Development of EMS-induced mutation population for amylose and resistant starch variation in bread wheat (Triticum aestivum) and identification of candidate genes responsible for amylose variation
Tóm tắt
Starch is a major part of cereal grain. It comprises two glucose polymer fractions, amylose (AM) and amylopectin (AP), that make up about 25 and 75 % of total starch, respectively. The ratio of the two affects processing quality and digestibility of starch-based food products. Digestibility determines nutritional quality, as high amylose starch is considered a resistant or healthy starch (RS type 2) and is highly preferred for preventive measures against obesity and related health conditions. The topic of nutrition security is currently receiving much attention and consumer demand for food products with improved nutritional qualities has increased. In bread wheat (Triticum aestivum L.), variation in amylose content is narrow, hence its limited improvement. Therefore, it is necessary to produce wheat lines or populations showing wide variation in amylose/resistant starch content. In this study, a set of EMS-induced M4 mutant lines showing dynamic variation in amylose/resistant starch content were produced. Furthermore, two diverse mutant lines for amylose content were used to study quantitative expression patterns of 20 starch metabolic pathway genes and to identify candidate genes for amylose biosynthesis. A population comprising 101 EMS-induced mutation lines (M4 generation) was produced in a bread wheat (Triticum aestivum) variety. Two methods of amylose measurement in grain starch showed variation in amylose content ranging from ~3 to 76 % in the population. The method of in vitro digestion showed variation in resistant starch content from 1 to 41 %. One-way ANOVA analysis showed significant variation (p < 0.05) in amylose and resistant starch content within the population. A multiple comparison test (Dunnett’s test) showed that significant variation in amylose and resistant starch content, with respect to the parent, was observed in about 89 and 38 % of the mutant lines, respectively. Expression pattern analysis of 20 starch metabolic pathway genes in two diverse mutant lines (low and high amylose mutants) showed higher expression of key genes of amylose biosynthesis (GBSSI and their isoforms) in the high amylose mutant line, in comparison to the parent. Higher expression of amylopectin biosynthesis (SBE) was observed in the low amylose mutant lines. An additional six candidate genes showed over-expression (BMY, SPA) and reduced-expression (SSIII, SBEI, SBEIII, ISA3) in the high amylose mutant line, indicating that other starch metabolic genes may also contribute to amylose biosynthesis. In this study a set of 101 EMS-induced mutant lines (M4 generation) showing variation in amylose and resistant starch content in seed were produced. This population serves as useful germplasm or pre-breeding material for genome-wide study and improvement of starch-based processing and nutrition quality in wheat. It is also useful for the study of the genetic and molecular basis of amylose/resistant starch variation in wheat. Furthermore, gene expression analysis of 20 starch metabolic genes in the two diverse mutant lines (low and high amylose mutants) indicates that in addition to key genes, several other genes (such as phosphorylases, isoamylases, and pullulanases) may also be involved in contributing to amylose/amylopectin biosynthesis.
Tài liệu tham khảo
Nakamura T, Yamamori M, Hirano H, Hidaka S. Identification of three Wx protein in wheat (Triticum aestivum L). Biochem Genet. 1993;31:75–86.
Nakamura Y, Yamamori M, Hirano H, Hidaka S, Nagamine T. Production of waxy (amylose-free) wheat. Mol Gen Genet. 1995;248:253–9.
Hoshino T, Ito S, Hatta K, Nakamura T, Yamamori M. Development of waxy common wheat by haploid breeding. Breed Sci. 1996;46:185–8.
Graybosch RA. Waxy wheats: origin, properties, and prospects. Trends Food Sci Tech. 1998;9:135–42.
Dong C, Dalton-Morgan J, Vincent K, Sharp P. A modified TILLING method for wheat breeding. Plant Genome. 2009;2:39–47.
Hazard B, Zhang X, Colasuonno P, Uauy C, Beckles DM, Dubcovsky J. Induced mutations in the starch branching enzyme II (SBEII) genes increase amylose and resistant starch content in durum wheat. Crop Sci. 2012;52:1754–66.
