<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang C</submitter><funding>Guangxi Science and Technology Base and Special Talents</funding><funding>Innovative Team for Traditional Chinese Medicinal Materials Quality of Guangxi</funding><funding>Natural Science Foundation of Guangxi Province</funding><funding>Key Laboratory Construction Program of Guangxi Health commission</funding><funding>Gaungxi Bagui Brilliance Visiting Scholar Program</funding><funding>Guangxi Traditional Chinese Medicine Appropriate Technology Development and Promotion Project</funding><funding>Natural Science Foundation of Guangxi Province (2023GXNSFAA026330), Gaungxi Bagui Brilliance Visiting Scholar Program (Lingyun Wan), Guangxi Science and Technology Base and Special Talents (Guike AD22035026), Innovative Team for Traditional Chinese Medici</funding><pagination>953</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12385686</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(8)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>&lt;i>Centella asiatica&lt;/i>, a medicinally important species that is rich in bioactive compounds, lacks a characterized mitochondrial genome, despite nuclear and chloroplast assemblies. We sequenced and annotated its mitochondrial genome to elucidate its genetic foundations and evolutionary mechanisms.&lt;h4>Methods&lt;/h4>Assembly using Illumina short-reads and Nanopore long-reads was used to characterize the mitochondrial genome. Analyses included structural characterization, codon usage bias, repetitive sequences, horizontal gene transfer (HGT), collinearity, and phylogeny. The resulting tissue-specific (root, stem, and leaf) long non-coding RNA (lncRNA) profiles identified RNA editing sites.&lt;h4>Results&lt;/h4>The complete mitochondrial genome (249,777 bp, 45.5% GC) comprises thr</pubmed_abstract><journal>Genes</journal><pubmed_title>Mitochondrial Genome and RNA Editing Tissue Specificity of &amp;lt;i&amp;gt;Centella asiatica&amp;lt;/i&amp;gt;.</pubmed_title><pmcid>PMC12385686</pmcid><funding_grant_id>GZKJ2305</funding_grant_id><funding_grant_id>GZSY23-02</funding_grant_id><funding_grant_id>(2023GXNSFAA026330); (Guike AD22035026); (GZKJ2305); (GZSY23-02); (ZJC2020003)</funding_grant_id><funding_grant_id>Guike AD22035026</funding_grant_id><funding_grant_id>ZJC2020003</funding_grant_id><funding_grant_id>2023GXNSFAA026330</funding_grant_id><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Liang W</pubmed_authors><pubmed_authors>Tan G</pubmed_authors><pubmed_authors>Wei S</pubmed_authors><pubmed_authors>Wan L</pubmed_authors><pubmed_authors>Gui L</pubmed_authors><pubmed_authors>Qin Y</pubmed_authors><pubmed_authors>El-Sappah AH</pubmed_authors><pubmed_authors>Huang Q</pubmed_authors><pubmed_authors>Yang C</pubmed_authors><pubmed_authors>Wei Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mitochondrial Genome and RNA Editing Tissue Specificity of &amp;lt;i&amp;gt;Centella asiatica&amp;lt;/i&amp;gt;.</name><description>&lt;h4>Background&lt;/h4>&lt;i>Centella asiatica&lt;/i>, a medicinally important species that is rich in bioactive compounds, lacks a characterized mitochondrial genome, despite nuclear and chloroplast assemblies. We sequenced and annotated its mitochondrial genome to elucidate its genetic foundations and evolutionary mechanisms.&lt;h4>Methods&lt;/h4>Assembly using Illumina short-reads and Nanopore long-reads was used to characterize the mitochondrial genome. Analyses included structural characterization, codon usage bias, repetitive sequences, horizontal gene transfer (HGT), collinearity, and phylogeny. The resulting tissue-specific (root, stem, and leaf) long non-coding RNA (lncRNA) profiles identified RNA editing sites.&lt;h4>Results&lt;/h4>The complete mitochondrial genome (249,777 bp, 45.5% GC) comprises thr</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-07-05T03:16:25.526Z</modification><creation>2026-07-05T03:12:20.103Z</creation></dates><accession>S-EPMC12385686</accession><cross_references><pubmed>40870001</pubmed><doi>10.3390/genes16080953</doi></cross_references></HashMap>