The plant ESCRT component FREE1 regulates peroxisome-mediated turnover of lipid droplets in germinating Arabidopsis seedlings

Author:

Huang Shuxian1ORCID,Liu Zhiqi1ORCID,Cao Wenhan1ORCID,Li Hongbo2ORCID,Zhang Wenxin1ORCID,Cui Yong3ORCID,Hu Shuai4ORCID,Luo Mengqian1ORCID,Zhu Ying1ORCID,Zhao Qiong5ORCID,Xie Lijuan6ORCID,Gao Caiji2ORCID,Xiao Shi7ORCID,Jiang Liwen189ORCID

Affiliation:

1. School of Life Sciences, Centre for Cell & Developmental Biology and State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong , Shatin, China

2. Guangdong Provincial Key Laboratory of Biotechnology for Plant Development, School of Life Sciences, South China Normal University (SCNU) , Guangzhou, 510631, China

3. School of Life Sciences, State Key Laboratory of Cellular Stress Biology, Xiamen University , Xiamen, 361102, China

4. State Key Laboratory of Subtropical Silviculture, Zhejiang A&F University , Hangzhou, China

5. School of Life Sciences, East China Normal University , Shanghai, 200062, China

6. College of Plant Protection, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, South China Agricultural University , Guangzhou, 510642, China

7. School of Life Sciences, State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory of Plant Resources, Sun Yat-sen University , Guangzhou, 510275, China

8. CUHK Shenzhen Research Institute , Shenzhen, 518057, China

9. Institute of Plant Molecular Biology and Agricultural Biotechnology, The Chinese University of Hong Kong , Shatin, China

Abstract

Abstract Lipid droplets (LDs) stored during seed development are mobilized and provide essential energy and lipids to support seedling growth upon germination. Triacylglycerols (TAGs) are the main neutral lipids stored in LDs. The lipase SUGAR DEPENDENT 1 (SDP1), which hydrolyzes TAGs in Arabidopsis thaliana, is localized on peroxisomes and traffics to the LD surface through peroxisomal extension, but the underlying mechanism remains elusive. Here, we report a previously unknown function of a plant-unique endosomal sorting complex required for transport (ESCRT) component FYVE DOMAIN PROTEIN REQUIRED FOR ENDOSOMAL SORTING 1 (FREE1) in regulating peroxisome/SDP1-mediated LD turnover in Arabidopsis. We showed that LD degradation was impaired in germinating free1 mutant; moreover, the tubulation of SDP1- or PEROXIN 11e (PEX11e)-marked peroxisomes and the migration of SDP1-positive peroxisomes to the LD surface were altered in the free1 mutant. Electron tomography analysis showed that peroxisomes failed to form tubules to engulf LDs in free1, unlike in the wild-type. FREE1 interacted directly with both PEX11e and SDP1, suggesting that these interactions may regulate peroxisomal extension and trafficking of the lipase SDP1 to LDs. Taken together, our results demonstrate a pivotal role for FREE1 in LD degradation in germinating seedlings via regulating peroxisomal tubulation and SDP1 targeting.

Funder

National Natural Science Foundation of China

Research Grants Council of Hong Kong

The Chinese University of Hong Kong

Research Committee and CAS-Croucher Funding Scheme for Joint Laboratories

Fok Ying-Tong Education Foundation for Young Teachers in the Higher Education Institutions of China

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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