A transcriptomic analysis of Chrysanthemum nankingense provides insights into the basis of low temperature tolerance
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  • 作者:Liping Ren (2) (3)
    Jing Sun (2)
    Sumei Chen (2)
    Jiaojiao Gao (2)
    Bin Dong (2)
    Yanan Liu (2)
    Xiaolong Xia (2)
    Yinjie Wang (2)
    Yuan Liao (2)
    Nianjun Teng (2)
    Weimin Fang (2)
    Zhiyong Guan (2)
    Fadi Chen (2) (3)
    Jiafu Jiang (2)

    2. College of Horticulture
    ; Nanjing Agricultural University ; Nanjing ; 210095 ; China
    3. Jiangsu Province Engineering Lab for Modern Facility Agriculture Technology & Equipment
    ; No. 1 Weigang ; Nanjing ; 210095 ; Jiangsu Province ; China
  • 关键词:Transcriptome ; RNA Sequencing ; Low temperature tolerance ; Ornamental plant
  • 刊名:BMC Genomics
  • 出版年:2014
  • 出版时间:December 2014
  • 年:2014
  • 卷:15
  • 期:1
  • 全文大小:931 KB
  • 参考文献:1. Liu, L, Zhu, K, Yang, Y, Wu, J, Chen, F, Yu, D (2008) Molecular cloning, expression profiling and trans-activation property studies of a DREB2-like gene from chrysanthemum (Dendranthema vestitum). J Plant Res 121: pp. 215-226 CrossRef
    2. da Silva JA, T, Shinoyama, H, Aida, R, Matsushita, Y, Raj, SK, Chen, F (2013) Chrysanthemum biotechnology: Quo Vadis?. Crit Rev Plant Sci 32: pp. 21-52 CrossRef
    3. Cheng, X, Chen, S, Chen, F, Fang, W, Deng, Y, She, L (2009) Interspecific hybrids between Dendranthema morifolium (Ramat.) Kitamura and D. nankingense (Nakai) Tzvel. achieved using ovary rescue and their cold tolerance characteristics. Euphytica 172: pp. 101-108 CrossRef
    4. Wang, H, Jiang, J, Chen, S, Qi, X, Peng, H, Li, P, Song, A, Guan, Z, Fang, W, Liao, Y (2013) Next-generation sequencing of the Chrysanthemum nankingense (Asteraceae) transcriptome permits large-scale unigene assembly and SSR marker discovery. PLoS One 8: pp. e62293 CrossRef
    5. Jansk谩, A, Mar拧铆k, P, Zelenkov谩, S, Ovesn谩, J (2010) Cold stress and acclimation鈥搘hat is important for metabolic adjustment?. Plant Biol 12: pp. 395-405 CrossRef
    6. Yang, T, Zhang, L, Zhang, T, Zhang, H, Xu, S, An, L (2005) Transcriptional regulation network of cold-responsive genes in higher plants. Plant Sci 169: pp. 987-995 CrossRef
    7. Chinnusamy, V, Zhu, J, Zhu, J-K (2007) Cold stress regulation of gene expression in plants. Trends Plant Sci 12: pp. 444-451 CrossRef
    8. Chinnusamy, V, Zhu, JK, Sunkar, R (2010) Gene regulation during cold stress acclimation in plants. Plant Stress Tolerance 639: pp. 39-55 CrossRef
    9. Yamaguchi-Shinozaki, K, Shinozaki, K (2006) Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses. Annu Rev Plant Biol 57: pp. 781-803 CrossRef
    10. Heidarvand, L, Amiri, RM (2010) What happens in plant molecular responses to cold stress?. Acta Physiol Plant 32: pp. 419-431 CrossRef
    11. Bohn, M, L眉thje, S, Sperling, P, Heinz, E, D枚rffling, K (2007) Plasma membrane lipid alterations induced by cold acclimation and abscisic acid treatment of winter wheat seedlings differing in frost resistance. J Plant Physiol 164: pp. 146-156 CrossRef
    12. Lynch, DV, Steponkus, PL (1987) Plasma membrane lipid alterations associated with cold acclimation of winter rye seedlings (Secale cereale L. cv Puma). Plant Physiol 83: pp. 761-767 CrossRef
    13. Uemura, M, Joseph, RA, Steponkus, PL (1995) Cold acclimation of Arabidopsis thaliana (effect on plasma membrane lipid composition and freeze-induced lesions). Plant Physiol 109: pp. 15-30
