转录因子TCP4参与植物生长发育和抗逆调节研究进展

doi:10.7668/hbnxb.20192025

摘要/Abstract

摘要： 转录因子TCP（TEOSINTE BRANCHED1，CYCLOIDEA，PROLIFERATING CELL FACTORS）家族具有bHLH（basic-Helix-Loop-Helix）二级结构域，根据结合位点碱基序列不同，将TCP家族分为两大类：Ι类（GGNCCCAC）和Ⅱ类（GTGGNCC）。转录因子TCP4是植物特有的转录因子Ⅱ类TCP家族成员之一，调控植物的生长发育，影响多种植物激素的合成，参与植物抗逆调节。本研究综述了转录因子TCP4与植物其他转录因子家族相互作用参与植物种子萌发、表皮毛分化、叶片形态、开花等重要植物生长发育过程，以此适应外界不断变化的生长环境。植物在生长发育过程中会遇到各种不利环境，从而对其造成逆境胁迫。在非生物胁迫下转录因子TCP4与功能基因的顺式作用元件结合调控其表达，调控植物激素的合成，从而参与植物抗逆。在植物发育过程中TCP4还具有时空限制的表达模式，这些表达模式提高了TCP4在局部触发或拮抗激素信号传导的可能性。为转录因子TCP4如何调控植物生长发育和精准的参与植物激素合成提供参考依据和理论基础，对植物生长调节和逆境下优良品种的选育有重要指导意义。

关键词: 转录因子TCP4, 生长发育, 抗逆调节, 植物激素

Abstract: The transcription factor TCP (TEOSINTE BRANCHED1, CYCLOIDEA, and PCF) family has bHLH (basic-Helix-Loop-Helix) secondary domain. According to the different base sequences of binding sites, the TCP family was divided into two categories:Ι Class (GGNCCCAC) and II class (GTGGNCC). The transcription factor TCP4 is one of the II class members of plant-specific transcription factors. TCP4 regulates the growth and development of plants, affects the synthesis of a variety of plant hormones, and participates in the regulation of plant resistance. This article reviews the involvement of transcription factor TCP4 interacts with other plant transcription factor families in plant seed germination, epidermal hair differentiation, leaf morphology, flowering and other important plant growth and development processes.So plants adapt to the changing growth environment of the outside world. Plants will encounter various environments in the process of growth and development, resulting in stress. Under abiotic stress, transcription factor TCP4 combines with cis acting elements of functional genes to regulate its expression and regulate the synthesis of plant hormones, so as to participate in plant stress resistance. During plant development, TCP4 also has spatio-temporal limited expression patterns, which improve the possibility of TCP4 triggering or antagonizing hormone signal transduction locally. It provides a reference and theoretical basis for how transcription factor TCP4 regulates plant growth and development and accurately participates in plant hormone synthesis, and has important guiding significance for plant growth regulation and breeding of excellent varieties under stress.

Key words: Transcription factor TCP4, Growth and development, Stress resistance regulation, Plant hormones

中图分类号:

Q945

雷其冬, 孙旭东, 徐慧妮. 转录因子TCP4参与植物生长发育和抗逆调节研究进展[J]. 华北农学报, 2021, 36(S1): 210-214. doi: 10.7668/hbnxb.20192025.

LEI Qidong, SUN Xudong, XU Huini. Research Progress in Transcription Factor TCP4 Participating in Plant Growth, Development and Stress Resistance Regulation[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2021, 36(S1): 210-214. doi: 10.7668/hbnxb.20192025.

