Evidence map›Paper›PMID 33434234›Full record

ArticlePloS one2021

Comparative RNA-Seq analysis unfolds a complex regulatory network imparting yellow mosaic disease resistance in mungbean [Vigna radiata (L.) R. Wilczek].

Uttarayan Dasgupta, Gyan Prakash Mishra, Harsh K Dikshit, Dwijesh C Mishra, Tejas Bosamia, Anirban Roy, Jyotika Bhati, Priti, Muraleedhar Aski, Ranjeet R Kumar and 6 more

Abstract readComparative Study
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

27 citing papers in PubMed.

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  7. Variable infection mechanisms of mungbean yellow mosaic India virus in diversePhysiology and molecular biology of plants : an international journal of functional plant biology · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Uttarayan DasguptaDivision of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Gyan Prakash MishraDivision of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, India.ORCID 0000-0002-7023-2638
Harsh K DikshitDivision of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Dwijesh C MishraAgricultural Bioinformatics, ICAR-Indian Agricultural Statistics Research Institute, New Delhi, India.
Tejas BosamiaCrop Improvement Division, ICAR-Directorate of Groundnut Research, Junagadh, Gujarat, India.
Anirban RoyDivision of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Jyotika BhatiAgricultural Bioinformatics, ICAR-Indian Agricultural Statistics Research Institute, New Delhi, India.ORCID 0000-0002-8719-181X
PritiDivision of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, India.ORCID 0000-0002-8719-181X
Muraleedhar AskiDivision of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Ranjeet R KumarDivision of Biochemistry, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Amit Kumar SinghGermplasm Evaluation Division, ICAR-National Bureau of Plant Genetic Resources, New Delhi, India.
Atul KumarDivision of Seed Science and Technology, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Subodh K SinhaICAR-National Institute for Plant Biotechnology, New Delhi, India.
Shiksha ChaurasiaDivision of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Shelly PraveenDivision of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Ramakrishnan M NairWorld Vegetable Center, South Asia, ICRISAT Campus Patancheru, Hyderabad, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Yellow Mosaic Disease (YMD) in mungbean [Vigna radiata (L.) R. Wilczek] is one of the most damaging diseases in Asia. In the northern part of India, the YMD is caused by Mungbean Yellow Mosaic India Virus (MYMIV), while in southern India this is caused by Mungbean Yellow Mosaic Virus (MYMV). The molecular mechanism of YMD resistance in mungbean remains largely unknown. In this study, RNA-seq analysis was conducted between a resistant (PMR-1) and a susceptible (Pusa Vishal) mungbean genotype under infected and control conditions to understand the regulatory network operating between mungbean-YMV. Overall, 76.8 million raw reads could be generated in different treatment combinations, while mapping rate per library to the reference genome varied from 86.78% to 93.35%. The resistance to MYMIV showed a very complicated gene network, which begins with the production of general PAMPs (pathogen-associated molecular patterns), then activation of various signaling cascades like kinases, jasmonic acid (JA) and brassinosteroid (BR), and finally the expression of specific genes (like PR-proteins, virus resistance and R-gene proteins) leading to resistance response. The function of WRKY, NAC and MYB transcription factors in imparting the resistance against MYMIV could be established. The string analysis also revealed the role of proteins involved in kinase, viral movement and phytoene synthase activity in imparting YMD resistance. A set of novel stress-related EST-SSRs are also identified from the RNA-Seq data which may be used to find the linked genes/QTLs with the YMD resistance. Also, 11 defence-related transcripts could be validated through quantitative real-time PCR analysis. The identified gene networks have led to an insight about the defence mechanism operating against MYMIV infection in mungbean which will be of immense use to manage the YMD resistance in mungbean.

Indexed as

Gene Expression Regulation, PlantBegomovirusDisease ResistanceGene Regulatory NetworksPlant DiseasesRNA-SeqTranscriptomeVigna

Identifiers

PMID33434234
PMCPMC7802970

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.