Acta Agronomica Sinica ›› 2022, Vol. 48 ›› Issue (6): 1401-1415.doi: 10.3724/SP.J.1006.2022.12032
• CROP GENETICS & BREEDING·GERMPLASM RESOURCES·MOLECULAR GENETICS • Previous Articles Next Articles
ZHOU Wen-Qi1,2(), QIANG Xiao-Xia3, WANG Sen4, JIANG Jing-Wen1, WEI Wan-Rong1,*()
[1] |
Farooq M, Wahid A, Lee D J, Ito O, Siddique K H M. Advances in drought resistance of rice. CRC Crit Rev Plant Sci, 2009, 28: 199-217.
doi: 10.1080/07352680902952173 |
[2] |
Lampayan R L, Rejesus R M, Singleton G R, Bouman B A M. Adoption and economics of alternate wetting and drying water management for irrigated lowland rice. Field Crops Res, 2015, 170: 95-108.
doi: 10.1016/j.fcr.2014.10.013 |
[3] | 饶玉春, 戴志俊, 朱怡彤, 姜嘉骥, 马若盈, 王予烨, 王跃星. 水稻抗干旱胁迫的研究进展. 浙江师范大学学报(自然科学版), 2020, 43: 417-429. |
Rao Y C, Dai Z J, Zhu Y T, Jiang J J, Ma R Y, Wang Y Y, Wang Y X. Advances in research of drought resistance in rice. J Zhejiang Norm Univ (Nat Sci Edn), 2020, 43: 417-429 (in Chinese with English abstract). | |
[4] | Sahebi M, Hanafi M M, Rafii M Y, Mahmud T M M, Azizi P, Osman M, Abiri R, Taheri S, Kalhori N, Shabanimofrad M, Miah G, Atabaki N. Improvement of drought tolerance in rice (Oryza sativa L.): genetics, genomic tools, and the WRKY gene family. Biomed Res Int, 2018, 2018: 3158474. |
[5] | 周玉乾, 孟思远, 周文期. 植物表皮形态建成的分子调控机制. 西北农业学报, 2018, 27: 609-616. |
Zhou Y Q, Meng S Y, Zhou W Q. Molecular mechanism for regulating epidermal morphogenesis in plants. Acta Agric Boreali-Occident Sin, 2018, 27: 609-616 (in Chinese with English abstract). | |
[6] |
Martin C, Glover B J. Functional aspects of cell patterning in aerial epidermis. Curr Opin Plant Biol, 2007, 10: 70-82.
doi: 10.1016/j.pbi.2006.11.004 |
[7] |
Yanagisawa M, Desyatova A S, Belteton S A, Mallery E L, Turner J A, Szymanski D B. Patterning mechanisms of cytoskeletal and cell wall systems during leaf trichome morphogenesis. Nat Plants, 2015, 1: 15014.
doi: 10.1038/nplants.2015.14 pmid: 27246881 |
[8] |
Luo L, Zhou W Q, Liu P, Luo L, Li C X, Hou S W. The development of stomata and other epidermal cells on the rice leaves. Biol Plant, 2012, 56: 521-527
doi: 10.1007/s10535-012-0045-y |
[9] |
Zhou W Q, Wang Y C, Wu Z L, Luo L, Liu P, Yan L F, Hou S W. Homologs of SCAR/WAVE complex components are required for epidermal cell morphogenesis in rice. J Exp Bot, 2016, 67: 4311-4323.
doi: 10.1093/jxb/erw214 |
[10] |
Brembu T, Winge P, Seem M, Bones A M. NAPP and PIRP encode subunits of a putative wave regulatory protein complex involved in plant cell morphogenesis. Plant Cell, 2004, 16: 2335-2349.
pmid: 15316111 |
[11] |
Yanagisawa M, Zhang C, Szymanski D B. ARP2/3-dependent growth in the plant kingdom: scars for life. Front Plant Sci, 2013, 4: 166.
doi: 10.3389/fpls.2013.00166 pmid: 23802001 |
[12] |
Zhu X, Xiong L. Putative megaenzyme DWA1 plays essential roles in drought resistance by regulating stress-induced wax deposition in rice. Proc Natl Acad Sci USA, 2013, 110: 17790-17795.
doi: 10.1073/pnas.1316412110 |
[13] |
Seo P J, Lee S B, Suh M C, Park M J, Go Y S, Park C M. The MYB96 transcription factor regulates cuticular wax biosynthesis under drought conditions in Arabidopsis. Plant Cell, 2011, 23: 1138-1152.
doi: 10.1105/tpc.111.083485 |
[14] |
Mauricio R. Costs of resistance to natural enemies in field populations of the annual plant Arabidopsis thaliana. Am Nat, 1998, 151: 20-28.
