LIL3, a light-harvesting-like protein, plays an essential role in chlorophyll and tocopherol biosynthesis

• DOI: 10.1073/pnas.1004699107
• Publication Date: 2010-09-08T02:21:32Z
• Authors: Ryouichi Tanaka; Maxi Rothbart; Seiko Oka; Atsushi Takabayashi; Kaori Takahashi; Masaru Shibata; Fumiyoshi Myouga; Reiko Motohashi; Kazuo Shinozaki; Bernhard Grimm; Ayumi Tanaka
• Keywords: Chlorophyll; 471; Molecular Sequence Data; Arabidopsis; Light-Harvesting Protein Complexes; Tocopherols; Genes, Plant; phytol; Chloroplast Proteins; 03 medical and health sciences; Enzyme Stability; Amino Acid Sequence; RNA, Messenger; Phylogeny; DNA Primers; 0303 health sciences; Base Sequence; Sequence Homology, Amino Acid; Arabidopsis Proteins; geranylgeranyl reductase; Mutagenesis, Insertional; RNA, Plant; Mutation; tetrapyrrole; Mutant Proteins; Oxidoreductases

The light-harvesting chlorophyll-binding (LHC) proteins are major constituents of eukaryotic photosynthetic machinery. In plants, six different groups of proteins, LHC-like proteins, share a conserved motif with LHC. Although the evolution of LHC and LHC-like proteins is proposed to be a key for the diversification of modern photosynthetic eukaryotes, our knowledge of the evolution and functions of LHC-like proteins is still limited. In this study, we aimed to understand specifically the function of one type of LHC-like proteins, LIL3 proteins, by analyzing Arabidopsis mutants lacking them. The Arabidopsis genome contains two gene copies for LIL3, LIL3:1 and LIL3:2 . In the lil3:1/lil3:2 double mutant, the majority of chlorophyll molecules are conjugated with an unsaturated geranylgeraniol side chain. This mutant is also deficient in α-tocopherol. These results indicate that reduction of both the geranylgeraniol side chain of chlorophyll and geranylgeranyl pyrophosphate, which is also an essential intermediate of tocopherol biosynthesis, is compromised in the lil3 mutants. We found that the content of geranylgeranyl reductase responsible for these reactions was severely reduced in the lil3 double mutant, whereas the mRNA level for this enzyme was not significantly changed. We demonstrated an interaction of geranylgeranyl reductase with both LIL3 isoforms by using a split ubiquitin assay, bimolecular fluorescence complementation, and combined blue-native and SDS polyacrylamide gel electrophoresis. We propose that LIL3 is functionally involved in chlorophyll and tocopherol biosynthesis by stabilizing geranylgeranyl reductase.