    14. Uemura, M, Tominaga, Y, Nakagawara, C, Shigematsu, S, Minami, A, Kawamura, Y (2006) Responses of the plasma membrane to low temperatures. Physiol Plant 126: pp. 81-89 CrossRef
    15. Komatsu, S, Yang, G, Khan, M, Onodera, H, Toki, S, Yamaguchi, M (2007) Over-expression of calcium-dependent protein kinase 13 and calreticulin interacting protein 1 confers cold tolerance on rice plants. Mol Gen Genomics 277: pp. 713-723 CrossRef
    16. Saijo, Y, Hata, S, Kyozuka, J, Shimamoto, K, Izui, K (2000) Over鈥抏xpression of a single Ca2+-dependent protein kinase confers both cold and salt/drought tolerance on rice plants. Plant J 23: pp. 319-327 CrossRef
    17. Lissarre, M, Ohta, M, Sato, A, Miura, K (2010) Cold-responsive gene regulation during cold acclimation in plants. Plant Signal Behav 5: pp. 948-952 CrossRef
    18. Yang, G, Zou, H, Wu, Y, Liu, H, Yuan, Y (2011) Identification and characterisation of candidate genes involved in chilling responses in maize (Zea mays L.). Plant Cell, Tissue and Organ Culture (PCTOC) 106: pp. 127-141 CrossRef
    19. Thomashow, MF (2010) Molecular basis of plant cold acclimation: insights gained from studying the CBF cold response pathway. Plant Physiol 154: pp. 571-577 CrossRef
    20. Dong, MA, Farr茅, EM, Thomashow, MF (2011) Circadian clock-associated 1 and late elongated hypocotyl regulate expression of the C-repeat binding factor (CBF) pathway in Arabidopsis. Proc Natl Acad Sci 108: pp. 7241-7246 CrossRef
    21. B-h, L, Henderson, DA, Zhu, J-K (2005) The Arabidopsis cold-responsive transcriptome and its regulation by ICE1. Plant Cell Online 17: pp. 3155-3175 CrossRef
    22. Dong, C-H, Agarwal, M, Zhang, Y, Xie, Q, Zhu, J-K (2006) The negative regulator of plant cold responses, HOS1, is a RING E3 ligase that mediates the ubiquitination and degradation of ICE1. Proc Natl Acad Sci 103: pp. 8281-8286 CrossRef
    23. Miura, K, Ohta, M (2010) SIZ1, a small ubiquitin-related modifier ligase, controls cold signaling through regulation of salicylic acid accumulation. J Plant Physiol 167: pp. 555-560 CrossRef
    24. Scott, IM, Clarke, SM, Wood, JE, Mur, LA (2004) Salicylate accumulation inhibits growth at chilling temperature in Arabidopsis. Plant Physiol 135: pp. 1040-1049 CrossRef
    25. Zhu, J, Dong, C-H, Zhu, J-K (2007) Interplay between cold-responsive gene regulation, metabolism and RNA processing during plant cold acclimation. Curr Opin Plant Biol 10: pp. 290-295 CrossRef
    26. Ma, H, Lu, Z, Liu, B, Qiu, Q, Liu, J (2013) Transcriptome analyses of a Chinese hazelnut species Corylus mandshurica. BMC Plant Biol 13: pp. 152 CrossRef
    27. Hornett, EA, Wheat, CW (2012) Quantitative RNA-Seq analysis in non-model species: assessing transcriptome assemblies as a scaffold and the utility of evolutionary divergent genomic reference species. BMC Genomics 13: pp. 361 CrossRef
    28. Wang, X-C, Zhao, Q-Y, Ma, C-L, Zhang, Z-H, Cao, H-L, Kong, Y-M, Yue, C, Hao, X-Y, Chen, L, Ma, J-Q (2013) Global transcriptome profiles of Camellia sinensis during cold acclimation. BMC Genomics 14: pp. 415 CrossRef
    29. Wang, H, Zou, Z, Wang, S, Gong, M (2013) Global analysis of transcriptome responses and gene expression profiles to cold stress of Jatropha curcas L. PLoS One 8: pp. e82817 CrossRef
    30. Tian, D-Q, Pan, X-Y, Yu, Y-M, Wang, W-Y, Zhang, F, Ge, Y-Y, Shen, X-L, Shen, F-Q, Liu, X-J (2013) De novo characterization of the Anthurium transcriptome and analysis of its digital gene expression under cold stress. BMC Genomics 14: pp. 827 CrossRef
