水稻耐低温研究重要进展

doi:10.11924/j.issn.1000-6850.casb20190800542

中国农学通报 ›› 2020, Vol. 36 ›› Issue (27): 1-5.doi: 10.11924/j.issn.1000-6850.casb20190800542

所属专题：水稻

• 农学·农业基础科学 • 下一篇

水稻耐低温研究重要进展

刘静妍(), 闫双勇, 张融雪, 苏京平, 孙玥, 孙林静()

天津市农作物研究所/天津市农作物遗传育种重点实验室,天津 300384

收稿日期:2019-08-15 修回日期:2019-09-27 出版日期:2020-09-25 发布日期:2020-09-23
通讯作者: 孙林静
作者简介:刘静妍,女,1986年出生,天津人,助理研究员,博士,博士后,从事水稻响应温度的功能研究。通信地址:300384 天津市西青区津静公路17公里处天津市农作物研究所,Tel:022-83744846,E-mail: liujingyan826@qq.com。
基金资助:
国家重点研发计划“华北及西北稻区优质高产高效新品种培育”(2017YFD0100505);天津市农业科学院青年科研人员创新研究与实验项目“水稻芽苗期耐寒基因克隆及功能研究”(2019001);天津市自然科学基金面上项目“水稻芽期耐寒基因的克隆和功能分析”(19JCYBJC29500);转基因专项“新株型超级稻”北方粳稻品种的培育(2016ZX08001004-002)

Low Temperature Tolerance of Rice: A Review

Liu Jingyan(), Yan Shuangyong, Zhang Rongxue, Su Jingping, Sun Yue, Sun Linjing()

Tianjin Crop Research Institute/Tianjin Key Laboratory of Crop Genetics and Breeding, Tianjin 300384

Received:2019-08-15 Revised:2019-09-27 Online:2020-09-25 Published:2020-09-23
Contact: Sun Linjing

摘要/Abstract

摘要：

水稻是中国最重要的粮食作物之一,低温寒害作为主要非生物胁迫,严重影响了水稻的产量和品质,对水稻的各个生长时期都有不同程度的危害。研究水稻耐低温的分子机制,培育高产优质的耐寒品种对保障中国粮食安全具有重要意义。为了进一步揭示水稻耐低温分子机制,本研究综述了近几十年来水稻低温信号途径研究方面的研究进展,发现在水稻的种子萌发期、幼苗期及孕穗期均克隆了若干个重要的耐低温基因,并初步解析了其基因功能和分子机制。但具体的作用机制及信号通路研究仍存在不足。今后的研究工作还需要发掘更多水稻耐寒基因及其作用机制,并鉴定重要的SNP位点,以期为水稻分子育种提供科学依据。

关键词: 水稻, 耐低温, 非生物胁迫, 分子机制, 分子育种

Abstract:

Rice (Oryza sativa L.) is one of the most important food crop in China. As the main abiotic stress, cold stress has affected the yield and quality of rice crop seriously, and makes different degrees of harm to rice in various growth stages. It is significant to study the molecular mechanism of low-temperature tolerance of rice and cultivate high-yield and high-quality cold-resistant varieties to ensure food security in China. In order to further reveal the molecular mechanism of low temperature tolerance in rice, this study reviewed the research progress of low temperature signaling pathway in rice in recent decades. It is found that several important genes with low temperature tolerance are cloned at the seed germination stage, seedling stage and booting stage of rice, and their gene functions and molecular mechanisms are preliminarily analyzed. However, there are still some deficiencies in the study of specific mechanisms and signal pathways. Further research should focus on identifying more cold-resistant genes and their mechanism in rice and important SNP sites, so as to provide a scientific basis for rice molecular breeding.

Key words: rice, low temperature tolerance, abiotic stress, mechanism, molecular breeding

中图分类号:

刘静妍, 闫双勇, 张融雪, 苏京平, 孙玥, 孙林静. 水稻耐低温研究重要进展[J]. 中国农学通报, 2020, 36(27): 1-5.

Liu Jingyan, Yan Shuangyong, Zhang Rongxue, Su Jingping, Sun Yue, Sun Linjing. Low Temperature Tolerance of Rice: A Review[J]. Chinese Agricultural Science Bulletin, 2020, 36(27): 1-5.