http://www.hbnxb.net/CN/Y2021/V36/IS1/210

参考文献

[1] Cubas P,Lauter N,Doebley J,Coen E. The TCP domain:a motif found in proteins regulating plant growth and development[J]. The Plant Journal,1999,18(2):215-222.doi:10.1046/j.1365-313X.1999.00444.x.
[2] Kosugi S,Ohashi Y. DNA binding and dimerization specificity and potential targets for the TCP protein family[J]. The Plant Journal,2002,30(3):337-348.doi:10.1046/j.1365-313x.2002.01294.x.
[3] 刘丽娟,高辉.TCP家族基因研究进展[J].生物技术通报,2016,32(9):14-22.doi:10.13560/j.cnki.biotech.bull.1985.2016.09.003.
Liu L J,Gao H. Research progress on the family of TCP genes[J]. Biotechnology Bulletin,2016,32(9):14-22.
[4] Koyama T,Mitsuda N,Seki M,Shinozaki K,Ohme-Takagi M. TCP transcription factors regulate the activities of ASYMMETRIC LEAVES1 and miR164,as well as the auxin response,during differentiation of leaves in Arabidopsis[J]. The Plant Cell,2010,22(11):3574-3588.doi:10.1105/tpc.110.075598.
[5] He Z M,Zhao X Y,Kong F N,Zuo Z C,Liu X M. TCP2 positively regulates HY5/HYH and photomorphogenesis in Arabidopsis[J]. Journal of Experimental Botany,2016,67(3):775-785.doi:10.1093/jxb/erv495.
[6] Kong Y Y,Zhu Y B,Gao C,She W J,Lin W Q,Chen Y,Han N,Bian H W,Zhu M Y,Wang J H.Tissue-specific expression of SMALL AUXIN UP RNA41 differentially regulates cell expansion and root meristem patterning in Arabidopsis[J]. Plant and Cell Physiology,2013,54(4):609-621.doi:10.1093/pcp/pct028.
[7] Sun N,Wang J,Gao Z,Dong J,He H,Terzaghi W,Wei N,Deng X W,Chen H. Arabidopsis SAURs are critical for differential light regulation of the development of various organs[J]. P Natl Acad Sci USA,2016,113(21):6071-6076.doi:10.1073/pnas.1604782113.
[8] Shi H,Lyu M H,Luo Y W,Liu S C,Li Y,He H,Wei N,Deng X W,Zhong S W. Genome-wide regulation of light-controlled seedling morphogenesis by three families of transcription factors[J]. Proceedings of the National Academy of Sciences of the United States of America,2018,115(25):6482-6487.doi:10.1073/pnas.1803861115.
[9] Zhang Y,Mayba O,Pfeiffer A,Shi H,Tepperman J M,Speed T P,Quail P H. A quartet of PIF bHLH factors provides a transcriptionally centered signaling hub that regulates seedling morphogenesis through differential expression-patterning of shared target genes in Arabidopsis[J]. PLoS Genetics,2013,9(1):e1003244.doi:10.1371/journal.pgen.1003244.
[10] Dong J,Sun N,Yang J,Deng Z G,Lan J Q,Qin G J,He H,Deng X W,Irish V F,Chen H D,Wei N. The transcription factors TCP4 and PIF3 antagonistically regulate organ-specific light induction of SAUR genes to modulate cotyledon opening during de-etiolation in Arabidopsis[J]. The Plant Cell,2019,31(5):1155-1170.doi:10.1105/tpc.18.00803.
[11] Nag A,King S,Jack T. miR319a targeting of TCP4 is critical for petal growth and development in Arabidopsis[J]. Proceedings of the National Academy of Sciences of the United States of America,2009,106(52):22534-22539.doi:10.1073/pnas.0908718106.
[12] Challa K R,Aggarwal P,Nath U. Activation of YUCCA5 by the transcription factor TCP4 integrates developmental and environmental signals to promote hypocotyl elongation in Arabidopsis[J]. The Plant Cell,2016,28(9):2117-2130.doi:10.1105/tpc.16.00360.
[13] Sarvepalli K,Nath U. Hyper-activation of the TCP4 transcription factor in Arabidopsis thaliana accelerates multiple aspects of plant maturation[J]. The Plant Journal,2011,67(4):595-607.doi:10.1111/j.1365-313x.2011.04616.x.
[14] Patra B,Pattanaik S,Yuan L. Ubiquitin protein ligase 3 mediates the proteasomal degradation of GLABROUS 3 and ENHANCER OF GLABROUS 3,regulators of trichome development and flavonoid biosynthesis in Arabidopsis[J]. Plant Journal,2013,74(3):435-447.doi:10.1111/tpj.12132.
[15] Kasili R,Huang C C,Walker J D,Simmons L A,Zhou J,Faulk C,H lskamp M,Larkin J C. BRANCHLESS TRICHOMES links cell shape and cell cycle control in Arabidopsis trichomes[J]. Development,2011,138(11):2379-2388.doi:10.1242/dev.058982.
