<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sakai Y</submitter><funding>Suntory Foundation for Life Sciences</funding><funding>Kyoto University Foundation</funding><funding>Ministry of Education, Culture, Sports, Science and Technology</funding><funding>Asahi Glass Foundation</funding><funding>Yamada Science Foundation</funding><funding>Ohsumi Frontier Science Foundation</funding><funding>Japan Science and Technology Agency</funding><funding>Japan Society for the Promotion of Science</funding><pagination>2678-2696</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12371152</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>247(6)</volume><pubmed_abstract>Many plants reproduce asexually by generating clonal progeny from vegetative tissues, a process known as vegetative reproduction. This reproduction mode contrasts with sexual reproduction, which enhances genetic diversity. The bryophyte Marchantia polymorpha L. adjusts its reproductive strategy in response to seasonal environmental cues, transitioning between vegetative and sexual reproduction. In this study, we identified a gene encoding the R2R3-MYB transcription factor SHOT GLASS (MpSTG) as a critical regulator of gemma cup development. MpSTG was predominantly expressed in the gemma cup, apical notch, and sexual reproductive organs (gametangiophores). MpSTG mutation resulted in the formation of abnormal shot-glass-shaped structures lacking gemmae, which replaced functional gemma cups. Additionally, MpSTG-disrupted plants failed to develop sexual reproductive organs, even under inductive conditions. In Arabidopsis thaliana, the MpSTG ortholog LATERAL ORGAN FUSION1 (AtLOF1) plays a pivotal role in lateral bud formation. We demonstrated that MpSTG can partially compensate for AtLOF1's function in lateral bud formation in A. thaliana. Our findings suggest that MpSTG is a key regulator of vegetative and sexual reproduction in M. polymorpha, and illustrate that evolutionarily conserved developmental mechanisms may function in both the gametophyte generation of bryophytes and the sporophyte generation of angiosperms.</pubmed_abstract><journal>The New phytologist</journal><pubmed_title>SHOT GLASS, an R2R3-MYB transcription factor, promotes gemma cup and gametangiophore development in Marchantia polymorpha.</pubmed_title><pmcid>PMC12371152</pmcid><funding_grant_id>KAKENHI 21K15125</funding_grant_id><funding_grant_id>KAKENHI 15H01233</funding_grant_id><funding_grant_id>KAKENHI 15H04391</funding_grant_id><funding_grant_id>KAKENHI 19H05673</funding_grant_id><funding_grant_id>KAKENHI 19H05670</funding_grant_id><funding_grant_id>J-PEAKS</funding_grant_id><funding_grant_id>KAKENHI 20H05780</funding_grant_id><funding_grant_id>KAKENHI 17H06472</funding_grant_id><funding_grant_id>KAKENHI25K09689</funding_grant_id><funding_grant_id>KAKENHI 19H03247</funding_grant_id><funding_grant_id>KAKENHI 21J40092</funding_grant_id><funding_grant_id>J‐PEAKS</funding_grant_id><funding_grant_id>KAKENHI 25119711</funding_grant_id><funding_grant_id>JPMJGX23B0</funding_grant_id><pubmed_authors>Kato H</pubmed_authors><pubmed_authors>Fukaki H</pubmed_authors><pubmed_authors>Sakai Y</pubmed_authors><pubmed_authors>Kohchi T</pubmed_authors><pubmed_authors>Yamaoka S</pubmed_authors><pubmed_authors>Ishizaki K</pubmed_authors><pubmed_authors>Takami H</pubmed_authors></additional><is_claimable>false</is_claimable><name>SHOT GLASS, an R2R3-MYB transcription factor, promotes gemma cup and gametangiophore development in Marchantia polymorpha.</name><description>Many plants reproduce asexually by generating clonal progeny from vegetative tissues, a process known as vegetative reproduction. This reproduction mode contrasts with sexual reproduction, which enhances genetic diversity. The bryophyte Marchantia polymorpha L. adjusts its reproductive strategy in response to seasonal environmental cues, transitioning between vegetative and sexual reproduction. In this study, we identified a gene encoding the R2R3-MYB transcription factor SHOT GLASS (MpSTG) as a critical regulator of gemma cup development. MpSTG was predominantly expressed in the gemma cup, apical notch, and sexual reproductive organs (gametangiophores). MpSTG mutation resulted in the formation of abnormal shot-glass-shaped structures lacking gemmae, which replaced functional gemma cups. Additionally, MpSTG-disrupted plants failed to develop sexual reproductive organs, even under inductive conditions. In Arabidopsis thaliana, the MpSTG ortholog LATERAL ORGAN FUSION1 (AtLOF1) plays a pivotal role in lateral bud formation. We demonstrated that MpSTG can partially compensate for AtLOF1's function in lateral bud formation in A. thaliana. Our findings suggest that MpSTG is a key regulator of vegetative and sexual reproduction in M. polymorpha, and illustrate that evolutionarily conserved developmental mechanisms may function in both the gametophyte generation of bryophytes and the sporophyte generation of angiosperms.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-08T10:53:15.728Z</modification><creation>2026-05-03T03:06:15.237Z</creation></dates><accession>S-EPMC12371152</accession><cross_references><pubmed>40734229</pubmed><doi>10.1111/nph.70337</doi></cross_references></HashMap>