Differential expression of structural genes for the late phase of phytic acid biosynthesis in developing seeds of wheat (Triticum aestivum L.)

Plant Science

Volumn 224, Issue , 2014, Pages 74-85

  Bhati, Kaushal Kumar ^a   Aggarwal, Sipla ^a   Sharma, Shivani ^a   Mantri, Shrikant ^a   Singh, Sudhir P ^a   Bhalla, Sherry ^a   Kaur, Jagdeep ^b   Tiwari, Siddharth ^a   Roy, Joy K ^a   Tuli, Rakesh ^a   Pandey, Ajay K ^a  

^a NATIONAL AGRI FOOD BIOTECHNOLOGY INSTITUTE   (India)

^b PANJAB UNIVERSITY   (India)

Author keywords

Gene expression; Inositol phosphate kinases; Multidrug resistance protein; Phytic acid pathway; Seed development; Triticum aestivum

Indexed keywords

INOSITOL PENTAKISPHOSPHATE KINASE; MESSENGER RNA; PHOSPHOTRANSFERASE; PHYTIC ACID; VEGETABLE PROTEIN;

BIOSYNTHESIS; GENE EXPRESSION REGULATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; PLANT GENE; PLANT SEED; WHEAT;

GENE EXPRESSION REGULATION, ENZYMOLOGIC; GENE EXPRESSION REGULATION, PLANT; GENES, PLANT; PHOSPHOTRANSFERASES; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); PHYTIC ACID; PLANT PROTEINS; RNA, MESSENGER; SEEDS; TRITICUM;

EID: 84899809696     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2014.04.009     Document Type: Article

References (44)

