玉米抗旱性的遗传解析

doi:10.11983/CBB24089

植物学报 ›› 2024, Vol. 59 ›› Issue (6): 883-902.DOI: 10.11983/CBB24089 cstr: 32102.14.CBB24089

所属专题：大食物观；粮食安全

玉米抗旱性的遗传解析

王子阳, 刘升学, 杨志蕊, 秦峰^*()

中国农业大学生物学院, 植物抗逆高效全国重点实验室, 北京 100193

收稿日期:2024-06-07 接受日期:2024-07-23 出版日期:2024-11-10 发布日期:2024-08-01
通讯作者: *秦峰, 2010-2016年在中国科学院植物研究所任研究员, 入选“百人计划”。2016年至今任中国农业大学生物学院教授。主要从事玉米抗旱性的遗传解析与基因克隆研究, 致力于为玉米抗旱性的遗传改良提供基因资源和基因编辑靶点。2014年获“杜邦青年教授奖”; 2015年获“第一届中国作物学会青年科技奖”; 2016年获得国家自然科学基金委“杰出青年”基金资助; 2018年获“卫志明青年创新奖”; 2019年入选“国家特殊支持计划” 科技创新领军人才。研究成果发表在Nature Genetics、Nature Communications、Molecular Plant、Genome Biology和Plant Cell等国际期刊上。目前担任《植物学报》、Plant Journal、Plant Molecular Biology和Molecular Breeding编委。E-mail: qinfeng@cau.edu.cn
基金资助:
国家自然科学基金(32171940);国家自然科学基金(32272024)

Genetic Dissection of Drought Resistance in Maize

Ziyang Wang, Shengxue Liu, Zhirui Yang, Feng Qin^*()

State Key Laboratory of Plant Environmental Resilience, College of Biological Sciences, China Agricultural University, Beijing 100193, China

Received:2024-06-07 Accepted:2024-07-23 Online:2024-11-10 Published:2024-08-01
Contact: *E-mail: qinfeng@cau.edu.cn

摘要/Abstract

摘要： 玉米(Zea mays)是我国第一大粮食作物, 干旱是玉米生长发育过程中主要的非生物胁迫因子, 直接造成玉米产量与品质降低, 甚至威胁粮食安全。目前全球气候变化导致极端天气事件频发, 加剧了对玉米生产的不良影响。因此, 鉴定玉米抗旱种质资源、解析干旱胁迫应答的分子机制和培育抗旱品种至关重要。该文总结了近年来运用全基因组关联分析、数量性状位点基因克隆和多组学联合分析等方法在玉米抗旱性遗传解析方面取得的研究进展, 介绍了玉米抗旱性遗传改良分子设计育种的可能途径, 并对玉米抗旱性遗传解析及改良的发展方向进行了展望。

关键词: 玉米, 抗旱性, 遗传解析, 基因克隆, 遗传改良

Abstract: Maize (Zea mays) is the main crop in China, and drought is a primary abiotic stress during its growth, resulting in direct reduction in grain yield and quality, thereby posing a threat to food security within the global climate context. At present, global climate change leads to extreme weather events, which aggravates the adverse effects on yield. Therefore, it is imperative to identify drought-resistant germplasm resources, elucidate the molecular mechanisms of drought stress response, and breed drought-resistant varieties. Here, we review recent advances in the genetic dissection of drought resistance in maize using methods such as genome-wide association study, quantitative trait locus gene cloning and multi-omics analysis. Additionally, we introduce potential strategies for genetic improvement of drought resistance by leveraging the identified genetic resources while discussing future perspectives within this research area.

Key words: maize, drought resistance, genetic dissection, gene cloning, genetic improvement

王子阳, 刘升学, 杨志蕊, 秦峰. 玉米抗旱性的遗传解析. 植物学报, 2024, 59(6): 883-902.

Ziyang Wang, Shengxue Liu, Zhirui Yang, Feng Qin. Genetic Dissection of Drought Resistance in Maize. Chinese Bulletin of Botany, 2024, 59(6): 883-902.

