An Insight Into Pentatricopeptide-Mediated Chloroplast Necrosis via microRNA395a During Rhizoctonia solani Infection

Author:

Srikakulam Nagesh,Guria Ashirbad,Karanthamalai Jeyalakshmi,Murugesan Vidya,Krishnan Vignesh,Sundaramoorthy Kasthuri,Saha Shakkhar,Singh Rudransh,Victorathisayam Thiveyarajan,Rajapriya Veeraputhiran,Sridevi Ganapathi,Pandi Gopal

Abstract

Sheath blight (ShB) disease, caused by Rhizoctonia solani, is one of the major biotic stress-oriented diseases that adversely affect the rice productivity worldwide. However, the regulatory mechanisms are not understood yet comprehensively. In the current study, we had investigated the potential roles of miRNAs in economically important indica rice variety Pusa Basmati-1 upon R. solani infection by carrying out in-depth, high-throughput small RNA sequencing with a total data size of 435 million paired-end raw reads from rice leaf RNA samples collected at different time points. Detailed data analysis revealed a total of 468 known mature miRNAs and 747 putative novel miRNAs across all the libraries. Target prediction and Gene Ontology functional analysis of these miRNAs were found to be unraveling various cellular, molecular, and biological functions by targeting various plant defense-related genes. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) was performed to validate the miRNAs and their putative target genes. Out of the selected miRNA-specific putative target genes, miR395a binding and its cleavage site on pentatricopeptide were determined by 5’ RACE-PCR. It might be possible that R. solani instigated chloroplast degradation by modulating the pentatricopeptide which led to increased susceptibility to fungal infection.

Funder

Department of Biotechnology, Ministry of Science and Technology, India

Publisher

Frontiers Media SA

Subject

Genetics (clinical),Genetics,Molecular Medicine

Reference95 articles.

1. Hairpin Priming Is Better Suited Than In Vitro Polyadenylation to Generate cDNA for Plant miRNA qPCR;Adhikari;Mol. Plant,2013

2. Detecting Sequence Signals in Targeting Peptides Using Deep Learning;Almagro Armenteros;Life Sci. Alliance,2019

3. Differential Expression Analysis for Sequence Count Data;Anders;Nat. Prec,2010

4. FastQC: a Quality Control Tool for High Throughput Sequence Data AndrewsS. 2010

5. Deciphering the Role of microRNAs during Pi54 Gene Mediated Magnaporthe Oryzae Resistance Response in Rice;Arora;Physiol. Mol. Biol. Plants,2021

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