参考文献 55

[1]	Gross B L, Zhao Z. Archaeological and genetic insights into the origins of domesticated rice[J]. Proc Natl Acad Sci USA, 2014,111(17):6190-6197. doi: 10.1073/pnas.1308942110 URL pmid: 24753573
[2]	Xie G, Kato H, Imai R. Biochemical identification of the OsMKK6-OsMPK3 signalling pathway for chilling stress tolerance in rice[J]. Biochem J, 2012,443(1):95-102. doi: 10.1042/BJ20111792 URL pmid: 22248149
[3]	Zhang Q, Chen Q, Wang S, et al. Rice and cold stress: methods for its evaluation and summary of cold tolerance-related quantitative trait loci[J]. Rice (N Y), 2014,7:24.
[4]	Zhao J, Zhang S, Yang T, et al. Global transcriptional profiling of a cold-tolerant rice variety under moderate cold stress reveals different cold stress response mechanisms[J]. Physiol Plant, 2015,154(3):381-394. URL pmid: 25263631
[5]	Liu C T, Wang W, Mao B G, et al. Cold stress tolerance in rice: physiological changes, molecular mechanism, and future prospects[J]. Yi Chuan, 2018,40(3):171-185. URL pmid: 29576541
[6]	Thomashow M F. PLANT COLD ACCLIMATION: Freezing Tolerance Genes and Regulatory Mechanisms[J]. Annu Rev Plant Physiol Plant Mol Biol, 1999,50:571-599. URL pmid: 15012220
[7]	Ding Y, Shi Y, Yang S. Advances and challenges in uncovering cold tolerance regulatory mechanisms in plants[J]. New Phytol, 2019,222(4):1690-1704. doi: 10.1111/nph.15696 URL pmid: 30664232
[8]	Liu J, Shi Y, Yang S. Insights into the regulation of C-repeat binding factors in plant cold signaling[J]. J Integr Plant Biol, 2018,60(9):780-795. URL pmid: 29667328
[9]	Medina J, Catala R, Salinas J. The CBFs: three arabidopsis transcription factors to cold acclimate[J]. Plant Sci, 2011,180(1):3-11. URL pmid: 21421341
[10]	Shi Y, Ding Y, Yang S. Molecular Regulation of CBF Signaling in Cold Acclimation[J]. Trends Plant Sci, 2018,23(7):623-637. doi: 10.1016/j.tplants.2018.04.002 URL pmid: 29735429
[11]	Miquel, M, James Jr D, Dooner H, et al. Arabidopsis requires polyunsaturated lipids for low-temperature survival[J]. Proc Natl Acad Sci U S A, 1993,90(13):6208-6212.
[12]	Thorlby G, Fourrier N, Warren G. The SENSITIVE TO FREEZING2 gene, required for freezing tolerance in Arabidopsis thaliana, encodes a beta-glucosidase[J]. Plant Cell, 2004,16(8):2192-2203. doi: 10.1105/tpc.104.024018 URL pmid: 15258268
[13]	Moellering E R, Muthan B, Benning C. Freezing tolerance in plants requires lipid remodeling at the outer chloroplast membrane[J]. Science, 2010,330(6001):226-228. doi: 10.1126/science.1191803 URL pmid: 20798281
[14]	Ma Y, Dai X, Xu Y, et al. COLD1 confers chilling tolerance in rice[J]. Cell, 2015,160(6):1209-1221. doi: 10.1016/j.cell.2015.01.046 URL pmid: 25728666
[15]	Kumar S V, Wigge P A. H2A.Z-containing nucleosomes mediate the thermosensory response in Arabidopsis[J]. Cell, 2010,140(1):136-147. doi: 10.1016/j.cell.2009.11.006 URL pmid: 20079334
[16]	Huang G T, Ma S L, Bai L P, et al. Signal transduction during cold, salt, and drought stresses in plants[J]. Mol Biol Rep, 2012,39(2):969-987. doi: 10.1007/s11033-011-0823-1 URL pmid: 21573796
[17]	Stockinger E J, Gilmour S J, Thomashow M F. Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit[J]. Proc Natl Acad Sci USA, 1997,94(3):1035-1040. doi: 10.1073/pnas.94.3.1035 URL pmid: 9023378
[18]	Liu Q, Kasuga M, Sakuma Y, et al. Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought- and low-temperature-responsive gene expression, respectively, in Arabidopsis[J]. Plant Cell, 1998,10(8):1391-1406. doi: 10.1105/tpc.10.8.1391 URL pmid: 9707537
[19]	Jia Y, Ding Y, Shi Y, et al. The cbfs triple mutants reveal the essential functions of CBFs in cold acclimation and allow the definition of CBF regulons in Arabidopsis[J]. New Phytol, 2016,212(2):345-353. doi: 10.1111/nph.14088 URL pmid: 27353960
