<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Martinho C</submitter><funding>RCUK | Biotechnology and Biological Sciences Research Council</funding><pagination>e2112240119</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9060480</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>119(13)</volume><pubmed_abstract>SignificanceParamutation involves the transfer of a repressive epigenetic mark between silent and active alleles. It is best known from exceptional non-Mendelian inheritance of conspicuous phenotypes in maize but also in other plants and animals. Recent genomic studies, however, indicate that paramutation may be less exceptional. It may be a consequence of wide-cross hybridization and may contribute to quantitative trait variation or unstable phenotypes in crops. Using the &lt;i>sulfurea&lt;/i> (&lt;i>sulf&lt;/i>) locus in tomato, we demonstrate that a self-reinforcing feedback loop involving DNA- and histone-methyl transferases CHROMOMETHYLTRANSFERASE3 (CMT3) and KRYPTONITE (KYP) is required for paramutation of &lt;i>sulf&lt;/i> and that there is a change in chromatin organization. These findings advance t</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pubmed_title>CHROMOMETHYLTRANSFERASE3/KRYPTONITE maintains the &lt;i>sulfurea&lt;/i> paramutation in &lt;i>Solanum lycopersicum&lt;/i>.</pubmed_title><pmcid>PMC9060480</pmcid><funding_grant_id>PDAG/387</funding_grant_id><pubmed_authors>Buddle S</pubmed_authors><pubmed_authors>Ghigi A</pubmed_authors><pubmed_authors>Yarur A</pubmed_authors><pubmed_authors>Gouil Q</pubmed_authors><pubmed_authors>Muller S</pubmed_authors><pubmed_authors>Stam M</pubmed_authors><pubmed_authors>Barbour F</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Martinho C</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Baulcombe DC</pubmed_authors></additional><is_claimable>false</is_claimable><name>CHROMOMETHYLTRANSFERASE3/KRYPTONITE maintains the &lt;i>sulfurea&lt;/i> paramutation in &lt;i>Solanum lycopersicum&lt;/i>.</name><description>SignificanceParamutation involves the transfer of a repressive epigenetic mark between silent and active alleles. It is best known from exceptional non-Mendelian inheritance of conspicuous phenotypes in maize but also in other plants and animals. Recent genomic studies, however, indicate that paramutation may be less exceptional. It may be a consequence of wide-cross hybridization and may contribute to quantitative trait variation or unstable phenotypes in crops. Using the &lt;i>sulfurea&lt;/i> (&lt;i>sulf&lt;/i>) locus in tomato, we demonstrate that a self-reinforcing feedback loop involving DNA- and histone-methyl transferases CHROMOMETHYLTRANSFERASE3 (CMT3) and KRYPTONITE (KYP) is required for paramutation of &lt;i>sulf&lt;/i> and that there is a change in chromatin organization. These findings advance t</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-04T21:33:27.715Z</modification><creation>2025-02-19T03:27:47.776Z</creation></dates><accession>S-EPMC9060480</accession><cross_references><pubmed>35324329</pubmed><doi>10.1073/pnas.2112240119</doi></cross_references></HashMap>