Arabidopsis RNA processing factor SERRATE regulates the transcription of intronless genes

Author:

Speth Corinna123,Szabo Emese Xochitl1234,Martinho Claudia123,Collani Silvio5ORCID,zur Oven-Krockhaus Sven1,Richter Sandra1,Droste-Borel Irina6,Macek Boris6,Stierhof York-Dieter1,Schmid Markus5,Liu Chang1ORCID,Laubinger Sascha1234ORCID

Affiliation:

1. Centre for Plant Molecular Biology (ZMBP), University of Tuebingen, Tuebingen, Germany

2. Chemical Genomics Centre (CGC) of the Max Planck Society, Dortmund, Germany

3. Max Planck Institute for Developmental Biology, Tuebingen, Germany

4. Institute for Biology and Environmental Science, University of Oldenburg, Oldenburg, Germany

5. Department of Plant Physiology, Umea Plant Science Centre, Umeå University, Umea, Sweden

6. Proteome Centre, University of Tuebingen, Tuebingen, Germany

Abstract

Intron splicing increases proteome complexity, promotes RNA stability, and enhances transcription. However, introns and the concomitant need for splicing extend the time required for gene expression and can cause an undesirable delay in the activation of genes. Here, we show that the plant microRNA processing factor SERRATE (SE) plays an unexpected and pivotal role in the regulation of intronless genes. Arabidopsis SE associated with more than 1000, mainly intronless, genes in a transcription-dependent manner. Chromatin-bound SE liaised with paused and elongating polymerase II complexes and promoted their association with intronless target genes. Our results indicate that stress-responsive genes contain no or few introns, which negatively affects their expression strength, but that some genes circumvent this limitation via a novel SE-dependent transcriptional activation mechanism. Transcriptome analysis of a Drosophila mutant defective in ARS2, the metazoan homologue of SE, suggests that SE/ARS2 function in regulating intronless genes might be conserved across kingdoms.

Funder

Deutsche Forschungsgemeinschaft

Max-Planck-Gesellschaft

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Cited by 34 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3