[20]	Novillo F, Alonso J M, Ecker J R, et al. CBF2/DREB1C is a negative regulator of CBF1/DREB1B and CBF3/DREB1A expression and plays a central role in stress tolerance in Arabidopsis[J]. Proc Natl Acad Sci U S A, 2004,101(11):3985-3990. URL pmid: 15004278
[21]	Novillo F, Medina J, Salinas J. Arabidopsis CBF1 and CBF3 have a different function than CBF2 in cold acclimation and define different gene classes in the CBF regulon[J]. Proc Natl Acad Sci U S A, 2007,104(52):21002-21007. URL pmid: 18093929
[22]	Yamaguchi-Shinozaki K, Shinozaki K. Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses[J]. Annu Rev Plant Biol, 2006,57:781-803. URL pmid: 16669782
[23]	Chinnusamy V, Ohta M, Kanrar S, et al. ICE1: a regulator of cold-induced transcriptome and freezing tolerance in Arabidopsis[J]. Genes Dev, 2003,17(8):1043-1054. doi: 10.1101/gad.1077503 URL pmid: 12672693
[24]	Dong C H, Agarwal M, Zhang Y, et al. The negative regulator of plant cold responses, HOS1, is a RING E3 ligase that mediates the ubiquitination and degradation of ICE1[J]. Proc Natl Acad Sci U S A, 2006,103(21):8281-8286. doi: 10.1073/pnas.0602874103 URL pmid: 16702557
[25]	Miura K, Jin J B, Lee J, et al. SIZ1-mediated sumoylation of ICE1 controls CBF3/DREB1A expression and freezing tolerance in Arabidopsis[J]. Plant Cell, 2007,19(4):1403-1414. doi: 10.1105/tpc.106.048397 URL pmid: 17416732
[26]	Ding Y, Li H, Zhang X, et al. OST1 kinase modulates freezing tolerance by enhancing ICE1 stability in Arabidopsis[J]. Dev Cell, 2015,32(3):278-289. doi: 10.1016/j.devcel.2014.12.023 URL pmid: 25669882
[27]	Li H, Ding Y, Shi Y, et al. MPK3- and MPK6-Mediated ICE1 Phosphorylation Negatively Regulates ICE1 Stability and Freezing Tolerance in Arabidopsis[J]. Dev Cell, 2017,43(5):630-642. doi: 10.1016/j.devcel.2017.09.025 URL pmid: 29056553
[28]	Zhao C, Wang P, Si T, et al. MAP Kinase Cascades Regulate the Cold Response by Modulating ICE1 Protein Stability[J]. Dev Cell, 2017,43(5):618-629. doi: 10.1016/j.devcel.2017.09.024 URL pmid: 29056551
[29]	Agarwal M, Hao Y, Kapoor A, et al. A R2R3 type MYB transcription factor is involved in the cold regulation of CBF genes and in acquired freezing tolerance[J]. J Biol Chem, 2006,281(49):37636-37645. doi: 10.1074/jbc.M605895200 URL pmid: 17015446
[30]	Doherty C J, Van Buskirk H A, Myers S J, et al. Roles for Arabidopsis CAMTA transcription factors in cold-regulated gene expression and freezing tolerance[J]. Plant Cell, 2009,21(3):972-984. doi: 10.1105/tpc.108.063958 URL pmid: 19270186
[31]	Fursova O V, Pogorelko G V, Tarasov V A. Identification of ICE2, a gene involved in cold acclimation which determines freezing tolerance in Arabidopsis thaliana[J]. Gene, 2009,429(1-2):98-103. doi: 10.1016/j.gene.2008.10.016 URL pmid: 19026725
[32]	Shi Y, Tian S, Hou L, et al. Ethylene signaling negatively regulates freezing tolerance by repressing expression of CBF and type-A ARR genes in Arabidopsis[J]. Plant Cell, 2012,24(6):2578-2595.
[33]	Vogel J T, Zarka D G, Van Buskirk H A, et al. Roles of the CBF2 and ZAT12 transcription factors in configuring the low temperature transcriptome of Arabidopsis[J]. Plant J, 2005,41(2):195-211. doi: 10.1111/j.1365-313X.2004.02288.x URL pmid: 15634197
[34]	Zhang Z, Li J, Li F, et al. OsMAPK3 Phosphorylates OsbHLH002/OsICE1 and Inhibits Its Ubiquitination to Activate OsTPP1 and Enhances Rice Chilling Tolerance[J]. Dev Cell, 2017,43(6):731-743. URL pmid: 29257952
[35]	Guo X, Liu D, Chong K. Cold signaling in plants: Insights into mechanisms and regulation[J]. J Integr Plant Biol, 2018,60(9):745-756. doi: 10.1111/jipb.12706 URL
[36]	Ramirez V E, Poppenberger B. MAP Kinase Signaling Turns to ICE[J]. Dev Cell, 2017,43(5):545-546. doi: 10.1016/j.devcel.2017.10.032 URL pmid: 29207256
[37]	Choi J Y, Platts A E, Fuller D Q, et al. The Rice Paradox: Multiple Origins but Single Domestication in Asian Rice[J]. Mol Biol Evol, 2017,34(4):969-979. doi: 10.1093/molbev/msx049 URL pmid: 28087768