Slade AJ, McGuire C, Loeffler D, Mullenberg J, Skinner W, Fazio G, Holm A, Brandt KA, Steine MN, Goodstal JF, Knauf VC. Development of high amylose wheat through TILLING. BMC Plant Biol. 2012;12:69.
Hogg AC, Gause K, Hofer P, Martin JM, Graybosch RA, Hansen LE, Giroux MJ. Creation of a high amylose durum wheat through mutagenesis of starch synthase II (SSIIa). J Cereal Sci. 2013;57:377–83.
Sestili F, Palombieri S, Botticella E, Mantovani P, Bovina R, Lafiandra D. TILLING mutants of durum wheat result in a high amylose phenotype and provide information on alternative splicing mechanisms. Plant Sci. 2015;233:127–33.
Botticella E, Sestili F, Hernandez-Lopez A, Phillips AD, Lafiandra D. High resolution melting analysis for the detection of EMS induced mutations in wheat SBEIIa genes. BMC Plant Biol. 2011;11:156.
Regina A, Berbezy P, Kosar-Hashemi B, Li S, Cmiel M, Larroque O, Bird AR, Swain SM, Cavanagh C, Jobling SA, Li Z, Morell M. A genetic strategy generating wheat with very high amylose content. Plant Biotechnol J. 2015;13:1276–86.
Uauy C, Paraiso F, Colasuonno P, Tran RK, Tsai H, Beradi S, Comai L, Dubcovsky J. A modified TILLING approach to detect in tetraploid and hexaploid wheat. BMC Plant Biol. 2009;9:115.
Regina A, Bird A, Topping D, Bowden S, Freeman J, Barsby T, Kosar-Hashemi B, Li Z, Rahman S, Morell M. High-amylose wheat generated by RNA interference improves indices of large-bowel health in rats. Proc Natl Acad Sci U S A. 2006;103:3546–51.
Fu FF, Ye R, Xu SP, Xue HW. Studies on rice seed quality through analysis of a large-scale T-DNA insertion population. Cell Res. 2009;19:380–91.
Birt DF, Boylston T, Hendrich S, Jane JL, Hollis J, Li L, McClelland J, Moore S, Phillips GJ, Rowling M, Schalinske K, Scott MP, Whitley EM. Resistant starch: promise for improving human health. Adv Nutr. 2013;4:587–601.
Hung PV, Maeda T, Yamuchi H, Morita N. Dough and breadmaking properties of various strong wheat grains cultivated in Japan. J Appl Glycosci. 2005;52:15–21.
Morell MK, Li Z, Regina A, Rahman SR, d’Hulst C, Ball SG. Control of starch biosynthesis in vascular plants and algae. Annual Plant Review. 2006;22:258–89.
Tetlow IJ, Blissett KJ, Emes MJ. Starch synthesis and carbohydrate oxidation in amyloplasts from developing wheat endosperm. Planta. 1994;194:454–60.
Singh A, Kumar P, Sharma M, Tuli R, Dhaliwal HS, Chaudhury A, Pal D, Roy J. Understanding the expression pattern of genes involved in starch biosynthesis during seed development in bread wheat (Triticum aestivum). Mol Breed. 2015;35:184.
Fu FF, Xue HW. Coexpression analysis identifies rice starch regulator, a rice AP2/EREBP family transcription factor, as a novel rice starch biosynthesis regulator. Plant Physiol. 2010;154:927–38.
Till BJ, Cooper J, Tai TH, Colowit P, Greene EA, Henikoff S, Comai L. Discovery of chemically induced mutations in rice by TILLING. BMC Plant Biol. 2007;7:19.
Greene EA, Codomo CA, Taylor NE, Henikoff JG, Till BJ, Reynolds SH, Enns LC, Burtner C, Johnson JE, Odden AR, Comai L, Henikoff S. Spectrum of chemically induced mutations from a large-scale reverse-genetic screen in Arabidopsis. Genetics. 2003;2003:164–731.
Slade AJ, Fuerstenberg SI, Loeffler D, Steine MN, Facciotti D. A reverse genetic, nontransgenic approach to wheat crop improvement by TILLING. Nat Biotechnol. 2005;23:75–81.
