The soybean immune receptor GmBIR1 regulates host transcriptome, spliceome, and immunity during cyst nematode infection

Author:

Hawk Tracy E.1ORCID,Piya Sarbottam1,Zadegan Sobhan Bahrami12,Li Peitong1,Rice John H.1,Hewezi Tarek1ORCID

Affiliation:

1. Department of Plant Sciences University of Tennessee Knoxville TN 37996 USA

2. UT‐ORNL Graduate School of Genome Science and Technology University of Tennessee Knoxville TN 37996 USA

Abstract

Summary BAK1‐INTERACTING RECEPTOR LIKE KINASE1 (BIR1) is a negative regulator of various aspects of disease resistance and immune responses. Here, we investigated the functional role of soybean (Glycine max) BIR1 (GmBIR1) during soybean interaction with soybean cyst nematode (SCN, Heterodera glycines) and the molecular mechanism through which GmBIR1 regulates plant immunity. Overexpression of wild‐type variant of GmBIR1 (WT‐GmBIR1) using transgenic soybean hairy roots significantly increased soybean susceptibility to SCN, whereas overexpression of kinase‐dead variant (KD‐GmBIR1) significantly increased plant resistance. Transcriptome analysis revealed that genes oppositely regulated in WT‐GmBIR1 and KD‐GmBIR1 upon SCN infection were enriched primarily in defense and immunity‐related functions. Quantitative phosphoproteomic analysis identified 208 proteins as putative substrates of the GmBIR1 signaling pathway, 114 of which were differentially phosphorylated upon SCN infection. In addition, the phosphoproteomic data pointed to a role of the GmBIR1 signaling pathway in regulating alternative pre‐mRNA splicing. Genome‐wide analysis of splicing events provided compelling evidence supporting a role of the GmBIR1 signaling pathway in establishing alternative splicing during SCN infection. Our results provide novel mechanistic insights into the function of the GmBIR1 signaling pathway in regulating soybean transcriptome and spliceome via differential phosphorylation of splicing factors and regulation of splicing events of pre‐mRNA decay‐ and spliceosome‐related genes.

Funder

National Institute of Food and Agriculture

Publisher

Wiley

Subject

Plant Science,Physiology

Reference98 articles.

1. The Plant Cytoskeleton Remodelling in Nematode Induced Feeding Sites

2. HTSeq--a Python framework to work with high-throughput sequencing data

3. In silico identification of MAPK3/6 substrates in WRKY, bZIP, MYB, MYB‐ related, NAC and AP‐2 transcription factor family in Arabidopsis thaliana;Avashthi H;International Journal of Computational Bioinformatics and In Silico Modeling,2014

4. Kill the messenger: mRNA decay and plant development

5. Phosphoproteomics reveals extensive in vivo phosphorylation of Arabidopsis proteins involved in RNA metabolism

Cited by 1 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