Identification, classification and bioinformatics expression analysis of NAC transcription factor gene family in Hordeum vulgare cv. Morex genome

Document Type : Research Paper

Authors

1 Associate Professor, Department of Agronomy & Plant Breeding, Faculty of Agriculture and Natural Resources, University of Mohaghegh Ardabili, Ardabil, Iran.

2 Assistant Professor, Department of Horticultural Sciences, Faculty of Agriculture and Natural Resources, University of Mohaghegh Ardabili, Ardabil, Iran.

3 Former M. Sc. student of Biotechnology, Department of Agriculture, Karaj Payam Noor University, Alborz, Iran

4 Associate Professor, Payame Noor University, Tehran, Iran.

5 Former Ph. D. student of Molecular Genetics, Department of Agronomy & Plant Breeding, Faculty of Agriculture and Natural Resources, University of Mohaghegh Ardabili, Ardabil, Iran.

Abstract

NAC gene family is one large family of plant-specific transcription factor that plays various roles in plant developmental stages and stress responses. The possibility of bioinformatics studies on NAC gene family in barley was provided with completion of the genome sequencing of Hordeum vulgare cv. Morex project. In this research using genome scanning, 73 non-redundant NAC-encoding genes in total were identified from the genomic sequences of Hordeum vulgare cv. Morex. A composite phylogenetic tree was constructed with HvNAC protein sequences and a number of known rice and Arabidopsis NAC protein sequences and tree was classified into 15 distinct subgroups. It is revealed the uneven distribution of the HvNAC genes on barley chromosomes. Most members of NAC genes were not located in groups (singletons) and few members of this family were located in groups with two or three genes. Most detected cis elements in upstream and downstream of HvNAC genes were involved in response to light, response to abiotic stresses and relatively low in response to biotic stresses. In silico gene expression analysis revealed that HvNAC genes were expressed in a wide range of tissues and is not highly expressed in developmental stages. Also, the HvNAC genes partly is expressed in stress conditions, especially in abiotic stresses and relatively less expressed in biotic stresses. This bioinformatics information provide a framework for genomics and functional studies of this gene family in barley.

