Arabidopsis cytosolic acyl-CoA-binding proteins ACBP4, ACBP5 and ACBP6 have overlapping but distinct roles in seed development
Eukaryotic cytosolic ACBPs (acyl-CoA-binding proteins) bind acyl-CoA esters and maintain a cytosolic acyl-CoA pool, but the thermodynamics of their protein–lipid interactions and physiological relevance in plants are not well understood. Arabidopsis has three cytosolic ACBPs which have been identif...
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Portland Press, Biochemical Society
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doaj-5a14ab3d594349219908c74d0b8cbc782020-11-25T00:42:45ZengPortland Press, Biochemical SocietyBioscience Reports1573-49352014-12-01346e0016510.1042/BSR20140139BSR20140139Arabidopsis cytosolic acyl-CoA-binding proteins ACBP4, ACBP5 and ACBP6 have overlapping but distinct roles in seed developmentAn‑Shan Hsiao0Richard P. Haslam1Louise V. Michaelson2Pan Liao3Qin‑Fang Chen4Sanjeewani Sooriyaarachchi5Sherry L. MowbrayJohnathan A. Napier6Julian A. Tanner7Mee‑Len Chye8 School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China Department of Biological Chemistry, Rothamsted Research, Harpenden, Hertfordshire AL5 2JQ, U.K. Department of Biological Chemistry, Rothamsted Research, Harpenden, Hertfordshire AL5 2JQ, U.K. School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China Department of Cell and Molecular Biology, Uppsala University, Box 596, Biomedical Center, 751 24 Uppsala, Sweden Department of Biological Chemistry, Rothamsted Research, Harpenden, Hertfordshire AL5 2JQ, U.K. ║Department of Biochemistry, The University of Hong Kong, Pokfulam, Hong Kong, China School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China Eukaryotic cytosolic ACBPs (acyl-CoA-binding proteins) bind acyl-CoA esters and maintain a cytosolic acyl-CoA pool, but the thermodynamics of their protein–lipid interactions and physiological relevance in plants are not well understood. Arabidopsis has three cytosolic ACBPs which have been identified as AtACBP4, AtACBP5 and AtACBP6, and microarray data indicated that all of them are expressed in seeds; AtACBP4 is expressed in early embryogenesis, whereas AtACBP5 is expressed later. ITC (isothermal titration calorimetry) in combination with transgenic Arabidopsis lines were used to investigate the roles of these three ACBPs from Arabidopsis thaliana. The dissociation constants, stoichiometry and enthalpy change of AtACBP interactions with various acyl-CoA esters were determined using ITC. Strong binding of recombinant (r) AtACBP6 with long-chain acyl-CoA (C16- to C18-CoA) esters was observed with dissociation constants in the nanomolar range. However, the affinity of rAtACBP4 and rAtACBP5 to these acyl-CoA esters was much weaker (dissociation constants in the micromolar range), suggesting that they interact with acyl-CoA esters differently from rAtACBP6. When transgenic Arabidopsis expressing AtACBP6pro::GUS was generated, strong GUS (β-glucuronidase) expression in cotyledonary-staged embryos and seedlings prompted us to measure the acyl-CoA contents of the acbp6 mutant. This mutant accumulated higher levels of C18:1-CoA and C18:1- and C18:2-CoAs in cotyledonary-staged embryos and seedlings, respectively, in comparison with the wild type. The acbp4acbp5acbp6 mutant showed the lightest seed weight and highest sensitivity to abscisic acid during germination, suggesting their physiological functions in seeds.http://www.bioscirep.org/bsr/034/e165/bsr034e165.htmacyl-CoA-binding proteinisothermal titration calorimetrylipid metabolismseed |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
