Sorbitol induces flower bud formation via the MADS‐box transcription factor EjCAL in loquat
ABSTRACT Sorbitol is an important signaling molecule in fruit trees. Here, we observed that sorbitol increased during flower bud differentiation (FBD) in loquat (Eriobotrya japonica Lindl.). Transcriptomic analysis suggested that bud formation was associated with the expression of the MADS‐box trans...
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Published in | Journal of integrative plant biology Vol. 65; no. 5; pp. 1241 - 1261 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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China (Republic : 1949- )
Wiley Subscription Services, Inc
01.05.2023
Institute of Horticulture,Zhejiang Academy of Agricultural Sciences,Hangzhou 310021,China%Beijing Advanced Innovation Center for Tree Breeding by Molecular Design,Beijing Forestry University,Beijing 100000,China College of Forestry,Beijing Forestry University,Beijing 100083,China |
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Abstract | ABSTRACT
Sorbitol is an important signaling molecule in fruit trees. Here, we observed that sorbitol increased during flower bud differentiation (FBD) in loquat (Eriobotrya japonica Lindl.). Transcriptomic analysis suggested that bud formation was associated with the expression of the MADS‐box transcription factor (TF) family gene, EjCAL. RNA fluorescence in situ hybridization showed that EjCAL was enriched in flower primordia but hardly detected in the shoot apical meristem. Heterologous expression of EjCAL in Nicotiana benthamiana plants resulted in early FBD. Yeast‐one‐hybrid analysis identified the ERF12 TF as a binding partner of the EjCAL promoter. Chromatin immunoprecipitation‐PCR confirmed that EjERF12 binds to the EjCAL promoter, and β‐glucuronidase activity assays indicated that EjERF12 regulates EjCAL expression. Spraying loquat trees with sorbitol promoted flower bud formation and was associated with increased expression of EjERF12 and EjCAL. Furthermore, we identified EjUF3GaT1 as a target gene of EjCAL and its expression was activated by EjCAL. Function characterization via overexpression and RNAi reveals that EjUF3GaT1 is a biosynthetic gene of flavonoid hyperoside. The concentration of the flavonoid hyperoside mirrored that of sorbitol during FBD and exogenous hyperoside treatment also promoted loquat bud formation. We identified a mechanism whereby EjCAL might regulate hyperoside biosynthesis and confirmed the involvement of EjCAL in flower bud formation in planta. Together, these results provide insight into bud formation in loquat and may be used in efforts to increase yield.
Sorbitol induces flower bud formation via the MADS‐box transcription factor EjCAL in loquat (Eriobotrya japonica). Sorbitol also promotes the accumulation of an important developmental flavonoid, hyperoside, and EjCAL regulates hyperoside biosynthesis. |
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AbstractList | Sorbitol is an important signaling molecule in fruit trees.Here,we observed that sorbitol increased during flower bud differentiation(FBD)in loquat(Eriobotrya japonica Lindl.).Transcriptomic analysis suggested that bud formation was associated with the expression of the MADS-box transcription factor(TF)family gene,EjCAL.RNA fluorescence in situ hybridization showed that EjCAL was enriched in flower primordia but hardly detected in the shoot apical meristem.Heterologous expression of EjCAL in Nicotiana benthamiana plants resulted in early FBD.Yeast-one-hybrid analysis identified the ERF12 TF as a binding partner of the EjCAL promoter.Chromatin immunoprecipitation-PCR confirmed that EjERF12 binds to the EjCAL pro-moter,and β-glucuronidase activity assays in-dicated that EjERF12 regulates EjCAL expression.Spraying loquat trees with sorbitol promoted flower bud formation and was associated with increased expression of EjERF12 and EjCAL.Furthermore,we identified EjUF3GaT1 as a target gene of EjCAL and its expression was activated by EjCAL.Function characterization via overexpression and RNAi re-veals that EjUF3GaT1 is a biosynthetic gene of fla-vonoid hyperoside.The concentration of