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LIF2 通过与多梳复合物成分 LHP1 结合的 RNA 结合伴侣控制开花和细胞命运。

Control of flowering and cell fate by LIF2, an RNA binding partner of the polycomb complex component LHP1.

机构信息

Institut J-P Bourgin, UMR1318 INRA-AgroParisTech, INRA Centre de Versailles-Grignon, Versailles, France.

出版信息

PLoS One. 2011 Jan 31;6(1):e16592. doi: 10.1371/journal.pone.0016592.

Abstract

Polycomb Repressive Complexes (PRC) modulate the epigenetic status of key cell fate and developmental regulators in eukaryotes. The chromo domain protein like heterochromatin protein1 (LHP1) is a subunit of a plant PRC1-like complex in Arabidopsis thaliana and recognizes histone H3 lysine 27 trimethylation, a silencing epigenetic mark deposited by the PRC2 complex. We have identified and studied an LHP1-Interacting Factor2 (LIF2). LIF2 protein has RNA recognition motifs and belongs to the large hnRNP protein family, which is involved in RNA processing. LIF2 interacts in vivo, in the cell nucleus, with the LHP1 chromo shadow domain. Expression of LIF2 was detected predominantly in vascular and meristematic tissues. Loss-of-function of LIF2 modifies flowering time, floral developmental homeostasis and gynoecium growth determination. lif2 ovaries have indeterminate growth and produce ectopic inflorescences with severely affected flowers showing proliferation of ectopic stigmatic papillae and ovules in short-day conditions. To look at how LIF2 acts relative to LHP1, we conducted transcriptome analyses in lif2 and lhp1 and identified a common set of deregulated genes, which showed significant enrichment in stress-response genes. By comparing expression of LHP1 targets in lif2, lhp1 and lif2 lhp1 mutants we showed that LIF2 can either antagonize or act with LHP1. Interestingly, repression of the FLC floral transcriptional regulator in lif2 mutant is accompanied by an increase in H3K27 trimethylation at the locus, without any change in LHP1 binding, suggesting that LHP1 is targeted independently from LIF2 and that LHP1 binding does not strictly correlate with gene expression. LIF2, involved in cell identity and cell fate decision, may modulate the activity of LHP1 at specific loci, during specific developmental windows or in response to environmental cues that control cell fate determination. These results highlight a novel link between plant RNA processing and Polycomb regulation.

摘要

多梳抑制复合物(PRC)调节真核生物中关键细胞命运和发育调节剂的表观遗传状态。类染色质域蛋白异染色质蛋白 1(LHP1)是拟南芥 PRC1 样复合物的一个亚基,可识别组蛋白 H3 赖氨酸 27 三甲基化,这是 PRC2 复合物沉积的沉默表观遗传标记。我们已经鉴定并研究了一个 LHP1 相互作用因子 2(LIF2)。LIF2 蛋白具有 RNA 识别基序,属于参与 RNA 加工的大型 hnRNP 蛋白家族。LIF2 在体内、细胞核内与 LHP1 染色质阴影域相互作用。LIF2 的表达主要在血管和分生组织中检测到。LIF2 功能丧失会改变开花时间、花发育的动态平衡和雌蕊生长的决定。lif2 子房生长不定,产生不定的花序,严重影响的花朵表现出异位柱头和短日照条件下短胚珠的增殖。为了研究 LIF2 相对于 LHP1 的作用,我们在 lif2 和 lhp1 中进行了转录组分析,鉴定出一组共同的失调基因,这些基因在应激反应基因中显著富集。通过比较 lif2、lhp1 和 lif2 lhp1 突变体中 LHP1 靶基因的表达,我们表明 LIF2 可以拮抗或与 LHP1 作用。有趣的是,lif2 突变体中 FLC 花转录调节剂的抑制伴随着该基因座处 H3K27 三甲基化的增加,而 LHP1 结合没有任何变化,这表明 LHP1 是独立于 LIF2 靶向的,并且 LHP1 结合与基因表达不严格相关。LIF2 参与细胞身份和细胞命运决定,可能在特定发育窗口或响应控制细胞命运决定的环境线索时,在特定基因座上调节 LHP1 的活性。这些结果突出了植物 RNA 处理和多梳调控之间的新联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b40d/3031606/d89d05406937/pone.0016592.g001.jpg

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