PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2019 | 41 | 09 |

Tytuł artykułu

Transformation of wheat Triticum aestivum with the HvBADH1 transgene from hulless barley improves salinity-stress tolerance

Autorzy

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Studies have shown that the stress tolerance of cereal plants to osmotic or salinity stresses can be improved to varying degrees by the overexpression of an introduced betaine aldehyde dehydrogenase (BADH) gene. In the present study, the HvBADH1 gene from Hordeum vulgare L. var. nudum Hook. f., encoding a cytosolic BADH, was transferred into Triticum aestivum via traditional Agrobacterium tumefaciens-mediated transformation. Molecular methods, such as PCR, Southern blot analysis, and real-time quantitative RT-PCR were used to identify the successful integration and expression of the HvBADH1 transgene in genetically transformed wheat lines. To detect the efficacy of the HvBADH1 transgene in the transformants, some pivotal physiological indicators that reflected abiotic stress tolerance were measured in individual transgenic plant lines. These indicators included intracellular K⁺ and Na⁺ contents or K⁺/Na⁺ ratio, relative conductivity, and malondialdehyde and glycine betaine (GB) concentrations in cells. The results revealed that all the tested transgenic lines could significantly increase the recruitments of K⁺ in their cytosol than the wild-type seedlings. Similarly, 11.59- to 21.82-fold greater accumulation of GB, 2.11–2.56 times higher calli relative growth rates, and 26.2–29.1% seedling survival rates were found in transgenic lines under 150 mM NaCl stressed conditions. Our results demonstrated that by overexpressing the HvBADH1 transgene in genetically transformed wheat, the overall salt tolerance of the target plants was significantly increased, and the damaging effects of high salinity were significantly reduced.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

41

Numer

09

Opis fizyczny

Article 155 [14p.], fig.,ref.

Twórcy

autor
  • Provincial Key Laboratory of Biotechnology of Shaanxi Province, Key Laboratory of Resource Biology and Biotechnology in Western China (Ministry of Education), Life Sciences School, Northwest University, Xi’an 710069, Shaanxi, China
autor
  • Provincial Key Laboratory of Biotechnology of Shaanxi Province, Key Laboratory of Resource Biology and Biotechnology in Western China (Ministry of Education), Life Sciences School, Northwest University, Xi’an 710069, Shaanxi, China
autor
  • Provincial Key Laboratory of Biotechnology of Shaanxi Province, Key Laboratory of Resource Biology and Biotechnology in Western China (Ministry of Education), Life Sciences School, Northwest University, Xi’an 710069, Shaanxi, China
autor
  • Provincial Key Laboratory of Biotechnology of Shaanxi Province, Key Laboratory of Resource Biology and Biotechnology in Western China (Ministry of Education), Life Sciences School, Northwest University, Xi’an 710069, Shaanxi, China
autor
  • Provincial Key Laboratory of Biotechnology of Shaanxi Province, Key Laboratory of Resource Biology and Biotechnology in Western China (Ministry of Education), Life Sciences School, Northwest University, Xi’an 710069, Shaanxi, China
autor
  • Provincial Key Laboratory of Biotechnology of Shaanxi Province, Key Laboratory of Resource Biology and Biotechnology in Western China (Ministry of Education), Life Sciences School, Northwest University, Xi’an 710069, Shaanxi, China
autor
  • Provincial Key Laboratory of Biotechnology of Shaanxi Province, Key Laboratory of Resource Biology and Biotechnology in Western China (Ministry of Education), Life Sciences School, Northwest University, Xi’an 710069, Shaanxi, China

