<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang X</submitter><funding>The technology integration and demonstration promotion project of “Zhi-Mi-AI” simplified and efficient cultivation of cotton in Jiangxi Province</funding><funding>The National Key Research and Development Program of China</funding><funding>The technology integration and demonstration promotion project of "Zhi-Mi-AI" simplified and efficient cultivation of cotton in Jiangxi Province</funding><funding>Guiding project of Agriculture, animal husbandry and fishery in Jiangxi Province</funding><pagination>312</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11036760</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>DNA methylation is an important epigenetic mode of genomic DNA modification and plays a vital role in maintaining epigenetic content and regulating gene expression. Cytosine-5 DNA methyltransferase (C5-MTase) are the key enzymes in the process of DNA methylation. However, there is no systematic analysis of the C5-MTase in cotton so far, and the function of DNMT2 genes has not been studied.&lt;h4>Methods&lt;/h4>In this study, the whole genome of cotton C5-MTase coding genes was identified and analyzed using a bioinformatics method based on information from the cotton genome, and the function of GhDMT6 was further validated by VIGS experiments and subcellular localization analysis.&lt;h4>Results&lt;/h4>33 C5-MTases were identified from three cotton genomes, and were divided into four subfamilies by systematic evolutionary analysis. After the protein domain alignment of C5-MTases in cotton, 6 highly conserved motifs were found in the C-terminus of 33 proteins involved in methylation modification, which indicated that C5-MTases had a basic catalytic methylation function. These proteins were divided into four classes based on the N-terminal difference, of which DNMT2 lacks the N-terminal regulatory domain. The expression of C5-MTases in different parts of cotton was different under different stress treatments, which indicated the functional diversity of cotton C5-MTase gene family. Among the C5-MTases, the GhDMT6 had a obvious up-regulated expression. After silencing GhDMT6 with VIGS, the phenotype of cotton seedlings under different stress treatments showed a significant difference. Compared with cotton seedlings that did not silence GhDMT6, cotton seedlings silencing GhDMT6 showed significant stress resistance.&lt;h4>Conclusion&lt;/h4>The results show that C5-MTases plays an important role in cotton stress response, which is beneficial to further explore the function of DNMT2 subfamily genes.</pubmed_abstract><journal>BMC plant biology</journal><pubmed_title>Genome-wide characterization of DNA methyltransferase family genes implies GhDMT6 improving tolerance of salt and drought on cotton.</pubmed_title><pmcid>PMC11036760</pmcid><funding_grant_id>No. 2022YFD1200300</funding_grant_id><funding_grant_id>NO.2023-14</funding_grant_id><funding_grant_id>No. CCRI 2023-17</funding_grant_id><pubmed_authors>Lu X</pubmed_authors><pubmed_authors>Han M</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Ye W</pubmed_authors><pubmed_authors>Bai Z</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Yin Z</pubmed_authors><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Sun L</pubmed_authors><pubmed_authors>Wang N</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Guo L</pubmed_authors><pubmed_authors>He Y</pubmed_authors><pubmed_authors>Feng K</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Zhang B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-wide characterization of DNA methyltransferase family genes implies GhDMT6 improving tolerance of salt and drought on cotton.</name><description>&lt;h4>Background&lt;/h4>DNA methylation is an important epigenetic mode of genomic DNA modification and plays a vital role in maintaining epigenetic content and regulating gene expression. Cytosine-5 DNA methyltransferase (C5-MTase) are the key enzymes in the process of DNA methylation. However, there is no systematic analysis of the C5-MTase in cotton so far, and the function of DNMT2 genes has not been studied.&lt;h4>Methods&lt;/h4>In this study, the whole genome of cotton C5-MTase coding genes was identified and analyzed using a bioinformatics method based on information from the cotton genome, and the function of GhDMT6 was further validated by VIGS experiments and subcellular localization analysis.&lt;h4>Results&lt;/h4>33 C5-MTases were identified from three cotton genomes, and were divided into four subfamilies by systematic evolutionary analysis. After the protein domain alignment of C5-MTases in cotton, 6 highly conserved motifs were found in the C-terminus of 33 proteins involved in methylation modification, which indicated that C5-MTases had a basic catalytic methylation function. These proteins were divided into four classes based on the N-terminal difference, of which DNMT2 lacks the N-terminal regulatory domain. The expression of C5-MTases in different parts of cotton was different under different stress treatments, which indicated the functional diversity of cotton C5-MTase gene family. Among the C5-MTases, the GhDMT6 had a obvious up-regulated expression. After silencing GhDMT6 with VIGS, the phenotype of cotton seedlings under different stress treatments showed a significant difference. Compared with cotton seedlings that did not silence GhDMT6, cotton seedlings silencing GhDMT6 showed significant stress resistance.&lt;h4>Conclusion&lt;/h4>The results show that C5-MTases plays an important role in cotton stress response, which is beneficial to further explore the function of DNMT2 subfamily genes.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-06-03T01:32:07.974Z</modification><creation>2026-04-22T03:13:29.364Z</creation></dates><accession>S-EPMC11036760</accession><cross_references><pubmed>38649800</pubmed><doi>10.1186/s12870-024-04985-x</doi></cross_references></HashMap>