<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu J</submitter><funding>and Science and Technology Specific Projects in Agricultural High-tech Industrial Demonstration Area of the Yellow River Delta</funding><funding>the Agricultural Variety Improvement Project of Shandong Province</funding><funding>Natural Science Foundation of Shandong Province</funding><funding>the China Agriculture Research System Foundation</funding><funding>Scholar Foundation of Shandong Province</funding><pagination>uhae031</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10933707</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(3)</volume><pubmed_abstract>Apple fruit skin color fading is not well understood although the molecular mechanism of skin color formation is well known. The red-fleshed apple cultivar 'Daihong' (DH) exhibited fading skin color during fruit development despite having a heterozygous R6 allele but lacking Red-TE for red fruit skin. In this study, transcriptomic analysis revealed the expression level of &lt;i>MdMYB10&lt;/i> increased with fruit development whereas reduced expression levels of &lt;i>MdMYBPA1&lt;/i>, &lt;i>MdCHS&lt;/i>, &lt;i>MdANS&lt;/i>, &lt;i>MdUFGT&lt;/i>, &lt;i>MdLAR&lt;/i>, and &lt;i>MdANR&lt;/i> were observed, consistent with decreased levels of chalcone, anthocyanin, catechin, epicatechin, and procyanidin B2. Whole-genome bisulfite sequencing (WGBS) indicated a global gain in cytosine methylation levels and increased methylation in 5' and 3' flanking regions of genes and transposable elements (TEs), and in TE bodies in all CG, CHG and CHH contexts, especially the mCHH context, during fruit development. The increased DNA methylation was attributed to reduced expression levels of DNA demethylase genes, including &lt;i>MdDME1&lt;/i>, &lt;i>MdROS1&lt;/i>, and &lt;i>MdROS2&lt;/i>. Association analysis revealed a significant negative correlation between promoter methylation levels of &lt;i>MdCHS&lt;/i>, &lt;i>MdCHI&lt;/i>, &lt;i>MdMYBPA1&lt;/i>, and their respective transcript levels, as well as a negative correlation between promoter methylation levels of &lt;i>MdCHS&lt;/i>, &lt;i>MdCHI&lt;/i>, &lt;i>MdANR&lt;/i>, and &lt;i>MdFLS&lt;/i>, and the content of chalcones, naringenin-7-glucoside, epicatechin, and quercetin. Treatment with the DNA demethylation agent 5-aza-2'-deoxycytidine verified the negative correlation between DNA methylation and gene expression within the flavonoid pathway. These findings suggest that hypermethylation in promoter regions of genes of the flavonoid biosynthesis pathway is associated with the reduction of gene expression and flavonoid content, and fruit skin color fading during DH apple development.</pubmed_abstract><journal>Horticulture research</journal><pubmed_title>Hypermethylation in the promoter regions of flavonoid pathway genes is associated with skin color fading during 'Daihong' apple fruit development.</pubmed_title><pmcid>PMC10933707</pmcid><funding_grant_id>CARS-27</funding_grant_id><funding_grant_id>tstp20221134</funding_grant_id><funding_grant_id>ZR2023MC169</funding_grant_id><funding_grant_id>2023LZGCQY007; 2021LZGC024; 2022LZGC010</funding_grant_id><funding_grant_id>2022SZX34</funding_grant_id><pubmed_authors>Yao JL</pubmed_authors><pubmed_authors>Xiong L</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Zhao P</pubmed_authors><pubmed_authors>Jiang H</pubmed_authors><pubmed_authors>Jiang S</pubmed_authors><pubmed_authors>Sun X</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>Xu J</pubmed_authors><pubmed_authors>Dong C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hypermethylation in the promoter regions of flavonoid pathway genes is associated with skin color fading during 'Daihong' apple fruit development.</name><description>Apple fruit skin color fading is not well understood although the molecular mechanism of skin color formation is well known. The red-fleshed apple cultivar 'Daihong' (DH) exhibited fading skin color during fruit development despite having a heterozygous R6 allele but lacking Red-TE for red fruit skin. In this study, transcriptomic analysis revealed the expression level of &lt;i>MdMYB10&lt;/i> increased with fruit development whereas reduced expression levels of &lt;i>MdMYBPA1&lt;/i>, &lt;i>MdCHS&lt;/i>, &lt;i>MdANS&lt;/i>, &lt;i>MdUFGT&lt;/i>, &lt;i>MdLAR&lt;/i>, and &lt;i>MdANR&lt;/i> were observed, consistent with decreased levels of chalcone, anthocyanin, catechin, epicatechin, and procyanidin B2. Whole-genome bisulfite sequencing (WGBS) indicated a global gain in cytosine methylation levels and increased methylation in 5' and 3' flanking regions of genes and transposable elements (TEs), and in TE bodies in all CG, CHG and CHH contexts, especially the mCHH context, during fruit development. The increased DNA methylation was attributed to reduced expression levels of DNA demethylase genes, including &lt;i>MdDME1&lt;/i>, &lt;i>MdROS1&lt;/i>, and &lt;i>MdROS2&lt;/i>. Association analysis revealed a significant negative correlation between promoter methylation levels of &lt;i>MdCHS&lt;/i>, &lt;i>MdCHI&lt;/i>, &lt;i>MdMYBPA1&lt;/i>, and their respective transcript levels, as well as a negative correlation between promoter methylation levels of &lt;i>MdCHS&lt;/i>, &lt;i>MdCHI&lt;/i>, &lt;i>MdANR&lt;/i>, and &lt;i>MdFLS&lt;/i>, and the content of chalcones, naringenin-7-glucoside, epicatechin, and quercetin. Treatment with the DNA demethylation agent 5-aza-2'-deoxycytidine verified the negative correlation between DNA methylation and gene expression within the flavonoid pathway. These findings suggest that hypermethylation in promoter regions of genes of the flavonoid biosynthesis pathway is associated with the reduction of gene expression and flavonoid content, and fruit skin color fading during DH apple development.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-30T03:10:28.47Z</modification><creation>2025-04-04T19:16:47.632Z</creation></dates><accession>S-EPMC10933707</accession><cross_references><pubmed>38481937</pubmed><doi>10.1093/hr/uhae031</doi></cross_references></HashMap>