Bibliografia

  • Ashraf M, Foolad MR (2007) Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environ Exp Bot 59:206–216
  • Battal A, Baloglu MC, Kavas M, Yucel M, Oktem HA (2012) Particle bombardment transformation of some Turkish wheat cultivars with TaNAC69-1 and TtNAMB2 genes. New Biotechnol 29:S173. https://doi.org/10.1016/j.nbt.2012.08.481
  • Chan MT, Chang HH, Ho SL, Tong WF, Yu SM (1993) Agrobacterium-mediated production of transgenic rice plants expressing a chimeric alpha-amylase promoter/beta-glucuronidase gene. Plant Mol Biol 22:491–506
  • Chandran P, Potty VP (2008) Induction of hairy roots through the mediation of four strains of Agrobacterium rhizogenes on five host plants. Indian J Biotechnol 7:122–128
  • Chang YF (1983) Plant regeneration in vitro from leaf tissues derived from cultured immature embryos of Zea mays L. Plant Cell Rep 2:183–185. https://doi.org/10.1007/BF00270098
  • Cheng M et al (1997) Genetic transformation of wheat mediated by Agrobacterium tumefaciens. Plant Physiol 115:971–980
  • Deng YS, Kong FY, Zhou B, Zhang S, Yue MM, Meng QW (2014) Heterology expression of the tomato LeLhcb2 gene confers elevated tolerance to chilling stress in transgenic tobacco. Plant Physiol Biochem 80:318–327
  • Finer KR, Finer JJ (2000) Use of Agrobacterium expressing green fluorescent protein to evaluate colonization of sonication-assisted Agrobacterium-mediated transformation-treated soybean cotyledons. Lett Appl Microbiol 30:406–410
  • Gamborg OL, Miller RA, Ojima K (1968) Nutrient requirements of suspension cultures of soybean root cells. Exp Cell Res 50:151–158
  • He Y et al (2010) Agrobacterium-mediated transformation of durum wheat (Triticum turgidum L. var. durum cv Stewart) with improved efficiency. J Exp Bot 61:1567–1581. https://doi.org/10.1093/jxb/erq035
  • He X et al (2015) A sucrose:fructan-6-fructosyltransferase (6-SFT) gene from Psathyrostachys huashanica confers abiotic stress tolerance in tobacco. Gene 570:239–247. https://doi.org/10.1016/j.gene.2015.06.023
  • Hiei Y, Ishida Y, Komari T (2014) Progress of cereal transformation technology mediated by Agrobacterium tumefaciens. Front Plant Sci 5:628. https://doi.org/10.3389/fpls.2014.00628
  • Hussain Wani SNBS, Haribhushan A, Iqbal Mir J (2013) Compatible solute engineering in plants for abiotic stress tolerance—role of glycine betaine. Curr Genom 14:157–165
  • Ishida Y, Saito H, Ohta S, Hiei Y, Komari T, Kumashiro T (1996) High efficiency transformation of maize (Zea mays L.) mediated by Agrobacterium tumefaciens. Nat Biotechnol 14:745–750. https://doi.org/10.1038/nbt0696-745
  • Li X, Lai P, Li P, Zhao Y (2016) Transformation of Cichorium intybus with the HvBADH1 gene enhanced the salinity tolerance of the transformants. S Afr J Bot 102:110–119. https://doi.org/10.1016/j.sajb.2015.07.009
  • Martinez SEV (1983) Simultaneous determination of choline and betaine in some fish materials. Analyst 108:1114–1119
  • Mehta R et al (2013) Coat protein-mediated transgenic resistance of peanut (Arachis hypogaea L.) to peanut stem necrosis disease through Agrobacterium-mediated genetic transformation. VirusDisease 24:205–213
  • Metris A, George SM, Mulholland F, Carter AT, Baranyi J (2014) E. coli under salt stress: metabolic shift in the presence of glycine betaine. Appl Environ Microbiol 80:4745–4756
  • Mitić N, Nikolić R, Ninković S, Miljuš-Djukić J, Nešković M (2004) Agrobacterium-mediated transformation and plant regeneration of Triticum aestivum L. Biol Plant 48:179–184
  • Munns R (2002) Munns, R.: Comparative physiology of salt and water stress. Plant Cell Environ. 28, 239-250. Plant Cell Environ 25:239–250
  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bio assays with tobacco tissue cultures. Physiol Plant 15:24. https://doi.org/10.1111/j.1399-3054.1962.tb08052.x
  • Murray MG, Thompson WF (1980) Rapid isolation of high molecular weight plant DNA. Nucleic Acids Res 8:4321–4325
  • Nakamura T, Nomura M, Mori H, Jagendorf AT, Ueda A, Takabe T (2001) An isozyme of betaine aldehyde dehydrogenase in barley. Plant Cell Physiol 42:1088–1092
  • Nguyen T, Thu T, Claeys MG (2007) Agrobacterium-mediated transformation of sorghum (Sorghum bicolor (L.) Moench) using an improved in vitro regeneration system. Plant Cell Tissue Organ Cult (PCTOC) 91:155–164
