A single-cell view of the transcriptome during lateral root initiation in Arabidopsis thaliana

Author:

Gala Hardik P.1ORCID,Lanctot Amy12ORCID,Jean-Baptiste Ken3ORCID,Guiziou Sarah1ORCID,Chu Jonah C.1ORCID,Zemke Joseph E.1ORCID,George Wesley1ORCID,Queitsch Christine3ORCID,Cuperus Josh T.3ORCID,Nemhauser Jennifer L.1ORCID

Affiliation:

1. Department of Biology, University of Washington, Seattle, WA 98195, USA

2. Molecular and Cellular Biology Program, University of Washington, Seattle, WA 98195, USA

3. Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA

Abstract

Abstract Root architecture is a major determinant of plant fitness and is under constant modification in response to favorable and unfavorable environmental stimuli. Beyond impacts on the primary root, the environment can alter the position, spacing, density, and length of secondary or lateral roots. Lateral root development is among the best-studied examples of plant organogenesis, yet there are still many unanswered questions about its earliest steps. Among the challenges faced in capturing these first molecular events is the fact that this process occurs in a small number of cells with unpredictable timing. Single-cell sequencing methods afford the opportunity to isolate the specific transcriptional changes occurring in cells undergoing this fate transition. Using this approach, we successfully captured the transcriptomes of initiating lateral root primordia in Arabidopsis thaliana and discovered many upregulated genes associated with this process. We developed a method to selectively repress target gene transcription in the xylem pole pericycle cells where lateral roots originate and demonstrated that the expression of several of these targets is required for normal root development. We also discovered subpopulations of cells in the pericycle and endodermal cell files that respond to lateral root initiation, highlighting the coordination across cell files required for this fate transition.

Funder

National Institutes of Health

Howard Hughes Medical Institute Faculty Scholars Program

National Science Foundation

NSF Graduate Research Fellowship

EMBO Post-doctoral Award (ALTF

University of Washington National Institutes of Health Big Data for Genomics and Neuroscience Training

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

Reference111 articles.

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