导出引用管理器 EndNote|Ris|BibTeX

链接本文: https://www.chinbullbotany.com/CN/10.11983/CBB24089

https://www.chinbullbotany.com/CN/Y2024/V59/I6/883

图/表 3

参考文献 123

[1]	高冠龙, 冯起, 张小由, 司建华, 鱼腾飞 (2018). 植物叶片光合作用的气孔与非气孔限制研究综述. 干旱区研究 35, 929-937. DOI
[2]	高辉, 张红芳, 袁思安, 李小婷 (2013). 植物内源激素对干旱胁迫的响应研究. 绿色科技 (11), 5-7.
[3]	高世斌, 冯质雷, 李晚忱, 荣廷昭 (2005). 干旱胁迫下玉米根系性状和产量的QTLs分析. 作物学报 31, 718-722.
[4]	国家统计局 (2023). 中国统计摘要-2023. 北京: 中国统计出版社. pp. 1-212.
[5]	郭莹, 化青春, 虎梦霞, 王勇, 袁俊秀, 杨芳萍 (2023). 分子标记辅助选择在作物育种中的应用及展望. 寒旱农业科学 2, 785-790.
[6]	金锐, 张从合, 朱全贵, 苏法 (2021). 分子标记辅助选择在玉米抗病和抗虫育种上的应用. 安徽农业科学 49(16), 10-15.
[7]	宋博研, 朱卫国 (2011). 组蛋白甲基化修饰效应分子的研究进展. 遗传 33, 285-292.
[8]	宋凤斌, 戴俊英 (2004). 干旱胁迫对玉米花粉和花丝表面超微结构及两者活力的影响. 吉林农业大学学报 26, 1-5.
[9]	尹立林, 马云龙, 项韬, 朱猛进, 余梅, 李新云, 刘小磊, 赵书红 (2019). 全基因组选择模型研究进展及展望. 畜牧兽医学报 50, 233-242.
[10]	赵坤 (2019). 我国玉米生产现状及发展趋势. 新农业 (12), 49.
[11]	周文期, 刘忠祥, 王晓娟, 何海军, 周玉乾, 杨彦忠, 连晓荣, 李永生 (2022). 利用BSA-Seq方法快速定位作物农艺性状QTL/基因概述. 甘肃农业科技 53(4), 1-10.
[12]	周文期, 周玉乾, 李永生, 何海军, 杨彦忠, 王晓娟, 连晓荣, 刘忠祥, 胡筑兵 (2023). 玉米ZmICE2基因调控气孔发育. 植物学报 58, 866-881. DOI
[13]	Apel K, Hirt H (2004). Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol 55, 373-399. PMID
[14]	Armstrong F, Leung J, Grabov A, Brearley J, Giraudat J, Blatt MR (1995). Sensitivity to abscisic acid of guard-cell K⁺ channels is suppressed by abi1-1, a mutant Arabidopsis gene encoding a putative protein phosphatase. Proc Natl Acad Sci USA 92, 9520-9524. PMID
[15]	Blankenagel S, Eggels S, Frey M, Grill E, Bauer E, Dawid C, Fernie AR, Haberer G, Hammerl R, Barbosa Medeiros D, Ouzunova M, Presterl T, Ruß V, Schäufele R, Schlüter U, Tardieu F, Urbany C, Urzinger S, Weber APM, Schön CC, Avramova V (2022). Natural alleles of the abscisic acid catabolism gene ZmAbh4 modulate water use efficiency and carbon isotope discrimination in maize. Plant Cell 34, 3860-3872.
[16]	Brugière N, Zhang WJ, Xu QZ, Scolaro EJ, Lu C, Kahsay RY, Kise R, Trecker L, Williams RW, Hakimi S, Niu XP, Lafitte R, Habben JE (2017). Overexpression of RING domain E3 ligase ZmXerico1 confers drought tolerance through regulation of ABA homeostasis. Plant Physiol 175, 1350-1369. DOI PMID
[17]	Caine RS, Yin XJ, Sloan J, Harrison EL, Mohammed U, Fulton T, Biswal AK, Dionora J, Chater CC, Coe RA, Bandyopadhyay A, Murchie EH, Swarup R, Quick WP, Gray JE (2019). Rice with reduced stomatal density conserves water and has improved drought tolerance under future climate conditions. New Phytol 221, 371-384. DOI PMID
[18]	Cao LR, Ma CC, Ye FY, Pang YY, Wang GR, Fahim AM, Lu XM (2023). Genome-wide identification of NF-Y gene family in maize (Zea mays L.) and the positive role of ZmNF-YC12 in drought resistance and recovery ability. Front Plant Sci 14, 1159955.
[19]	Castorina G, Domergue F, Chiara M, Zilio M, Persico M, Ricciardi V, Horner DS, Consonni G (2020). Drought- responsive ZmFDL1/MYB94 regulates cuticle biosynthesis and cuticle-dependent leaf permeability. Plant Physiol 184, 266-282. DOI PMID
[20]	de Carvalho MHC (2008). Drought stress and reactive oxygen species: production, scavenging and signaling. Plant Signal Behav 3, 156-165. DOI PMID
[21]	Doudna JA, Charpentier E (2014). Genome editing. The new frontier of genome engineering with CRISPR-Cas9. Science 346, 1258096.
[22]	Du LY, Huang XL, Ding L, Wang ZX, Tang DL, Chen B, Ao LJY, Liu YL, Kang ZS, Mao HD (2023). TaERF87 and TaAKS1 synergistically regulate TaP5CS1/TaP5CR1-mediated proline biosynthesis to enhance drought tolerance in wheat. New Phytol 237, 232-250.
[23]	Feng XJ, Jia L, Cai YT, Guan HR, Zheng D, Zhang WX, Xiong H, Zhou HM, Wen Y, Hu Y, Zhang XM, Wang QJ, Wu FK, Xu J, Lu YL (2022). ABA-inducible DEEPER ROOTING 1 improves adaptation of maize to water deficiency. Plant Biotechnol J 20, 2077-2088.
[24]	Flint-Garcia SA, Thornsberry JM, Buckler ES (2003). Structure of linkage disequilibrium in plants. Annu Rev Plant Biol 54, 357-374. PMID
[25]	Fujii H, Chinnusamy V, Rodrigues A, Rubio S, Antoni R, Park SY, Cutler SR, Sheen J, Rodriguez PL, Zhu JK (2009). In vitro reconstitution of an abscisic acid signaling pathway. Nature 462, 660-664.
[26]	Gaffney J, Schussler J, Löffler C, Cai WG, Paszkiewicz S, Messina C, Groeteke J, Keaschall J, Cooper M (2015). Industry-scale evaluation of maize hybrids selected for increased yield in drought-stress conditions of the US corn belt. Crop Sci 55, 1608-1618.
[27]	Gao HJ, Cui JJ, Liu SX, Wang SH, Lian YY, Bai YT, Zhu TF, Wu HH, Wang YJ, Yang SP, Li XF, Zhuang JH, Chen LM, Gong ZZ, Qin F (2022). Natural variations of ZmSRO1d modulate the trade-off between drought resistance and yield by affecting ZmRBOHC-mediated stomatal ROS production in maize. Mol Plant 15, 1558-1574.
[28]	Gill SS, Tuteja N (2010). Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48, 909-930.
[29]	Gulzar F, Fu JY, Zhu CY, Yan J, Li XL, Meraj TA, Shen QQ, Hassan B, Wang Q (2021). Maize WRKY transcription factor ZmWRKY79 positively regulates drought tolerance through elevating ABA biosynthesis. Int J Mol Sci 22, 10080.
[30]	Guo YZ, Shi YB, Wang YL, Liu F, Li Z, Qi JS, Wang Y, Zhang JB, Yang SH, Wang Y, Gong ZZ (2023). The clade F PP2C phosphatase ZmPP84 negatively regulates drought tolerance by repressing stomatal closure in maize. New Phytol 237, 1728-1744.
[31]	Gupta A, Rico-Medina A, Caño-Delgado AI (2020). The physiology of plant responses to drought. Science 368, 266-269. DOI PMID
[32]	Gusev A, Ko A, Shi H, Bhatia G, Chung W, Penninx BW, Jansen R, de Geus EJ, Boomsma DI, Wright FA, Sullivan PF, Nikkola E, Alvarez M, Civelek M, Lusis AJ, Lehtimäki T, Raitoharju E, Kähönen M, Seppälä I, Raitakari OT, Kuusisto J, Laakso M, Price AL, Pajukanta P, Pasaniuc B (2016). Integrative approaches for large-scale transcriptome-wide association studies. Nat Genet 48, 245-252. DOI PMID
[33]	He ZH, Zhong JW, Sun XP, Wang BC, Terzaghi W, Dai MQ (2018). The maize ABA receptors ZmPYL8, 9, and 12 facilitate plant drought resistance. Front Plant Sci 9, 422. DOI PMID
[34]	Heffner EL, Sorrells ME, Jannink JL (2009). Genomic selection for crop improvement. Crop Sci 49, 1-12.
[35]	Hetherington AM, Woodward FI (2003). The role of stomata in sensing and driving environmental change. Nature 424, 901-908.
[36]	Hou X, Xie KB, Yao JL, Qi ZY, Xiong LZ (2009). A homolog of human ski-interacting protein in rice positively regulates cell viability and stress tolerance. Proc Natl Acad Sci USA 106, 6410-6415. DOI PMID
[37]	Huang WZ, Ma XR, Wang QL, Gao YF, Xue Y, Niu XL, Yu GR, Liu YS (2008). Significant improvement of stress tolerance in tobacco plants by overexpressing a stress- responsive aldehyde dehydrogenase gene from maize (Zea mays). Plant Mol Biol 68, 451-463.