1. Loewus F.A., Murthy P.P.N. Myo-Inositol metabolism in plants. Plant Sci. 2000, 15:1-19.
2. Hegeman C.E., Good L.L., Grabau E.A. Expression of d-myo-inositol-3-phosphate synthase in soybean. Implications for phytic acid biosynthesis. Plant Physiol. 2001, 125:1941-19948.
3. Doria E., Galleschi L., Calucci L., Pinzino C., Pilu R., Cassani E., Nielsen E. Phytic acid prevents oxidative stress in seeds: evidence from a maize (Zea mays L.) low phytic acid mutant. J. Exp. Bot. 2009, 60:967-978.
4. Rasmussen S.R., Ingvardsen C.R., Torp A.M. Mutations in genes controlling the biosynthesis and accumulation of inositol phosphates in seeds. Biochem. Soc. Trans. 2010, 38:689-694.
5. Bouis H.E., Hotz C., McClafferty B., Meenakshi J.V., Pfeiffer W.H. Biofortification: a new tool to reduce micronutrient malnutrition. Food Nutr. Bull. 2011, 32:S31-S40.
6. Bohn L., Meyer A.S., Rasmussen S.K. Phytate: impact on environment and human nutrition. A challenge for molecular breeding. J. Zhejiang Univ. Sci. 2008, B9:165-191.
7. Raboy V. Approaches and challenges to engineering see phytate and total phosphorus. Plant Sci. 2009, 79:281-296.
8. Borg S., Brinch-Pedersen H., Tauris B., Holm P.B. Iron transport, deposition and bioavailability in the wheat and barley grain. Plant Soil 2009, 325:15-24.
9. Brinch-Pedersen H., Hatzack F., Stoger E., Arcalis E., Pontopidan K., Homl P.B. Heat-stable phytases in transgenic wheat (Triticum aestivum L.): deposition pattern, thermo stability and phytate hydrolysis. J. Agric. Food Chem. 2006, 54:4624-4632.
10. Drakakaki G., Marcel S., Glahn R.P., Lund E.K., Pariagh S., Fischer R., Christou P., Stöger E. Endosperm-specific co-expression of recombinant soybean ferritin and Aspergillus phytase in maize results in significant increases in the levels of bioavailable iron. Plant Mol. Biol. 2005, 59:869-880.
11. Masuda H., Kobayashi T., Ishimaru Y., Takahashi M., Aung M.S., Nakanishi H., Mori S., Nishizawa N.K. Iron-biofortification in rice by the introduction of three barley genes participated in mugineic acid biosynthesis with soybean ferritin gene. Front. Plant Sci. 2013, 4:132.
12. Lee S., Kim Y.S., Jeon U.S., Kim Y.K., Schjoerring J.K., An G. Activation of rice nicotianamine synthase 2 (OsNAS2) enhances iron availability for biofortification. Mol. Cell 2012, 33:269-275.
13. Shi J., Wang W., Schellin K., Li B., Faller M., Styoop J.M., Meeley R.B., Ertl D.S., Ranch J.P., Glassman K. Embryo-specific silencing of a transporter reduces phytic acid content of maize and soybean seeds. Nat. Biotechnol. 2007, 25:930-937.
14. Stiles A.R., Qian X., Shears S.B., Grabau E.A. Metabolic and signaling properties of an Itpk gene family in Glycine max. FEBS Lett. 2008, 582:1853-1858.
15. González B., Baños-Sanz J.I., Villate M., Brearley C.A., Sanz-Aparicio J. Inositol 1,3,4,5,6-pentakisphosphate 2-kinase is a distant IPK member with a singular inositide binding site for axial 2-OH recognition. Proc. Natl. Acad. Sci. U.S.A. 2010, 107:9608-9613.
16. Shi J., Wang H., Wu Y., Hazebroek J., Meeley R.B., Ertl D.S. The maize low-phytic acid mutant lpa2 is caused by mutation in an inositol phosphate kinase gene. Plant Physiol. 2003, 131:507-515.
17. Suzuki M., Tanaka K., Kuwano M., Yoshida K.T. Expression pattern of inositol phosphate-related enzymes in rice (Oryza sativa L.): implications for the phytic acid biosynthetic pathway. Gene 2007, 405:55-64.
18. Dorsch J.A., Cook A., Young K.A., Anderson J.M., Bauman A.T., Volkmann C.J., Murthy P.P., Raboy V. Seed phosphorus and inositol phosphate phenotype of barley low phytic acid genotypes. Phytochemistry 2003, 62:691-706.
19. Odom A.R., Stahlberg A., Wente S.R., York J.D. A role for nuclear inositol 1,4,5-trisphosphate kinase in transcriptional control. Science 2000, 287(5460):2026-2029.
20. Stevenson-Paulik J., Bastidas R.J., Chiou S.T., Frye R.A., York J.D. Generation of phytate free seeds in Arabidopsis through disruption of inositol polyphosphate kinases. Proc. Natl. Acad. Sci. U.S.A. 2005, 102:12612-12617.
21. Sun Y., Thompson M., Lin G., Butler H., Gao Z., Thornburgh S., Yau K., Smith D.A., Shukla V.K. Inositol 1,3,4,5,6-pentakisphosphate 2-kinase from maize. Molecular and biochemical characterization. Plant Physiol. 2007, 144:1278-1291.
22. Sweetman D., Sue Johnson S.E.K., Caddick D.E., Hanke C.A., Brearley Characterization of an Arabidopsis inositol 1,3,4,5,6-pentakisphosphate 2-kinase (AtIPK1). Biochem. J. 2006, 394:95-103.
23. Yuan F.J., Zhu D.H., Tan Y.Y., Dong D.K., Fu X.J., Zhu S.L., Li B.Q., Shu Q.Y. Identification and characterization of the soybean IPK1 ortholog of a low phytic acid mutant reveals an exon-excluding splice-site mutation. Theor. Appl. Genet. 2012, 125:1413-1423.
