Evidence map›Paper›PMID 30465114›Full record

ArticlePlanta2019

Abiotic stress regulates expression of galactinol synthase genes post-transcriptionally through intron retention in rice.

Sritama Mukherjee, Sonali Sengupta, Abhishek Mukherjee, Papri Basak, Arun Lahiri Majumder

Abstract read
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In one paragraph

Article in Planta, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 44 citations in OpenAlex.

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  7. Transcriptomic Analyses Reveal ThatInternational journal of molecular sciences · 2024
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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

5 authors at 3 institutions in 2 countries.

Sritama MukherjeeDivision of Plant Biology, Bose Institute (Centenary Campus), Kolkata, West Bengal, 700054, India.
Sonali SenguptaDivision of Plant Biology, Bose Institute (Centenary Campus), Kolkata, West Bengal, 700054, India. sonalisengupta2000@yahoo.co.in.
Abhishek MukherjeeDivision of Plant Biology, Bose Institute (Centenary Campus), Kolkata, West Bengal, 700054, India.
Papri BasakDivision of Plant Biology, Bose Institute (Centenary Campus), Kolkata, West Bengal, 700054, India.
Arun Lahiri MajumderDivision of Plant Biology, Bose Institute (Centenary Campus), Kolkata, West Bengal, 700054, India. lahiri@jcbose.ac.in.ORCID http://orcid.org/0000-0002-8581-9589
Bose Institute · INBotanical Survey of India · INLouisiana State University Agricultural Center · US

Funding

Department of Atomic Energy, Government of India D.O No. 10/25/2010/RRF-R & D-II/3118Department of Biotechnology, Ministry of Science and Technology DBT654BT/AB/05/02/2007-III
6 · The paper itself

Abstract

MAIN

conclusionExpression of the Galactinol synthase genes in rice is regulated through post-transcriptional intron retention in response to abiotic stress and may be linked to Raffinose Family Oligosaccharide synthesis in osmotic perturbation. Galactinol synthase (GolS) is the first committed enzyme in raffinose family oligosaccharide (RFO) synthesis pathway and synthesizes galactinol from UDP-galactose and inositol. Expression of GolS genes has long been implicated in abiotic stress, especially drought and salinity. A non-canonical regulation mechanism controlling the splicing and maturation of rice GolS genes was identified in rice photosynthetic tissue. We found that the two isoforms of Oryza sativa GolS (OsGolS) gene, located in chromosomes 3(OsGolS1) and 7(OsGolS2) are interspersed by conserved introns harboring characteristic premature termination codons (PTC). During abiotic stress, the premature and mature transcripts of both isoforms were found to accumulate in a rhythmic manner for very small time-windows interrupted by phases of complete absence. Reporter gene assay using GolS promoters under abiotic stress does not reflect this accumulation profile, suggesting that this regulation occurs post-transcriptionally. We suggest that this may be due to a surveillance mechanism triggering the degradation of the premature transcript preventing its accumulation in the cell. The suggested mechanism fits the paradigm of PTC-induced Nonsense-Mediated Decay (NMD). In support of our hypothesis, when we pharmacologically blocked NMD, the full-length pre-mRNAs were increasingly accumulated in cell. To this end, our work suggests that a combined transcriptional and post transcriptional control exists in rice to regulate GolS expression under stress. Concurrent detection and processing of prematurely terminating transcripts coupled to repressed splicing can be described as a form of Regulated Unproductive Splicing and Translation (RUST) and may be linked to the stress adaptation of the plant, which is an interesting future research possibility.

Indexed as

ArabidopsisGalactosyltransferasesGene Expression Regulation, PlantGenes, PlantIntronsOryzaPlants, Genetically ModifiedReal-Time Polymerase Chain ReactionRNA Processing, Post-TranscriptionalSequence AlignmentStress, PhysiologicalGalactosyltransferasesinositol 1-alpha-galactosyltransferaseAbiotic stressGolSRegulationRiceRUSTSplicing

Identifiers

PMID30465114
OpenAlexW2901548973

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Registered trials

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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.