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Main Subjects


Aida M, Ishida T, Fukaki H, Fujisawa H, Tasaka M (1997) Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon Mutant. Plant Cell Online. 9: 841–857.
Chen X, Wang Y, Lv B, Li JLuo LLu SZhang XMa HMing F (2014) The NAC family transcription factor OsNAP confers abiotic stress response through the ABA pathway. Plant Cell Physiol 55: 604–619.
Demura T, Fukuda H (2007) Transcriptional regulation in wood formation. Trends Plant Sci. 12:64–70.
Finn RD, Clements J, Eddy SR (2011) HMMER web server: interactive sequence similarity searching. Nucleic Acids Res. 39: 29–37.
Gubler F, Kalla R, Roberts JK, Jacobsen JV (1995) Gibberellin-regulated expression of a myb gene in barley aleurone cells: evidence for Myb transactivation of a high-pl [alpha]-amylase gene promoter. Plant Cell Online 7: 1879–1891.
Gubler F, Raventos D, Keys M,  Watts RMundy JJacobsen JV (1999) Target genes and regulatory domains of the GAMYB transcriptional activator in cereal aleurone. Plant J. 17: 1–9.
Hendelman A, Stav R, Zemach H, Arazi T (2013) The tomato NAC transcription factor SlNAM2 is involved in flower-boundary morphogenesis. J. Exp. Bot. 64: 5497–5507.
Jeong JS, Kim YS, Baek KH, Jung HHa SHDo Choi YKim MReuzeau CKim JK (2010) Root-specific expression of OsNAC10 improves drought tolerance and grain yield in rice under field drought conditions. Plant Physiol. 153: 185–197.
Jupe F, Pritchard L, Etherington GJ,   MacKenzie K, Cock PJA, Wright F, Sharma SK, Bolser D, Bryan GJ,  Jones JDJ, Hein I (2012) Identification and localisation of the NB-LRR gene family within the potato genome. BMC Genomics 13:75.
Kato H, Motomura T, Komeda Y, Saito TKato A (2010) Overexpression of the NAC transcription factor family gene ANAC036 results in a dwarf phenotype in Arabidopsis thaliana. J Plant Physiol 167: 571–577.
Kim YS, Kim SG, Park JE, Park HYLim MHChua NHPark CM (2006) A membrane-bound NAC transcription factor regulates cell division in Arabidopsis. Plant Cell Online 18: 3132–3144.
Kozik A, Kochetkova E, Michelmore R (2002) GenomePixelizer--a visualization program for comparative genomics within and between species. Bioinformatics 18: 335–336.
Lozano R, Ponce O, Ramirez M, Mostajo N, Orjeda G (2012) Genome-wide identification and mapping of NBS-encoding resistance genes in Solanum tuberosum group Phureja. PLoS One 7:e34775.
Mallory AC, Dugas D V, Bartel DP, Bartel B (2004) MicroRNA regulation of NAC-domain targets is required for proper formation and separation of adjacent embryonic, vegetative, and floral organs. Curr. Biol. 14: 1035–1046.
Mao C, Ding W, Wu Y, Yu JHe XShou HWu P (2007) Overexpression of a NAC-domain protein promotes shoot branching in rice. New Phytol. 176:288–298.
Mitsuda N, Iwase A, Yamamoto H, et al (2007) NAC transcription factors, NST1 and NST3, are key regulators of the formation of secondary walls in woody tissues of Arabidopsis. Plant Cell Online 19:270–280.
Nakashima K, Tran LSP, Van Nguyen D, Fujita MMaruyama KTodaka DIto YHayashi NShinozaki K, Yamaguchi-Shinozaki K (2007) Functional analysis of a NAC-type transcription factor OsNAC6 involved in abiotic and biotic stress-responsive gene expression in rice. Plant J. 51: 617-30.
Nuruzzaman M, Manimekalai R, Sharoni AM, Satoh KKondoh HOoka HKikuchi S (2010) Genome-wide analysis of NAC transcription factor family in rice. Gene. 465: 30–44.
Olsen AN, Ernst HA, Leggio LL, Skriver K (2005) NAC transcription factors: structurally distinct, functionally diverse. Trends Plant Sci. 10: 79–87.
Park J, Kim YS, Kim SG, Jung JHWoo JCPark CM (2011) Integration of auxin and salt signals by the NAC transcription factor NTM2 during seed germination in Arabidopsis. Plant Physiol. 156: 537–549.
Puranik S, Bahadur RP, Srivastava PS, Prasad M (2011) Molecular cloning and characterization of a membrane associated NAC family gene, SiNAC from foxtail millet [Setaria italica (L.) P. Beauv.]. Mol. Biotechnol. 49: 138–150.
Quach TN, Tran LSP, Valliyodan B, Nguyen HTKumar RNeelakandan AKGuttikonda SKSharp RENguyen HT (2014) Functional analysis of water stress-responsive soybean GmNAC003 and GmNAC004 transcription factors in lateral root development in Arabidopsis. PLoS One 9:e84886.
Ramaswamy M, Narayanan J, Manickavachagam G, Athiappan S, Arun M, Gomathi R, Ram B (2017) Genome wide analysis of NAC gene family “sequences” in sugarcane and its comparative phylogenetic relationship with rice, sorghum, maize and Arabidopsis for prediction of stress associated NAC genes. Agri Gene 3: 1–11.
Redillas MC, Jeong JS, Kim YS, Jung HBang SWChoi YDHa SHReuzeau CKim JK (2012) The overexpression of OsNAC9 alters the root architecture of rice plants enhancing drought resistance and grain yield under field conditions. Plant Biotechnol. J. 10: 792–805.
