Two modes of gene regulation by TFL1 mediate its dual function in flowering time and shoot determinacy of Arabidopsis

Author:

Cerise Martina1ORCID,da Silveira Falavigna Vítor1ORCID,Rodríguez-Maroto Gabriel1ORCID,Signol Antoine1ORCID,Severing Edouard1ORCID,Gao He1ORCID,van Driel Annabel1ORCID,Vincent Coral1ORCID,Wilkens Sandra1,Iacobini Francesca Romana1ORCID,Formosa-Jordan Pau1ORCID,Pajoro Alice123ORCID,Coupland George1ORCID

Affiliation:

1. Max Planck Institute for Plant Breeding Research 1 Department of Plant Developmental Biology , , Cologne 50829 , Germany

2. Institute of Molecular Biology and Pathology, National Research Council 2 , c/o Department Biology and , Rome 00185 , Italy

3. Biotechnology ‘C. Darwin’ Sapienza University 2 , c/o Department Biology and , Rome 00185 , Italy

Abstract

ABSTRACT Plant organ primordia develop successively at the shoot apical meristem (SAM). In Arabidopsis, primordia formed early in development differentiate into vegetative leaves, whereas those formed later generate inflorescence branches and flowers. TERMINAL FLOWER 1 (TFL1), a negative regulator of transcription, acts in the SAM to delay flowering and to maintain inflorescence meristem indeterminacy. We used confocal microscopy, time-resolved transcript profiling and reverse genetics to elucidate this dual role of TFL1. We found that TFL1 accumulates dynamically in the SAM reflecting its dual function. Moreover, TFL1 represses two major sets of genes. One set includes genes that promote flowering, expression of which increases earlier in tfl1 mutants. The other set is spatially misexpressed in tfl1 inflorescence meristems. The misexpression of these two gene sets in tfl1 mutants depends upon FD transcription factor, with which TFL1 interacts. Furthermore, the MADS-box gene SEPALLATA 4, which is upregulated in tfl1, contributes both to the floral transition and shoot determinacy defects of tfl1 mutants. Thus, we delineate the dual function of TFL1 in shoot development in terms of its dynamic spatial distribution and different modes of gene repression.

Funder

Max-Planck-Gesellschaft

Deutsche Forschungsgemeinschaft

Ministero dell'Istruzione, dell'Università e della Ricerca

Alexander von Humboldt-Stiftung

H2020 Marie Skłodowska-Curie Actions

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3