    31. Mortazavi, A, Williams, BA, McCue, K, Schaeffer, L, Wold, B (2008) Mapping and quantifying mammalian transcriptomes by RNA-Seq. Nat Methods 5: pp. 621-628 CrossRef
    32. Audic, S, Claverie, J-M (1997) The significance of digital gene expression profiles. Genome Res 7: pp. 986-995
    33. Xu, L, Zhu, L, Tu, L, Liu, L, Yuan, D, Jin, L, Long, L, Zhang, X (2011) Lignin metabolism has a central role in the resistance of cotton to the wilt fungus Verticillium dahliae as revealed by RNA-Seq-dependent transcriptional analysis and histochemistry. J Exp Bot 62: pp. 5607-5621 CrossRef
    34. Reddy, AS, Ali, GS, Celesnik, H, Day, IS (2011) Coping with stresses: roles of calcium-and calcium/calmodulin-regulated gene expression. Plant Cell Online 23: pp. 2010-2032 CrossRef
    35. Miura, K, Furumoto, T (2013) Cold signaling and cold response in plants. Int J Mol Sci 14: pp. 5312-5337 CrossRef
    36. Boudsocq, M, Sheen, J (2013) CDPKs in immune and stress signaling. Trends Plant Sci 18: pp. 30-40 CrossRef
    37. Morris, ER, Walker, JC (2003) Receptor-like protein kinases: the keys to response. Curr Opin Plant Biol 6: pp. 339-342 CrossRef
    38. Lehti-Shiu, MD, Zou, C, Hanada, K, Shiu, S-H (2009) Evolutionary history and stress regulation of plant receptor-like kinase/pelle genes. Plant Physiol 150: pp. 12-26 CrossRef
    39. McCormack, E, Braam, J (2003) Calmodulins and related potential calcium sensors of Arabidopsis. New Phytol 159: pp. 585-598 CrossRef
    40. Xu, G-Y, Rocha, PS, Wang, M-L, Xu, M-L, Cui, Y-C, Li, L-Y, Zhu, Y-X, Xia, X (2011) A novel rice calmodulin-like gene, OsMSR2, enhances drought and salt tolerance and increases ABA sensitivity in Arabidopsis. Planta 234: pp. 47-59 CrossRef
    41. Hashimoto, K, Kudla, J (2011) Calcium decoding mechanisms in plants. Biochimie 93: pp. 2054-2059 CrossRef
    42. Schulz, P, Herde, M, Romeis, T (2013) Calcium-dependent protein kinases: hubs in plant stress signaling and development. Plant Physiol 163: pp. 523-530 CrossRef
    43. Chen, J, Xue, B, Xia, X, Yin, W (2013) A novel calcium-dependent protein kinase gene from Populus euphratica, confers both drought and cold stress tolerance. Biochem Biophys Res Commun 441: pp. 630-636 CrossRef
    44. Singh, KB, Foley, RC, O帽ate-S谩nchez, L (2002) Transcription factors in plant defense and stress responses. Curr Opin Plant Biol 5: pp. 430-436 CrossRef
    45. Mizoi, J, Shinozaki, K, Yamaguchi Shinozaki, K (2012) AP2/ERF family transcription factors in plant abiotic stress responses. Biochim Biophysica Acta (BBA)-Gene Regulatory Mechanisms 1819: pp. 86-96 CrossRef
    46. Sakuma, Y, Liu, Q, Dubouzet, JG, Abe, H, Shinozaki, K, Yamaguchi-Shinozaki, K (2002) DNA-binding specificity of the ERF/AP2 domain of Arabidopsis DREBs, transcription factors involved in dehydration-and cold-inducible gene expression. Biochem Biophys Res Commun 290: pp. 998-1009 CrossRef
    47. Li, X, Zhang, D, Li, H, Wang, Y, Zhang, Y, Wood, AJ (2014) EsDREB2B, a novel truncated DREB2-type transcription factor in the desert legume Eremosparton songoricum, enhances tolerance to multiple abiotic stresses in yeast and transgenic tobacco. BMC Plant Biol 14: pp. 44 CrossRef
    48. Szabados, L, Savour茅, A (2010) Proline: a multifunctional amino acid. Trends Plant Sci 15: pp. 89-97 CrossRef
    49. Kang, H-G, Kim, J, Kim, B, Jeong, H, Choi, SH, Kim, EK, Lee, H-Y, Lim, PO (2011) Overexpression of FTL1/ DDF1, an AP2 transcription factor, enhances tolerance to cold, drought, and heat stresses in Arabidopsis thaliana. Plant Sci 180: pp. 634-641 CrossRef
