<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Song X</submitter><funding>Wancang Sun</funding><funding>Gang Yang</funding><funding>Junyan Wu</funding><funding>Wangtian Wang</funding><pagination>2737</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11942965</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(6)</volume><pubmed_abstract>Glyoxalase I (GLYI) is a key enzyme that detoxifies methylglyoxal, a toxic byproduct of glycolysis, and is essential for plant pollination. However, the genome-wide identification and functional analysis of &lt;i>GLYI&lt;/i> in &lt;i>Brassica rapa&lt;/i> L. (&lt;i>B. rapa&lt;/i>) remain limited. This study identified 17 &lt;i>BrGLYI&lt;/i> genes (&lt;i>BrGLYI1&lt;/i>-&lt;i>BrGLYI17&lt;/i>) from the &lt;i>B. rapa&lt;/i> genome. The self-compatible line 039-1 and the self-incompatible line GAU-28-5 were used as experimental materials, and Real-Time Quantitative Reverse Transcription PCR (RT-qPCR) was performed to examine the effect of &lt;i>BrGLYI&lt;/i> genes on self-compatibility in winter &lt;i>B. rapa&lt;/i>. Preliminary results showed that &lt;i>BrGLYI13&lt;/i> exhibited significant tissue specificity, with higher expression in the flowers of 03</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Cloning and Functional Analysis of Glyoxalase I Gene &amp;lt;i&amp;gt;BrGLYI 13&amp;lt;/i&amp;gt; in &amp;lt;i&amp;gt;Brassica rapa&amp;lt;/i&amp;gt; L.</pubmed_title><pmcid>PMC11942965</pmcid><funding_grant_id>CARS-12-09</funding_grant_id><funding_grant_id>GAU-KYQD-2022-09</funding_grant_id><funding_grant_id>Grant No. 2024YFD2300204-08</funding_grant_id><funding_grant_id>22ZD6NA009</funding_grant_id><pubmed_authors>Zhang F</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Yang G</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Ma L</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Tao X</pubmed_authors><pubmed_authors>Pu Y</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Sun W</pubmed_authors><pubmed_authors>Song X</pubmed_authors><pubmed_authors>Fan T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cloning and Functional Analysis of Glyoxalase I Gene &amp;lt;i&amp;gt;BrGLYI 13&amp;lt;/i&amp;gt; in &amp;lt;i&amp;gt;Brassica rapa&amp;lt;/i&amp;gt; L.</name><description>Glyoxalase I (GLYI) is a key enzyme that detoxifies methylglyoxal, a toxic byproduct of glycolysis, and is essential for plant pollination. However, the genome-wide identification and functional analysis of &lt;i>GLYI&lt;/i> in &lt;i>Brassica rapa&lt;/i> L. (&lt;i>B. rapa&lt;/i>) remain limited. This study identified 17 &lt;i>BrGLYI&lt;/i> genes (&lt;i>BrGLYI1&lt;/i>-&lt;i>BrGLYI17&lt;/i>) from the &lt;i>B. rapa&lt;/i> genome. The self-compatible line 039-1 and the self-incompatible line GAU-28-5 were used as experimental materials, and Real-Time Quantitative Reverse Transcription PCR (RT-qPCR) was performed to examine the effect of &lt;i>BrGLYI&lt;/i> genes on self-compatibility in winter &lt;i>B. rapa&lt;/i>. Preliminary results showed that &lt;i>BrGLYI13&lt;/i> exhibited significant tissue specificity, with higher expression in the flowers of 03</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-07-02T03:04:50.425Z</modification><creation>2025-07-02T03:04:50.425Z</creation></dates><accession>S-EPMC11942965</accession><cross_references><pubmed>40141379</pubmed><doi>10.3390/ijms26062737</doi></cross_references></HashMap>