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全基因组结合分析转录因子水稻不定 1 揭示了一个复杂的网络控制水稻花转变。

Genome-wide binding analysis of transcription factor Rice Indeterminate 1 reveals a complex network controlling rice floral transition.

机构信息

National Key Laboratory of Crop Genetic Improvement and National Center of Plant Gene Research (Wuhan), Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, 430070, China.

出版信息

J Integr Plant Biol. 2022 Sep;64(9):1690-1705. doi: 10.1111/jipb.13325. Epub 2022 Aug 26.

Abstract

RICE INDETERMINATE 1 (RID1) plays a critical role in controlling floral transition in rice (Oryza sativa). However, the molecular basis for this effect, particularly the target genes and regulatory specificity, remains largely unclear. Here, we performed chromatin immunoprecipitation followed by sequencing (ChIP-seq) in young leaves at the pre-floral-transition stage to identify the target genes of RID1, identifying 2,680 genes associated with RID1 binding sites genome-wide. RID1 binding peaks were highly enriched for TTTGTC, the direct binding motif of the INDETERMINATE DOMAIN protein family that includes RID1. Interestingly, CACGTG and GTGGGCCC, two previously uncharacterized indirect binding motifs, were enriched through the interactions of RID1 with the novel flowering-promoting proteins OsPIL12 and OsTCP11, respectively. Moreover, the ChIP-seq data demonstrated that RID1 bound to numerous rice heading-date genes, such as HEADING DATE 1 (HD1) and FLAVIN-BINDING, KELCH REPEAT, F-BOX 1 (OsFKF1). Notably, transcriptome sequencing (RNA-seq) analysis revealed roles of RID1 in diverse developmental pathways. Genetic analysis combined with genome-wide ChIP-seq and RNA-seq results showed that RID1 directly binds to the promoter of OsERF#136 (a repressor of rice flowering) and negatively regulates its expression. Overall, our findings provide new insights into the molecular and genetic mechanisms underlying rice floral transition and characterize OsERF#136 as a previously unrecognized direct target of RID1.

摘要

RICE INDETERMINATE 1 (RID1) 在控制水稻(Oryza sativa)的花发育转变中起着关键作用。然而,其作用的分子基础,尤其是靶基因和调控特异性,在很大程度上仍不清楚。在这里,我们在预花发育转变阶段的幼叶中进行了染色质免疫沉淀测序(ChIP-seq),以鉴定 RID1 的靶基因,在全基因组范围内鉴定了 2680 个与 RID1 结合位点相关的基因。RID1 结合峰高度富集 TTTGTC,这是包括 RID1 在内的 INDETERMINATE DOMAIN 蛋白家族的直接结合基序。有趣的是,CACGTG 和 GTGGGCCC,这两个以前未被描述的间接结合基序,分别通过 RID1 与新型促进开花的蛋白质 OsPIL12 和 OsTCP11 的相互作用而被富集。此外,ChIP-seq 数据表明,RID1 结合到许多水稻开花期基因上,如 HEADING DATE 1 (HD1) 和 FLAVIN-BINDING, KELCH REPEAT, F-BOX 1 (OsFKF1)。值得注意的是,转录组测序(RNA-seq)分析显示 RID1 在多种发育途径中发挥作用。遗传分析结合全基因组 ChIP-seq 和 RNA-seq 结果表明,RID1 直接结合到 OsERF#136(水稻开花的抑制剂)的启动子上,并负调控其表达。总的来说,我们的研究结果为水稻花发育转变的分子和遗传机制提供了新的见解,并将 OsERF#136 鉴定为 RID1 的一个以前未被识别的直接靶标。

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