    50. Yokotani, N, Sato, Y, Tanabe, S, Chujo, T, Shimizu, T, Okada, K, Yamane, H, Shimono, M, Sugano, S, Takatsuji, H (2013) WRKY76 is a rice transcriptional repressor playing opposite roles in blast disease resistance and cold stress tolerance. J Exp Bot 64: pp. 5085-5097 CrossRef
    51. H-h, P, Shan, W, Kuang, J-f, Lu, W-j, Chen, J-y (2013) Molecular characterization of cold-responsive basic helix-loop-helix transcription factors MabHLHs that interact with MaICE1 in banana fruit. Planta 238: pp. 937-953 CrossRef
    52. Yang, A, Dai, X, Zhang, W-H (2012) A R2R3-type MYB gene, OsMYB2, is involved in salt, cold, and dehydration tolerance in rice. J Exp Bot 63: pp. 2541-2556 CrossRef
    53. Kang, H, Park, SJ, Kwak, KJ (2012) Plant RNA chaperones in stress response. Trends Plant Sci 18: pp. 100-106 CrossRef
    54. Fowler, S, Thomashow, MF (2002) Arabidopsis transcriptome profiling indicates that multiple regulatory pathways are activated during cold acclimation in addition to the CBF cold response pathway. Plant Cell Online 14: pp. 1675-1690 CrossRef
    55. Kreps, JA, Wu, Y, Chang, H-S, Zhu, T, Wang, X, Harper, JF (2002) Transcriptome changes for Arabidopsis in response to salt, osmotic, and cold stress. Plant Physiol 130: pp. 2129-2141 CrossRef
    56. Lim, J, Thomas, T, Cavicchioli, R (2000) Low temperature regulated DEAD-box RNA helicase from the antarctic archaeon, Methanococcoides burtonii. J Mol Biol 297: pp. 553-567 CrossRef
    57. Chamot, D, Owttrim, GW (2000) Regulation of cold shock-induced RNA helicase gene expression in the cyanobacterium Anabaena sp. strain PCC 7120. J Bacteriol 182: pp. 1251-1256 CrossRef
    58. Kim, JS, Kim, KA, Oh, TR, Park, CM, Kang, H (2008) Functional characterization of DEAD-box RNA helicases in Arabidopsis thaliana under abiotic stress conditions. Plant Cell Physiol 49: pp. 1563-1571 CrossRef
    59. Guan, Q, Wu, J, Zhang, Y, Jiang, C, Liu, R, Chai, C, Zhu, J (2013) A DEAD box RNA helicase is critical for pre-mRNA splicing, cold-responsive gene regulation, and cold tolerance in Arabidopsis. Plant Cell Online 25: pp. 342-356 CrossRef
    60. Asakura, Y, Galarneau, E, Watkins, KP, Barkan, A, van Wijk, KJ (2012) Chloroplast RH3 DEAD box RNA helicases in maize and Arabidopsis function in splicing of specific group II introns and affect chloroplast ribosome biogenesis. Plant Physiol 159: pp. 961-974 CrossRef
    61. Karunatilaka, KS, Solem, A, Pyle, AM, Rueda, D (2010) Single-molecule analysis of Mss116-mediated group II intron folding. Nature 467: pp. 935-939 CrossRef
    62. Bhaskaran, H, Russell, R (2007) Kinetic redistribution of native and misfolded RNAs by a DEAD-box chaperone. Nature 449: pp. 1014-1018 CrossRef
    63. Liu, Y, Wang, L, Xing, X, Sun, L, Pan, J, Kong, X, Zhang, M, Li, D (2013) ZmLEA3, a multifunctional group 3 LEA protein from maize (Zea mays L.), is involved in biotic and abiotic stresses. Plant Cell Physiol 54: pp. 944-959 CrossRef
    64. Sasaki, K, Christov, NK, Tsuda, S, Imai, R (2014) Identification of a novel LEA protein involved in freezing tolerance in wheat. Plant Cell Physiol 55: pp. 136-147 CrossRef
    65. Eriksson, SK, Kutzer, M, Procek, J, Gr枚bner, G, Harryson, P (2011) Tunable membrane binding of the intrinsically disordered dehydrin Lti30, a cold-induced plant stress protein. Plant Cell Online 23: pp. 2391-2404 CrossRef
