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A J-Like Protein Influences Fatty Acid Composition of Chloroplast Lipids in Arabidopsis
A comprehensive understanding of the lipid and fatty acid metabolic machinery is needed for optimizing production of oils and fatty acids for fuel, industrial feedstocks and nutritional improvement in plants. T-DNA mutants in the poorly annotated Arabidopsis thaliana gene At1g08640 were identified a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196505/ https://www.ncbi.nlm.nih.gov/pubmed/22028775 http://dx.doi.org/10.1371/journal.pone.0025368 |
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author | Ajjawi, Imad Coku, Ardian Froehlich, John E. Yang, Yue Osteryoung, Katherine W. Benning, Christoph Last, Robert L. |
author_facet | Ajjawi, Imad Coku, Ardian Froehlich, John E. Yang, Yue Osteryoung, Katherine W. Benning, Christoph Last, Robert L. |
author_sort | Ajjawi, Imad |
collection | PubMed |
description | A comprehensive understanding of the lipid and fatty acid metabolic machinery is needed for optimizing production of oils and fatty acids for fuel, industrial feedstocks and nutritional improvement in plants. T-DNA mutants in the poorly annotated Arabidopsis thaliana gene At1g08640 were identified as containing moderately high levels (50–100%) of 16∶1Δ7 and 18∶1Δ9 leaf fatty acids and subtle decreases (5–30%) of 16∶3 and 18∶3 (http://www.plastid.msu.edu/). TLC separation of fatty acids in the leaf polar lipids revealed that the chloroplastic galactolipids monogalactosyldiacylglycerol (MGDG) and digalactosyldiacylglycerol (DGDG) were the main lipid types affected by this mutation. Analysis of the inferred amino acid sequence of At1g08640 predicted the presence of a transit peptide, three transmembrane domains and an N-terminal J-like domain, and the gene was named CJD1 for Chloroplast J-like Domain 1. GFP reporter experiments and in vitro chloroplast import assays demonstrated CJD1 is a chloroplast membrane protein. Screening of an Arabidopsis cDNA library by yeast-2-hybrid (Y2H) using the J-like domain of CJD1 as bait identified a plastidial inner envelope protein (Accumulation and Replication of Chloroplasts 6, ARC6) as the primary interacting partner in the Y2H assay. ARC6 plays a central role in chloroplast division and binds CJD1 via its own J-like domain along with an adjacent conserved region whose function is not fully known. These results provide a starting point for future investigations of how mutations in CJD1 affect lipid composition. |
format | Online Article Text |
id | pubmed-3196505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31965052011-10-25 A J-Like Protein Influences Fatty Acid Composition of Chloroplast Lipids in Arabidopsis Ajjawi, Imad Coku, Ardian Froehlich, John E. Yang, Yue Osteryoung, Katherine W. Benning, Christoph Last, Robert L. PLoS One Research Article A comprehensive understanding of the lipid and fatty acid metabolic machinery is needed for optimizing production of oils and fatty acids for fuel, industrial feedstocks and nutritional improvement in plants. T-DNA mutants in the poorly annotated Arabidopsis thaliana gene At1g08640 were identified as containing moderately high levels (50–100%) of 16∶1Δ7 and 18∶1Δ9 leaf fatty acids and subtle decreases (5–30%) of 16∶3 and 18∶3 (http://www.plastid.msu.edu/). TLC separation of fatty acids in the leaf polar lipids revealed that the chloroplastic galactolipids monogalactosyldiacylglycerol (MGDG) and digalactosyldiacylglycerol (DGDG) were the main lipid types affected by this mutation. Analysis of the inferred amino acid sequence of At1g08640 predicted the presence of a transit peptide, three transmembrane domains and an N-terminal J-like domain, and the gene was named CJD1 for Chloroplast J-like Domain 1. GFP reporter experiments and in vitro chloroplast import assays demonstrated CJD1 is a chloroplast membrane protein. Screening of an Arabidopsis cDNA library by yeast-2-hybrid (Y2H) using the J-like domain of CJD1 as bait identified a plastidial inner envelope protein (Accumulation and Replication of Chloroplasts 6, ARC6) as the primary interacting partner in the Y2H assay. ARC6 plays a central role in chloroplast division and binds CJD1 via its own J-like domain along with an adjacent conserved region whose function is not fully known. These results provide a starting point for future investigations of how mutations in CJD1 affect lipid composition. Public Library of Science 2011-10-18 /pmc/articles/PMC3196505/ /pubmed/22028775 http://dx.doi.org/10.1371/journal.pone.0025368 Text en Ajjawi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ajjawi, Imad Coku, Ardian Froehlich, John E. Yang, Yue Osteryoung, Katherine W. Benning, Christoph Last, Robert L. A J-Like Protein Influences Fatty Acid Composition of Chloroplast Lipids in Arabidopsis |
title | A J-Like Protein Influences Fatty Acid Composition of Chloroplast Lipids in Arabidopsis |
title_full | A J-Like Protein Influences Fatty Acid Composition of Chloroplast Lipids in Arabidopsis |
title_fullStr | A J-Like Protein Influences Fatty Acid Composition of Chloroplast Lipids in Arabidopsis |
title_full_unstemmed | A J-Like Protein Influences Fatty Acid Composition of Chloroplast Lipids in Arabidopsis |
title_short | A J-Like Protein Influences Fatty Acid Composition of Chloroplast Lipids in Arabidopsis |
title_sort | j-like protein influences fatty acid composition of chloroplast lipids in arabidopsis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196505/ https://www.ncbi.nlm.nih.gov/pubmed/22028775 http://dx.doi.org/10.1371/journal.pone.0025368 |
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