[38]	Jiang SS, Zhang D, Wang L, Pan JW, Liu Y, Kong XP, Zhou Y, Li DQ (2013). A maize calcium-dependent protein kinase gene, ZmCPK4, positively regulated abscisic acid signaling and enhanced drought stress tolerance in transgenic Arabidopsis. Plant Physiol Biochem 71, 112-120.
[39]	Jiao P, Jiang ZZ, Miao M, Wei XT, Wang CL, Liu SY, Guan SY, Ma YY (2024). Zmhdz9, an HD-Zip transcription factor, promotes drought stress resistance in maize by modulating ABA and lignin accumulation. Int J Biol Macromol 258, 128849.
[40]	Kazan K, Manners JM (2013). MYC2: the master in action. Mol Plant 6, 686-703. DOI PMID
[41]	Kim TH, Böhmer M, Hu HH, Nishimura N, Schroeder JI (2010). Guard cell signal transduction network: advances in understanding abscisic acid, CO₂, and Ca²⁺ signaling. Annu Rev Plant Biol 61, 561-591.
[42]	Kooyers NJ (2015). The evolution of drought escape and avoidance in natural herbaceous populations. Plant Sci 234, 155-162. DOI PMID
[43]	Kramp RE, Liancourt P, Herberich MM, Saul L, Weides S, Tielbörger K, Májeková M (2022). Functional traits and their plasticity shift from tolerant to avoidant under extreme drought. Ecology 103, e3826.
[44]	Krannich CT, Maletzki L, Kurowsky C, Horn R (2015). Network candidate genes in breeding for drought tolerant crops. Int J Mol Sci 16, 16378-16400. DOI PMID
[45]	Lebaudy A, Pascaud F, Véry AA, Alcon C, Dreyer I, Thibaud JB, Lacombe B (2010). Preferential KAT1-KAT2 heteromerization determines inward K⁺ current properties in Arabidopsis guard cells. J Biol Chem 285, 6265-6274. DOI PMID
[46]	Li CH, Guo J, Wang DM, Chen XJ, Guan HH, Li YX, Zhang DF, Liu XY, He GH, Wang TY, Li Y (2023). Genomic insight into changes of root architecture under drought stress in maize. Plant Cell Environ 46, 1860-1872.
[47]	Li DL, Liu Q, Schnable PS (2021a). TWAS results are complementary to and less affected by linkage disequilibrium than GWAS. Plant Physiol 186, 1800-1811.
[48]	Li DX, Wang MW, Zhang TP, Chen X, Li CY, Liu Y, Brestic M, Chen THH, Yang XH (2021b). Glycinebetaine mitigated the photoinhibition of photosystem II at high temperature in transgenic tomato plants. Photosynth Res 147, 301-315.
[49]	Li L, Du YC, He C, Dietrich CR, Li JK, Ma XL, Wang R, Liu Q, Liu SZ, Wang GY, Schnable PS, Zheng J (2019a). Maize glossy6 is involved in cuticular wax deposition and drought tolerance. J Exp Bot 70, 3089-3099.
[50]	Li ZX, Liu C, Zhang Y, Wang BM, Ran QJ, Zhang JR (2019b). The bHLH family member ZmPTF1 regulates drought tolerance in maize by promoting root development and abscisic acid synthesis. J Exp Bot 70, 5471-5486.
[51]	Liang YN, Jiang YL, Du M, Li BY, Chen L, Chen MC, Jin DM, Wu JD (2019). ZmASR3 from the maize ASR gene family positively regulates drought tolerance in transgenic Arabidopsis. Int J Mol Sci 20, 2278.
[52]	Liu BX, Zhang B, Yang ZR, Liu Y, Yang SP, Shi YL, Jiang CF, Qin F (2021a). Manipulating ZmEXPA4 expression ameliorates the drought-induced prolonged anthesis and silking interval in maize. Plant Cell 33, 2058-2071.
[53]	Liu L, Gallagher J, Arevalo ED, Chen R, Skopelitis T, Wu QY, Bartlett M, Jackson D (2021b). Enhancing grain- yield-related traits by CRISPR-Cas9 promoter editing of maize CLE genes. Nat Plants 7, 287-294.
[54]	Liu SX, Li CP, Wang HW, Wang SH, Yang SP, Liu XH, Yan JB, Li BL, Beatty M, Zastrow-Hayes G, Song SH, Qin F (2020). Mapping regulatory variants controlling gene expression in drought response and tolerance in maize. Genome Biol 21, 163. DOI PMID
[55]	Liu SX, Liu XH, Zhang XM, Chang SJ, Ma C, Qin F (2022). Co-expression of ZmVPP1 with ZmNAC111 confers robust drought resistance in maize. Genes (Basel) 14, 8.
[56]	Liu YQ, Li AQ, Liang MN, Zhang Q, Wu JD (2023). Overexpression of the maize genes ZmSKL1 and ZmSKL2 positively regulates drought stress tolerance in transgenic Arabidopsis. Plant Cell Rep 42, 521-533.
[57]	Lu FZ, Li WC, Peng YL, Cao Y, Qu JT, Sun FA, Yang QQ, Lu YL, Zhang XH, Zheng LJ, Fu FL, Yu HQ (2022). ZmPP2C26 alternative splicing variants negatively regulate drought tolerance in maize. Front Plant Sci 13, 85-1531.
[58]	Lu HF, Lin T, Klein J, Wang SH, Qi JJ, Zhou Q, Sun JJ, Zhang ZH, Weng YQ, Huang SW (2014). QTL-seq identifies an early flowering QTL located near Flowering Locus T in cucumber. Theor Appl Genet 127, 1491-1499.
[59]	Lynch J (1995). Root architecture and plant productivity. Plant Physiol 109, 7-13. DOI PMID
[60]	Ma HZ, Liu C, Li ZX, Ran QJ, Xie GN, Wang BM, Fang S, Chu JF, Zhang JR (2018). ZmbZIP4 contributes to stress resistance in maize by regulating ABA synthesis and root development. Plant Physiol 178, 753-770. DOI PMID
[61]	Ma Y, Szostkiewicz I, Korte A, Moes D, Yang Y, Christmann A, Grill E (2009). Regulators of PP2C phosphatase activity function as abscisic acid sensors. Science 324, 1064-1068. DOI PMID
[62]	Mao HD, Wang HW, Liu SX, Li ZG, Yang XH, Yan JB, Li JS, Tran LSP, Qin F (2015). A transposable element in a NAC gene is associated with drought tolerance in maize seedlings. Nat Commun 6, 8326.
[63]	Massman JM, Gordillo A, Lorenzana RE, Bernardo R (2013). Genomewide predictions from maize single-cross data. Theor Appl Genet 126, 13-22. DOI PMID
[64]	Mei FM, Chen B, Du LY, Li SM, Zhu DH, Chen N, Zhang YF, Li FF, Wang ZX, Cheng XX, Ding L, Kang ZS, Mao HD (2022). A gain-of-function allele of a DREB transcription factor gene ameliorates drought tolerance in wheat. Plant Cell 34, 4472-4494.
[65]	Miao ZY, Zhang T, Qi YH, Song J, Han ZX, Ma C (2020). Evolution of the RNA N⁶-methyladenosine methylome mediated by genomic duplication. Plant Physiol 182, 345-360.
[66]	Mittler R, Vanderauwera S, Suzuki N, Miller G, Tognetti VB, Vandepoele K, Gollery M, Shulaev V, Van Breusegem F (2011). ROS signaling: the new wave? Trends Plant Sci 16, 300-309. DOI PMID
[67]	Nakaya A, Isobe SN (2012). Will genomic selection be a practical method for plant breeding? Ann Bot 110, 1303-1316.
[68]	Nelson DE, Repetti PP, Adams TR, Creelman RA, Wu JR, Warner DC, Anstrom DC, Bensen RJ, Castiglioni PP, Donnarummo MG, Hinchey BS, Kumimoto RW, Maszle DR, Canales RD, Krolikowski KA, Dotson SB, Gutterson N, Ratcliffe OJ, Heard JE (2007). Plant nuclear factor Y (NF-Y) B subunits confer drought tolerance and lead to improved corn yields on water-limited acres. Proc Natl Acad Sci USA 104, 16450-16455. DOI PMID