[16] Vadde B V L,Challa K R,Nath U. The TCP4 transcription factor regulates trichome cell differentiation by directly activating GLABROUS INFLORESCENCE STEMS in Arabidopsis thaliana[J]. The Plant Journal,2018,93(2):259-269.doi:10.1111/tpj.13772.
[17] Schommer C,Debernardi J M,Bresso E G,Rodriguez R E,Palatnik J F. Repression of cell proliferation by miR319-regulated TCP4[J]. Molecular Plant,2014,7(10):1533-1544.doi:10.1093/mp/ssu084.
[18] Rodriguez R E,Mecchia M A,Debernardi J M,Schommer C,Weigel D,Palatnik J F. Control of cell proliferation in Arabidopsis thaliana by microRNA miR396[J]. Development,2010,137(1):103-112.doi:10.1242/dev.043067.
[19] Bresso E G,Chorostecki U,Rodriguez R E,Palatnik J F,Schommer C. Spatial control of gene expression by miR319-regulated TCP transcription factors in leaf development[J]. Plant Physiology,2018,176(2):1694-1708.doi:10.1104/pp.17.00823.
[20] Johansson M,Staiger D. Time to flower:Interplay between photoperiod and the circadian clock[J]. Journal of Experimental Botany,2015,66(3):719-730.doi:10.1093/jxb/eru441.
[21] Shim J S,Kubota A,Imaizumi T. Circadian clock and photoperiodic flowering in Arabidopsis:CONSTANS is a hub for signal integration[J]. Plant Physiology,2017,173(1):5-15.doi:10.1104/pp.16.01327.
[22] Fornara F,Panigrahi K C S,Gissot L,Sauerbrunn N,R hl M,Jarillo J A,Coupland G. Arabidopsis DOF transcription factors act redundantly to reduce CONSTANS expression and are essential for a photoperiodic flowering response[J]. Developmental Cell,2009,17(1):75-86.doi:10.1016/j.devcel.2009.06.015.
[23] Ito S,Song Y H,Josephson-Day A R,Miller R J,Breton G,Olmstead R G,Imaizumi T. FLOWERING BHLH transcriptional activators control expression of the photoperiodic flowering regulator CONSTANS in Arabidopsis[J]. Proceedings of the National Academy of Sciences of the United States of America,2012,109(9):3582-3587.doi:10.1073/pnas.1118876109.
[24] Cubas P,Lauter N,Doebley J,Coen E. The TCP domain:a motif found in proteins regulating plant growth and development[J]. The Plant Journal,1999,18(2). 215-222.doi:10.1046/j.1365-313X.1999.00444.x.
[25] Kubota A,Ito S,Shim J S,Johnson R S,Song Y H,Breton G,Goralogia G S,Kwon M S,Laboy Cintr n D,Koyama T,Ohme-Takagi M,Pruneda-Paz J L,Kay S A,MacCoss M J,Imaizumi T.TCP4-dependent induction of CONSTANS transcription requires GIGANTEA in photoperiodic flowering in Arabidopsis[J]. PLoS Genetics,2017,13(6):e1006856.doi:10.1371/journal.pgen.1006856.
[26] 王瑞元. 中国食用植物油加工业的现状与发展趋势[J].粮油食品科技,2017,25(3):4-9.doi:10.16210/j.cnki.1007-7561.2017.03.002.
Wang R Y. The current situation and development trend of China's edible vegetable oil processing industry[J]. Science and Technology of Cereals, Oils and Foods,2017,25(3):4-9.
[27] 滕红梅,王艳萍,闫丽清,曹发昊,郝浩永. 中条山区域野生油脂植物资源及特征分析[J].中国油脂,2020,45(9):137-144.doi:10.12166/j.zgyz.1003-7969/2020.09.026.
Teng H M,Wang Y P,Yan L Q,Cao F H,Hao H Y. Resources and characteristics of wild oil plants in Zhongtiaoshan area[J]. China Oils and Fats,2020,45(9):137-144.
[28] Chapman K D,Ohlrogge J B. Compartmentation of triacylglycerol accumulation in plants[J]. Journal of Biological Chemistry,2012,287(4):2288-2294.doi:10.1074/jbc.R111.290072.
[29] Focks N,Benning C. wrinkled1:A novel,low-seed-oil mutant of Arabidopsis with a deficiency in the seed-specific regulation of carbohydrate metabolism[J]. Plant Physiology,1998,118(1):91-101.doi:10.1104/pp.118.1.91.
[30] Kong Q,Singh S K,Mantyla J J,Pattanaik S,Guo L,Yuan L,Benning C,Ma W. TEOSINTE BRANCHED1/CYCLOIDEA/PROLIFERATING CELL FACTOR4 interacts with WRINKLED1 to mediate seed oil biosynthesis[J]. Plant Physiology,2020,184(2):658-665.doi:10.1104/pp.20.00547.
