Identification of tissue-specific and cold-responsive lncRNAs in Medicago truncatula by high-throughput RNA sequencing

• Published in: BMC plant biology Vol. 20; no. 1; p. 99
• Main Authors: Zhao, Mingui, Wang, Tianzuo, Sun, Tianyang, Yu, Xiaoxi, Tian, Rui, Zhang, Wen-Hao
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 06-03-2020; BioMed Central; BMC
• Subjects: Alfalfa; Biochemistry; CBFs; Chromosomes; Cold; Cold stress; Datasets; Gene expression; Gene sequencing; Genes; Genetic aspects; Genetic research; Genomes; Genomics; Growth; Identification; Kinases; Legumes; Long non-coding RNAs; Medicago truncatula; Methods; MtCIR1; Non-coding RNA; Nucleic acids; Plant hardiness; Quantitative genetics; Ribonucleic acid; RNA; RNA sequencing; Transcription (Genetics); China; Medicago truncatula; Long non-coding RNAs; CBFs; Cold stress; MtCIR1
• ISSN: 1471-2229; 1471-2229
• DOI: 10.1186/s12870-020-2301-1

Long non-coding RNAs (lncRNAs) play important roles in the regulation of plant responses to environmental stress by acting as essential regulators of gene expression. However, whether and how lncRNAs are involved in cold acclimation-dependent freezing tolerance in plants remains largely unknown. Medicago truncatula is a prominent model for studies of legume genomics, and distinguished by its cold-acclimation characteristics. To determine the roles of lncRNAs in plant cold stress response, we conducted genome-wide high-throughput sequencing in the legume model plant M. truncatula.
RNA-seq data were generated from twelve samples for the four treatments, i.e., non-cold treated leaves and roots, cold-treated leaves and roots of M. truncatula Jemalong A17 seedlings. A total of 1204 million raw reads were generated. Of them, 1150 million filtered reads after quality control (QC) were subjected to downstream analysis. A large number of 24,368 unique lncRNAs were identified from the twelve samples. Among these lncRNAs, 983 and 1288 were responsive to cold treatment in the leaves and roots, respectively. We further found that the intronic-lncRNAs were most sensitive to the cold treatment. The cold-responsive lncRNAs were unevenly distributed across the eight chromosomes in M. truncatula seedlings with obvious preferences for locations. Further analyses revealed that the cold-responsive lncRNAs differed between leaves and roots. The putative target genes of the lncRNAs were predicted to mainly involve the processes of protein translation, transport, metabolism and nucleic acid transcription. Furthermore, the networks of a tandem array of CBF/DREB1 genes that were reported to be located in a major freezing tolerance QTL region on chromosome 6 and their related lncRNAs were dissected based on their gene expression and chromosome location.
We identified a comprehensive set of lncRNAs that were responsive to cold treatment in M. truncatula seedlings, and discovered tissue-specific cold-responsive lncRNAs in leaves and roots. We further dissected potential regulatory networks of CBF Intergenic RNA (MtCIR1) and MtCBFs that play critical roles in response and adaptation of M. truncatula to cold stress.