Isolation and expression analysis of glycerol-3-phosphate acyltransferase genes from peanuts (Arachis hypogaea L.)

Authors

  • X. Chi Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture, Oil Crops Research Institute, Chinese Academy of Agricultural Sciences - Shandong Peanut Research Institute
  • Q. Yang College of food science and engineering of Qingdao agricultural university
  • L. Pan Shandong Peanut Research Institute
  • N. Chen Shandong Peanut Research Institute
  • T. Wang Shandong Peanut Research Institute
  • M. Wang Shandong Peanut Research Institute
  • Z. Yang Shandong Peanut Research Institute
  • X. Guan School of Ocean Sciences, China University of Geosciences
  • S. Yu Shandong Peanut Research Institute

DOI:

https://doi.org/10.3989/gya.1190142

Keywords:

Glycerol-3-phosphate acyltransferase, Peanuts (Arachis hypogaea L.), Phylogenetic analysis, Quantitative real-time RT-PCR

Abstract


sn-Glycerol-3-phosphate acyltransferase (GPAT) catalyzes the committed step in the production of glycerolipids. The functions of GPAT genes have been intensively studied in Arabidopsis, but not in peanuts (Arachis hypogaea L.). In this study, six AhGPAT genes were isolated from peanuts. Quantitative real-time RT-PCR analysis indicated that the AhGPAT9 transcript was more abundant in the stems, flowers, and seeds, whereas the transcript abundances of five other genes were higher in the leaves or flowers than in the other tissues examined. During seed development, the transcript levels of AhGPAT9 gradually increased, whereas the transcript levels of the other five genes decreased. In addition, the levels of AhGPAT2 transcript were distinctly enhanced after exposure to all four kinds of stress treatments except for ABA-treated leaves. The transcripts of AhGPAT1, AhGPAT6, AhGPAT8 and AhATS1 increased substantially in roots exposed to salt, drought, and ABA stress. The expressions of AhGPAT6, AhGPAT8, AhGPAT9 and AhATS1 were slightly higher in leaves under certain stress conditions than under normal conditions. The present study provides significant information for modifying oil deposition and improving the abiotic stress resistance of peanuts through molecular breeding.

Downloads

Download data is not yet available.

References

Ariizumi T, Kishitani S, Inatsugi R. 2002. An increase in unsaturation of fatty acids in phosphatidylglycerol from leaves improves the rates of photosynthesis and growth at low temperatures in transgenic rice seedlings. Plant. Cell. Physiol. 43, 751–758. http://dx.doi.org/10.1093/pcp/pcf087 PMid:12154137

Beisson F, Li Y, Bonaventure G, Pollard M, Ohlrogge JB. 2007. The acyltransferase GPAT5 is required for the synthesis of suberin in seed coat and root of Arabidopsis. Plant. Cell. 19, 351–368. http://dx.doi.org/10.1105/tpc.106.048033 PMid:17259262 PMCid:PMC1820950

Burroughs AM, Allen KN, Dunaway-Mariano D, Aravind L. 2006. Evolutionary genomics of the HAD superfamily: understanding the structural adaptations and catalytic diversity in a superfamily of phosphoesterases and allied enzymes. J. Mol. Biol. 361, 1003–1034. http://dx.doi.org/10.1016/j.jmb.2006.06.049 PMid:16889794

Cao J, Li JL, Li D, Tobin JF, Gimeno RE. 2006. Molecular identification of microsomal acyl-CoA: glycerol-3-phosphate acyltransferase, a key enzyme in de novo triacylglycerol synthesis. Proc. Natl. Acad. Sci. USA. 103, 19695–19700. http://dx.doi.org/10.1073/pnas.0609140103 PMid:17170135 PMCid:PMC1702318

Chen X, Snyder CL, Truksa M, Shah S, Weselake RJ. 2011a. sn-Glycerol-3-phosphate acyltransferases in plants. Plant Signaling Behavior. 6, 1695–1699. http://dx.doi.org/10.4161/psb.6.11.17777 PMid:22057337 PMCid:PMC3329339

Chen X, Truksa M, Snyder CL, El-Mezawy A, Shah S, Weselake RJ. 2011b. Three Homologous genes encoding sn-glycerol- 3-phosphate acyltransferase 4 exhibit different expression patterns and functional divergence in Brassica napus. Plant Physiol. 155, 851–865. http://dx.doi.org/10.1104/pp.110.169482 PMid:21173024 PMCid:PMC3032471