[69]	Nemali KS, Bonin C, Dohleman FG, Stephens M, Reeves WR, Nelson DE, Castiglioni P, Whitsel JE, Sammons B, Silady RA, Anstrom D, Sharp RE, Patharkar OR, Clay D, Coffin M, Nemeth MA, Leibman ME, Luethy M, Lawson M (2015). Physiological responses related to increased grain yield under drought in the first biotechnology-derived drought-tolerant maize. Plant Cell Environ 38, 1866-1880.
[70]	Nica AC, Dermitzakis ET (2013). Expression quantitative trait loci: present and future. Philos Trans R Soc Lond B Biol Sci 368, 20120362.
[71]	Nuccio ML, Wu J, Mowers R, Zhou HP, Meghji M, Primavesi LF, Paul MJ, Chen X, Gao Y, Haque E, Basu SS, Lagrimini LM (2015). Expression of trehalose- 6-phosphate phosphatase in maize ears improves yield in well-watered and drought conditions. Nat Biotechnol 33, 862-869.
[72]	Ogura T, Goeschl C, Filiault D, Mirea M, Slovak R, Wolhrab B, Satbhai SB, Busch W (2019). Root system depth in Arabidopsis is shaped by EXOCYST70A3 via the dynamic modulation of auxin transport. Cell 178, 400-412.
[73]	Pan ZY, Liu M, Zhao HL, Tan ZD, Liang K, Sun Q, Gong DM, He HJ, Zhou WQ, Qiu FZ (2020). ZmSRL5 is involved in drought tolerance by maintaining cuticular wax structure in maize. J Integr Plant Biol 62, 1895-1909.
[74]	Park SY, Fung P, Nishimura N, Jensen DR, Fujii H, Zhao Y, Lumba S, Santiago J, Rodrigues A, Chow TFF, Alfred SE, Bonetta D, Finkelstein R, Provart NJ, Desveaux D, Rodriguez PL, McCourt P, Zhu JK, Schroeder JI, Volkman BF, Cutler SR (2009). Abscisic acid inhibits type 2C protein phosphatases via the PYR/PYL family of START proteins. Science 324, 1068-1071.
[75]	Pourghayoumi M, Bakhshi D, Rahemi M, Kamgar- Haghighi AA, Aalami A (2017). The physiological responses of various pomegranate cultivars to drought stress and recovery in order to screen for drought tolerance. Sci Hortic 217, 164-172.
[76]	Qi JS, Song CP, Wang BS, Zhou JM, Kangasjärvi J, Zhu JK, Gong ZZ (2018). Reactive oxygen species signaling and stomatal movement in plant responses to drought stress and pathogen attack. J Integr Plant Biol 60, 805-826. DOI
[77]	Qin LM, Sun L, Wei L, Yuan JR, Kong FF, Zhang Y, Miao X, Xia GM, Liu SW (2021). Maize SRO1e represses anthocyanin synthesis through regulating the MBW complex in response to abiotic stress. Plant J 105, 1010-1025.
[78]	Reguera M, Peleg Z, Blumwald E (2012). Targeting metabolic pathways for genetic engineering abiotic stress-tolerance in crops. Biochim Biophys Acta 1819, 186-194. DOI PMID
[79]	Ren W, Zhao LF, Liang JX, Wang LF, Chen LM, Li PC, Liu ZG, Li XJ, Zhang ZH, Li JP, He KH, Zhao Z, Ali F, Mi GH, Yan JB, Zhang FS, Chen FJ, Yuan LX, Pan QC (2022). Genome-wide dissection of changes in maize root system architecture during modern breeding. Nat Plants 8, 1408-1422. DOI PMID
[80]	Ribaut JM, Ragot M (2007). Marker-assisted selection to improve drought adaptation in maize: the backcross approach, perspectives, limitations, and alternatives. J Exp Bot 58, 351-360.
[81]	Schneider KA, Brothers ME, Kelly JD (1997). Marker- assisted selection to improve drought resistance in common bean. Crop Sci 37, 51-60.
[82]	Shavrukov Y, Kurishbayev A, Jatayev S, Shvidchenko V, Zotova L, Koekemoer F, de Groot S, Soole K, Langridge P (2017). Early flowering as a drought escape mechanism in plants: how can it aid wheat production? Front Plant Sci 8, 1950. DOI PMID
[83]	Shi JR, Gao HR, Wang HY, Lafitte HR, Archibald RL, Yang MZ, Hakimi SM, Mo H, Habben JE (2017). ARGOS8 variants generated by CRISPR-Cas9 improve maize grain yield under field drought stress conditions. Plant Biotechnol J 15, 207-216. DOI PMID
[84]	Singh D, Laxmi A (2015). Transcriptional regulation of drought response: a tortuous network of transcriptional factors. Front Plant Sci 6, 895. DOI PMID
[85]	Soma F, Takahashi F, Suzuki T, Shinozaki K, Yamaguchi-Shinozaki K (2020). Plant Raf-like kinases regulate the mRNA population upstream of ABA-unresponsive SnRK2 kinases under drought stress. Nat Commun 11, 1373. DOI PMID
[86]	Sun XP, Xiang YL, Dou NN, Zhang H, Pei SR, Franco AV, Menon M, Monier B, Ferebee T, Liu T, Liu SY, Gao YC, Wang JB, Terzaghi W, Yan JB, Hearne S, Li L, Li F, Dai MQ (2023). The role of transposon inverted repeats in balancing drought tolerance and yield-related traits in maize. Nat Biotechnol 41, 120-127.
[87]	Takagi H, Abe A, Yoshida K, Kosugi S, Natsume S, Mitsuoka C, Uemura A, Utsushi H, Tamiru M, Takuno S, Innan H, Cano LM, Kamoun S, Terauchi R (2013). QTL-seq: rapid mapping of quantitative trait loci in rice by whole genome resequencing of DNA from two bulked populations. Plant J 74, 174-183.
[88]	Tang Q, Lv HZ, Li QM, Zhang XY, Li L, Xu J, Wu FK, Wang QJ, Feng XJ, Lu YL (2022). Characteristics of microRNAs and target genes in maize root under drought stress. Int J Mol Sci 23, 4968.
[89]	Tian T, Wang SH, Yang SP, Yang ZR, Liu SX, Wang YJ, Gao HJ, Zhang SS, Yang XH, Jiang CF, Qin F (2023). Genome assembly and genetic dissection of a prominent drought-resistant maize germplasm. Nat Genet 55, 496-506. DOI PMID
[90]	Uga Y, Sugimoto K, Ogawa S, Rane J, Ishitani M, Hara N, Kitomi Y, Inukai Y, Ono K, Kanno N, Inoue H, Takehisa H, Motoyama R, Nagamura Y, Wu JZ, Matsumoto T, Takai T, Okuno K, Yano M (2013). Control of root system architecture by DEEPER ROOTING 1 increases rice yield under drought conditions. Nat Genet 45, 1097-1102.
[91]	Van Dooren TJM, Silveira AB, Gilbault E, Jiménez-Gómez JM, Martin A, Bach L, Tisné S, Quadrana L, Loudet O, Colot V (2020). Mild drought in the vegetative stage induces phenotypic, gene expression, and DNA methylation plasticity in Arabidopsis but no transgenerational effects. J Exp Bot 71, 3588-3602. DOI PMID
[92]	Virlouvet L, Jacquemot MP, Gerentes D, Corti H, Bouton S, Gilard F, Valot B, Trouverie J, Tcherkez G, Falque M, Damerval C, Rogowsky P, Perez P, Noctor G, Zivy M, Coursol S (2011). The ZmASR1 protein influences branched-chain amino acid biosynthesis and maintains kernel yield in maize under water-limited conditions. Plant Physiol 157, 917-936. DOI PMID
[93]	Wainberg M, Sinnott-Armstrong N, Mancuso N, Barbeira AN, Knowles DA, Golan D, Ermel R, Ruusalepp A, Quertermous T, Hao K, Björkegren JLM, Im HK, Pa-saniuc B, Rivas MA, Kundaje A (2019). Opportunities and challenges for transcriptome-wide association stu-dies. Nat Genet 51, 592-599. DOI PMID
[94]	Wan LY, Zhang JF, Zhang HW, Zhang ZJ, Quan RD, Zhou SR, Huang RF (2011). Transcriptional activation of OsDERF1 in OsERF3 and OsAP2-39 negatively modulates ethylene synthesis and drought tolerance in rice. PLoS One 6, e25216.
