<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yin Y</submitter><funding>Guangzhou Science and Technology Program</funding><funding>Forestry Grassland Ecological Protection and Restoration Program</funding><funding>Linzhi Science and Technology Program</funding><funding>Guangdong Basic and Applied Basic Research Foundation</funding><funding>Guangdong Science and Technology Plan Project</funding><funding>Science and Technology Projects in Guangzhou</funding><pagination>241</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11849335</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Paphiopedilum orchids have a high ornamental value, and flower abundance is a key horticultural trait. Most Paphiopedilum plants exhibit weak tillering ability, with their tiller buds often entering a dormant state post-formation. Tiller production plays a crucial role in enhancing flower abundance and is potentially regulated by plant hormones. However, the effect of hormones on tillering in Paphiopedilum plants is still unclear.&lt;h4>Results&lt;/h4>In this study, we investigated the promotion of tillering in P. callosum through exogenous root irrigation of benzylaminopurine (BAP). We observed a dose-dependent promotion of tiller production by BAP, with the strongest effect observed at a concentration of 400 mg/L. By comparing the expression of key genes in P. 'SCBG Yingchun' (with strong tiller ability) and P callosum (with weak tiller ability), we found that BAP promotes tillering by interacting with abscisic acid (ABA). This interaction involves down-regulation of the ABA degradation gene PcCYP707A, leading to a reduction in ABA content, and the subsequent down-regulation of dormancy-associated genes (PcDRMH1, PcSVP) to release bud dormancy. Additionally, BAP promotes sustained outgrowth of tiller buds by increasing the level of indole-3-acetic acid (IAA) through up-regulation of the IAA synthesis gene PcYUC2 and the transport gene PcPINIC.&lt;h4>Conclusions&lt;/h4>Our results indicated that the application of BAP promotes lateral bud outgrowth and increases tiller production in P. callosum. Through transcriptome analysis, we found that the BAP-promotion of tillering involves not only changes in endogenous IAA, ABA, and CTKs content but is also associated with the regulation of metabolism-related genes and dormancy-associated genes. This study presents the first comprehensive report of BAP-promoted tillering in P. callosum, providing a foundational basis for further mechanistic studies on tiller development in Paphiopedilum species and other non-model plants.</pubmed_abstract><journal>BMC plant biology</journal><pubmed_title>BAP regulates lateral bud outgrowth to promote tillering in Paphiopedilum callosum (Orchidaceae).</pubmed_title><pmcid>PMC11849335</pmcid><funding_grant_id>2023E04J0004, 2024B03J1129</funding_grant_id><funding_grant_id>2024A1515012952</funding_grant_id><funding_grant_id>E33309</funding_grant_id><funding_grant_id>2023-QYCX-02</funding_grant_id><funding_grant_id>2023B1212060046</funding_grant_id><funding_grant_id>E436070011</funding_grant_id><pubmed_authors>Yin Y</pubmed_authors><pubmed_authors>Wu K</pubmed_authors><pubmed_authors>Zeng S</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Zhong R</pubmed_authors><pubmed_authors>Guo B</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Fang L</pubmed_authors><pubmed_authors>Ma G</pubmed_authors></additional><is_claimable>false</is_claimable><name>BAP regulates lateral bud outgrowth to promote tillering in Paphiopedilum callosum (Orchidaceae).</name><description>&lt;h4>Background&lt;/h4>Paphiopedilum orchids have a high ornamental value, and flower abundance is a key horticultural trait. Most Paphiopedilum plants exhibit weak tillering ability, with their tiller buds often entering a dormant state post-formation. Tiller production plays a crucial role in enhancing flower abundance and is potentially regulated by plant hormones. However, the effect of hormones on tillering in Paphiopedilum plants is still unclear.&lt;h4>Results&lt;/h4>In this study, we investigated the promotion of tillering in P. callosum through exogenous root irrigation of benzylaminopurine (BAP). We observed a dose-dependent promotion of tiller production by BAP, with the strongest effect observed at a concentration of 400 mg/L. By comparing the expression of key genes in P. 'SCBG Yingchun' (with strong tiller ability) and P callosum (with weak tiller ability), we found that BAP promotes tillering by interacting with abscisic acid (ABA). This interaction involves down-regulation of the ABA degradation gene PcCYP707A, leading to a reduction in ABA content, and the subsequent down-regulation of dormancy-associated genes (PcDRMH1, PcSVP) to release bud dormancy. Additionally, BAP promotes sustained outgrowth of tiller buds by increasing the level of indole-3-acetic acid (IAA) through up-regulation of the IAA synthesis gene PcYUC2 and the transport gene PcPINIC.&lt;h4>Conclusions&lt;/h4>Our results indicated that the application of BAP promotes lateral bud outgrowth and increases tiller production in P. callosum. Through transcriptome analysis, we found that the BAP-promotion of tillering involves not only changes in endogenous IAA, ABA, and CTKs content but is also associated with the regulation of metabolism-related genes and dormancy-associated genes. This study presents the first comprehensive report of BAP-promoted tillering in P. callosum, providing a foundational basis for further mechanistic studies on tiller development in Paphiopedilum species and other non-model plants.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-04T09:08:51.964Z</modification><creation>2025-04-04T09:08:51.964Z</creation></dates><accession>S-EPMC11849335</accession><cross_references><pubmed>39988668</pubmed><doi>10.1186/s12870-025-06256-9</doi></cross_references></HashMap>