Arabidopsis ACYL CARRIER PROTEIN4 and RHOMBOID LIKE10 act independently in chloroplast phosphatidate synthesis

Author:

Xu Yang1ORCID,Kambhampati Shrikaar2ORCID,Morley Stewart A23ORCID,Cook Ron14ORCID,Froehlich John14ORCID,Allen Doug K23ORCID,Benning Christoph145ORCID

Affiliation:

1. DOE-Plant Research Laboratory, Michigan State University , East Lansing, MI 48824 , USA

2. Donald Danforth Plant Science Center , St. Louis, MO 63132 , USA

3. United States Department of Agriculture, Agriculture Research Service , St. Louis, MO 63132 , USA

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

5. Department of Plant Biology, Michigan State University , East Lansing, MI 48824 , USA

Abstract

Abstract ACYL CARRIER PROTEIN4 (ACP4) is the most abundant ACP isoform in Arabidopsis (Arabidopsis thaliana) leaves and acts as a scaffold for de novo fatty acid biosynthesis and as a substrate for acyl-ACP-utilizing enzymes. Recently, ACP4 was found to interact with a protein-designated plastid RHOMBOID LIKE10 (RBL10) that affects chloroplast monogalactosyldiacylglycerol (MGDG) biosynthesis, but the cellular function of this interaction remains to be explored. Here, we generated and characterized acp4 rbl10 double mutants to explore whether ACP4 and RBL10 directly interact in influencing chloroplast lipid metabolism. Alterations in the content and molecular species of chloroplast lipids such as MGDG and phosphatidylglycerol were observed in the acp4 and rbl10 mutants, which are likely associated with the changes in the size and profiles of diacylglycerol (DAG), phosphatidic acid (PA), and acyl-ACP precursor pools. ACP4 contributed to the size and profile of the acyl-ACP pool and interacted with acyl-ACP-utilizing enzymes, as expected for its role in fatty acid biosynthesis and chloroplast lipid assembly. RBL10 appeared to be involved in the conversion of PA to DAG precursors for MGDG biosynthesis as evidenced by the increased 34:x PA and decreased 34:x DAG in the rbl10 mutant and the slow turnover of radiolabeled PA in isolated chloroplasts fed with [14C] acetate. Interestingly, the impaired PA turnover in rbl10 was partially reversed in the acp4 rbl10 double mutant. Collectively, this study shows that ACP4 and RBL10 affect chloroplast lipid biosynthesis by modulating substrate precursor pools and appear to act independently.

Funder

Division of Chemical Sciences, Geosciences and Biosciences

Office of Basic Energy Sciences of the United States Department of Energy

National Institute of Health

Department of Agriculture, Agriculture Research Service

Michigan State University AgBioResearch

US Department of Energy

Office of Science

Office of Biological and Environmental Research

Genomic Science Program

National Science Foundation

Orbitrap Fusion Lumos LC-MS/MS

QTRAP LC-MS/MS

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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