Systems Biology Approach in Chlamydomonas Reveals Connections between Copper Nutrition and Multiple Metabolic Steps

Author:

Castruita Madeli1,Casero David23,Karpowicz Steven J.1,Kropat Janette1,Vieler Astrid4,Hsieh Scott I.1,Yan Weihong1,Cokus Shawn2,Loo Joseph A.135,Benning Christoph4,Pellegrini Matteo23,Merchant Sabeeha S.13

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095

2. Department of Molecular, Cell, and Developmental Biology, University of California, Los Angeles, California 90095

3. Institute of Genomics and Proteomics, University of California, Los Angeles, California 90095

4. Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824

5. Department of Biological Chemistry, University of California, Los Angeles, California 90095

Abstract

Abstract In this work, we query the Chlamydomonas reinhardtii copper regulon at a whole-genome level. Our RNA-Seq data simulation and analysis pipeline validated a 2-fold cutoff and 10 RPKM (reads per kilobase of mappable length per million mapped reads) (~1 mRNA per cell) to reveal 63 CRR1 targets plus another 86 copper-responsive genes. Proteomic and immunoblot analyses captured 25% of the corresponding proteins, whose abundance was also dependent on copper nutrition, validating transcriptional regulation as a major control mechanism for copper signaling in Chlamydomonas. The impact of copper deficiency on the expression of several O2-dependent enzymes included steps in lipid modification pathways. Quantitative lipid profiles indicated increased polyunsaturation of fatty acids on thylakoid membrane digalactosyldiglycerides, indicating a global impact of copper deficiency on the photosynthetic apparatus. Discovery of a putative plastid copper chaperone and a membrane protease in the thylakoid suggest a mechanism for blocking copper utilization in the chloroplast. We also found an example of copper sparing in the N assimilation pathway: the replacement of copper amine oxidase by a flavin-dependent backup enzyme. Forty percent of the targets are previously uncharacterized proteins, indicating considerable potential for new discovery in the biology of copper.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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