Unique Features of the m6A Methylome and Its Response to Salt Stress in the Roots of Sugar Beet (Beta vulgaris)

被引:3
|
作者
Li, Junliang [1 ,2 ]
Pang, Qiuying [2 ,3 ]
Yan, Xiufeng [1 ]
机构
[1] Wenzhou Univ, Inst Ecoenvironm Res Sanyang Wetland, Natl & Local Joint Engn Res Ctr Ecol Treatment Tec, Coll Life & Environm Sci,Zhejiang Prov Key Lab Wat, Zhong Xin St, Wenzhou 325035, Peoples R China
[2] Northeast Forestry Univ, Postdoctoral Res Stn, Harbin 150040, Peoples R China
[3] Northeast Forestry Univ, Coll Life Sci, Key Lab Saline Alkali Vegetat Ecol Restorat, Minist Educ, Harbin 150040, Peoples R China
关键词
m(6)A-sequencing; differentially methylated peaks; mRNA stability; salt stress; sugar beet; RED-BEET; SODIUM; TOLERANCE; GLYCOLYSIS; METABOLISM; REVEALS; ENZYMES;
D O I
10.3390/ijms241411659
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Salt is one of the most important environmental factors in crop growth and development. N-6-methyladenosine (m(6)A) is an epigenetic modification that regulates plant-environment interaction at transcriptional and translational levels. Sugar beet is a salt-tolerant sugar-yielding crop, but how m(6)A modification affects its response to salt stress remains unknown. In this study, m(6)A-seq was used to explore the role of m(6)A modification in response to salt stress in sugar beet (Beta vulgaris). Transcriptome-wide m(6)A methylation profiles and physiological responses to high salinity were investigated in beet roots. After treatment with 300 mM NaCl, the activities of peroxidase and catalase, the root activity, and the contents of Na+, K+, and Ca2+ in the roots were significantly affected by salt stress. Compared with the control plants, 6904 differentially expressed genes (DEGs) and 566 differentially methylated peaks (DMPs) were identified. Association analysis revealed that 243 DEGs contained DMP, and 80% of these DEGs had expression patterns that were negatively correlated with the extent of m(6)A modification. Further analysis verified that m(6)A methylation may regulate the expression of some genes by controlling their mRNA stability. Functional analysis revealed that m(6)A modifications primarily affect the expression of genes involved in energy metabolism, transport, signal transduction, transcription factors, and cell wall organization. This study provides evidence that a post-transcriptional regulatory mechanism mediates gene expression during salt stress by affecting the stability of mRNA in the root.
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页数:16
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