[95]	Wang BM, Li ZX, Ran QJ, Li P, Peng ZH, Zhang JR (2018a). ZmNF-YB16 overexpression improves drought resistance and yield by enhancing photosynthesis and the antioxidant capacity of maize plants. Front Plant Sci 9, 709.
[96]	Wang CT, Ru JN, Liu YW, Li M, Zhao D, Yang JF, Fu JD, Xu ZS (2018b). Maize WRKY transcription factor ZmWRKY106 confers drought and heat tolerance in transgenic plants. Int J Mol Sci 19, 3046.
[97]	Wang CT, Ru JN, Liu YW, Yang JF, Li M, Xu ZS, Fu JD (2018c). The maize WRKY transcription factor ZmWRKY40 confers drought resistance in transgenic Arabidopsis. Int J Mol Sci 19, 2580.
[98]	Wang N, Cheng M, Chen Y, Liu BJ, Wang XN, Li GJ, Zhou YH, Luo P, Xi ZY, Yong HJ, Zhang DG, Li MS, Zhang XC, Vicente FS, Hao ZF, Li XH (2021). Natural variations in the non-coding region of ZmNAC080308 contributes maintaining grain yield under drought stress in maize. BMC Plant Biol 21, 305. DOI PMID
[99]	Wang XL, Wang HW, Liu SX, Ferjani A, Li JS, Yan JB, Yang XH, Qin F (2016). Genetic variation in ZmVPP1 contributes to drought tolerance in maize seedlings. Nat Genet 48, 1233-1241.
[100]	Wang YG, Fu FL, Yu HQ, Hu T, Zhang YY, Tao Y, Zhu JK, Zhao Y, Li WC (2018d). Interaction network of core ABA signaling components in maize. Plant Mol Biol 96, 245-263.
[101]	Wen WW, Li D, Li X, Gao YQ, Li WQ, Li HH, Liu J, Liu HJ, Chen W, Luo J, Yan JB (2014). Metabolome-based genome-wide association study of maize kernel leads to novel biochemical insights. Nat Commun 5, 3438. DOI PMID
[102]	Wu JD, Jiang YL, Liang YN, Chen L, Chen WJ, Cheng BJ (2019). Expression of the maize MYB transcription factor ZmMYB3R enhances drought and salt stress tolerance in transgenic plants. Plant Physiol Biochem 137, 179-188.
[103]	Wu X, Feng H, Wu D, Yan SJ, Zhang P, Wang WB, Zhang J, Ye JL, Dai GX, Fan Y, Li WK, Song BX, Geng ZD, Yang WL, Chen GX, Qin F, Terzaghi W, Stitzer M, Li L, Xiong LZ, Yan JB, Buckler E, Yang WN, Dai MQ (2021). Using high-throughput multiple optical phenotyping to decipher the genetic architecture of maize drought tolerance. Genome Biol 22, 185. DOI PMID
[104]	Xia ZL, Liu QJ, Wu JY, Ding JQ (2012). ZmRFP1, the putative ortholog of SDIR1, encodes a RING-H2 E3 ubiquitin ligase and responds to drought stress in an ABA-dependent manner in maize. Gene 495, 146-153. DOI PMID
[105]	Xiang YL, Sun XP, Gao S, Qin F, Dai MQ (2017). Deletion of an endoplasmic reticulum stress response element in a ZmPP2C-A gene facilitates drought tolerance of maize seedlings. Mol Plant 10, 456-469. DOI PMID
[106]	Xu HX, Cao YW, Xu YF, Ma PT, Ma FF, Song LP, Li LH, An DG (2017). Marker-assisted development and evaluation of near-isogenic lines for broad-spectrum powdery mildew resistance gene Pm2b introgressed into different genetic backgrounds of wheat. Front Plant Sci 8, 1322.
[107]	Xu YB, Lu YL, Xie CX, Gao SB, Wan JM, Prasanna BM (2012). Whole-genome strategies for marker-assisted plant breeding. Mol Breed 29, 833-854.
[108]	Yang Y, Shi JX, Chen LM, Xiao WH, Yu JJ (2022a). ZmEREB46, a maize ortholog of Arabidopsis WAX INDUCER1/SHINE1, is involved in the biosynthesis of leaf epicuticular very-long-chain waxes and drought tolerance. Plant Sci 321, 111256.
[109]	Yang YL, Wang BM, Wang JM, He CM, Zhang DF, Li P, Zhang JR, Li ZX (2022b). Transcription factors ZmNF- YA1 and ZmNF-YB16 regulate plant growth and drought tolerance in maize. Plant Physiol 190, 1506-1525.
[110]	Young TE, Meeley RB, Gallie DR (2004). ACC synthase expression regulates leaf performance and drought tolerance in maize. Plant J 40, 813-825. PMID
[111]	Yu J, Xu F, Wei ZW, Zhang XX, Chen T, Pu L (2020). Epigenomic landscape and epigenetic regulation in maize. Theor Appl Genet 133, 1467-1489. DOI PMID
[112]	Yu P, Li CH, Li M, He XM, Wang DN, Li HJ, Marcon C, Li Y, Perez-Limón S, Chen XP, Delgado-Baquerizo M, Koller R, Metzner R, van Dusschoten D, Pflugfelder D, Borisjuk L, Plutenko I, Mahon A, Resende MFR, Salvi S, Akale A, Abdalla M, Ahmed MA, Bauer FM, Schnepf A, Lobet G, Heymans A, Suresh K, Schreiber L, McLaughlin CM, Li CJ, Mayer M, Schön CC, Bernau V, von Wirén N, Sawers RJH, Wang TY, Hochholdinger F (2024). Seedling root system adaptation to water availability during maize domestication and global expansion. Nat Genet 56, 1245-1256.
[113]	Zhang C, Yang RJ, Zhang TT, Zheng DY, Li XL, Zhang ZB, Li LG, Wu ZY (2023a). ZmTIFY16, a novel maize TIFY transcription factor gene, promotes root growth and development and enhances drought and salt tolerance in Arabidopsis and Zea mays. Plant Growth Regul 100, 149-160.
[114]	Zhang F, Wu JF, Sade N, Wu S, Egbaria A, Fernie AR, Yan JB, Qin F, Chen W, Brotman Y, Dai MQ (2021). Genomic basis underlying the metabolome-mediated drought adaptation of maize. Genome Biol 22, 260. DOI PMID
[115]	Zhang H, Xiang YL, He N, Liu XG, Liu HB, Fang LP, Zhang F, Sun XP, Zhang DL, Li XW, Terzaghi W, Yan JB, Dai MQ (2020a). Enhanced vitamin C production mediated by an ABA-induced PTP-like nucleotidase improves plant drought tolerance in Arabidopsis and maize. Mol Plant 13, 760-776.
[116]	Zhang K, Xue M, Qin F, He Y, Zhou YY (2023b). Natural polymorphisms in ZmIRX15A affect water-use efficiency by modulating stomatal density in maize. Plant Biotechnol J 21, 2560-2573.
[117]	Zhang M, Chen YH, Xing HY, Ke WS, Shi YL, Sui Z, Xu RB, Gao LL, Guo GG, Li JS, Xing JW, Zhang YR (2023c). Positional cloning and characterization reveal the role of a miRNA precursor gene ZmLRT in the regulation of lateral root number and drought tolerance in maize. J Integr Plant Biol 65, 772-790.
[118]	Zhang W, Han ZX, Guo QL, Liu Y, Zheng YX, Wu FL, Jin WB (2014). Identification of maize long non-coding RNAs responsive to drought stress. PLoS One 9, e98958.
[119]	Zhang XM, Mi Y, Mao HD, Liu SX, Chen LM, Qin F (2020b). Genetic variation in ZmTIP1 contributes to root hair elongation and drought tolerance in maize. Plant Biotechnol J 18, 1271-1283.
[120]	Zhao Y, Ma Q, Jin XL, Peng XJ, Liu JY, Deng L, Yan HW, Sheng L, Jiang HY, Cheng BJ (2014). A novel maize homeodomain-leucine zipper (HD-Zip) I gene, Zmhdz10, positively regulates drought and salt tolerance in both rice and Arabidopsis. Plant Cell Physiol 55, 1142-1156.
[121]	Zhao YS, Zeng J, Fernando R, Reif JC (2013). Genomic prediction of hybrid wheat performance. Crop Sci 53, 802-810.
[122]	Zhu JK (2002). Salt and drought stress signal transduction in plants. Annu Rev Plant Biol 53, 247-273.
[123]	Zhu YQ, Liu Y, Zhou KM, Tian CY, Aslam M, Zhang BL, Liu WJ, Zou HW (2022). Overexpression of ZmEREBP60 enhances drought tolerance in maize. J Plant Physiol 275, 153763.

