Polycomb group (PcG) protein TERMINAL FLOWER 2 (TFL2, also known as LIKE HETEROCHROMATIN PROTEIN 1, LHP1) at the WUS locus; however, the mechanism by which WUS is repressed remains unclear. Here, using chromosome conformation capture (3C) and chromatin immunoprecipitation 3C, we found that two specific regions flanking the WUS gene body bound by AG and TFL2 form a chromatin loop that is directly promoted by AG during flower development in a manner independent of the physical distance and sequence content of the intervening region. Moreover, AG physically interacts with TFL2, and TFL2 binding to the chromatin loop is dependent on AG. Transgenic and CRISPR/Cas9-edited lines showed that the WUS chromatin loop represses gene expression by blocking the recruitment of RNA polymerase II at the locus. The findings uncover the WUS chromatin loop as another regulatory mechanism controlling WUS expression, and also shed light on the factors required for chromatin conformation change and their recruitment.
WUSCHEL(WUS)对于拟南芥的植物分生组织维持和确定性至关重要,其时空表达模式的调节非常复杂。我们之前发现,AGAMOUS(AG),花器官身份和花分生组织确定性的关键 MADS 结构域转录因子,可通过募集多梳组(PcG)蛋白 TERMINAL FLOWER 2(TFL2,也称为 LIKE HETEROCHROMATIN PROTEIN 1,LHP1),直接抑制 WUS 的表达在 WUS 基因座;然而,WUS 被抑制的机制仍不清楚。在这里,我们使用染色质构象捕获(3C)和染色质免疫沉淀 3C,发现 AG 和 TFL2 结合的 WUS 基因体两侧的两个特定区域形成一个染色质环,该染色质环在花发育过程中由 AG 直接促进,而与间隔区的物理距离和序列内容无关。此外,AG 与 TFL2 发生物理相互作用,并且 TFL2 结合到染色质环依赖于 AG。转基因和 CRISPR/Cas9 编辑系表明,WUS 染色质环通过阻止 RNA 聚合酶 II 在基因座上的募集来抑制基因表达。这些发现揭示了 WUS 染色质环作为另一种调控机制来控制 WUS 的表达,也为染色质构象变化及其募集所需的因素提供了线索。