24. Gillman J.D., Pantalone V.R., Bilyeu K. The low phytic acid phenotype in soybean line CX1834 is due to mutation in two homologs of the maize low phytic acid gene. Plant Genome 2009, 2:179-190.
25. Kim S., Tai T.H. Identification of genes necessary for wild-type levels of seed phytic acid in Arabidopsis thaliana using a reverse genetics approach. Mol. Genet. Genomics 2011, 286:119-133.
26. Panzeri D., Cassani E., Doria E., Tagliabue G., Forti L., Campion B., Bollini R., Brearley C.A., Pilu R., Nielsen E., Sparvoli F. A defective ABC transporter of the MRP family, responsible for the bean lpa1 mutation, affects the regulation of the phytic acid pathway, reduces seed myo-inositol and alters ABA sensitivity. New Phytol. 2011, 191:70-83.
27. Aluru M.R., Rodermel S.R., Reddy M.B. Genetic modification of low phytic acid1-1 maize to enhance iron content and bioavailability. J. Agric. Food Chem. 2011, 59:12954-12962.
28. Frelet-Barrand A., Kolukisaoglu H.Ü., Plaza S., Rüffer M., Azevedo L., Hörtensteiner S., Marinova K., Weder B., Schulz B., Klein M. Comparative mutant analysis of Arabidopsis ABCC-type ABC transporters: AtMRP2 contributes to detoxification, vacuolar organic anion transport and chlorophyll degradation. Plant Cell Physiol. 2008, 49:557-569.
29. Nagy R., Grob H., Weder B., Green P., Klein M., Frelet-Barrand A., Schjoerring J.K., Brearley C., Martinoia E. The Arabidopsis ATP-binding cassette protein AtMRP5/AtABCC5 is a high affinity inositol hexakisphosphate transporter involved in guard cell signaling and phytate storage. J. Biol. Chem. 2009, 284:33614-33622.
30. Ye H., Zhang X.Q., Broughton S., Westcott S., Wu D., Reg L., Li C. A nonsense mutation in a putative sulphate transporter gene results in low phytic acid in barley. Funct. Integr. Genomics 2011, 11:103-110.
31. Ali N., Paul S., Gayen D., Sarkar S.N., Datta K., Datta S.K. Development of low phytate rice by RNAi mediated seed-specific silencing of inositol 1,3,4,5,6-pentakisphosphate 2-kinase gene (IPK1). PLoS ONE 2013, 8:e68161.
32. Laudencia-Chingcuanco D.L., Stamova B.S., You F.M., Lazo G.R., Beckles D.M., Anderson O.D. Transcriptional profiling of wheat caryopsis development using cDNA microarrays. Plant Mol. Biol. 2007, 63:651-668.
33. Wan Y., Poole R.L., Huttly A.K., Toscano-Underwood C., Feeney K., Welham S., Gooding M.J., Mills C., Edwards K.J., Shewry P.R., Mitchell R.A.C. Transcriptome analysis of grain development in hexaploid wheat. BMC Genomics 2008, 9:121.
34. Thompson J.D., Higgins D.G., Gibson T.J. CLUSTALW: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994, 22:4673-4680.
35. Livak, Schmitteng Analysis of relative gene expression data using a real time quantitative PCR and 2-(Delta Delta C (T)) method. Methods 2001, 25:402-408.
36. Verbsky J.W., Wilson M.P., Kisseleva M.V., Majerus P.W., Wente S.R. The synthesis of inositol hexakisphosphate. Characterization of human inositol 1,3,4,5,6-pentakisphosphate 2-kinase. J. Biol. Chem. 2002, 277:31857-31862.
37. Singh S.P., Vogel-Mikuš K., Arčon I., Vavpetič P., Jeromel L., Pelicon P., Kumar J., Tuli R. Pattern of iron distribution in maternal and filial tissues in wheat grains with contrasting levels of iron. J. Exp. Bot. 2013, 64:3249-3260.
38. Li Z.S., Szczypka M., Lu Y.P., Thiele D.J., Rea P.A. The yeast cadmium factor protein (YCF1) is a vacuolar glutathione S-conjugate pump. J. Biol. Chem. 2006, 271:6509-6517.
39. Ma D., Zuo Y., Sun D., Wang C., Guo T. Characterization of the TaMIPS gene from winter wheat (Triticum aestivum L.) and changes in its expression pattern with phytic acid accumulation in seeds during grain filing. J. Cereal Sci. 2013, 57:437-443.
40. Salunke R., Neelam K., Rawat N., Tiwari V.K., Randhawa G.S., Dhaliwal H.S., Roy P. Bioavailability of iron from wheat Aegilops derivatives selected for high grain iron and protein contents. J. Agric. Food Chem. 2011, 59:7465-7473.
41. Guttieri M., Bowen D., Dorsch J.A., Raboy V., Souza E. Identification and characterization of a low phytic acid wheat. Crop Sci. 2004, 44:418-424.
42. Josefsen L., Bohn L., Soerensen M.B., Rasmussen S.K. Characterization of a multifunctional inositol phosphate kinase from rice and barley belonging to the ATP-grasp superfamily. Gene 2007, 397:114-125.
43. Feng X., Yoshida K.T. Molecular approaches for producing low-phytic-acid grains in rice. Plant Biotechnol. 2004, 21:183-189.
44. Sharma K.G., Kaur R., Bachhawat A.K. The glutathione-mediated detoxification pathway in yeast: an analysis using the red pigment that accumulates in certain adenine biosynthetic mutants of yeasts reveals the involvement of novel genes. Arch. Microbiol. 2003, 180:108-117.