Evidence map›Paper›PMID 41078113›Full record

ArticlePlant biotechnology journal2026

Trans-QTL Alliance of HKT1 and PHL7 Modulate Salinity Stress Tolerance and Enhance Crop Yield Endurance.

Jitendra K Mohanty, Antima Yadav, Laxmi Narnoliya, Virevol Thakro, Deepanshi Rathore, Shailesh Tripathi, Senjuti Sinharoy, Pinky Agarwal, Swarup K Parida

Abstract read
In one paragraph

Article in Plant biotechnology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Jitendra K MohantyBiotechnology Research and Innovation Council-National Institute of Plant Genome Research (BRIC-NIPGR), New Delhi, India.
Antima YadavBiotechnology Research and Innovation Council-National Institute of Plant Genome Research (BRIC-NIPGR), New Delhi, India.
Laxmi NarnoliyaBiotechnology Research and Innovation Council-National Institute of Plant Genome Research (BRIC-NIPGR), New Delhi, India.
Virevol ThakroBiotechnology Research and Innovation Council-National Institute of Plant Genome Research (BRIC-NIPGR), New Delhi, India.ORCID https://orcid.org/0000-0002-1642-7530
Deepanshi RathoreBiotechnology Research and Innovation Council-National Institute of Plant Genome Research (BRIC-NIPGR), New Delhi, India.
Shailesh TripathiIndian Institute of Pulses Research (IIPR), Kanpur, Uttar Pradesh, India.
Senjuti SinharoyBiotechnology Research and Innovation Council-National Institute of Plant Genome Research (BRIC-NIPGR), New Delhi, India.
Pinky AgarwalBiotechnology Research and Innovation Council-National Institute of Plant Genome Research (BRIC-NIPGR), New Delhi, India.ORCID https://orcid.org/0000-0002-1219-1735
Swarup K ParidaBiotechnology Research and Innovation Council-National Institute of Plant Genome Research (BRIC-NIPGR), New Delhi, India.ORCID https://orcid.org/0000-0001-7843-3031

Funding

Department of Biotechnology, Ministry of Science and Technology, India
6 · The paper itself

Abstract

Salinity stress can cause significant yield losses in crops because of its major impact on reproductive success. The complexity of salinity stress responses, particularly their tissue- and cell-specific regulation, continues to challenge the translation of molecular insights into tangible crop yield improvements. In the present study, the authors deployed a genomic strategy combining a genome-wide association study, regional association analysis, QTL mapping, fine mapping, and map-based cloning to delineate a pair of novel CaPHL7 and CaHKT1 alleles that regulate yield under salinity stress. The selected contrasting accessions, developed near-isogenic lines (NILs), overexpressed chickpea lines and complemented Arabidopsis lines collectively underscore the functional significance of the identified alleles in relaying yield endurance under salinity stress conditions. Functional characterisation of the genes revealed the intricate transcriptional regulation of CaHKT1 by CaPHL7, which influences the degree of salinity stress tolerance. Furthermore, in our efforts to enhance yield endurance, we discovered a novel regulatory role for the phosphorus (P) starvation-responsive gene (PHL7) in legumes, facilitating salinity stress adaptation. This study provides the first functional validation of a trans-QTL regulatory model in chickpea, where CaPHL7, located on one chromosome, transcriptionally activates CaHKT1 on a separate chromosome. The regulatory mechanism plays a key role in excluding sodium from the transpiration stream, thereby protecting reproductive processes from salinity-induced damage and mitigating yield penalties. This inter-locus regulation explains yield stability and offers useful insights that may be considered in future efforts to enhance salt resilience in chickpea.

Indexed as

Cation Transport ProteinsCicerCrops, AgriculturalPlant ProteinsQuantitative Trait LociSalt StressSalt ToleranceSymportersArabidopsisChromosome MappingGene Expression Regulation, PlantGenome-Wide Association StudyCation Transport ProteinsPlant ProteinsSymporterschickpeaGWASHKT1PHL7QTLsalinitySNP

Identifiers

PMID41078113
PMCPMC12946503

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.