    66. Fern谩ndez, M, Valenzuela, S (2011) Isolation, characterization and genes expression analysis of three dehydrin genes during cold acclimation of Eucalyptus globulus. BMC Proceedings 5: pp. 81 CrossRef
    67. Wang, W, Vinocur, B, Shoseyov, O, Altman, A (2004) Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci 9: pp. 244-252 CrossRef
    68. Chen, B, Zhong, D, Monteiro, A (2006) Comparative genomics and evolution of the HSP90 family of genes across all kingdoms of organisms. BMC Genomics 7: pp. 156 CrossRef
    69. Wheeler, DL, Barrett, T, Benson, DA, Bryant, SH, Canese, K, Chetvernin, V, Church, DM, DiCuccio, M, Edgar, R, Federhen, S, Geer, LY, Helmberg, W, Kapustin, Y, Kenton, DL, Khovayko, O, Lipman, DJ, Madden, TL, Maglott, DR, Ostell, J, Pruitt, KD, Schuler, GD, Schriml, LM, Sequeira, E, Sherry, ST, Sirotkin, K, Souvorov, A, Starchenko, G, Suzek, TO, Tatusov, R, Tatusova, TA (2008) Database resources of the National Center for Biotechnology Information. Nucleic Acids Res 36: pp. D13-D21 CrossRef
    70. Li, R, Yu, C, Li, Y, Lam, T-W, Yiu, S-M, Kristiansen, K, Wang, J (2009) SOAP2: an improved ultrafast tool for short read alignment. Bioinformatics 25: pp. 1966-1967 CrossRef
    71. Conesa, A, G枚tz, S, Garc铆a-G贸mez, JM, Terol, J, Tal贸n, M, Robles, M (2005) Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics 21: pp. 3674-3676 CrossRef
    72. Kanehisa, M, Araki, M, Goto, S, Hattori, M, Hirakawa, M, Itoh, M, Katayama, T, Kawashima, S, Okuda, S, Tokimatsu, T (2008) KEGG for linking genomes to life and the environment. Nucleic Acids Res 36: pp. D480-D484
    73. Livak, KJ, Schmittgen, TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2- 螖螖CT Method. Methods 25: pp. 402-408 CrossRef
  • 刊物主题:Life Sciences, general; Microarrays; Proteomics; Animal Genetics and Genomics; Microbial Genetics and Genomics; Plant Genetics & Genomics;
  • 出版者:BioMed Central
  • ISSN:1471-2164
文摘
Background A major constraint affecting the quality and productivity of chrysanthemum is the unusual period of low temperature occurring during early spring, late autumn, and winter. Yet, there has been no systematic investigation on the genes underlying the response to low temperature in chrysanthemum. Herein, we used RNA-Seq platform to characterize the transcriptomic response to low temperature by comparing different transcriptome of Chrysanthemum nankingense plants and subjecting them to a period of sub-zero temperature, with or without a prior low temperature acclimation. Results Six separate RNA-Seq libraries were generated from the RNA samples of leaves and stems from six different temperature treatments, including one cold acclimation (CA), two freezing treatments without prior CA, two freezing treatments with prior CA and the control. At least seven million clean reads were obtained from each library. Over 77% of the reads could be mapped to sets of C. nankingense unigenes established previously. The differentially transcribed genes (DTGs) were identified as low temperature sensing and signalling genes, transcription factors, functional proteins associated with the abiotic response, and low temperature-responsive genes involved in post-transcriptional regulation. The differential transcription of 15 DTGs was validated using quantitative RT-PCR. Conclusions The large number of DTGs identified in this study, confirmed the complexity of the regulatory machinery involved in the processes of low temperature acclimation and low temperature/freezing tolerance.

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