The underlying molecular conservation and diversification of dioecious flower and leaf buds provide insights into the development, dormancy breaking, flowering, and sex association of willows
As harbingers of bursting growth, flower buds and leaf buds generally show similar surface morphologies but different structural and functional changes. Dioecious plants further generate four types of Female/Male Flower/Leaf Buds (FFB, FLB, MFB, and MLB), showing a complex regulation. However, littl...
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Veröffentlicht in: | Plant physiology and biochemistry 2021-10, Vol.167, p.651-664 |
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description | As harbingers of bursting growth, flower buds and leaf buds generally show similar surface morphologies but different structural and functional changes. Dioecious plants further generate four types of Female/Male Flower/Leaf Buds (FFB, FLB, MFB, and MLB), showing a complex regulation. However, little is known about their underlying molecular mechanisms. Here, we exemplify the woody dioecious Salix linearistipularis to investigate their morphological characteristics and potential molecular mechanisms by combining cytological, physiological, phenological, and transcriptomic datasets. First, FFB and MFB have simultaneous development dynamics and so do FLB and MLB. Interestingly, FLB and MLB show very similar expression profiles preparing for photosynthesis and stress-tolerance, whereas FFB and MFB show great similarities but also striking sexual differences. Comparing flower buds and leaf buds after their revival from dormancy shows different cold- and vernalization-responsive genes (e.g. SliVRN1, SliAGL19, and SliAGL24), implying different programming processes for dormancy breaking between the buds. Moreover, except SliAP3, the expression of ABCDE model genes is consistent with their roles in the buds, suggesting a conserved mechanism of flower development between dioecious Salix and hermaphrodite Arabidopsis. Finally, considering sex-associated genes (e.g. SliCLE25, SliTPS21, and SliARR9) on Salix chromosomes and other reports, we hypothesize a dynamic model of sex determination on chromosomes 15 and 19 in the last ancestor of Salix and Populus but evolutionarily on 15 in Salix after their divergence. Together, our study provides new insights into the molecular mechanisms of dioecious four-type buds by showing the genes involved in their development, dormancy breaking, flowering, and sexual association.
•S. linearistipularis FFB/MFB have simultaneous development dynamics; so do FLB/MLB.•FLB/MLB show similar expression, while FFB/MFB show similarity but sexual difference.•LB/FB have different programming of dormancy breaking by regulating different genes.•The ABCDE model of flower development is conserved in the dioecious Salix.•A dynamic sex determination is assumed on Chr 15/19 in the ancestor of Salix/Populus. |
doi_str_mv | 10.1016/j.plaphy.2021.08.044 |
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•S. linearistipularis FFB/MFB have simultaneous development dynamics; so do FLB/MLB.•FLB/MLB show similar expression, while FFB/MFB show similarity but sexual difference.•LB/FB have different programming of dormancy breaking by regulating different genes.•The ABCDE model of flower development is conserved in the dioecious Salix.•A dynamic sex determination is assumed on Chr 15/19 in the ancestor of Salix/Populus.</description><identifier>ISSN: 0981-9428</identifier><identifier>EISSN: 1873-2690</identifier><identifier>DOI: 10.1016/j.plaphy.2021.08.044</identifier><language>eng</language><publisher>Elsevier Masson SAS</publisher><subject>ABCDE model ; Dioecy ; Flower bud ; Leaf bud ; Sex determination ; Transcriptome ; Vernalization</subject><ispartof>Plant physiology and biochemistry, 2021-10, Vol.167, p.651-664</ispartof><rights>2021 Elsevier Masson SAS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c269t-58d6a1224483dc8609c5ee4b93e53f0257ba169071f3939e4ae88d86b24718333</citedby><cites>FETCH-LOGICAL-c269t-58d6a1224483dc8609c5ee4b93e53f0257ba169071f3939e4ae88d86b24718333</cites><orcidid>0000-0001-7818-299X ; 0000-0003-2996-8675</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.plaphy.2021.08.044$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Ye, Xiaoxue</creatorcontrib><creatorcontrib>Zhao, Xijuan</creatorcontrib><creatorcontrib>Sun, Yajun</creatorcontrib><creatorcontrib>Zhang, Meijiao</creatorcontrib><creatorcontrib>Feng, Shuang</creatorcontrib><creatorcontrib>Zhou, Aimin</creatorcontrib><creatorcontrib>Wu, Wenwu</creatorcontrib><creatorcontrib>Ma, Shurong</creatorcontrib><creatorcontrib>Liu, Shenkui</creatorcontrib><title>The