doi: 10.1086/286099 |
[15] |
Frank M J, Smith L G. A small, novel protein highly conserved in plants and animals promotes the polarized growth and division of maize leaf epidermal cells. Curr Biol, 2002, 12: 849-853.
pmid: 12015123 |
[16] |
Buckley T N. The control of stomata by water balance. New Phytol, 2005, 168: 275-291.
pmid: 16219068 |
[17] |
Bergmann D C, Sack F D. Stomatal development. Annu Rev Plant Biol, 2007, 58: 163-181.
doi: 10.1146/arplant.2007.58.issue-1 |
[18] |
Liu T, Ohashi-Ito K, Bergmann D C. Orthologs of Arabidopsis thaliana stomatal bHLH genes and regulation of stomatal development in grasses. Development, 2009, 136: 2265-2276.
doi: 10.1242/dev.032938 |
[19] |
Kamiya N, Itoh J, Morikami A, Nagato Y, Matsuoka M. The SCARECROW gene’s role in asymmetric cell divisions in rice plants. Plant J, 2003, 36: 45-54.
doi: 10.1046/j.1365-313X.2003.01856.x |
[20] | Apostolakos P, Livanos P, Giannoutsou E, Panteris E, Galatis B. The intracellular and intercellular cross-talk during subsidiary cell formation in Zea mays: existing and novel components orchestrating cell polarization and asymmetric division. Ann Bot, 2018, 122: 679-696. |
[21] |
Wu Z L, Chen Li, Yu Q, Zhou W Q, Gou X P, Li J, Hou S W. Multiple transcriptional factors control stomata development in rice. New Phytol, 2019, 223: 220-232.
doi: 10.1111/nph.2019.223.issue-1 |
[22] |
Chater C C C, Caine R S, Fleming A J, Gray J E. Origins and evolution of stomatal development. Plant Physiol, 2017, 174: 624-638.
doi: 10.1104/pp.17.00183 |
[23] |
Deeks M J, Kaloriti D, Davies B, Malho R, Hussey P J. Arabidopsis NAP1 is essential for Arp2/3-dependent trichome morphogenesis. Curr Biol, 2004, 14: 1410-1414.
doi: 10.1016/j.cub.2004.06.065 |
[24] |
Zhang C, Mallery E L, Schlueter J, Huang S, Fan Y, Brankle S, Staiger C J, Szymanski D B. Arabidopsis SCARs function interchangeably to meet actin-related protein 2/3 activation thresholds during morphogenesis. Plant Cell, 2008, 20: 995-1011.
doi: 10.1105/tpc.107.055350 |
[25] | Jorgens C I, Grunewald N, Hulskamp M, Uhrig J F. A role for ABIL3 in plant cell morphogenesis. Plant J, 2010, 62: 925-935. |
[26] |
Bai J T, Zhu X D, Wang Q, Zhang J, Chen H, Dong G, Zhu L, Zheng H, Xie Q, Nian J, Chen F, Fu Y, Qian Q, Zuo J. Rice TUTOU1 encodes a suppressor of camp receptor-like protein that is important for actin organization and panicle development. Plant Physiol, 2015, 169: 1179-1191.
doi: 10.1104/pp.15.00229 |
[27] |
Rao Y C, Yang Y L, Xu J, Li X, Leng Y, Dai L, Huang L, Shao G, Ren D, Hu J, Guo L, Pan J, Zeng D. EARLY SENESCENCE1 encodes a SCAR-LIKE PROTEIN2 that affects water loss in rice. Plant Physiol, 2015, 169: 1225-1239.
doi: 10.1104/pp.15.00991 |
[28] |
Eden S, Rohatgi R, Podtelejnikov A V, Mann M, Kirschner M W. Mechanism of regulation of WAVE1-induced actin nucleation by Rac1 and Nck. Nature, 2002, 418: 790-793.
doi: 10.1038/nature00859 |
[29] |
Welch M D, Mullins R D. Cellular control of actin nucleation. Annu Rev Cell Dev Biol, 2002, 18: 247-288.
doi: 10.1146/cellbio.2002.18.issue-1 |
[30] |
Kotchoni S O, Zakharova T, Mallery E L, Le J, El-Assal S E D, Szymanski D B. The association of the Arabidopsis actin- related protein 2/3 complex with cell membranes is linked to its assembly status but not its activation. Plant Physiol, 2009, 151: 2095-2109.
doi: 10.1104/pp.109.143859 pmid: 19801398 |
[31] |
Frank M J. Three BRICK genes have distinct functions in a common pathway promoting polarized cell division and cell morphogenesis in the maize leaf epidermis. Development, 2003, 130: 753-762.