[31] Li B S,Qin Y R,Duan H,Yin W L,Xia X L. Genome-wide characterization of new and drought stress responsive microRNAs in Populus euphratica[J]. Journal of Experimental Botany,2011,62(11):3765-3779.doi:10.1093/jxb/err051.
[32] Yu X,Wang H,Lu Y Z,de Ruiter M,Cariaso M,Prins M,van Tunen A,He Y K. Identification of conserved and novel microRNAs that are responsive to heat stress in Brassica rapa[J]. Journal of Experimental Botany,2012,63(2):1025-1038.doi:10.1093/jxb/err337.
[33] Waters B M,McInturf S A,Stein R J. Rosette iron deficiency transcript and microRNA profiling reveals links between copper and iron homeostasis in Arabidopsis thaliana[J]. Journal of Experimental Botany,2012,63(16):5903-5918.doi:10.1093/jxb/ers239.
[34] Hewezi T,Howe P,Maier T R,Baum T J. Arabidopsis small RNAs and their targets during cyst nematode parasitism[J]. Molecular Plant-Microbe Interactions,2008,21(12):1622-1634.doi:10.1094/mpmi-21-12-1622.
[35] Thiebaut F,Rojas C A,Almeida K L,Grativol C,Domiciano G C,Lamb C R C,Engler J D A,Hemerly A S,Ferreira P C G. Regulation of miR319 during cold stress in sugarcane[J]. Plant, Cell & Environment,2012,35(3):502-512.doi:10.1111/j.1365-3040.2011.02430.x.
[36] Zhao W C,Li Z L,Fan J W,Hu C L,Yang R,Qi X,Chen H,Zhao F K,Wang S H. Identification of jasmonic acid-associated microRNAs and characterization of the regulatory roles of the miR319/TCP4 module under root-knot nematode stress in tomato[J]. Journal of Experimental Botany,2015,66(15):4653-4667.doi:10.1093/jxb/erv238.
[37] Mahajan S,Tuteja N. Cold,salinity and drought stresses:An overview[J]. Archives of Biochemistry and Biophysics,2005,444(2):139-158.doi:10.1016/j.abb.2005.10.018.
[38] 刘春浩,梁楠松,于磊,赵兴堂,刘颖,孙爽,王紫晴,詹亚光. 水曲柳TCP4转录因子克隆及胁迫和激素下的表达分析[J].北京林业大学学报,2017,39(6):22-31.doi:10.13332/j.1000-1522.20160359.
Liu C H,Liang N S,Yu L,Zhao X T,Liu Y,Sun S,Wang Z Q,Zhan Y G. Cloning,analysing and homologous expression of TCP4 transcription factor under abiotic stress and hormone signal in Fraxinus mandschurica[J]. Journal of Beijing Forestry University,2017,39(6):22-31.
[39] Zhang S,Zhao Q C,Zeng D X,Xu J H,Zhou H G,Wang F L,Ma N,Li Y H. RhMYB108,an R2R3-MYB transcription factor,is involved in ethylene-and JA-induced petal senescence in rose plants[J]. Horticulture Research,2019,6:131.doi:10.1038/s41438-019-0221-8.
[40] Wang N,Yang H Z,Yin Z Y,Liu W T,Sun L Y,Wu Y F. Phytoplasma effector SWP1 induces witches' broom symptom by destabilizing the TCP transcription factor BRANCHED1[J]. Molecular Plant Pathology,2018,19(12):2623-2634.doi:10.1111/mpp.12733.
[41] Tiwari P,Indoliya Y,Chauhan A S,Pande V,Chakrabarty D. Over-expression of rice R1-type MYB transcription factor confers different abiotic stress tolerance in transgenic Arabidopsis[J]. Ecotoxicology and Environmental Safety,2020,206:11136.doi:10.1016/j.ecoenv.2020.111361.
[42] Pecher P,Moro G,Canale M C,Capdevielle S,Singh A,MacLean A,Sugio A,Kuo C H,Lopes J R S,Hogenhout S A. Phytoplasma SAP11 effector destabilization of TCP transcription factors differentially impact development and defence of Arabidopsis versus maize[J]. PLoS Pathogens,2019,15(9):e1008035.doi:10.1371/journal.ppat.1008035.
[43] Leng B Y,Wang X,Yuan F,Zhang H N,Lu C X,Chen M,Wang B S. Heterologous expression of the Limonium bicolor MYB transcription factor LbTRY in Arabidopsis thaliana increases salt sensitivity by modifying root hair development and osmotic homeostasis[J]. Plant Science:an International Journal of Experimental Plant Biology,2021,302:110704-110704.doi:10.1016/j.plantsci.2020.110704.
[44] Capdevielle S,Pecher P,Moro G,Al-Subhi A,Mathers T C,Huang W,Al-Sadi A M,Hogenhout S A. Phytoplasma SAP11 effector homologs have evolved to differentially interact with plant TCP transcription factor subclasses[J]. Molecular Plant-Microbe Interactions,2019,32(10):3-3.doi:10.1371/journal.ppat.1008035.

选择文件类型/文献管理软件名称

选择包含的内容