the fla-vonoid hyperoside mirrored that of sorbitol during FBD and exogenous hyperoside treatment also promoted loquat bud formation.We identified a mechanism whereby EjCAL might regulate hypero-side biosynthesis and confirmed the involvement of EjCAL in flower bud formation in planta.Together,these results provide insight into bud formation in loquat and may be used in efforts to increase yield. Sorbitol is an important signaling molecule in fruit trees. Here, we observed that sorbitol increased during flower bud differentiation (FBD) in loquat (Eriobotrya japonica Lindl.). Transcriptomic analysis suggested that bud formation was associated with the expression of the MADS-box transcription factor (TF) family gene, EjCAL. RNA fluorescence in situ hybridization showed that EjCAL was enriched in flower primordia but hardly detected in the shoot apical meristem. Heterologous expression of EjCAL in Nicotiana benthamiana plants resulted in early FBD. Yeast-one-hybrid analysis identified the ERF12 TF as a binding partner of the EjCAL promoter. Chromatin immunoprecipitation-PCR confirmed that EjERF12 binds to the EjCAL promoter, and β-glucuronidase activity assays indicated that EjERF12 regulates EjCAL expression. Spraying loquat trees with sorbitol promoted flower bud formation and was associated with increased expression of EjERF12 and EjCAL. Furthermore, we identified EjUF3GaT1 as a target gene of EjCAL and its expression was activated by EjCAL. Function characterization via overexpression and RNAi reveals that EjUF3GaT1 is a biosynthetic gene of flavonoid hyperoside. The concentration of the flavonoid hyperoside mirrored that of sorbitol during FBD and exogenous hyperoside treatment also promoted loquat bud formation. We identified a mechanism whereby EjCAL might regulate hyperoside biosynthesis and confirmed the involvement of EjCAL in flower bud formation in planta. Together, these results provide insight into bud formation in loquat and may be used in efforts to increase yield. ABSTRACT Sorbitol is an important signaling molecule in fruit trees. Here, we observed that sorbitol increased during flower bud differentiation (FBD) in loquat (Eriobotrya japonica Lindl.). Transcriptomic analysis suggested that bud formation was associated with the expression of the MADS‐box transcription factor (TF) family gene, EjCAL. RNA fluorescence in situ hybridization showed that EjCAL was enriched in flower primordia but hardly detected in the shoot apical meristem. Heterologous expression of EjCAL in Nicotiana benthamiana plants resulted in early FBD. Yeast‐one‐hybrid analysis identified the ERF12 TF as a binding partner of the EjCAL promoter. Chromatin immunoprecipitation‐PCR confirmed that EjERF12 binds to the EjCAL promoter, and β‐glucuronidase activity assays indicated that EjERF12 regulates EjCAL expression. Spraying loquat trees with sorbitol promoted flower bud formation and was associated with increased expression of EjERF12 and EjCAL. Furthermore, we identified EjUF3GaT1 as a target gene of EjCAL and its expression was activated by EjCAL. Function characterization via overexpression and RNAi reveals that EjUF3GaT1 is a biosynthetic gene of flavonoid hyperoside. The concentration of the flavonoid hyperoside mirrored that of sorbitol during FBD and exogenous hyperoside treatment also promoted loquat bud formation. We identified a mechanism whereby EjCAL might regulate hyperoside biosynthesis and confirmed the involvement of EjCAL in flower bud formation in planta. Together, these results provide insight into bud formation in loquat and may be used in efforts to increase yield. Sorbitol induces flower bud formation via the MADS‐box transcription factor EjCAL in loquat (Eriobotrya japonica). Sorbitol also promotes the accumulation of an important developmental flavonoid, hyperoside, and EjCAL regulates hyperoside biosynthesis. Sorbitol is an important signaling molecule in fruit trees. Here, we observed that sorbitol increased during flower bud differentiation (FBD) in loquat ( Eriobotrya japonica Lindl.). Transcriptomic analysis suggested that bud formation was associated with the expression of the MADS‐box transcription factor (TF) family gene, EjCAL . RNA fluorescence in situ hybridization showed that EjCAL was enriched in flower primordia but hardly detected in the shoot apical meristem. Heterologous expression of EjCAL in Nicotiana benthamiana plants resulted in early FBD. Yeast‐one‐hybrid analysis identified the ERF12 TF as a binding partner of the EjCAL promoter. Chromatin immunoprecipitation‐PCR confirmed that EjERF12 binds to the EjCAL promoter, and β‐glucuronidase activity assays indicated that EjERF12 regulates EjCAL expression. Spraying loquat trees with sorbitol promoted flower bud formation and was associated with increased expression of EjERF12 and EjCAL . Furthermore, we identified EjUF3GaT1 as a target gene of EjCAL and its expression was activated by EjCAL. Function characterization via overexpression and RNAi reveals that EjUF3GaT1 is a biosynthetic gene of flavonoid hyperoside. The concentration of the flavonoid hyperoside mirrored that of sorbitol during FBD and exogenous hyperoside treatment also promoted loquat bud formation. We identified a mechanism whereby EjCAL might regulate hyperoside biosynthesis and confirmed the involvement of EjCAL in flower bud formation in planta. Together, these results provide insight into bud formation in loquat and may be used in efforts to increase yield. Sorbitol is an important signaling molecule in fruit trees. Here, we observed that sorbitol increased during flower bud differentiation (FBD) in loquat (Eriobotrya japonica Lindl.). Transcriptomic analysis suggested that bud formation was associated with the expression of the MADS-box transcription factor (TF) family gene, EjCAL. RNA fluorescence in situ hybridization showed that EjCAL was enriched in flower primordia but hardly detected in the shoot apical meristem. Heterologous expression of EjCAL in Nicotiana benthamiana plants resulted in early FBD. Yeast-one-hybrid analysis identified the ERF12 TF as a binding partner of the EjCAL promoter. Chromatin immunoprecipitation-PCR confirmed that EjERF12 binds to the EjCAL promoter, and β-glucuronidase activity assays indicated that EjERF12 regulates EjCAL expression. Spraying loquat trees with sorbitol promoted flower bud formation and was associated with increased expression of EjERF12 and EjCAL. Furthermore, we identified EjUF3GaT1 as a target gene of EjCAL and its expression was activated by EjCAL. Function characterization via overexpression and RNAi reveals that EjUF3GaT1 is a biosynthetic gene of flavonoid hyperoside. The concentration of the flavonoid hyperoside mirrored that of sorbitol during FBD and exogenous hyperoside treatment also promoted loquat bud formation. We identified a mechanism whereby EjCAL might regulate hyperoside biosynthesis and confirmed the involvement of EjCAL in flower bud formation in planta. Together, these results provide insight into bud formation in loquat and may be used in efforts to increase yield.Sorbitol is an important signaling molecule in fruit trees. Here, we observed that sorbitol increased during flower bud differentiation (FBD) in loquat (Eriobotrya japonica Lindl.). Transcriptomic analysis suggested that bud formation was associated with the expression of the MADS-box transcription factor (TF) family gene, EjCAL. RNA fluorescence in situ hybridization showed that EjCAL was enriched in flower primordia but hardly detected in the shoot apical meristem. Heterologous expression of EjCAL in Nicotiana benthamiana plants resulted in early FBD. Yeast-one-hybrid analysis identified the ERF12 TF as a binding partner of the EjCAL promoter. Chromatin immunoprecipitation-PCR confirmed that EjERF12 binds to the EjCAL promoter, and β-glucuronidase activity assays indicated that EjERF12 regulates EjCAL expression. Spraying loquat trees with sorbitol promoted flower bud formation and was associated with increased expression of EjERF12 and EjCAL. Furthermore, we identified EjUF3GaT1 as a target gene of EjCAL and its expression was activated by EjCAL. Function characterization via overexpression and RNAi reveals that EjUF3GaT1 is a biosynthetic gene of flavonoid hyperoside. The concentration of the flavonoid hyperoside mirrored that of sorbitol during FBD and exogenous hyperoside treatment also promoted loquat bud formation. We identified a mechanism whereby EjCAL might regulate hyperoside biosynthesis and confirmed the involvement of EjCAL in flower bud formation in planta. Together, these results provide insight into bud formation in loquat and may be used in efforts to increase yield. |
