Fluctuations of the transcription factor ATML1 generate the pattern of giant cells in the Arabidopsis sepal

Author:

Meyer Heather M12ORCID,Teles José3ORCID,Formosa-Jordan Pau3ORCID,Refahi Yassin3ORCID,San-Bento Rita4,Ingram Gwyneth4,Jönsson Henrik356ORCID,Locke James C W378ORCID,Roeder Adrienne H K129ORCID

Affiliation:

1. Weill Institute for Cell and Molecular Biology, Cornell University, United States

2. The graduate field of Genetics, Genomics, and Development, Cornell University, Ithaca, United States

3. Sainsbury Laboratory, University of Cambridge, Cambridge, United Kingdom

4. Laboratoire Reproduction et Développement des Plantes, Univ Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRA, Lyon, France

5. Computational Biology and Biological Physics, Lund University, Lund, Sweden

6. Department of Applied Mathematics and Theoretical Physics, University of Cambridge, Cambridge, United Kingdom

7. Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom

8. Microsoft Research, Cambridge, United Kingdom

9. Section of Plant Biology, School of Integrative Plant Science, Cornell University, Ithaca, United States

Abstract

Multicellular development produces patterns of specialized cell types. Yet, it is often unclear how individual cells within a field of identical cells initiate the patterning process. Using live imaging, quantitative image analyses and modeling, we show that during Arabidopsis thaliana sepal development, fluctuations in the concentration of the transcription factor ATML1 pattern a field of identical epidermal cells to differentiate into giant cells interspersed between smaller cells. We find that ATML1 is expressed in all epidermal cells. However, its level fluctuates in each of these cells. If ATML1 levels surpass a threshold during the G2 phase of the cell cycle, the cell will likely enter a state of endoreduplication and become giant. Otherwise, the cell divides. Our results demonstrate a fluctuation-driven patterning mechanism for how cell fate decisions can be initiated through a random yet tightly regulated process.

Funder

National Science Foundation

Gatsby Charitable Foundation

Vetenskapsrådet

Herchel Smith Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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