4.7 Article

Maize DNA Methylation in Response to Drought Stress Is Involved in Target Gene Expression and Alternative Splicing

Journal

Publisher

MDPI
DOI: 10.3390/ijms22158285

Keywords

DNA methylation; drought stress; gene regulation; maize

Funding

  1. Key Research and Development Program of Sichuan Province, China [2020YFH0116, 2020YJ0350]
  2. National Special Support Program for High-level Talent of China
  3. National Natural Science Foundation of China [31871640, 32072074]
  4. Foundation of International Cooperation in Science and Technology of Chengdu, China [2020-GH02-00027-HZ]

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In maize roots, DNA methylation levels change under water stress, with more stable methylomes in drought-tolerant inbred lines. Different responses to stress were observed among inbred lines with varying drought sensitivities. DNA methylation showed a negative correlation with gene expression and a positive correlation with exon splicing events, while a positive correlation was also observed between small interfering RNA (siRNA) and DNA methylation, consistent with the differential DNA methylation response under water stress.
DNA methylation is important for plant growth, development, and stress response. To understand DNA methylation dynamics in maize roots under water stress (WS), we reanalyzed DNA methylation sequencing data to profile DNA methylation and the gene expression landscape of two inbred lines with different drought sensitivities, as well as two of their derived recombination inbred lines (RILs). Combined with genotyping-by-sequencing, we found that the inheritance pattern of DNA methylation between RILs and parental lines was sequence-dependent. Increased DNA methylation levels were observed under WS and the methylome of drought-tolerant inbred lines were much more stable than that of the drought-sensitive inbred lines. Distinctive differentially methylated genes were found among diverse genetic backgrounds, suggesting that inbred lines with different drought sensitivities may have responded to stress in varying ways. Gene body DNA methylation showed a negative correlation with gene expression but a positive correlation with exon splicing events. Furthermore, a positive correlation of a varying extent was observed between small interfering RNA (siRNA) and DNA methylation, which at different genic regions. The response of siRNAs under WS was consistent with the differential DNA methylation. Taken together, our data can be useful in deciphering the roles of DNA methylation in plant drought-tolerance variations and in emphasizing its function in alternative splicing.

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