<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Su K</submitter><funding>Natural Science Research Project of Anhui Province</funding><pagination>409</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12027353</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Cucumber (&lt;i>Cucumis sativus&lt;/i> L.) is an important economic crop worldwide. Response regulators (RRs) play crucial roles in plant growth, development, and responses to both biotic and abiotic stresses.&lt;h4>Methods&lt;/h4>Combined analysis of 182 re-sequencing and transcriptome datasets was conducted to investigate &lt;i>CsRR&lt;/i> variations, with subsequent RT-qPCR experiments confirming its functional significance.&lt;h4>Results&lt;/h4>In this study, 18 &lt;i>CsRR&lt;/i> genes were identified and classified into three groups according to their protein structures: A-ARRs (3), B-ARRs (8), and PRRs (7). Resequencing uncovered critical mutations (non-synonymous SNPs, frameshift, and stop-gain variants) in &lt;i>CsRR&lt;/i> genes. Transcriptome data revealed that five genes responded to abiotic stress and four responded to biotic stress. &lt;i>CsPRR1&lt;/i> was upregulated in both resistant and susceptible lines at five dpi, downregulated in resistant plants at nine dpi, and showed no significant difference at 11 dpi. &lt;i>CsPRR2&lt;/i> was consistently upregulated in both lines at 5, 9, and 11 dpi. &lt;i>CsPRR3&lt;/i> was upregulated in resistant lines at nine dpi but downregulated at 11 dpi. &lt;i>CsARR8&lt;/i> was significantly downregulated in both lines at 9 and 11 dpi. Notably, &lt;i>CsPRR2&lt;/i> demonstrated dual functionality related to (i) the regulation of immature fruit skin color via a stop-gain InDel and (ii) resistance to Foc, as the gene was upregulated in both resistant and susceptible lines after inoculation with the pathogen.&lt;h4>Conclusions&lt;/h4>This study integrated resequencing and transcriptomic data to comprehensively characterize &lt;i>CsRR&lt;/i> genes, establishing a foundation for further exploration of their functional mechanisms in cucumber.</pubmed_abstract><journal>Genes</journal><pubmed_title>Resequencing and Transcriptome Analyses Reveal Variations and Expression Patterns of the RR Gene Family in Cucumber.</pubmed_title><pmcid>PMC12027353</pmcid><funding_grant_id>2023AH051056</funding_grant_id><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Gao Y</pubmed_authors><pubmed_authors>Su K</pubmed_authors><pubmed_authors>Ao W</pubmed_authors><pubmed_authors>Sun Z</pubmed_authors><pubmed_authors>Gan D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Resequencing and Transcriptome Analyses Reveal Variations and Expression Patterns of the RR Gene Family in Cucumber.</name><description>&lt;h4>Background&lt;/h4>Cucumber (&lt;i>Cucumis sativus&lt;/i> L.) is an important economic crop worldwide. Response regulators (RRs) play crucial roles in plant growth, development, and responses to both biotic and abiotic stresses.&lt;h4>Methods&lt;/h4>Combined analysis of 182 re-sequencing and transcriptome datasets was conducted to investigate &lt;i>CsRR&lt;/i> variations, with subsequent RT-qPCR experiments confirming its functional significance.&lt;h4>Results&lt;/h4>In this study, 18 &lt;i>CsRR&lt;/i> genes were identified and classified into three groups according to their protein structures: A-ARRs (3), B-ARRs (8), and PRRs (7). Resequencing uncovered critical mutations (non-synonymous SNPs, frameshift, and stop-gain variants) in &lt;i>CsRR&lt;/i> genes. Transcriptome data revealed that five genes responded to abiotic stress and four responded to biotic stress. &lt;i>CsPRR1&lt;/i> was upregulated in both resistant and susceptible lines at five dpi, downregulated in resistant plants at nine dpi, and showed no significant difference at 11 dpi. &lt;i>CsPRR2&lt;/i> was consistently upregulated in both lines at 5, 9, and 11 dpi. &lt;i>CsPRR3&lt;/i> was upregulated in resistant lines at nine dpi but downregulated at 11 dpi. &lt;i>CsARR8&lt;/i> was significantly downregulated in both lines at 9 and 11 dpi. Notably, &lt;i>CsPRR2&lt;/i> demonstrated dual functionality related to (i) the regulation of immature fruit skin color via a stop-gain InDel and (ii) resistance to Foc, as the gene was upregulated in both resistant and susceptible lines after inoculation with the pathogen.&lt;h4>Conclusions&lt;/h4>This study integrated resequencing and transcriptomic data to comprehensively characterize &lt;i>CsRR&lt;/i> genes, establishing a foundation for further exploration of their functional mechanisms in cucumber.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-07-03T03:27:13.192Z</modification><creation>2025-07-07T03:08:49.417Z</creation></dates><accession>S-EPMC12027353</accession><cross_references><pubmed>40282369</pubmed><doi>10.3390/genes16040409</doi></cross_references></HashMap>