抗旱基因	基因功能	参考文献
ABH4	编码脱落酸8'-羟化酶, 调控脱落酸的水平	Blankenagel et al., 2022
ACS6	编码ACC合酶	Young et al., 2004
ALDH22A1	编码醛脱氢酶	Huang et al., 2008
ARGOS8	乙烯反应的负调控因子	Shi et al., 2017
ASR1	调控支链氨基酸的生物合成	Virlouvet et al., 2011
ALKBH10	编码m⁶A脱甲基酶	Miao et al., 2020
bZIP4	促进侧根数量增加和主根伸长	Ma et al., 2018
CIPK3	提高干旱胁迫下种子根的长度	Li et al., 2023
cPGM2	编码磷酸葡萄糖变位酶, 参与糖代谢	Wu et al., 2021
CPK4	参与钙信号转导及脱落酸介导的气孔关闭	Jiang et al., 2013
DRESH8	产生siRNA, 调控干旱应答和种子大小基因的表达	Sun et al., 2023
DRO1	根尖向重力性和根系构型	Feng et al., 2022
EREB46	叶片表皮蜡质积累	Yang et al., 2022a
EXPA4	促进雌穂生长, 减小干旱诱导产生的散粉和吐丝时间间隔	Liu et al., 2021a
FAB1A	编码1-磷脂酰肌醇-4-磷酸-5-激酶, 参与磷酸肌醇代谢	Wu et al., 2021
GLK44	调控玉米的色氨酸合成	Zhang et al., 2021
IRX15A	负调控叶片的气孔密度	Zhang et al., 2023b
LRT	抑制玉米侧根的起始和伸长	Zhang et al., 2023c
NAC111	调控气孔关闭, 提高水分利用效率	Mao et al., 2015
NF-YA1	茉莉酸信号转导、组蛋白修饰和染色质重塑	Yang et al., 2022b
PP2C26	负调控脱落酸信号转导	Lu et al., 2022
PP84	抑制气孔关闭	Guo et al., 2023
PTF1	促进根系发育和脱落酸合成	Li et al., 2019b
PTPN	编码新型核苷酸酶	Zhang et al., 2020a
RBOHC	编码NADPH氧化酶	Gao et al., 2022
RFP1	编码E3连接酶	Xia et al., 2012
Rtn16	编码网状蛋白, 增强液泡H⁺-ATPase活性	Tian et al., 2023
SKL1/2	减少干旱下活性氧(reactive oxygen species, ROS)的积累	Liu et al., 2023
SRL5	参与角质层蜡质结构的形成	Pan et al., 2020
SRO1d	提高气孔的ROS含量, 促进气孔关闭	Gao et al., 2022
TIFY16	与茉莉酸信号途径的MYC2互作	Zhang et al., 2023a
TIP1	编码S-酰基转移酶, 促进根毛伸长	Zhang et al., 2020b
VPP1	编码质膜H⁺-ATPase, 促进根系发育	Wang et al., 2016
WRKY106	增强抗氧化相关酶活性, 降低ROS含量	Wang et al., 2018b
WRKY40	增强抗氧化相关酶活性, 降低ROS含量	Wang et al., 2018c
WRKY79	促进脱落酸的生物合成	Gulzar et al., 2021
Xerico1	调控脱落酸的代谢稳态	Brugière et al., 2017