underlying molecular conservation and diversification of dioecious flower and leaf buds provide insights into the development, dormancy breaking, flowering, and sex association of willows</title><title>Plant physiology and biochemistry</title><description>As harbingers of bursting growth, flower buds and leaf buds generally show similar surface morphologies but different structural and functional changes. Dioecious plants further generate four types of Female/Male Flower/Leaf Buds (FFB, FLB, MFB, and MLB), showing a complex regulation. However, little is known about their underlying molecular mechanisms. Here, we exemplify the woody dioecious Salix linearistipularis to investigate their morphological characteristics and potential molecular mechanisms by combining cytological, physiological, phenological, and transcriptomic datasets. First, FFB and MFB have simultaneous development dynamics and so do FLB and MLB. Interestingly, FLB and MLB show very similar expression profiles preparing for photosynthesis and stress-tolerance, whereas FFB and MFB show great similarities but also striking sexual differences. Comparing flower buds and leaf buds after their revival from dormancy shows different cold- and vernalization-responsive genes (e.g. SliVRN1, SliAGL19, and SliAGL24), implying different programming processes for dormancy breaking between the buds. Moreover, except SliAP3, the expression of ABCDE model genes is consistent with their roles in the buds, suggesting a conserved mechanism of flower development between dioecious Salix and hermaphrodite Arabidopsis. Finally, considering sex-associated genes (e.g. SliCLE25, SliTPS21, and SliARR9) on Salix chromosomes and other reports, we hypothesize a dynamic model of sex determination on chromosomes 15 and 19 in the last ancestor of Salix and Populus but evolutionarily on 15 in Salix after their divergence. Together, our study provides new insights into the molecular mechanisms of dioecious four-type buds by showing the genes involved in their development, dormancy breaking, flowering, and sexual association.
•S. linearistipularis FFB/MFB have simultaneous development dynamics; so do FLB/MLB.•FLB/MLB show similar expression, while FFB/MFB show similarity but sexual difference.•LB/FB have different programming of dormancy breaking by regulating different genes.•The ABCDE model of flower development is conserved in the dioecious Salix.•A dynamic sex determination is assumed on Chr 15/19 in the ancestor of Salix/Populus.</description><subject>ABCDE model</subject><subject>Dioecy</subject><subject>Flower bud</subject><subject>Leaf bud</subject><subject>Sex determination</subject><subject>Transcriptome</subject><subject>Vernalization</subject><issn>0981-9428</issn><issn>1873-2690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9UU1v1DAQtRCVWNr-gx585NAEO06yzgUJVXxJlbiUs-XYk64Xxw6eJGV_HX8Nb1Nx5DSj0Zs3894j5IazkjPevj-Wk9fT4VRWrOIlkyWr61dkx-VeFFXbsddkxzrJi66u5BvyFvHIGKvqvdiRPw8HoEuwkPzJhUc6Rg9m8TpREwNCWvXsYqA6WGrdCgnd4Mw2i0MeRTAuLkgHH58gPeM86IH2i0U6pbg6C9QFdI-HGXMzRzrnixZW8HEaIcy31MY06mBOtE-gf-Yvbl_ontszJcJvqhGjcf9OPzmfMXhFLgbtEa5f6iX58fnTw93X4v77l293H-8Lkw2Yi0baVvOqqmsprJEt60wDUPedgEYMrGr2vebZqT0fRCc6qDVIaWXbZ5e4FEJckncbb9b0awGc1ejQgPc6QNavMgPj2eS2ydB6g5oUERMMakpu1OmkOFPnvNRRbXmpc16KSZXzymsftjXIMlYHSaFxEAxYl8DMykb3f4K_rVelqg</recordid><startdate>202110</startdate><enddate>202110</enddate><creator>Ye, Xiaoxue</creator><creator>Zhao, Xijuan</creator><creator>Sun, Yajun</creator><creator>Zhang, Meijiao</creator><creator>Feng, Shuang</creator><creator>Zhou, Aimin</creator><creator>Wu, Wenwu</creator><creator>Ma, Shurong</creator><creator>Liu, Shenkui</creator><general>Elsevier Masson SAS</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7818-299X</orcidid><orcidid>https://orcid.org/0000-0003-2996-8675</orcidid></search><sort><creationdate>202110</creationdate><title>The underlying molecular conservation and diversification of dioecious flower and leaf buds provide insights into the development, dormancy breaking, flowering, and sex association of willows</title><author>Ye, Xiaoxue ; Zhao, Xijuan ; Sun, Yajun ; Zhang, Meijiao ; Feng, Shuang ; Zhou, Aimin ; Wu, Wenwu ; Ma, Shurong ; Liu, Shenkui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c269t-58d6a1224483dc8609c5ee4b93e53f0257ba169071f3939e4ae88d86b24718333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>ABCDE model</topic><topic>Dioecy</topic><topic>Flower bud</topic><topic>Leaf bud</topic><topic>Sex determination</topic><topic>Transcriptome</topic><topic>Vernalization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ye, Xiaoxue</creatorcontrib><creatorcontrib>Zhao, Xijuan</creatorcontrib><creatorcontrib>Sun, Yajun</creatorcontrib><creatorcontrib>Zhang, Meijiao</creatorcontrib><creatorcontrib>Feng, Shuang</creatorcontrib><creatorcontrib>Zhou, Aimin</creatorcontrib><creatorcontrib>Wu, Wenwu</creatorcontrib><creatorcontrib>Ma, Shurong</creatorcontrib><creatorcontrib>Liu, Shenkui</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Plant physiology and biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ye, Xiaoxue</au><au>Zhao, Xijuan</au><au>Sun, Yajun</au><au>Zhang, Meijiao</au><au>Feng, Shuang</au><au>Zhou, Aimin</au><au>Wu, Wenwu</au><au>Ma, Shurong</au><au>Liu, Shenkui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The underlying molecular conservation and diversification of dioecious flower and leaf buds provide insights into the development, dormancy breaking, flowering, and sex association of willows</atitle><jtitle>Plant physiology and biochemistry</jtitle><date>2021-10</date><risdate>2021</risdate><volume>167</volume><spage>651</spage><epage>664</epage><pages>651-664</pages><issn>0981-9428</issn><eissn>1873-2690</eissn><abstract>As harbingers of bursting growth, flower buds and leaf buds generally show similar surface morphologies but different structural and functional changes. Dioecious plants further generate four types of Female/Male Flower/Leaf Buds (FFB, FLB, MFB, and MLB), showing a complex regulation. However, little is known about their underlying molecular mechanisms. Here, we exemplify the woody dioecious Salix linearistipularis to investigate their morphological characteristics and potential molecular mechanisms by combining cytological, physiological, phenological, and transcriptomic datasets. First, FFB and MFB have simultaneous development dynamics and so do FLB and MLB. Interestingly, FLB and MLB show very similar expression profiles preparing for photosynthesis and stress-tolerance, whereas FFB and MFB show great similarities but also striking sexual differences. Comparing flower buds and leaf buds after their revival from dormancy shows different cold- and vernalization-responsive genes (e.g. SliVRN1, SliAGL19, and SliAGL24), implying different programming processes for dormancy breaking between the buds. Moreover, except SliAP3, the expression of ABCDE model genes is consistent with their roles in the buds, suggesting a conserved mechanism of flower development between dioecious Salix and hermaphrodite Arabidopsis. Finally, considering sex-associated genes (e.g. SliCLE25, SliTPS21, and SliARR9) on Salix chromosomes and other reports, we hypothesize a dynamic model of sex determination on chromosomes 15 and 19 in the last ancestor of Salix and Populus but evolutionarily on 15 in Salix after their divergence. Together, our study provides new insights into the molecular mechanisms of dioecious four-type buds by showing the genes involved in their development, dormancy breaking, flowering, and sexual association.
•S. linearistipularis FFB/MFB have simultaneous development dynamics; so do FLB/MLB.•FLB/MLB show similar expression, while FFB/MFB show similarity but sexual difference.•LB/FB have different programming of dormancy breaking by regulating different genes.•The ABCDE model of flower development is conserved in the dioecious Salix.•A dynamic sex determination is assumed on Chr 15/19 in the ancestor of Salix/Populus.</abstract><pub>Elsevier Masson SAS</pub><doi>10.1016/j.plaphy.2021.08.044</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-7818-299X</orcidid><orcidid>https://orcid.org/0000-0003-2996-8675</orcidid></addata></record> |
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subjects | ABCDE model Dioecy Flower bud Leaf bud Sex determination Transcriptome Vernalization |
title | The underlying molecular conservation and diversification of dioecious flower and leaf buds provide insights into the development, dormancy breaking, flowering, and sex association of willows |
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