[38]	Civan P, Craig H, Cox C J, et al. Three geographically separate domestications of Asian rice[J]. Nat Plants, 2015,1:15164. doi: 10.1038/nplants.2015.164 URL pmid: 27251535
[39]	Huang X, Kurata N, Wei X, et al. A map of rice genome variation reveals the origin of cultivated rice[J]. Nature, 2012,490(7421):497-501. doi: 10.1038/nature11532 URL pmid: 23034647
[40]	Lu G, Wu F Q, Wu W, et al. Rice LTG1 is involved in adaptive growth and fitness under low ambient temperature[J]. Plant J, 2014,78(3):468-480. doi: 10.1111/tpj.12487 URL pmid: 24635058
[41]	Lv Y, Guo Z, Li X, et al. New insights into the genetic basis of natural chilling and cold shock tolerance in rice by genome-wide association analysis[J]. Plant Cell Environ, 2016,39(3):556-570. doi: 10.1111/pce.12635 URL pmid: 26381647
[42]	Shakiba E, Edwards J D, Jodari F, et al. Genetic architecture of cold tolerance in rice (Oryza sativa) determined through high resolution genome-wide analysis[J]. PLoS One, 2017,12(3):e0172133. doi: 10.1371/journal.pone.0172133 URL pmid: 28282385
[43]	Wang D, Liu J, Li C, et al. Genome-wide Association Mapping of Cold Tolerance Genes at the Seedling Stage in Rice[J]. Rice (N Y), 2016,9(1):61.
[44]	Fujino K, Sekiguchi H, Matsuda Y, et al. Molecular identification of a major quantitative trait locus, qLTG3-1, controlling low-temperature germinability in rice[J]. Proc Natl Acad Sci USA, 2008,105(34):12623-12628. doi: 10.1073/pnas.0805303105 URL pmid: 18719107
[45]	Wang X, Zou B, Shao Q, et al. Natural variation reveals that OsSAP16 controls low-temperature germination in rice[J]. J Exp Bot, 2018,69(3):413-421. doi: 10.1093/jxb/erx413 URL pmid: 29237030
[46]	Civan P, Brown T A. Role of genetic introgression during the evolution of cultivated rice (Oryza sativa L.)[J]. BMC Evol Biol, 2018,18:57. doi: 10.1186/s12862-018-1180-7 URL pmid: 29688851
[47]	Wang W, Mauleon R, Hu Z, et al. Genomic variation in 3,010 diverse accessions of Asian cultivated rice[J]. Nature, 2018,557(7703):43-49. URL pmid: 29695866
[48]	Wang P, Yang C, Chen H, et al. Exploring transcription factors reveals crucial members and regulatory networks involved in different abiotic stresses in Brassica napus L.[J]. BMC Plant Biol, 2018,18:202. doi: 10.1186/s12870-018-1417-z URL pmid: 30231862
[49]	E Z G, Zhang Y P, Zhou J H, et al. Mini review roles of the bZIP gene family in rice[J]. Genet Mol Res, 2014,13(2):3025-3036. doi: 10.4238/2014.April.16.11 URL
[50]	Jakoby M, Weisshaar B, Droge-Laser W, et al. bZIP transcription factors in Arabidopsis[J]. Trends Plant Sci, 2002,7(3):106-111. doi: 10.1016/s1360-1385(01)02223-3 URL pmid: 11906833
[51]	Kawahara Y, de la Bastide M, Hamilton J P, et al. Improvement of the Oryza sativa Nipponbare reference genome using next generation sequence and optical map data[J]. Rice (N Y), 2013,6:4.
[52]	Nijhawan A, Jain M, Tyagi A K, et al. Genomic survey and gene expression analysis of the basic leucine zipper transcription factor family in rice[J]. Plant Physiol, 2008,146(2):333-350. doi: 10.1104/pp.107.112821 URL pmid: 18065552
[53]	Sornaraj P, Luang S, Lopato S, et al. Basic leucine zipper (bZIP) transcription factors involved in abiotic stresses: A molecular model of a wheat bZIP factor and implications of its structure in function[J]. Biochim Biophys Acta, 2016,1860(1 Pt A):46-56. doi: 10.1016/j.bbagen.2015.10.014 URL pmid: 26493723
[54]	Liu C, Ou S, Mao B, et al. Early selection of bZIP73 facilitated adaptation of japonica rice to cold climates[J]. Nat Commun, 2018,9:3302. doi: 10.1038/s41467-018-05753-w URL pmid: 30120236
[55]	Zhang Z, Li J, Pan Y, et al. Natural variation in CTB4a enhances rice adaptation to cold habitats[J]. Nat Commun, 2017,8:14788. doi: 10.1038/ncomms14788 URL pmid: 28332574

水稻耐低温研究重要进展

Low Temperature Tolerance of Rice: A Review

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