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作物学报 ›› 2017, Vol. 43 ›› Issue (07): 1021-1029.doi: 10.3724/SP.J.1006.2017.01021

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

玉米热激转录因子基因ZmHsf25的克隆、特性与耐热性功能分析

赵立娜1,2,**.段硕楠1,**.张华宁1.郭秀林1,*.李国良1,*   

  1. 1 河北省农林科学院遗传生理研究所 / 河北省植物转基因中心重点实验室,河北石家庄 050051;2 河北师范大学生命科学学院,河北石家庄 050024
  • 收稿日期:2016-11-08 修回日期:2017-03-02 出版日期:2017-07-12 网络出版日期:2017-03-17
  • 通讯作者: 李国良,E-mail: guolianglili@163.com, Tel: 0311-87652117; 郭秀林,E-mail: myhf2002@163.com, Tel: 0311-87269032
  • 基金资助:

    本研究由河北省自然科学基金项目(C2017301065),河北省博士基金项目(2017039349),渤海粮仓科技工程项目(F16C14001)和河北省高层次人才项目(A201500130)资助。

Cloning, Characteristics and Regulating Role in Thermotolerance of Heat Shock Transcription Factor (ZmHsf25) in Zea mays L.

ZHAO Li-Na1,2,**,DUAN Shuo-Nan1,**,ZHANG Hua-Ning1,GUO Xiu-Lin1,*,LI Guo-Liang1,*   

  1. 1 Institute of Genetics and Physiology, Hebei Academy of Agriculture and Forestry Sciences / Plant Genetic Engineering Center of Hebei Province, Shijiazhuang 050051, China; 2 College of Life Science, Hebei Normal University, Shijiazhuang 050024, China?
  • Received:2016-11-08 Revised:2017-03-02 Published:2017-07-12 Published online:2017-03-17
  • Contact: Li Guoliang,E-mail: guolianglili@163.com, Tel: 0311-87652117;LI Guoliang,E-mail: myhf2002@163.com, Tel: 0311-87269032
  • Supported by:

    This study was financially supported by the Natural Science Foundation of Hebei Province (C2017301065), the Doctoral Foundation of Hebei Province (2017039349), the Bohai Barn Science and Technology Project (F16C14001) and the High-level Talent Project of Hebei Province (A201500130).

摘要:

植物热激转录因子(heat shock transcription factor, Hsf)对下游热激蛋白基因及耐热性相关基因的表达起关键调控作用。玉米中至少有30个Hsf家族成员,其中B族有7个。在前期对玉米A1亚族热激转录因子基因ZmHsf06克隆及特性、抗旱耐热性功能分析的基础上,从玉米幼叶中克隆到B族热激转录因子基因ZmHsf25的完整编码序列,序列全长957 bp,编码318个氨基酸残基。蛋白质序列含有DNA结合结构域、核定位信号序列和核输出信号序列,同源分析结果显示,ZmHsf25与高粱Sb06g025710的相似性最高,达92%。荧光定量分析表明,正常生长条件下,ZmHsf25在玉米多个组织器官中表达,幼嫩花粉中高表达,幼嫩根系和雌穗中表达量较低。42℃热胁迫能显著上调根系和叶片ZmHsf25的表达,叶片中上升幅度高于根系,处理50 min达到峰值;正常条件下,水杨酸和H2O2处理均使根系和叶片ZmHsf25表达下调,而热激条件下却表现为显著上调。通过在洋葱表皮细胞中瞬时表达并观察GFP荧光,确定ZmHsf25定位在细胞核。通过转化酵母并进行热胁迫处理发现,热胁迫同时降低正常和转ZmHsf25酵母的耐热性,但与转空载体对照相比,转基因酵母的耐热性更强。推测ZmHsf25参与玉米热胁迫响应和花粉的发育过程,可能是水杨酸热激信号转导途径的下游组分。研究结果为进一步探明玉米热激转录因子家族成员的特性与功能提供了依据。

关键词: 玉米, 热激转录因子基因ZmHsf25, 表达, 亚细胞定位, 耐热性

Abstract:

Heat shock transcription factors (Hsfs) are key components of signal transduction pathways involved in the activation of genes in response to heat shock stress in plants. There are at least 30 Hsf members in maize and seven of which belong to class B. In our previous work, we obtained ZmHsf06, which belongs to subclass A1, and investigated the characteristics of expression, subcellular localization, and regulating roles in thermotolerance and drought-stress tolerance of ZmHsf06. In the present study, ZmHsf25 was isolated from maize (Zea mays L.) young leaves treated by heat shock at 42°C for 1 h using homologous cloning methods. The sequencing analysis showed that the coding sequence (CDS) of ZmHsf25 was 957 bp and encoded a protein of 318 amino acids. The amino acid sequence analysis demonstrated that ZmHsf25 contained a DNA-binding domain (DBD), a nuclear localization signal (NLS) of KRLR peptide and a nuclear export signal (NES) of VLTLSV peptide. The identity of amino acid between ZmHsf25 and Sb060g025710 of sorghum was the highest, which was 92%. ZmHsf25 was expressed in multiple tissues and organs of maize, and transcription expression level of ZmHsf25 was the highest in pollens compared with root, stem, functional leaf, immature embryo and ear. qRT-PCR results showed that ZmHsf25 was up-regulated by 42°C heat shock in both leaves and roots. Under normal conditions, ZmHsf25 was down-regulated by both SA and H2O2, but significantly up-regulated by heat stress at 42°C. Through transient reporter assay with onion (Allium cepa L.) epidermal cells, we found that ZmHsf25 was localized in nuclei. ZmHsf25 overexpressed yeast showed stronger thermotolerance than the controls after heat shock (HS), though yeast thermotolerance was both decreased by HS. The results revealed that ZmHsf25 perhaps is one of downstream elements of SA signal pathway to play a key role in regulating the response to heat stress and pollen development. These results will provide a theoretical basis for analyzing biological characteristics and functions of maize Hsf members further.