Rundle RE, French D. The configuration of starch and the starch-iodine complex. II. Optical properties of crystalline starch fractions. J Am Chem Soc. 1943;65:558–561.
Zhu T, Jackson DS, Wehling RL, Geera B. Comparison of amylose determination methods and development of dual wavelength iodine binding technique. Cereal Chem. 2008;85:51–8.
Roy JK, Smith KP, Muehlbauer GJ, Chao S, Close TJ, Steffenson BJ. Association mapping of spot blotch resistance in wild barley. Mol Breed. 2010;26:243–56.
Upadhyay SK, Kumar J, Tuli R. RNA-guided genome editing for target gene mutations in wheat. G3 Genes Genomes Genet. 2013;3:2233–8.
Bahar B, Akkaya MS. Effects of EMS treatment on seed germination in wheat. J Appl Biol Sci. 2009;3:59–64.
Rawat N, Sehgal SK, Joshi A, Rothe N, Wilson DL, McGraw N, Vadlani PV, Li W, Gill BS. A diploid wheat TILLING resource for wheat functional genomics. BMC Plant Biol. 2012;12:205.
Bovina R, Brunazzi A, Gasparini G, Sestili F, Palombieri S, Botticella E, Lafiandra D, Mantovani P, Massi A. Development of a TILLING resource in durum wheat for reverse- and forward-genetic analysis. Crop Pasture Sci. 2014;65:112–4.
Sestili F, Janni M, Doherty A, Boticella E, DOvidio R, Masci S, Jones HD, Lafiandra D. Increasing the amylose content of durum wheat through silencing of SBEIIa genes. BMC Plant Biol. 2010;10:144.
Agasimani S, Selvakumar G, Joel AJ, Ganesh RS. A simple and rapid single kernel screening method to estimate amylose content in rice grains. Phytochem Anal. 2012;24:569–73.
Mohammadkhani A, Stoddard FL, Marshall DR, Nizamuddin M, Zhao X. Starch extraction and amylose analysis from half seeds. Starch. 1999;51:62–6.
Kumar I, Khush GH. Gene dose effect of amylose content in rice endosperm. J Genet. 1988;61:559–68.
South JB, Morrison WR. Isolation and analysis of starch from single kernels of wheat and barley. J Cereal Sci. 1990;12:43–51.
Yamamori M, Fujita S, Hayakawa K, Matsuki J, Yasui T. Genetic elimination of a starch granule protein, SGP-1, of wheat generates an altered starch with apparent high amylose. Theor Appl Genet. 2000;101:21–9.
Yasui T, Matsuki J, Sasaki T, Yamamori M. Waxy endosperm mutants of bread wheat (triticum aestivum L.) and their starch properties. Breed Sci. 1997;47:161–3.
Martln C, Smlth AM. Starch biosynthesis. Plant Cell. 1995;7:971–85.
Itoh K, Ozaki H, Okada K, Hori H, Takeda Y, Mitsui T. Introduction of Wx transgene into rice wx mutants leads to both high- and low-amylose rice. Plant Cell Physiol. 2003;44:473–80.
Fujita N, Hasegawa H, Taira T. The isolation and characterization of a waxy mutant of diploid wheat (Triticum monococcum L.). Plant Sci. 2001;160:595–602.
Wang JC, Xu H, Zhu Y, Liu QQ, Cai XL. OsbZIP58, a basic leucine zipper transcription factor, regulates starch biosynthesis in rice endosperm. J Exp Bot. 2013;64:3453–66.
Gao M, Wanat J, Stinard PS, James MG, Myers AM. Characterization of dull1, a maize gene coding for a novel starch synthase. Plant Cell. 1998;10:399–412.
Fujita N, Kubo A, Suh D-S, Wong K-S, Jane J-L, Ozawa K, Takaiwa F, Inaba Y, Nakamura Y. Antisense inhibition of isoamylase alters the structure of amylopectin and the physicochemical properties of starch in rice endosperm. Plant and Cell Physiol. 2003;44:607–18.
Schwall GP, Safford R, Westcott RJ, Jeffcoat R, Tayal A, Shi YC, Gidley MJ, Jobling SA. Production of very-high-amylose potato starch by inhibition of SBE A and B. Nature Biotechnol. 2000;18:551–4.
