5ea7bdb3365856d16875464042d3d8bd plaphy_a2025m6v198n2pkiaf160.pdf 001752b14fac939533bbb4eed3f3a6c983bf1301 plaphy_a2025m6v198n2pkiaf160.pdf b6e7f13869eb725a04e368a9c82ccb7e43dcbc7598c1e44b8915decc237c769e plaphy_a2025m6v198n2pkiaf160.pdf Title: The transcriptional regulator VAL1 promotes Arabidopsis flowering by repressing the organ boundary genes BOP1 and BOP2 Subject: DOI: 10.1093/plphys/kiaf160; Plant Physiology, 198, 2, 2025-04-24.; Abstract: The transition to reproductive development is a critical step in the plant lifecycle and relies on the integration of intrinsic and environmental signals. Several different pathways controlling flowering time function downstream of the perception of environmental cues such as day length (photoperiodic pathway) and seasonal temperature (vernalization and ambient temperature pathways). In addition, the phytohormone gibberellin (GA) induces the floral transition under noninductive photoperiod. In the model plant Arabidopsis (Arabidopsis thaliana), the transcriptional repressor VIVIPAROUS1/ABSCISIC ACID INSENTIVE3 (ABI3)-LIKE1 (VAL1) triggers the stable repression of the floral repressor FLOWERING LOCUS C (FLC) during vernalization. However, the involvement of VAL1 in other flowering pathways remains unclear. In this work, we combined genetic and transcriptomic approaches to investigate the requirement of VAL1 for flowering activation under different day lengths. We found that VAL1, but not its sister protein VAL2, is required to induce the floral transition both under long and short days. The delayed flowering time of val1 mutant plants was fully bypassed by exogenous GA application. We demonstrated that VAL1-mediated induction of flowering occurs partially via the direct epigenetic repression of the organ boundary genes BLADE-ON-PETIOLE1 (BOP1) and BOP2. Our work thus expands the repertoire of VAL target genes and further demonstrates the pleiotropic role of VAL factors in regulating Arabidopsis development. Keywords: Author: Yajiao Cheng Creator: Servigistics Arbortext Advanced Print Publisher 11.1.4546/W-x64 Producer: PDFlib+PDI 9.0.7p3 (C++/Win64); modified using iTextSharp.LGPLv2.Core 3.7.4.0 CreationDate: Tue Jun 10 06:07:35 2025 CEST ModDate: Thu Jun 18 16:17:50 2026 CEST Custom Metadata: yes Metadata Stream: yes Tagged: yes UserProperties: no Suspects: no Form: AcroForm JavaScript: no Pages: 16 Encrypted: no Page size: 595.276 x 782.362 pts Page rot: 0 File size: 2916825 bytes Optimized: no PDF version: 1.6 name type encoding emb sub uni object ID ------------------------------------ ----------------- ---------------- --- --- --- --------- FOMHGS+CaeciliaLTStd-LightItalic Type 1C Custom yes yes yes 41 0 WLGXPJ+CaeciliaLTStd-Light Type 1C Custom yes yes yes 39 0 OTOFLH+CaeciliaLTStd-Bold Type 1C Custom yes yes yes 38 0 EHJTAL+CaeciliaLTStd-BoldItalic Type 1C Custom yes yes yes 108 0 UOVOHW+CaeciliaLTStd-Heavy Type 1C Custom yes yes yes 40 0 HJRETX+ArialMT TrueType WinAnsi yes yes no 1 0 HXMYSJ+STIXGeneral-Regular Type 1C Custom yes yes yes 109 0 Helvetica-Bold Type 1 Custom no no no 114 0 Helvetica-Bold Type 1 Custom no no no 138 0 SXDQKJ+TimesNewRomanPS-ItalicMT CID TrueType Identity-H yes yes yes 181 0 Helvetica-Bold Type 1 Custom no no no 183 0 Helvetica-Bold Type 1 Custom no no no 242 0 Helvetica-Bold Type 1 Custom no no no 323 0 Helvetica-Bold Type 1 Custom no no no 333 0 Jhove (Rel. 1.28.0, 2023-05-18) Date: 2026-06-19 04:34:24 CEST RepresentationInformation: plaphy_a2025m6v198n2pkiaf160.pdf ReportingModule: PDF-hul, Rel. 1.12.4 (2023-03-16) LastModified: 2026-06-18 16:21:37 CEST Size: 2916825 Format: PDF Version: 1.6 Status: Well-Formed and valid SignatureMatches: PDF-hul MIMEtype: application/pdf Profile: Tagged PDF PDFMetadata: Objects: 1949 FreeObjects: 1 IncrementalUpdates: 0 DocumentCatalog: ViewerPreferences: HideToolbar: false HideMenubar: false HideWindowUI: false FitWindow: false CenterWindow: false DisplayDocTitle: true NonFullScreenPageMode: UseNone Direction: L2R ViewArea: CropBox ViewClip: CropBox PrintArea: CropBox PageClip: CropBox PageLayout: OneColumn PageMode: UseOutlines Language: en Outlines: Item: Title: The transcriptional regulator VAL1 promotes Arabidopsis flowering by repressing the organ boundary genes BOP1 and BOP2 Destination: head1 Children: Item: Title: Introduction Destination: seckiaf160-s1 Item: Title: Results Destination: seckiaf160-s2 Children: Item: Title: VAL1 protein is required for Arabidopsis flowering both under inductive and noninductive photoperiod Destination: seckiaf160-s2.1 Item: Title: VAL1 accelerates flowering under noninductive photoperiod partially through the repression of FLC Destination: seckiaf160-s2.2 Item: Title: GA suppresses the late-flowering phenotype of val1 mutant Destination: seckiaf160-s2.3 Item: Title: Transcriptional responses in shoot apices of val mutant plants grown in SD Destination: seckiaf160-s2.4 Item: Title: VAL1 regulates flowering genes in Arabidopsis SAM Destination: seckiaf160-s2.5 Item: Title: Epigenetic repression of the organ boundary genes BOP1 and BOP2 requires VAL1 function