抗旱基因	基因功能	参考文献
ABH4	编码脱落酸8'-羟化酶, 调控脱落酸的水平	Blankenagel et al., 2022
ACS6	编码ACC合酶	Young et al., 2004
ALDH22A1	编码醛脱氢酶	Huang et al., 2008
ARGOS8	乙烯反应的负调控因子	Shi et al., 2017
ASR1	调控支链氨基酸的生物合成	Virlouvet et al., 2011
ALKBH10	编码m⁶A脱甲基酶	Miao et al., 2020
bZIP4	促进侧根数量增加和主根伸长	Ma et al., 2018
CIPK3	提高干旱胁迫下种子根的长度	Li et al., 2023
cPGM2	编码磷酸葡萄糖变位酶, 参与糖代谢	Wu et al., 2021
CPK4	参与钙信号转导及脱落酸介导的气孔关闭	Jiang et al., 2013
DRESH8	产生siRNA, 调控干旱应答和种子大小基因的表达	Sun et al., 2023
DRO1	根尖向重力性和根系构型	Feng et al., 2022
EREB46	叶片表皮蜡质积累	Yang et al., 2022a
EXPA4	促进雌穂生长, 减小干旱诱导产生的散粉和吐丝时间间隔	Liu et al., 2021a
FAB1A	编码1-磷脂酰肌醇-4-磷酸-5-激酶, 参与磷酸肌醇代谢	Wu et al., 2021
GLK44	调控玉米的色氨酸合成	Zhang et al., 2021
IRX15A	负调控叶片的气孔密度	Zhang et al., 2023b
LRT	抑制玉米侧根的起始和伸长	Zhang et al., 2023c
NAC111	调控气孔关闭, 提高水分利用效率	Mao et al., 2015
NF-YA1	茉莉酸信号转导、组蛋白修饰和染色质重塑	Yang et al., 2022b
PP2C26	负调控脱落酸信号转导	Lu et al., 2022
PP84	抑制气孔关闭	Guo et al., 2023
PTF1	促进根系发育和脱落酸合成	Li et al., 2019b
PTPN	编码新型核苷酸酶	Zhang et al., 2020a
RBOHC	编码NADPH氧化酶	Gao et al., 2022
RFP1	编码E3连接酶	Xia et al., 2012
Rtn16	编码网状蛋白, 增强液泡H⁺-ATPase活性	Tian et al., 2023
SKL1/2	减少干旱下活性氧(reactive oxygen species, ROS)的积累	Liu et al., 2023
SRL5	参与角质层蜡质结构的形成	Pan et al., 2020
SRO1d	提高气孔的ROS含量, 促进气孔关闭	Gao et al., 2022
TIFY16	与茉莉酸信号途径的MYC2互作	Zhang et al., 2023a
TIP1	编码S-酰基转移酶, 促进根毛伸长	Zhang et al., 2020b
VPP1	编码质膜H⁺-ATPase, 促进根系发育	Wang et al., 2016
WRKY106	增强抗氧化相关酶活性, 降低ROS含量	Wang et al., 2018b
WRKY40	增强抗氧化相关酶活性, 降低ROS含量	Wang et al., 2018c
WRKY79	促进脱落酸的生物合成	Gulzar et al., 2021
Xerico1	调控脱落酸的代谢稳态	Brugière et al., 2017