Key words: Maize, ZmHsf25, Expression, Subcelullar-localization, Thermotolerance

[1] Nover L, Scharf K D, Gagliardi D, Vergne P, Czarnecka-Verner E, Gurley W B. The HSF world: classification and properties of plant heat stress transcription factors. Cell Stress Chaperones, 1996, 1: 215–223 [2] Nover L, Bharti K, D?ring P, Mishra S K, Ganguli A, Scharf K D. Arabidopsis and the heat stress transcription factor world: how many heat stress transcription factors do we need. Cell Stress Chaperones, 2001, 6: 177–189 [3] Guo M, Liu H J. Ma X, Luo D X, Gong Z H, Lu M H. The plant heat stress transcription factors (HSFs): structure, regulation and function in response to aboitic stresses. Front Plant Sci, 2016, 7: 114 [4] Scharf K D, Rose S, Zott W. Three tomato genes code for heat stress transcription factors with a region of remarkable homology to the DNA-binding domain of the yeast HSF. EMBO J, 1990, 9: 4495–4501 [5] Xue G P, Sadat S, Drenth J, Mclntyre C L. The heat shock factor family from Triticum aestivum in response to heat and other major abiotic stresses and their role in regulation of heat shock protein genes. J Exp Bot, 2014, 65: 539–557 [6] Liu H C, Charng Y Y. Common and distinct functions of Arabidopsis class A1 and A2 heat shock factors in diverse abiotic stress responses and development. Plant Physiol, 2013, 163: 276–290 [7] Mishra S K, Tripp J, Winkelhaus S, Tschiersch B, Theres K, Nover L, Scharf K D. In the complex family of heat stress transcription factors, HsfA1 has a unique role as master regulator of thermotolerance in tomato. Genes and Development, 2002, 16: 1555–1567 [8] Kotak S, Port M, Ganguli A, Bicker F, von Koskull-Doüring P. Characterization of C-terminal domains of Arabidopsis heat stress transcription factors (Hsfs) and identification of a new signature combination of plant class A Hsfs with AHA and NES motifs essential for activator function and intracellular localization. Plant J, 2004, 39: 98–112 [9] Wunderlich M, Gro?-Hardt R, Sch?ff F. Heat shock factor HSFB2a involved in gametophyte development of Arabidopsis thaliana and its expression is controlled by a heat-inducible long non-coding antisense RNA. Plant Mol Biol, 85: 541–550 [10] Ikeda M, Mitsuda N, Ohme-Takagi M. Arabidopsis HsfB1 and HsfB2b act as repressors for the expression of heat-inducible Hsfs but positively regulate the acquired thermotolerance. Plant Physiol, 2011, 157: 1243–1254 [11] Ma H, Wang C T, Yang B, Cheng H Y , Wang Z, Mijiti A, Ren C, Qu G H, Zhang H, Ma L. CarHSFB2, a Class B heat shock transcription factor, is involved in different developmental processes and various stress responses in chickpea (Cicer Arietinum L.). Plant Mol Biol Rep, 2016, 34: 1–14 [12] Kumar M, Busch W, Birke H, Kemmerling B, Nürnberger T, Sch?ffl F. Heat shock factors HsfB1 and HsfB2b are involved in the regulation of Pdf1.2 expression and pathogen resistance in Arabidopsis. Mol Plant, 2009, 2: 152–165 [13] Zhu X, Thalor S K, Takahashi Y, Berberich T, Kusano T. An inhibitory effect of the sequence-conserved upstream open-reading frame on the translation of the main open-reading frame of HsfB1 transcripts in Arabidopsis. Plant Cell Environ, 2012, 35: 2014–2030 [14] Kolmos E, Chowa B Y, Pruneda-Pazb J L, Kay S A. Kolmos HsfB2b-mediated repression of PRR7 directs abiotic stress responses of the circadian clock. Proc Natl Acad Sci USA, 2014, 111: 16173–16177 [15] Bharti K, Von KoskullD?ring P, Bharti S, Kumar P, Tintschlk?rbitzer A, Treuter E, Nover L. Tomato heat stress transcription factor HsfB1 represents a novel type of general transcription coactivator with a histone-like motif interacting with HAC1/CBP. Plant Cell, 2004, 16: 1521–1535 [16] Hahn A, Bublak D, Schleiff E, Scharf K D. Crosstalk between Hsp90 and Hsp70 chaperones and heat stress transcription factors in tomato. Plant Cell, 2011, 23: 741–755 [17] Begum T, Reuter R, Sch?ff F. Overexpression of AtHsfB4 induces specific effects on root development of Arabidopsis. Mech Dev, 2012, 130: 54–60 [18] Mittal D, Chakrabarti S, Sarkar A, Singh A, Grover A. Heat shock factor gene family in rice: genomic organization and transcript expression profiing in response to high temperature, low temperature and oxidative stresses. Plant Physiol Biochem, 2009, 47: 785–795 [19] 李慧聪, 李国良, 郭秀林. 玉米热激转录因子基因ZmHsf-Like对逆境胁迫响应的信号途径. 作物学报, 2014, 40: 622–628 Li H C, Li G L, Guo X L. Signal transduction pathway of ZmHsf-Like gene responding to different abiotic stresses. Acta Agron Sin, 2014, 40: 622–628 (in Chinese with English abstract). [20] Lin Y X, Jiang H Y, Chu Z X, Tang X L, Zhu S W, Cheng B J. Genome-wide identifiation, classifiation and analysis of heat shock transcription factor family in maize. BMC Genomics, 2011, 12: 76–89 [21] Li H X, Fan R C, Li L B, Wei B, Li G L, Gu L Q, Wang X P, Zhang X Q. Identification and characterization of a novel copper transporter gene family TaCT1 in common wheat. Plant Cell Environ, 2014, 37: 1561–1573 [22] 李慧聪, 李国良, 郭秀林. 玉米热激转录因子基因(ZmHsf06)的克隆、表达和定位分析. 农业生物技术学报, 2015, 23(1): 41–51 Li H C, Li G L, Guo X L. Cloning, expression characteristics and subcellular-location of heat shock transcription factor ZmHsf06 in Zea mays. J Agric Biotechnol, 2015, 23: 41–51 (in Chinese with English abstract). [23] Gietz D, Jean A S, Woods R A, Schiestl R H. Improved method for high transformation of intact yeast cells. Nucleic Acids Res, 1992, 20: 1425 [24] Li H C, Zhang H N, Li G L, Liu Z H, Zhang Y M, Zhang H M. Expression of maize heat shock transcription factor gene ZmHsf06 enhances the thermotolerance and drought-stress tolerance of transgenic Arabidopsis. Funct Plant Biol, 2015, 42: 1080–1090 [25] Czarnecka-Verner E, Pan S, Salem T, Gurley W B. Plant class B HSFs inhibit transcription and exhibit affinity for TFIIB and TBP. Plant Mol Biol, 2004, 56: 57–75 [26] Ikeda M, Ohme-Takagi M. A novel group of transcriptional repressors in Arabidopsis. Plant Cell Physiol, 2009, 50: 970–975 [27] Bharti K, von Koskull-D?ring P, Bharti S, Kumar P, Tintschl-Korbitzer A, Treuter E, Nover L. Tomato heat stress transcription factor HsfB1 represents a novel type of general transcription coactivator with a histone-like motif interacting with the plant CREB binding protein ortholog HAC1. Plant Cell, 2004, 16: 1521–1535 [28] Xiang J, Ran J, Zou J, Zhou X, Liu A. Heat shock factor OsHsfB2b negatively regulates drought and salt tolerance in rice. Plant Cell Rep, 2013, 32: 1795–1806 [29] Gaffney T, Friedrich L, Vernooij B, Negrotto D, Nye G, Uknes S, Ward E, Ryals J. Requirement of salicylic acid for the induction of systemic acquired resistance. Science, 1993, 261: 6 [30] Larkindale J, Hall J D, Knight M R, Vierling E. Heat stress phenotypes of Arabidopsis mutants implicate multiple signaling pathways in the acquisition of thermotolerance. Plant Physiol, 2005, 138: 882–886 [31] Snyman M, Cronjé M J. Modulation of heat shock factors accompanies salicylic acid-mediated potentiation of Hsp70 in tomato seedlings. J Exp Bot, 2008, 59: 2125–2132 [32] Ayarpadikannan S, Chung E, Cho C W, So H A, Kim S O, Jeon J M, Kwak M H, Lee S W, Lee J H. Exploration for the salt stress tolerance genes from a salt-treated halophyte, Suaeda asparagoides. Plant Cell Rep, 2012, 31: 35–48

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