Destination: seckiaf160-s2.6 Item: Title: VAL1 controls flowering partially through the repression of BOP1 and BOP2 Destination: seckiaf160-s2.7 Item: Title: Discussion Destination: seckiaf160-s3 Item: Title: Materials and methods Destination: seckiaf160-s4 Children: Item: Title: Plant material and growth conditions Destination: seckiaf160-s4.1 Item: Title: Flowering time analysis Destination: seckiaf160-s4.2 Item: Title: GA3 treatment Destination: seckiaf160-s4.3 Item: Title: GA4 content analysis Destination: seckiaf160-s4.4 Item: Title: Generation of Arabidopsis transgenic lines Destination: seckiaf160-s4.5 Item: Title: GUS staining analysis Destination: seckiaf160-s4.6 Item: Title: Quantitative RT-qPCR analysis Destination: seckiaf160-s4.7 Item: Title: RNA-Seq analysis Destination: seckiaf160-s4.8 Item: Title: ChIP analysis Destination: seckiaf160-s4.9 Item: Title: Electrophoretic mobility shift assay Destination: seckiaf160-s4.10 Item: Title: In situ hybridization Destination: seckiaf160-s4.11 Item: Title: Statistical analysis Destination: seckiaf160-s4.12 Item: Title: Accession numbers Destination: seckiaf160-s4.13 Item: Title: Acknowledgments Destination: acknow Item: Title: Author contributions Destination: seckiaf160-s5 Item: Title: Supplementary data Destination: seckiaf160-s6 Item: Title: Funding Destination: seckiaf160-s7 Item: Title: References Destination: reflist Info: Title: The transcriptional regulator VAL1 promotes Arabidopsis flowering by repressing the organ boundary genes BOP1 and BOP2 Author: Yajiao Cheng Subject: DOI: 10.1093/plphys/kiaf160; Plant Physiology, 198, 2, 2025-04-24.; Abstract: The transition to reproductive development is a critical step in the plant lifecycle and relies on the integration of intrinsic and environmental signals. Several different pathways controlling flowering time function downstream of the perception of environmental cues such as day length (photoperiodic pathway) and seasonal temperature (vernalization and ambient temperature pathways). In addition, the phytohormone gibberellin (GA) induces the floral transition under noninductive photoperiod. In the model plant Arabidopsis (Arabidopsis thaliana), the transcriptional repressor VIVIPAROUS1/ABSCISIC ACID INSENTIVE3 (ABI3)-LIKE1 (VAL1) triggers the stable repression of the floral repressor FLOWERING LOCUS C (FLC) during vernalization. However, the involvement of VAL1 in other flowering pathways remains unclear. In this work, we combined genetic and transcriptomic approaches to investigate the requirement of VAL1 for flowering activation under different day lengths. We found that VAL1, but not its sister protein VAL2, is required to induce the floral transition both under long and short days. The delayed flowering time of val1 mutant plants was fully bypassed by exogenous GA application. We demonstrated that VAL1-mediated induction of flowering occurs partially via the direct epigenetic repression of the organ boundary genes BLADE-ON-PETIOLE1 (BOP1) and BOP2. Our work thus expands the repertoire of VAL target genes and further demonstrates the pleiotropic role of VAL factors in regulating Arabidopsis development. 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Tremblay Vicente Balanzà Alvaro S. Larran Julia I. Qüesta DOI: 10.1093/plphys/kiaf160; Plant Physiology, 198, 2, 2025-04-24.; Abstract: The transition to reproductive development is a critical step in the plant lifecycle and relies on the integration of intrinsic and environmental signals. Several different pathways controlling flowering time function downstream of the perception of environmental cues such as day length (photoperiodic pathway) and seasonal temperature (vernalization and ambient temperature pathways). In addition, the phytohormone gibberellin (GA) induces the floral transition under noninductive photoperiod. In the model plant Arabidopsis (Arabidopsis thaliana), the transcriptional repressor VIVIPAROUS1/ABSCISIC ACID INSENTIVE3 (ABI3)-LIKE1 (VAL1) triggers the stable repression of the floral repressor FLOWERING LOCUS C (FLC) during vernalization. However, the involvement of VAL1 in other flowering pathways remains unclear. In this work, we combined genetic and transcriptomic approaches to investigate the requirement of VAL1 for flowering activation under different day lengths. We found that VAL1, but not its sister protein VAL2, is required to induce the floral transition both under long and short days. The delayed flowering time of val1 mutant plants was fully bypassed by exogenous GA application. We demonstrated that VAL1-mediated induction of flowering occurs partially via the direct epigenetic repression of the organ boundary genes BLADE-ON-PETIOLE1 (BOP1) and BOP2. Our work thus expands the repertoire of VAL target genes and further demonstrates the pleiotropic role of VAL factors in regulating Arabidopsis development. © The Author(s) 2025. Published by Oxford University Press on behalf of American Society of Plant Biologists. Journal Plant Physiology © The Author(s) 2025. 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