<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Huang H</submitter><funding>the Guangdong Provincial Special Fund for Modern Agriculture Industry Technology Innovation Teams, Department of Agriculture and Rural Affairs of Guangdong Province</funding><funding>the Laboratory of Lingnan Modern Agriculture Project</funding><funding>the Earmarked Fund for CARS</funding><funding>the Research Fund of Maoming Branch, Guangdong Laboratory for Lingnan Modern Agriculture</funding><funding>the Guangdong Science and Technology Project:</funding><funding>the Science and Technology Department of Guangdong Province</funding><pagination>3420</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10970408</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(6)</volume><pubmed_abstract>Modern plant breeding relies heavily on the deployment of susceptibility and resistance genes to defend crops against diseases. The expression of these genes is usually regulated by transcription factors including members of the AP2/ERF family. While these factors are a vital component of the plant immune response, little is known of their specific roles in defense against &lt;i>Fusarium oxysporum&lt;/i> f. sp. &lt;i>cubense&lt;/i> tropical race 4 (&lt;i>Foc&lt;/i> TR4) in banana plants. In this study, we discovered that MaERF12, a pathogen-induced ERF in bananas, acts as a resistance gene against &lt;i>Foc&lt;/i> TR4. The yeast two-hybrid assays and protein-protein docking analyses verified the interaction between this gene and MaSMG7, which plays a role in nonsense-mediated RNA decay. The transient expression of MaERF12 in &lt;i>Nicotiana benthamiana&lt;/i> was found to induce strong cell death, which could be inhibited by MaSMG7 during co-expression. Furthermore, the immunoblot analyses have revealed the potential degradation of MaERF12 by MaSMG7 through the 26S proteasome pathway. These findings demonstrate that MaSMG7 acts as a susceptibility factor and interferes with MaERF12 to facilitate &lt;i>Foc&lt;/i> TR4 infection in banana plants. Our study provides novel insights into the biological functions of the MaERF12 as a resistance gene and MaSMG7 as a susceptibility gene in banana plants. Furthermore, the first discovery of interactions between MaERF12 and MaSMG7 could facilitate future research on disease resistance or susceptibility genes for the genetic improvement of bananas.</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>MaSMG7-Mediated Degradation of MaERF12 Facilitates &lt;i>Fusarium oxysporum&lt;/i> f. sp. &lt;i>cubense&lt;/i> Tropical Race 4 Infection in &lt;i>Musa acuminata&lt;/i>.</pubmed_title><pmcid>PMC10970408</pmcid><funding_grant_id>2022A1515110433</funding_grant_id><funding_grant_id>2021TDQD003</funding_grant_id><funding_grant_id>2023KJ109</funding_grant_id><funding_grant_id>NT2021004</funding_grant_id><funding_grant_id>CARS-31</funding_grant_id><funding_grant_id>2023A0505090004</funding_grant_id><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Huo Y</pubmed_authors><pubmed_authors>Huang H</pubmed_authors><pubmed_authors>Tian Y</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Yi G</pubmed_authors></additional><is_claimable>false</is_claimable><name>MaSMG7-Mediated Degradation of MaERF12 Facilitates &lt;i>Fusarium oxysporum&lt;/i> f. sp. &lt;i>cubense&lt;/i> Tropical Race 4 Infection in &lt;i>Musa acuminata&lt;/i>.</name><description>Modern plant breeding relies heavily on the deployment of susceptibility and resistance genes to defend crops against diseases. The expression of these genes is usually regulated by transcription factors including members of the AP2/ERF family. While these factors are a vital component of the plant immune response, little is known of their specific roles in defense against &lt;i>Fusarium oxysporum&lt;/i> f. sp. &lt;i>cubense&lt;/i> tropical race 4 (&lt;i>Foc&lt;/i> TR4) in banana plants. In this study, we discovered that MaERF12, a pathogen-induced ERF in bananas, acts as a resistance gene against &lt;i>Foc&lt;/i> TR4. The yeast two-hybrid assays and protein-protein docking analyses verified the interaction between this gene and MaSMG7, which plays a role in nonsense-mediated RNA decay. The transient expression of MaERF12 in &lt;i>Nicotiana benthamiana&lt;/i> was found to induce strong cell death, which could be inhibited by MaSMG7 during co-expression. Furthermore, the immunoblot analyses have revealed the potential degradation of MaERF12 by MaSMG7 through the 26S proteasome pathway. These findings demonstrate that MaSMG7 acts as a susceptibility factor and interferes with MaERF12 to facilitate &lt;i>Foc&lt;/i> TR4 infection in banana plants. Our study provides novel insights into the biological functions of the MaERF12 as a resistance gene and MaSMG7 as a susceptibility gene in banana plants. Furthermore, the first discovery of interactions between MaERF12 and MaSMG7 could facilitate future research on disease resistance or susceptibility genes for the genetic improvement of bananas.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-04T23:53:44.444Z</modification><creation>2025-04-04T23:53:44.444Z</creation></dates><accession>S-EPMC10970408</accession><cross_references><pubmed>38542394</pubmed><doi>10.3390/ijms25063420</doi></cross_references></HashMap>