Author | Xu, Hong‐Xia Chen, Jun‐Wei Qi, Meng Ge, Hang Chen, Ting Li, Xiao‐Ying Meng, Dong Yang, Qing |
AuthorAffiliation | Institute of Horticulture,Zhejiang Academy of Agricultural Sciences,Hangzhou 310021,China%Beijing Advanced Innovation Center for Tree Breeding by Molecular Design,Beijing Forestry University,Beijing 100000,China;College of Forestry,Beijing Forestry University,Beijing 100083,China |
AuthorAffiliation_xml | – name: Institute of Horticulture,Zhejiang Academy of Agricultural Sciences,Hangzhou 310021,China%Beijing Advanced Innovation Center for Tree Breeding by Molecular Design,Beijing Forestry University,Beijing 100000,China;College of Forestry,Beijing Forestry University,Beijing 100083,China |
Author_xml | – sequence: 1 givenname: Hong‐Xia surname: Xu fullname: Xu, Hong‐Xia organization: Zhejiang Academy of Agricultural Sciences – sequence: 2 givenname: Dong surname: Meng fullname: Meng, Dong organization: Beijing Forestry University – sequence: 3 givenname: Qing surname: Yang fullname: Yang, Qing organization: Beijing Forestry University – sequence: 4 givenname: Ting surname: Chen fullname: Chen, Ting organization: Beijing Forestry University – sequence: 5 givenname: Meng surname: Qi fullname: Qi, Meng organization: Beijing Forestry University – sequence: 6 givenname: Xiao‐Ying surname: Li fullname: Li, Xiao‐Ying organization: Zhejiang Academy of Agricultural Sciences – sequence: 7 givenname: Hang surname: Ge fullname: Ge, Hang organization: Zhejiang Academy of Agricultural Sciences – sequence: 8 givenname: Jun‐Wei surname: Chen fullname: Chen, Jun‐Wei email: chenjunwei@zaas.ac.cn organization: Zhejiang Academy of Agricultural Sciences |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36541724$$D View this record in MEDLINE/PubMed |
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Keywords | flower bud differentiation hyperoside EjCAL sorbitol loquat |
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Snippet | ABSTRACT
Sorbitol is an important signaling molecule in fruit trees. Here, we observed that sorbitol increased during flower bud differentiation (FBD) in... Sorbitol is an important signaling molecule in fruit trees. Here, we observed that sorbitol increased during flower bud differentiation (FBD) in loquat (... Sorbitol is an important signaling molecule in fruit trees. Here, we observed that sorbitol increased during flower bud differentiation (FBD) in loquat... Sorbitol is an important signaling molecule in fruit trees.Here,we observed that sorbitol increased during flower bud differentiation(FBD)in loquat(Eriobotrya... |
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SubjectTerms | apical meristems Biosynthesis Chromatin EjCAL Eriobotrya - genetics Eriobotrya - metabolism Eriobotrya japonica Flavonoids Flavonoids - metabolism flower bud differentiation flower buds flower primordia Flowers Flowers - genetics Flowers - metabolism fluorescence Fluorescence in situ hybridization Fruit trees fruits Gene Expression Regulation, Plant genes heterologous gene expression hybridization hyperoside Immunoprecipitation In Situ Hybridization, Fluorescence loquat loquats Meristems Nicotiana benthamiana Plant Proteins - genetics Plant Proteins - metabolism Primordia RNA RNA-mediated interference Sorbitol Sorbitol - metabolism Spraying Transcription factors Transcription Factors - metabolism Transcriptomics Trees Yeast |
Title | Sorbitol induces flower bud formation via the MADS‐box transcription factor EjCAL in loquat |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjipb.13439 https://www.ncbi.nlm.nih.gov/pubmed/36541724 https://www.proquest.com/docview/2812379704 https://www.proquest.com/docview/2756669581 https://www.proquest.com/docview/2834213692 https://d.wanfangdata.com.cn/periodical/zwxb202305010 |
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