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THO/TREX复合体的超重组在拟南芥中对乙烯敏感性恢复基因1的转录调控中发挥作用。

HYPER RECOMBINATION1 of the THO/TREX complex plays a role in controlling transcription of the REVERSION-TO-ETHYLENE SENSITIVITY1 gene in Arabidopsis.

作者信息

Xu Congyao, Zhou Xin, Wen Chi-Kuang

机构信息

National Key Laboratory of Plant Molecular Genetics and National Center for Plant Gene Research (Shanghai), Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.

出版信息

PLoS Genet. 2015 Feb 13;11(2):e1004956. doi: 10.1371/journal.pgen.1004956. eCollection 2015 Feb.

Abstract

Arabidopsis REVERSION-TO-ETHYLENE SENSITIVITY1 (RTE1) represses ethylene hormone responses by promoting ethylene receptor ETHYLENE RESPONSE1 (ETR1) signaling, which negatively regulates ethylene responses. To investigate the regulation of RTE1, we performed a genetic screening for mutations that suppress ethylene insensitivity conferred by RTE1 overexpression in Arabidopsis. We isolated HYPER RECOMBINATION1 (HPR1), which is required for RTE1 overexpressor (RTE1ox) ethylene insensitivity at the seedling but not adult stage. HPR1 is a component of the THO complex, which, with other proteins, forms the TRanscription EXport (TREX) complex. In yeast, Drosophila, and humans, the THO/TREX complex is involved in transcription elongation and nucleocytoplasmic RNA export, but its role in plants is to be fully determined. We investigated how HPR1 is involved in RTE1ox ethylene insensitivity in Arabidopsis. The hpr1-5 mutation may affect nucleocytoplasmic mRNA export, as revealed by in vivo hybridization of fluorescein-labeled oligo(dT)45 with unidentified mRNA in the nucleus. The hpr1-5 mutation reduced the total and nuclear RTE1 transcript levels to a similar extent, and RTE1 transcript reduction rate was not affected by hpr1-5 with cordycepin treatment, which prematurely terminates transcription. The defect in the THO-interacting TEX1 protein of TREX but not the mRNA export factor SAC3B also reduced the total and nuclear RTE1 levels. SERINE-ARGININE-RICH (SR) proteins are involved mRNA splicing, and we found that SR protein SR33 co-localized with HPR1 in nuclear speckles, which agreed with the association of human TREX with the splicing machinery. We reveal a role for HPR1 in RTE1 expression during transcription elongation and less likely during export. Gene expression involved in ethylene signaling suppression was not reduced by the hpr1-5 mutation, which indicates selectivity of HPR1 for RTE1 expression affecting the consequent ethylene response. Thus, components of the THO/TREX complex appear to have specific roles in the transcription or export of selected genes.

摘要

拟南芥乙烯敏感性恢复1(RTE1)通过促进乙烯受体乙烯反应1(ETR1)信号传导来抑制乙烯激素反应,而ETR1信号传导对乙烯反应起负调控作用。为了研究RTE1的调控机制,我们在拟南芥中进行了一项遗传筛选,以寻找能够抑制RTE1过表达所导致的乙烯不敏感的突变。我们分离出了超重组1(HPR1),它是RTE1过表达植株(RTE1ox)在幼苗期而非成年期乙烯不敏感所必需的。HPR1是THO复合物的一个组成部分,该复合物与其他蛋白质一起形成转录输出(TREX)复合物。在酵母、果蝇和人类中,THO/TREX复合物参与转录延伸和核质RNA输出,但其在植物中的作用尚待完全确定。我们研究了HPR1如何参与拟南芥中RTE1ox的乙烯不敏感现象。hpr1 - 5突变可能会影响核质mRNA输出,这通过荧光素标记的寡聚(dT)45与细胞核中未鉴定的mRNA的体内杂交得以揭示。hpr1 - 5突变使RTE1的总转录本水平和核转录本水平降低的程度相似,并且用虫草素处理(过早终止转录)时,hpr1 - 5对RTE1转录本降低率没有影响。TREX中与THO相互作用的TEX1蛋白而非mRNA输出因子SAC3B的缺陷也降低了RTE1的总水平和核水平。富含丝氨酸 - 精氨酸(SR)的蛋白质参与mRNA剪接,我们发现SR蛋白SR33与HPR1在核斑点中共定位,这与人类TREX与剪接机制的关联一致。我们揭示了HPR1在转录延伸过程中对RTE1表达起作用,而在输出过程中作用较小。hpr1 - 5突变并未降低参与乙烯信号抑制的基因表达,这表明HPR1对RTE1表达具有选择性,从而影响随后的乙烯反应。因此,THO/TREX复合物的组分似乎在特定基因的转录或输出中具有特定作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c99/4334170/0cb46d7c0f20/pgen.1004956.g001.jpg

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