Genome-wide identification of RNA recognition motif (RRM1) in Brassica rapa and functional analysis of RNA-binding protein (BrRBP) under low-temperature stress.


Journal

BMC plant biology
ISSN: 1471-2229
Titre abrégé: BMC Plant Biol
Pays: England
ID NLM: 100967807

Informations de publication

Date de publication:
07 Dec 2023
Historique:
received: 09 08 2023
accepted: 29 11 2023
medline: 11 12 2023
pubmed: 7 12 2023
entrez: 6 12 2023
Statut: epublish

Résumé

The RNA recognition motif (RRM) is primarily engaged in the processing of mRNA and rRNA following gene transcription as well as the regulation of RNA transport; it is critical in preserving RNA stability. In this study, we identified 102 members of the RRM1 gene family in Brassica rapa, which were dispersed across 10 chromosomes with the ninth chromosome being the most extensively distributed. The RRM1 gene family members of Brassica rapa and Arabidopsis thaliana were grouped into 14 subclades (I-XIV) using phylogenetic analysis. Moreover, the results of transcriptome analysis and RT-qPCR indicated that the expression of Brapa05T000840 was upregulated in the cultivars 'Longyou 7' and 'Longyou 99' following exposure to cold stress at a temperature of 4 °C for 24 h. The levels of expression in the leaves and growth cones of the 'Longyou 7' variety were found to be significantly higher than those observed in the 'Longyou 99' variety under conditions of low temperature and NaCl stress. It illustrates the involvement of the RRM1 gene in the physiological response to both low temperature and salt stress. In addition, it was observed that the survival rate of transgenic BrRBP (Brapa05T000840) Arabidopsis thaliana plants was notably higher compared to that of wild-type plants when subjected to varying durations of low temperature treatment. Furthermore, the expression of the BrRBP gene in transgenic plants exhibited an upward trend as the duration of low temperature treatment increased, reaching its peak at 24 h. The in-vivo enzymatic activity of reactive oxygen species-scavenging enzymes were found to be significantly elevated in comparison to wild-type plants, suggesting that the BrRBP gene may enhance the cold tolerance of Arabidopsis thaliana. This study offers a significant foundation for comprehending the regulation mechanism of the RRM1 gene family in winter Brassica rapa subjected to cold stress, as well as for finding key genes associated with cold resistance.

Sections du résumé

BACKGROUND BACKGROUND
The RNA recognition motif (RRM) is primarily engaged in the processing of mRNA and rRNA following gene transcription as well as the regulation of RNA transport; it is critical in preserving RNA stability.
RESULTS RESULTS
In this study, we identified 102 members of the RRM1 gene family in Brassica rapa, which were dispersed across 10 chromosomes with the ninth chromosome being the most extensively distributed. The RRM1 gene family members of Brassica rapa and Arabidopsis thaliana were grouped into 14 subclades (I-XIV) using phylogenetic analysis. Moreover, the results of transcriptome analysis and RT-qPCR indicated that the expression of Brapa05T000840 was upregulated in the cultivars 'Longyou 7' and 'Longyou 99' following exposure to cold stress at a temperature of 4 °C for 24 h. The levels of expression in the leaves and growth cones of the 'Longyou 7' variety were found to be significantly higher than those observed in the 'Longyou 99' variety under conditions of low temperature and NaCl stress. It illustrates the involvement of the RRM1 gene in the physiological response to both low temperature and salt stress. In addition, it was observed that the survival rate of transgenic BrRBP (Brapa05T000840) Arabidopsis thaliana plants was notably higher compared to that of wild-type plants when subjected to varying durations of low temperature treatment. Furthermore, the expression of the BrRBP gene in transgenic plants exhibited an upward trend as the duration of low temperature treatment increased, reaching its peak at 24 h. The in-vivo enzymatic activity of reactive oxygen species-scavenging enzymes were found to be significantly elevated in comparison to wild-type plants, suggesting that the BrRBP gene may enhance the cold tolerance of Arabidopsis thaliana.
CONCLUSIONS CONCLUSIONS
This study offers a significant foundation for comprehending the regulation mechanism of the RRM1 gene family in winter Brassica rapa subjected to cold stress, as well as for finding key genes associated with cold resistance.

Identifiants

pubmed: 38057714
doi: 10.1186/s12870-023-04639-4
pii: 10.1186/s12870-023-04639-4
pmc: PMC10701981
doi:

Substances chimiques

RNA-Binding Proteins 0
Plant Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

621

Subventions

Organisme : National Natural Science Foundation of China
ID : 32260519
Organisme : China Agriculture Research System of MOF and MARA
ID : CARS-12
Organisme : Science and Technology Program of Gansu Province
ID : 22ZD6NA009
Organisme : Gansu Province Modern Cold and Arid Agriculture Science and Technology Support
ID : KJZC-2023-12

Informations de copyright

© 2023. The Author(s).

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Auteurs

Li Ma (L)

State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, 730070, China.

Xiaolei Tao (X)

State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, 730070, China.
College of Agronomy, Gansu Agricultural University, Lanzhou, 730070, China.

Wangtian Wang (W)

State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, 730070, China.

Jintang Jiao (J)

State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, 730070, China.
College of Agronomy, Gansu Agricultural University, Lanzhou, 730070, China.

Yuanyuan Pu (Y)

State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, 730070, China.
College of Agronomy, Gansu Agricultural University, Lanzhou, 730070, China.

Gang Yang (G)

State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, 730070, China.
College of Agronomy, Gansu Agricultural University, Lanzhou, 730070, China.

Lijun Liu (L)

State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, 730070, China.

Yan Fang (Y)

State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, 730070, China.

Junyan Wu (J)

State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, 730070, China. wujuny@gsau.edu.cn.
College of Agronomy, Gansu Agricultural University, Lanzhou, 730070, China. wujuny@gsau.edu.cn.

Wancang Sun (W)

State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, 730070, China. sunwanc@gsau.edu.cn.
College of Agronomy, Gansu Agricultural University, Lanzhou, 730070, China. sunwanc@gsau.edu.cn.

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Classifications MeSH