Genome-wide identification and expression analysis of the trihelix transcription factor family in sesame (Sesamum indicum L.) under abiotic stress.


Journal

Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 27 03 2023
accepted: 27 06 2023
medline: 26 9 2023
pubmed: 16 8 2023
entrez: 16 8 2023
Statut: ppublish

Résumé

The plant trihelix gene family is among the earliest discovered transcription factor families, and it is vital in modulating light, plant growth, and stress responses. The identification and characterization of trihelix family members in the sesame genome were analyzed by bioinformatics methods, and the expression patterns of sesame trihelix genes were assessed by quantitative real-time PCR. There were 34 trihelix genes discovered in the genome of sesame, which were irregularly distributed among 10 linkage groups. Also, the genome contained 5 duplicate gene pairs. The 34 trihelix genes were divided into six sub-families through a phylogenetic study. A tissue-specific expression revealed that SiTH genes exhibited spatial expression patterns distinct from other trihelix genes in the same subfamily. The cis-element showed that the SiTHs gene promoter contained various elements associated with responses to hormones and multiple abiotic stresses. Additionally, the expression patterns of 8 SiTH genes in leaves under abiotic stresses demonstrated that all selected genes were significantly upregulated or downregulated at least once in the stress period. Furthermore, the SiTH4 gene was significantly induced in response to drought and salt stress, showing that SiTH genes may be engaged in the stress response mechanisms of sesame. These findings establish a foundation for further investigation of the trihelix gene-mediated response to abiotic stress in sesame.

Sections du résumé

BACKGROUND BACKGROUND
The plant trihelix gene family is among the earliest discovered transcription factor families, and it is vital in modulating light, plant growth, and stress responses.
METHODS METHODS
The identification and characterization of trihelix family members in the sesame genome were analyzed by bioinformatics methods, and the expression patterns of sesame trihelix genes were assessed by quantitative real-time PCR.
RESULTS RESULTS
There were 34 trihelix genes discovered in the genome of sesame, which were irregularly distributed among 10 linkage groups. Also, the genome contained 5 duplicate gene pairs. The 34 trihelix genes were divided into six sub-families through a phylogenetic study. A tissue-specific expression revealed that SiTH genes exhibited spatial expression patterns distinct from other trihelix genes in the same subfamily. The cis-element showed that the SiTHs gene promoter contained various elements associated with responses to hormones and multiple abiotic stresses. Additionally, the expression patterns of 8 SiTH genes in leaves under abiotic stresses demonstrated that all selected genes were significantly upregulated or downregulated at least once in the stress period. Furthermore, the SiTH4 gene was significantly induced in response to drought and salt stress, showing that SiTH genes may be engaged in the stress response mechanisms of sesame.
CONCLUSION CONCLUSIONS
These findings establish a foundation for further investigation of the trihelix gene-mediated response to abiotic stress in sesame.

Identifiants

pubmed: 37584845
doi: 10.1007/s11033-023-08640-w
pii: 10.1007/s11033-023-08640-w
pmc: PMC10519867
doi:

Substances chimiques

Transcription Factors 0
Plant Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8281-8295

Subventions

Organisme : China Agriculture Research System
ID : CARS-14

Informations de copyright

© 2023. The Author(s).

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Auteurs

Yunyan Zhao (Y)

College of Agriculture, Yangtze University, Jingzhou, 434025, China.
Jiangxi Province Key Laboratory of Oilcrops Biology / Nanchang Branch of National Center of Oilcrops Improvement, Crops Research Institute of Jiangxi Academy of Agricultural Sciences, Nanchang, 330200, China.

Junchao Liang (J)

Jiangxi Province Key Laboratory of Oilcrops Biology / Nanchang Branch of National Center of Oilcrops Improvement, Crops Research Institute of Jiangxi Academy of Agricultural Sciences, Nanchang, 330200, China.

Zhiqi Wang (Z)

Jiangxi Province Key Laboratory of Oilcrops Biology / Nanchang Branch of National Center of Oilcrops Improvement, Crops Research Institute of Jiangxi Academy of Agricultural Sciences, Nanchang, 330200, China.

Tingxian Yan (T)

Jiangxi Province Key Laboratory of Oilcrops Biology / Nanchang Branch of National Center of Oilcrops Improvement, Crops Research Institute of Jiangxi Academy of Agricultural Sciences, Nanchang, 330200, China.

Xiaowen Yan (X)

Jiangxi Province Key Laboratory of Oilcrops Biology / Nanchang Branch of National Center of Oilcrops Improvement, Crops Research Institute of Jiangxi Academy of Agricultural Sciences, Nanchang, 330200, China.

Wenliang Wei (W)

College of Agriculture, Yangtze University, Jingzhou, 434025, China.

Meiwang Le (M)

Jiangxi Province Key Laboratory of Oilcrops Biology / Nanchang Branch of National Center of Oilcrops Improvement, Crops Research Institute of Jiangxi Academy of Agricultural Sciences, Nanchang, 330200, China. mwyuecarl@163.com.

Jian Sun (J)

Jiangxi Province Key Laboratory of Oilcrops Biology / Nanchang Branch of National Center of Oilcrops Improvement, Crops Research Institute of Jiangxi Academy of Agricultural Sciences, Nanchang, 330200, China. whsunjian@aliyun.com.

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Classifications MeSH