  • Puniran-Hartley N, Hartley J, Shabala L, Shabala S (2014) Salinity-induced accumulation of organic osmolytes in barley and wheat leaves correlates with increased oxidative stress tolerance: in planta evidence for cross-tolerance. Plant Physiol Biochem PPB 83:32–39. https://doi.org/10.1016/j.plaphy.2014.07.005
  • Pushpavalli R, Quealy J, Colmer TD, Turner NC, Siddique KHM, Rao MV, Vadez V (2015) Salt stress delayed flowering and reduced reproductive success of chickpea (Cicer arietinum L.), a response associated with Na + accumulation in leaves. J Agron Crop Sci 202:125–138
  • Sarker RH, Biswas A (2002) In vitro plantlet regeneration and agrobacterium mediated genetic transformation of wheat (Triticum aestivum L.). Plant Tissue Cult Biotechnol 12:155–165
  • Shavrukov Y (2013) Salt stress or salt shock: which genes are we studying? J Exp Bot 64:119–127. https://doi.org/10.1093/jxb/ers316
  • Shirasawa K, Takabe T, Takabe T, Kishitani S (2006) Accumulation of glycinebetaine in rice plants that overexpress choline monooxygenase from Spinach and evaluation of their tolerance to abiotic stress. Ann Bot 98:565–571
  • Shrawat AK, Becker D, LöRz H (2007) Agrobacterium tumefaciens-mediated genetic transformation of barley (Hordeum vulgare L.). Plant Sci 172:281–290
  • Tang W et al (2014) RNAi-directed downregulation of betaine aldehyde dehydrogenase 1 (OsBADH1) results in decreased stress tolerance and increased oxidative markers without affecting glycine betaine biosynthesis in rice (Oryza sativa). Plant Mol Biol 86:443–454. https://doi.org/10.1007/s11103-014-0239-0
  • Vasil V, Castillo AM, Fromm ME, Vasil IK (1992) Herbicide resistant fertile transgenic wheat plants obtained by microprojectile bombardment of regenerable embryogenic callus. Nat Biotechnol 10:667–674
  • Wang A, Yu Z, Ding Y (2009) Genetic diversity analysis of wild close relatives of barley from Tibet and the Middle East by ISSR and SSR markers. Compt Rendus Biol 332:393–403. https://doi.org/10.1016/j.crvi.2008.11.007
  • Wang YC, Qu GZ, Li HY, Wu YJ, Wang C, Liu GF, Yang CP (2010) Enhanced salt tolerance of transgenic poplar plants expressing a manganese superoxide dismutase from Tamarix androssowii. Mol Biol Rep 37:1119–1124
  • Wang JY, Lai LD, Tong SM, Li QL (2013) Constitutive and salt-inducible expression of SlBADH gene in transgenic tomato (Solanum lycopersicum L. cv. Micro-Tom) enhances salt tolerance. Biochem Biophys Res Commun 432:262–267. https://doi.org/10.1016/j.bbrc.2013.02.001
  • Wang Z, Zhao X, Wang B, Liu E, Chen N, Zhang W, Liu H (2016) Overexpression of an Arabidopsis heterogeneous nuclear ribonucleoprotein gene, AtRNP1, affects plant growth and reduces plant tolerance to drought and salt stresses. Biochem Biophys Res Commun 472:353–359
  • Watson DJ, Thorne GN, French SAW (1963) Analysis of growth and yield of winter and spring wheats. Ann Bot 27:1–22
  • Wood AJ, Saneoka H, Rhodes D, Joly RJ, Goldsbrough PB (1996) Betaine aldehyde dehydrogenase in sorghum. Molecular cloning and expression of two related genes. Plant Physiol 110:1301–1308
  • Wu H, Doherty A, Jones HD (2009) Agrobacterium-mediated transformation of bread and durum wheat using freshly isolated immature embryos. Methods Mol Biol 478:93–103. https://doi.org/10.1007/978-1-59745-379-0_5
  • Yang C et al (2015) SpBADH of the halophyte Sesuvium portulacastrum strongly confers drought tolerance through ROS scavenging in transgenic Arabidopsis. Plant Physiol Biochem 96:377–387
  • Zárate-Romero A, Murillo-Melo Darío S, Mújica-Jiménez C, Montiel C, Muñoz-Clares Rosario A (2016) Reversible, partial inactivation of plant betaine aldehyde dehydrogenase by betaine aldehyde: mechanism and possible physiological implications. Biochem J 473:873–885. https://doi.org/10.1042/bj20151084
  • Zhang F, Li X, Lai P, Li P, Zhao Y (2015) Comparison of salt tolerance between Cichorium intybus L. transformed with AtNHX1 or HvBADH1. Acta Physiol Plant 37:8. https://doi.org/10.1007/s11738-014-1755-x
  • Zheng X et al (2007) The cauliflower mosaic virus (CaMV) 35S promoter sequence alters the level and patterns of activity of adjacent tissue- and organ-specific gene promoters. Plant Cell Rep 26:1195–1203. https://doi.org/10.1007/s00299-007-0307-x

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-3d6ee4e7-a116-4576-ba59-421b02f05e3a
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.