Identification, genomic localization, and functional validation of salt-stress-related lncRNAs in Indian Mustard (Brassica juncea L.)

被引:0
|
作者
Tribhuvan, Kishor U. [1 ]
Shivakumaraswamy, M. [1 ]
Mishra, Twinkle [1 ]
Kaur, Simardeep [2 ]
Sarkar, Biplab [1 ]
Pattanayak, A. [1 ]
Singh, Binay K. [1 ,2 ]
机构
[1] ICAR Indian Inst Agr Biotechnol, Ranchi 834003, Jharkhand, India
[2] ICAR Res Complex NEH Reg, Umiam 793103, Meghalaya, India
来源
BMC GENOMICS | 2024年 / 25卷 / 01期
关键词
<italic>Brassica juncea</italic>; lncRNA; eTMs; Salt stress; Salt shock; R2R3-MYB TRANSCRIPTION FACTOR; LONG NONCODING RNAS; ARABIDOPSIS-THALIANA; EXPRESSION; GENE; PROTEIN; ROLES; YIELD; SHOCK; RICE;
D O I
10.1186/s12864-024-10964-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Indian Mustard (Brassica juncea L.) is a globally cultivated winter oilseed crop of the rapeseed-mustard group. It is predominantly grown in the semi-arid northwest agroclimatic zone of India, characterized by high soil salinity. Enhancing tolerance to salt stress in B. juncea is therefore crucial for sustaining its production in this region. Long non-coding RNAs (lncRNAs) play critical roles in coordinating gene expression under various abiotic stresses, including salt stress, but their involvement in the salt stress response in B. juncea remains largely unknown. In this study, we conducted RNA-seq analysis on control, salt-stressed, and salt-shocked young leaves of the salt-tolerant B. juncea cv CS-52. We identified a total of 3,602 differentially expressed transcripts between stress versus control and shock versus control samples. Among these, 61 were identified as potential lncRNAs, with 21 specific to salt stress and 40 specific to salt shock. Of the 21 lncRNAs specific to salt stress, 15 were upregulated and six were downregulated, while all 40 lncRNAs unique to salt shock were downregulated. Chromosomal distribution analysis of the lncRNAs revealed their uneven placement across 18 chromosomes in B. juncea. RNA-RNA interaction analysis between salt stress-upregulated lncRNAs and salt stress-related miRNAs identified 26 interactions between 10 lncRNAs and 23 miRNAs and predicted 13 interactions between six miRNAs and 13 mRNAs. Finally, six lncRNA-miRNA-mRNA interaction networks were established, involving five lncRNAs, 13 miRNAs, and 23 mRNAs. RT-qPCR analysis revealed the upregulation of four out of five lncRNAs, along with their target mRNAs, supporting their involvement in the salt stress response in B. juncea.
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页数:12
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