Tickle P, Burrell MM, Coates SA, Emes MJ, Tetlow IJ, Bowsher CG. Characterization of plastidial starch phosphorylase in triticum aestivum L. Endosperm. J Plant Physiol. 2009;166:1465–78.
Satoh H, Shibahara K, Tokunaga T, Nishi A, Tasaki M, Hwang SK, Okita TW, Kaneko N, Fujita N, Yoshida M, Hosaka Y, Sato A, Utsumi Y, Ohdan T, Nakamura Y. Mutation of the plastidial alpha-glucan phosphorylase gene in rice affects the synthesis and structure of starch in the endosperm. Plant Cell. 2008; 1833–1849
Orawetz T, Malinova I, Orzechowski S, Fettke J. Reduction of plastidial phosphorylase in potato (Solanum tuberosum L) reveals impact on storage starch structure during growth at low temperature. Plant Physiol Biochem. 2016;100:141–9.
Whan A, Dielen AS, Mieog J, Bowerman AF, Robinson HM, Byrne K, Colgrave M, Larkin PJ, Howitt CA, Morell MK, Ral JP. Engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development. J Exp Bot. 2014;65:5443–57.
McMaugh SJ, Thistleton JL, Anschaw E, Luo J, Konik-Rose C, Wang H, Min Huang M, Larroque O, Regina A, Jobling SA, Morell MK, Li Z. Suppression of starch synthase I expression affects the granule morphology and granule size and fine structure of starch in wheat endosperm. J Exp Bot. 2014;65:2189–201.
Brummell DA, Watson LM, Zhou J, McKenzie MJ, Hallett IC, Simmons L, Carpenter M, Timmerman-Vaughan GM. Over-expression of starch branching enzyme II increases short-chain branching of amylopectin and alters the physicochemical properties of starch from potato tuber. BMC Biotechnol. 2015;15:28.
Sestili F, Boticella E, Proietti G, Janni M, D’Ovidio R, Lafiendra D. Amylose content is not affected by overexpression of the Wx-B1gene in durum wheat. Plant Breed. 2012;131:700–6.
Lafiandra D, Sestili F, D’Ovidio R, Janni M, Botticella E, Ferrazzano G, Silvestri M, Ranieri R, De Ambrogio E. Approaches for the modification of starch composition in durum wheat. Cereal Chem. 2010;87:28–34.
Rahman S, Regina A, Li ZY, Mukai Y, Yamamoto M, Kosar-Hashemi B, Abrahams S, Morell MK. Comparison of starch-branching enzyme genes reveals evolutionary relationships among isoforms. Characterization of a gene for starch-branching enzyme IIa from the wheat D genome donor aegilops tauschii. Plant Physiol. 2001;125:1314–24.
Bhatnagar T, Sachdev A, Johari RP. Molecular characterization of glutenins in wheat varieties differing in chapatti quality characteristics. J Plant Biochem Biotech. 2002;11:33–6.
Juliano BO. A simplified assay for milled-rice amylose. Cereal Sci Today. 1971;16:334–40.
Peng M, Gao M, Abdel-Aal ESM, Hucl P, Chibbar RN. Separation and characterization of A- and B-type starch granules in wheat endosperm. Cereal Chem. 1999;76:375–9.
Yun SH, Matheson NK. Estimation of amylose content of starches after precipitation of amylopectin by concanavalin-A. Starch-Starke. 1990;42:302–5.
McCleary BV, Gibson TS, Mugford DC. Measurement of total starch in cereal products by amyloglucosidase - α-amylase method: Collaborative study. J AOAC Int. 1997;80:571–9.
Miller GL. Use of dinitrosalicylic acid reagent for determination of reducing sugar. Anal Chem. 1955;31:426–8.
Singh A, Mantri S, Sharma M, Chaudhury A, Tuli R, Roy J. Genome-wide transcriptome study in wheat identified candidate genes related to processing quality, majority of them showing interaction (quality x development) and having temporal and spatial distributions. BMC Genomics. 2014;15:29.
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2[−Delta DeltaC(T)] method. Methods. 2001;25:402–8.