An‑Shan Hsiao Richard P. Haslam Louise V. Michaelson Pan Liao Qin‑Fang Chen Sanjeewani Sooriyaarachchi Sherry L. Mowbray Johnathan A. Napier Julian A. Tanner Mee‑Len Chye |
spellingShingle |
An‑Shan Hsiao Richard P. Haslam Louise V. Michaelson Pan Liao Qin‑Fang Chen Sanjeewani Sooriyaarachchi Sherry L. Mowbray Johnathan A. Napier Julian A. Tanner Mee‑Len Chye Arabidopsis cytosolic acyl-CoA-binding proteins ACBP4, ACBP5 and ACBP6 have overlapping but distinct roles in seed development Bioscience Reports acyl-CoA-binding protein isothermal titration calorimetry lipid metabolism seed |
author_facet |
An‑Shan Hsiao Richard P. Haslam Louise V. Michaelson Pan Liao Qin‑Fang Chen Sanjeewani Sooriyaarachchi Sherry L. Mowbray Johnathan A. Napier Julian A. Tanner Mee‑Len Chye |
author_sort |
An‑Shan Hsiao |
title |
Arabidopsis cytosolic acyl-CoA-binding proteins ACBP4, ACBP5 and ACBP6 have overlapping but distinct roles in seed development |
title_short |
Arabidopsis cytosolic acyl-CoA-binding proteins ACBP4, ACBP5 and ACBP6 have overlapping but distinct roles in seed development |
title_full |
Arabidopsis cytosolic acyl-CoA-binding proteins ACBP4, ACBP5 and ACBP6 have overlapping but distinct roles in seed development |
title_fullStr |
Arabidopsis cytosolic acyl-CoA-binding proteins ACBP4, ACBP5 and ACBP6 have overlapping but distinct roles in seed development |
title_full_unstemmed |
Arabidopsis cytosolic acyl-CoA-binding proteins ACBP4, ACBP5 and ACBP6 have overlapping but distinct roles in seed development |
title_sort |
arabidopsis cytosolic acyl-coa-binding proteins acbp4, acbp5 and acbp6 have overlapping but distinct roles in seed development |
publisher |
Portland Press, Biochemical Society |
series |
Bioscience Reports |
issn |
1573-4935 |
publishDate |
2014-12-01 |
description |
Eukaryotic cytosolic ACBPs (acyl-CoA-binding proteins) bind acyl-CoA esters and maintain a cytosolic acyl-CoA pool, but the thermodynamics of their protein–lipid interactions and physiological relevance in plants are not well understood. Arabidopsis has three cytosolic ACBPs which have been identified as AtACBP4, AtACBP5 and AtACBP6, and microarray data indicated that all of them are expressed in seeds; AtACBP4 is expressed in early embryogenesis, whereas AtACBP5 is expressed later. ITC (isothermal titration calorimetry) in combination with transgenic Arabidopsis lines were used to investigate the roles of these three ACBPs from Arabidopsis thaliana. The dissociation constants, stoichiometry and enthalpy change of AtACBP interactions with various acyl-CoA esters were determined using ITC. Strong binding of recombinant (r) AtACBP6 with long-chain acyl-CoA (C16- to C18-CoA) esters was observed with dissociation constants in the nanomolar range. However, the affinity of rAtACBP4 and rAtACBP5 to these acyl-CoA esters was much weaker (dissociation constants in the micromolar range), suggesting that they interact with acyl-CoA esters differently from rAtACBP6. When transgenic Arabidopsis expressing AtACBP6pro::GUS was generated, strong GUS (β-glucuronidase) expression in cotyledonary-staged embryos and seedlings prompted us to measure the acyl-CoA contents of the acbp6 mutant. This mutant accumulated higher levels of C18:1-CoA and C18:1- and C18:2-CoAs in cotyledonary-staged embryos and seedlings, respectively, in comparison with the wild type. The acbp4acbp5acbp6 mutant showed the lightest seed weight and highest sensitivity to abscisic acid during germination, suggesting their physiological functions in seeds. |
topic |
acyl-CoA-binding protein isothermal titration calorimetry lipid metabolism seed |
url |
http://www.bioscirep.org/bsr/034/e165/bsr034e165.htm |
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