Stromule extension along microtubules coordinated with actin-mediated anchoring guides perinuclear chloroplast movement during innate immunity

Author:

Kumar Amutha Sampath1,Park Eunsook23ORCID,Nedo Alexander14,Alqarni Ali145,Ren Li5,Hoban Kyle14,Modla Shannon1,McDonald John H4,Kambhamettu Chandra56,Dinesh-Kumar Savithramma P23ORCID,Caplan Jeffrey Lewis145ORCID

Affiliation:

1. Delaware Biotechnology Institute, University of Delaware, Newark, United States

2. Department of Plant Biology, College of Biological Sciences, University of California, Davis, Davis, United States

3. The Genome Center, College of Biological Sciences, University of California, Davis, Davis, United States

4. Department of Biological Sciences, College of Arts and Sciences, University of Delaware, Newark, United States

5. Department of Plant and Soil Sciences, College of Agriculture and Natural Resources, University of Delaware, Newark, United States

6. Department of Computer and Information Sciences, College of Engineering, University of Delaware, Newark, United States

Abstract

Dynamic tubular extensions from chloroplasts called stromules have recently been shown to connect with nuclei and function during innate immunity. We demonstrate that stromules extend along microtubules (MTs) and MT organization directly affects stromule dynamics since stabilization of MTs chemically or genetically increases stromule numbers and length. Although actin filaments (AFs) are not required for stromule extension, they provide anchor points for stromules. Interestingly, there is a strong correlation between the direction of stromules from chloroplasts and the direction of chloroplast movement. Stromule-directed chloroplast movement was observed in steady-state conditions without immune induction, suggesting it is a general function of stromules in epidermal cells. Our results show that MTs and AFs may facilitate perinuclear clustering of chloroplasts during an innate immune response. We propose a model in which stromules extend along MTs and connect to AF anchor points surrounding nuclei, facilitating stromule-directed movement of chloroplasts to nuclei during innate immunity.

Funder

National Institutes of Health

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