Chi XY, Hu RB, Yang QL, Zhang XW, Pan LJ, Chen N, Chen MN, Yang Z, Wang T, He YN, Yu SL. 2012. Validation of reference genes for gene expression studies in peanut by quantitative real-time RT-PCR. Mol. Genet. Genomics. 287, 167–176. http://dx.doi.org/10.1007/s00438-011-0665-5 PMid:22203160

Chi XY, Yang QL, Pan LJ, Chen MN, He YN, Yang Z, Yu SL. 2011. Isolation and characterization of fatty acid desaturase genes from peanut (Arachis hypogaea L.). Plant. Cell. Rep. 30, 1393–1404. http://dx.doi.org/10.1007/s00299-011-1048-4 PMid:21409552

Gidda SK, Shockey JM, Rothstein SJ, Dyer JM, Mullen RT. 2009. Arabidopsis thaliana GPAT8 and GPAT9 are localized to the ER and possess distinct ER retrieval signals: functional divergence of the dilysine ER retrieval motif in plant cells. Plant. Physiol. Biochem. 47, 867–879. http://dx.doi.org/10.1016/j.plaphy.2009.05.008 PMid:19539490

Gonzalez-Baró MR, Lewin TM, Coleman RA. 2007. Regulation of Triglyceride Metabolism II. Function of mitochondrial GPAT1 in the regulation of triacylglycerol biosynthesis and insulin action. Am. J. Physiol. Gastrointest. Liver. Physiol. 292, G1195–G1199. http://dx.doi.org/10.1152/ajpgi.00553.2006 PMid:17158253 PMCid:PMC2819211

Harwood H. 1984. Oleochemicals as a fuel. Mechanical and economic feasibility. J. Am. Oil Chem. Soc. 61, 315–324. http://dx.doi.org/10.1007/BF02678788

Livak KJ, Schmittgen TD. 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods. 25, 402–408. http://dx.doi.org/10.1006/meth.2001.1262 PMid:11846609

Li XC, Zhu J, Yang J, Zhang GR, Xing WF, Zhang S, Yang ZN. 2011. Glycerol-3-phosphate acyltransferase 6 (GPAT6) is important for tapetum development in Arabidopsis and plays multiple roles in plant fertility. Molecular Plant. 5, 131–142. http://dx.doi.org/10.1093/mp/ssr057 PMid:21746699

Li Y, Beisson F, Koo AJ, Molina I, Pollard M, Ohlrogge J. 2007b. Identification of acyltransferases required for cutin biosynthesis and production of cutin with suberin-like monomers. Proc. Natl. Acad. Sci. USA. 104, 18339–18344. http://dx.doi.org/10.1073/pnas.0706984104 PMid:17991776 PMCid:PMC2084344

Li Y, Beisson F, Ohlrogge J, Pollard M. 2007a. Monoacylglycerols are components of root waxes and can be produced in the aerial cuticle by ectopic expression of a suberin-associated acyltransferase. Plant. Physiol. 144, 1267–1277. http://dx.doi.org/10.1104/pp.107.099432 PMid:17496107 PMCid:PMC1914122

Li-Beisson Y, Pollard M, Sauveplane V, Pinot F, Ohlrogge J, Beisson F. 2009. Nanoridges that characterize the surface morphology of flowers require the synthesis of cutin polyester. Proc. Natl. Acad. Sci. USA. 106, 22008–22013. http://dx.doi.org/10.1073/pnas.0909090106 PMid:19959665 PMCid:PMC2788479

Ma-as-Fernández A, Li-Beisson Y, Alonso DL, García-Maroto F. 2010. Cloning and molecular characterization of a glycerol-3-phosphate O-acyltransferase (GPAT) gene from Echium (Boraginaceae) involved in the biosynthesis of cutin polyesters. Planta. 232, 987–997. http://dx.doi.org/10.1007/s00425-010-1232-8 PMid:20658148

Murata N, Ishizaki-Nishizawa O, Higashi S, Hayashi H, Tasaka Y, Nishida I. 1992. Genetically engineered alteration in the chilling sensitivity of plants. Nature. 365, 710–713. http://dx.doi.org/10.1038/356710a0

