Structural and functional regulation of Chlamydomonas lysosome-related organelles during environmental changes

Author:

Long Huan123ORCID,Fang Jinhua4ORCID,Ye Lian13ORCID,Zhang Baolong1ORCID,Hui Colleen256ORCID,Deng Xuan1ORCID,Merchant Sabeeha S2ORCID,Huang Kaiyao13ORCID

Affiliation:

1. Key Laboratory of Algal Biology, Institute of Hydrobiology, Chinese Academy of Sciences , Wuhan, Hubei Province 430072 , China

2. California Institute for Quantitative Biosciences (QB3), University of California , Berkeley, CA 94720 , USA

3. University of Chinese Academy of Sciences , Beijing 100049 , China

4. College of Life Science and Technology, Huazhong Agricultural University , Wuhan, Hubei Province 430072 , China

5. Department of Chemistry and Biochemistry, University of California , Los Angeles, CA 90095 , USA

6. Chemical Sciences Division, Lawrence Livermore National Laboratory , Livermore, CA 94550 , USA

Abstract

Abstract Lysosome-related organelles (LROs) are a class of heterogeneous organelles conserved in eukaryotes that primarily play a role in storage and secretion. An important function of LROs is to mediate metal homeostasis. Chlamydomonas reinhardtii is a model organism for studying metal ion metabolism; however, structural and functional analyses of LROs in C. reinhardtii are insufficient. Here, we optimized a method for purifying these organelles from 2 populations of cells: stationary phase or overloaded with iron. The morphology, elemental content, and lysosomal activities differed between the 2 preparations, even though both have phosphorus and metal ion storage functions. LROs in stationary phase cells had multiple non-membrane-bound polyphosphate granules to store phosphorus. Those in iron-overloaded cells were similar to acidocalcisomes (ACs), which have a boundary membrane and contain 1 or 2 large polyphosphate granules to store more phosphorus. We established a method for quantifying the capacity of LROs to sequester individual trace metals. Based on a comparative proteomic analysis of these 2 types of LROs, we present a comprehensive AC proteome and identified 113 putative AC proteins. The methods and protein inventories provide a framework for studying the biogenesis and modification of LROs and the mechanisms by which they participate in regulating metal ion metabolism.

Funder

National Key R&D Program of China

NIH

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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