AAE13 encodes a dual‐localized malonyl‐CoA synthetase that is crucial for mitochondrial fatty acid biosynthesis. (3rd March 2016)

• Record Type: Journal Article
• Authors: Guan, Xin; Nikolau, Basil J.
• Is Part Of: Plant journal. Volume 85:Number 5(2016:Mar.)
• Page Start: 581
• Page End: 593
• Publication Date: 2016-03-03
• Subjects: malonyl‐CoA synthetase -- mitochondrial fatty acid synthase -- lipoic acid -- glycine decarboxylase -- photorespiration -- Arabidopsis thaliana; Plant molecular biology -- Periodicals; Plant cells and tissues -- Periodicals; Botany -- Periodicals; 580
• DOI: 10.1111/tpj.13130
• Languages: English
• ISSNs: 0960-7412

Abstract

Summary: Malonyl‐CoA is a key intermediate in a number of metabolic processes associated with its role as a substrate in acylation and condensation reactions. These types of reactions occur in plastids, the cytosol and mitochondria, and although carboxylation of acetyl‐CoA is the known mechanism for generating the distinct plastidial and cytosolic pools, the metabolic origin of the mitochondrial malonyl‐CoA pool is still unclear. In this study we demonstrate that malonyl‐CoA synthetase encoded by the Arabidopsis AAE13 ( AT3G16170 ) gene is localized in both the cytosol and the mitochondria. These isoforms are translated from two types of transcripts, one that contains and one that does not contain a mitochondrial‐targeting pre‐sequence. Whereas the cytosolic AAE13 protein is not essential, due to the presence of a redundant malonyl‐CoA generating system provided by a cytosolic acetyl‐CoA carboxylase, the mitochondrial AAE13 protein is essential for plant growth. Phenotypes of the aae13‐1 mutant are transgenically reversed only if the mitochondrial pre‐sequence is present in the ectopically expressed AAE13 proteins. The aae13‐1 mutant exhibits typical metabolic phenotypes associated with a deficiency in the mitochondrial fatty acid synthase system, namely depleted lipoylation of the H subunit of the photorespiratory enzyme glycine decarboxylase, increased accumulation of glycine and glycolate and reduced levels of sucrose. Most of these metabolic alterations, and associated morphological changes, are reversed when the aae13‐1 mutant is grown in a non‐photorespiratory condition (i.e. a 1% CO2 atmosphere), demonstrating that they are a consequence of the deficiency in photorespiration due to the inability to generate lipoic acid from mitochondrially synthesized fatty acids. Significance Statement: Malonyl‐CoA is a key intermediate in a number of metabolic processes that occur in plastids, the cytosol and mitochondria, but the origin of the mitochondrial malonyl‐CoA pool was unclear. Here we show that the mitochondrial fatty acid synthase system uses malonyl‐CoA generated by a mitochondrially located malonyl‐CoA synthetase.