Evidence map›Paper›PMID 42298105›Full record

ReviewFunctional & integrative genomics2026

Genome-wide analysis of the SWEET gene family in quinoa and functional study of CqSWEET14 in drought resistance.

Zhu Xiaolin, Wang Baoqiang, Zhao Ying, Wei Xiaohong

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Review in Functional & integrative genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Zhu XiaolinCollege of Life Science and Technology, Gansu Agricultural University, Lanzhou, 730070, China.
Wang BaoqiangCollege of Life Science and Technology, Gansu Agricultural University, Lanzhou, 730070, China.
Zhao YingCollege of Life Science and Technology, Gansu Agricultural University, Lanzhou, 730070, China.
Wei XiaohongCollege of Life Science and Technology, Gansu Agricultural University, Lanzhou, 730070, China. weixh@gsau.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SWEET gene family plays important roles in various physiological processes, including sugar transport and regulation, plant development, and environmental adaptation. This study conducted a genome-wide identification, expression analysis, and functional investigation of the SWEET gene family in quinoa. The results revealed a total of 29 CqSWEET genes identified in quinoa, with most CqSWEET proteins being alkaline hydrophobic proteins. Gene structure analysis showed that the number of exons ranged from 1 to 9. The conserved motifs Motif1-7 were highly conserved among family members. Analysis of promoter cis-acting elements revealed that multiple genes contain elements related to hormone responses (ABA, JA) and abiotic stress responses (e.g., drought, low temperature). Chromosomal localization mapping indicated a non-uniform distribution of the genes, and collinearity analysis identified seven pairs of duplicated genes, with their evolution predominantly driven by purifying selection. qRT-PCR analysis showed that under drought stress, CqSWEET genes exhibited diverse expression patterns in leaf and root tissues. Among them, ten genes, including CqSWEET04, 05, 12-14, 19-21, and 27-29, were significantly upregulated in leaves, while genes such as CqSWEET14 and 21 also showed strong responses to drought in roots. Further functional validation demonstrated that overexpression of the CqSWEET14 gene in Arabidopsis significantly enhanced the plants' drought resistance: under mannitol-simulated drought conditions, the root length of transgenic plants increased significantly; under prolonged drought stress, their photosynthetic efficiency (Fv/Fm, Pn, Gs, Tr) and chlorophyll content were significantly higher than those of wild-type plants, while the intercellular CO₂ concentration (Ci) was lower. Additionally, the activities of antioxidant enzymes (SOD, POD, CAT) in transgenic plants were significantly elevated, and malondialdehyde (MDA) content was significantly reduced, indicating enhanced reactive oxygen species scavenging capacity to mitigate oxidative damage. In summary, this study systematically elucidated the fundamental characteristics of the CqSWEET gene family in quinoa, revealed its potential role in drought stress responses, and validated the function of the CqSWEET14 gene in improving plant drought resistance, providing important candidate genes and theoretical foundations for the genetic improvement of stress tolerance in quinoa.

Indexed as

Chenopodium quinoaDrought ResistancePlant ProteinsDroughtsGene Expression Regulation, PlantMultigene FamilyPhylogenyPromoter Regions, GeneticStress, PhysiologicalPlant ProteinsCqSWEET14drought stressquinoaSWEET gene family

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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.