玉米抗旱性的遗传解析

Genetic Dissection of Drought Resistance in Maize

RichHTML

PDF (PC)

可视化

摘要/Abstract

引用本文

使用本文

图/表 3

参考文献 123

相关文章 15

编辑推荐

Metrics

本文评价

[1]	杨文丽, 李钊, 刘志铭, 张志华, 杨今胜, 吕艳杰, 王永军. 不同熟期玉米叶片衰老特性及其对叶际细菌的影响[J]. 植物学报, 2024, 59(6): 1024-1040.
[2]	王涛, 冯敬磊, 张翠. 高温胁迫影响玉米生长发育的分子机制研究进展[J]. 植物学报, 2024, 59(6): 963-977.
[3]	郑名敏, 黄强, 张鹏, 刘孝伟, 赵卓凡, 易洪杨, 荣廷昭, 曹墨菊. 玉米细胞质雄性不育及育性恢复研究进展[J]. 植物学报, 2024, 59(6): 999-1006.
[4]	吴锁伟, 安学丽, 万向元. 玉米雄性不育机理及其在工程核不育制种中的应用[J]. 植物学报, 2024, 59(6): 932-949.
[5]	杜庆国, 李文学. lncRNA调控玉米生长发育和非生物胁迫研究进展[J]. 植物学报, 2024, 59(6): 950-962.
[6]	张强, 赵振宇, 李平华. 基因编辑技术在玉米中的研究进展[J]. 植物学报, 2024, 59(6): 978-998.
[7]	李园, 范开建, 安泰, 李聪, 蒋俊霞, 牛皓, 曾伟伟, 衡燕芳, 李虎, 付俊杰, 李慧慧, 黎亮. 玉米自然群体自交系农艺性状的多环境全基因组预测初探[J]. 植物学报, 2024, 59(6): 1041-1053.
[8]	闫恒宇, 李朝霞, 李玉斌. 高温对玉米生长的影响及中国耐高温玉米筛选研究进展[J]. 植物学报, 2024, 59(6): 1007-1023.
[9]	杨娟, 赵月磊, 陈晓远, 王宝宝, 王海洋. 玉米开花期调控机理及育种应用[J]. 植物学报, 2024, 59(6): 912-931.
[10]	廖星鑫, 牛祎, 多兴武, 阿克也得力·居玛哈孜, 买热哈巴·阿不都克尤木, 热孜瓦尼姑丽·胡甫尔, 兰海燕, 曹婧. 异源表达异子蓬SaPEPC2基因提高烟草抗旱性和光合特性(长英文摘要）[J]. 植物学报, 2024, 59(4): 585-599.
[11]	何璐梅, 马伯军, 陈析丰. 植物执行者抗病基因研究进展[J]. 植物学报, 2024, 59(4): 671-680.
[12]	王贺萍, 孙震, 刘雨辰, 苏彦龙, 杜锦瑜, 赵彦, 赵竑博, 王召明, 苑峰, 刘亚玲, 吴振映, 何峰, 付春祥. 蒙古冰草肉桂醇脱氢酶基因序列鉴定及功能分析[J]. 植物学报, 2024, 59(2): 204-216.
[13]	于熙婷, 黄学辉. 现代玉米起源新见解——两类大刍草的混血[J]. 植物学报, 2023, 58(6): 857-860.
[14]	周文期, 周玉乾, 李永生, 何海军, 杨彦忠, 王晓娟, 连晓荣, 刘忠祥, 胡筑兵. 玉米ZmICE2基因调控气孔发育[J]. 植物学报, 2023, 58(6): 866-881.
[15]	张蕾, 姜鹏飞, 王一鸣, 兰婷, 刘妍婧, 曾庆银. 苦杨×小叶杨杂交F₁代苗期抗旱性比较研究[J]. 植物学报, 2023, 58(4): 519-534.