Murata N, Tasaka Y. 1997. Glycerol-3-phosphate acyltransferase in plants. Biochim. Biophys. Acta. 1348 (1–2), 10–16. http://dx.doi.org/10.1016/S0005-2760(97)00115-X

Nishida I, Tasaka Y, Shiraishi H, Murata N. 1993. The gene and the RNA for the precursor to the plastid-located glycerol-3-phosphate acyltransferase of Arabidopsis thaliana. Plant. Mol. Biol. 21, 267–277. http://dx.doi.org/10.1007/BF00019943 PMid:7678766

Pellon-Maison M, Coleman RA, Gonzalez-Baró MR. 2006. The C-terminal region of mitochondrial glycerol-3-phosphate acyltransferase-1 interacts with the active site region and is required for activity. Arch. Biochem. Biophys. 450, 157–166. http://dx.doi.org/10.1016/j.abb.2006.03.009 PMid:16620760

Schreiber L. 2010. Transport barriers made of cutin, suberin and associated waxes. Trends. Plant. Sci. 15, 546–553. http://dx.doi.org/10.1016/j.tplants.2010.06.004 PMid:20655799

Sui N, Li M, Zhao SJ, Li F, Liang H, Meng QW. 2007. Overexpression of glycerol-3-phosphate acyltransferase gene improves chilling tolerance in tomato. Planta. 226, 1097–1108. http://dx.doi.org/10.1007/s00425-007-0554-7 PMid:17541789

Takeuchi K, Reue K. 2009. Biochemistry, physiology, and genetics of GPAT, AGPAT, and lipin enzymes in triglyceride synthesis. Am. J. Physiol. Endocrinol. Metab. 296, E1195–E1209. http://dx.doi.org/10.1152/ajpendo.90958.2008 PMid:19336658 PMCid:PMC2692402

Tamura K, Dudley J, Nei M, Kumar S. 2007. MEGA4: Molecular evolutionary genetics analysis (MEGA) software version 4.0. Molecular Biology and Evolution. 24, 1596–1599. http://dx.doi.org/10.1093/molbev/msm092 PMid:17488738

Thompson JD, Higgins DG, Gibson TJ. 1994. CLUSTALW: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic. Acids. Res. 22, 4673–4680. http://dx.doi.org/10.1093/nar/22.22.4673 PMid:7984417 PMCid:PMC308517

Xu C, Cornish AJ, Froehlich JE, Benning C. 2006. Phosphatidylglycerol biosynthesis in chloroplasts of Arabidopsis mutants deficient in acyl-ACP glycerol-3-phosphate acyltransferase. Plant. J. 47, 296–309. http://dx.doi.org/10.1111/j.1365-313X.2006.02790.x PMid:16774646

Yan K, Chen N, Qu YY, Dong XC, Meng QW, Zhao SJ. 2008. Overexpression of sweet pepper glycerol-3-phosphate acyltransferase gene enhanced thermotolerance of photosynthetic apparatus in transgenic tobacco. J. Integrative Plant Biol. 50 613–621. http://dx.doi.org/10.1111/j.1744-7909.2008.00652.x PMid:18713430

Yang WL, Simpson JP, Li-Beisson YH, Beisson F, Pollard M, Ohlrogge JB. 2012. A land-plant-specific glycerol-3-phosphate acyltransferase family in Arabidopsis: substrate specificity, sn-2 preference and evolution. Plant Physiol. 160, 638–652. http://dx.doi.org/10.1104/pp.112.201996 PMid:22864585 PMCid:PMC3461545

Zheng Z, Xia Q, Dauk M, Shen W, Selvaraj G, Zou J. 2003. Arabidopsis AtGPAT1, a member of the membranebound glycerol-3-phosphate acyltransferase gene family, is essential for tapetum differentiation and male fertility. Plant Cell. 15, 1872–1887. http://dx.doi.org/10.1105/tpc.012427 PMid:12897259 PMCid:PMC167176

Published

2015-09-30

How to Cite

1.
Chi X, Yang Q, Pan L, Chen N, Wang T, Wang M, Yang Z, Guan X, Yu S. Isolation and expression analysis of glycerol-3-phosphate acyltransferase genes from peanuts (Arachis hypogaea L.). Grasas aceites [Internet]. 2015Sep.30 [cited 2024Apr.19];66(3):e093. Available from: https://grasasyaceites.revistas.csic.es/index.php/grasasyaceites/article/view/1559

Issue

Section

Research

Most read articles by the same author(s)