Riechmann J, Heard J, Martin G, Reuber LJiang CKeddie JAdam LPineda ORatcliffe OJSamaha RRCreelman RPilgrim MBroun PZhang JZGhandehari DSherman BKYu G (2000) Arabidopsis transcription factors: genome-wide comparative analysis among eukaryotes. Science  290: 2105–2110.
Saad ASI, Li X, Li HP, Huang TGao CSGuo MWCheng WZhao GYLiao YC (2013) A rice stress-responsive NAC gene enhances tolerance of transgenic wheat to drought and salt stresses. Plant Sci. 203–204: 33–40.
Saga H, Ogawa T, Kai K, Suzuki HOgata YSakurai NShibata D, Ohta D (2012) Identification and characterization of ANAC042, a transcription factor family gene involved in the regulation of camalexin biosynthesis in Arabidopsis. Mol. Plant-Microbe Interact. 25: 684–696.
Shah ST, Pang C, Fan S,  Song MArain SYu S (2013) Isolation and expression profiling of GhNAC transcription factor genes in cotton (Gossypium hirsutum L.) during leaf senescence and in response to stresses. Gene 531: 220–234.
Souer E, Van Houwelingen A, Kloos D, Mol JKoes R (1996) The no apical meristem gene of petunia is required for pattern formation in embryos and flowers and is expressed at meristem and primordia boundaries. Cell 85: 159-170.
Takasaki HMaruyama KKidokoro SIto YFujita YShinozaki KYamaguchi-Shinozaki KNakashima K (2010) The abiotic stress-responsive NAC-type transcription factor OsNAC5 regulates stress-inducible genes and stress tolerance in rice. Mol. Genet. Genomics 284: 173–183.
Tamura K, Stecher G, Peterson DFilipski AKumar S (2013) MEGA6: Molecular evolutionary genetics analysis version 6.0. Mol. Biol. Evol. 30: 2725–2729.
Uauy C, Distelfeld A, Fahima T,  Blechl ADubcovsky J (2006) A NAC gene regulating senescence improves grain protein, zinc, and iron content in Wheat. Science 314: 1298–1301.
Voitsik A-M, Muench S, Deising HB, Voll LM (2013) Two recently duplicated maize NAC transcription factor paralogs are induced in response to Colletotrichum graminicola infection. BMC Plant Biol. 13:85.
Wei S, Gao L, Zhang Y, Zhang FYang XHuang D (2016) Genome-wide investigation of the NAC transcription factor family in melon (Cucumis melo L.) and their expression analysis under salt stress. Plant Cell Rep. 35: 1827-1839.
Xia N,  Zhang GLiu XYDeng LCai GLZhang YWang XJZhao JHuang LLKang ZS (2010a) Characterization of a novel wheat NAC transcription factor gene involved in defense response against stripe rust pathogen infection and abiotic stresses. Mol. Biol. Rep. 37: 3703–3712.
Xia N, Zhang G, Sun YF, Zhu L, Xu LS, Chen XM, Liu B, Yu YT, Wang XJ, Huang LL, Kang ZS (2010b) TaNAC8, a novel NAC transcription factor gene in wheat, responds to stripe rust pathogen infection and abiotic stresses. Physiol Mol. Plant Pathol. 74: 394–402.
Xie Q, Frugis G, Colgan D, Chua N (2000) Arabidopsis NAC1 transduces auxin signal downstream of TIR1 to promote lateral root development. Genes Dev. 14: 3024–3036.
Xie Q, Guo H., Dallman G,  Fang S, Weissman AM, Chua NH (2002) SINAT5 promotes ubiquitin-related degradation of NAC1 to attenuate auxin signals. Nature 419: 167–170.
Xiong Y, Liu T, Tian CSun SLi JChen M (2005) Transcription factors in rice: a genome-wide comparative analysis between monocots and eudicots. Plant Mol. Biol. 59: 191–203.
Yamaguchi M, Ohtani M,  Mitsuda NKubo MOhme-Takagi MFukuda HDemura T (2010) VND-INTERACTING2, a NAC domain transcription factor, negatively regulates xylem vessel formation in Arabidopsis. Plant Cell 22: 1249–1263.
Yang SD, Seo PJ, Yoon HK, Park CM (2011) The Arabidopsis NAC transcription factor VNI2 integrates abscisic acid signals into leaf senescence via the COR / RD genes. Plant Cell 23: 2155–2168.
Yokotani N, Tsuchida-Mayama T,  Ichikawa HMitsuda NOhme-Takagi MKaku HMinami ENishizawa Y (2014) OsNAC111, a blast disease–responsive transcription factor in rice, positively regulates the expression of defense-related genes. Mol. Plant-Microbe Interact. 27: 1027–1034.
Zhao Q, Gallego-Giraldo L,  Wang HZeng YDing SYChen FDixon RA (2010) An NAC transcription factor orchestrates multiple features of cell wall development in Medicago truncatula. Plant J. 63: 100–114.
Zhao Y, Sun J, Xu P, Zhang R, Li L (2014) Intron-mediated alternative splicing of WOOD-ASSOCIATED NAC TRANSCRIPTION FACTOR1B regulates cell wall thickening during fiber development in Populus Species. Plant Physiol. 164: 765–776.
Zheng X, Chen B, Lu G, Han B (2009) Overexpression of a NAC transcription factor enhances rice drought and salt tolerance. Biochem. Biophys. Res. Commun. 379: 985–989.
Zhong R, Lee C, Zhou J, McCarthy RL, Ye ZH (2008) A battery of transcription factors involved in the regulation of secondary cell wall biosynthesis in Arabidopsis. Plant Cell Online 20: 2763–2782.
Zhong R, Ye ZH (2007) Regulation of cell wall biosynthesis. Curr. Opin. Plant Biol. 10: 564–572.