pmid: 12506005 |
[32] |
Djakovic S, Dyachok J, Burke M, Frank M J, Smith L G. BRICK1/HSPC300 functions with SCAR and the ARP2/3 complex to regulate epidermal cell shape in Arabidopsis. Development, 2006, 133: 1091-1100.
pmid: 16481352 |
[33] |
Basu D, El-Assal S E, Le J, Mallery E L, Szymanski D B. Interchangeable functions of Arabidopsis PIROGI and the human WAVE complex subunit SRA1 during leaf epidermal development. Development, 2004, 131: 4345-4355.
doi: 10.1242/dev.01307 |
[34] |
Basu D, Le J, Zakharova T, Mallery E L, Szymanski D B. A SPIKE1 signaling complex controls actin-dependent cell morphogenesis through the heteromeric WAVE and ARP2/3 complexes. Proc Natl Acad Sci USA, 2008, 105: 4044-4049.
doi: 10.1073/pnas.0710294105 |
[35] |
Jiang K, Sorefan K, Deeks M J, Bevan M W, Hussey P J, Hetherington A M. The ARP2/3 complex mediates guard cell actin reorganization and stomatal movement in Arabidopsis. Plant Cell, 2012, 24: 2031-2040.
doi: 10.1105/tpc.112.096263 |
[36] | Singh D and Laxmi A. Transcriptional regulation of drought response: a tortuous network of transcriptional factors. Front Plant Sci, 2015, 6: 895. |
[37] | 周文期. 调控水稻叶表皮发育的LPL2和DSP1基因克隆与功能分析. 兰州大学博士学位论文, 甘肃兰州, 2015. |
Zhou W Q. The Cloning and Functional Analysis of LPL2 and DSP1, Two Genes, That Regulate the Epidermal Cell Development in Rice. PhD Dissertation of Lanzhou University, Lanzhou, Gansu, China, 2015 (in Chinese with English abstract). | |
[38] |
Huang X Y, Chao D Y, Gao J P, Zhu M Z, Shi M, Lin H X. A previously unknown zinc finger protein, DST, regulates drought and salt tolerance in rice via stomatal aperture control. Genes Dev, 2009, 23: 1805-1817.
doi: 10.1101/gad.1812409 |
[39] | 周文期, 寇思荣, 连晓荣, 杨彦忠, 刘忠祥, 王晓娟, 何海军, 周玉乾. 水稻和玉米叶表皮突变体的筛选和鉴定. 植物生理学报, 2020, 56: 189-199. |
Zhou W Q, Kou S R, Lian X R, Yang Y Z, Liu Z X, Wang X J, He H J, Zhou Y Q. Screening and identification of leaf epidermal mutants in rice and maize. Plant Physiol J, 2020, 56: 189-199 (in Chinese with English abstract). | |
[40] | 周文期, 强晓霞, 聂永鑫, 卫万荣. 水稻OsPP1a基因克隆和RNAi-OsPP1a遗传转化分析. 植物生理学报, 2020, 56: 1561-1572. |
Zhou W Q, Qiang X X, Nie Y X, Wei W R. Cloning of OsPP1a from rice and analysis of its RNAi-OsPP1a genetic transformation. Plant Physiol J, 2020, 56: 1561-1572 (in Chinese with English abstract). | |
[41] |
Chen Z, Borek D, Padrick S B, Gomez T S, Metlagel Z, Ismail A M, Umetani J, Billadeau D D, Otwinowski Z, Rosen M K. Structure and control of the actin regulatory WAVE complex. Nature, 2010, 468: 533-538.
doi: 10.1038/nature09623 |
[42] |
Huang L, Chen L, Wang L, Yang Y, Rao Y, Ren D, Dai L, Gao Y, Zou W, Lu X, Zhang G, Zhu L, Hu J, Chen G, Shen L, Dong G, Gao Z, Guo L, Qian Q, Zeng D. A Nck-associated protein 1-like protein affects drought sensitivity by its involvement in leaf epidermal development and stomatal closure in rice. Plant J, 2019, 98: 884-897.
doi: 10.1111/tpj.2019.98.issue-5 |
[43] |
Gao Y, Wu M, Zhang M, Jiang W, Liang E, Zhang D, Zhang C, Xiao N, Chen J. Roles of a maize phytochrome-interacting factors protein ZmPIF3 in regulation of drought stress responses by controlling stomatal closure in transgenic rice without yield penalty. Plant Mol Biol, 2018, 97: 311-323.
doi: 10.1007/s11103-018-0739-4 |
[44] |
Higaki T, Kutsuna N, Sano T, Kondo N, Hasezawa S. Quantification and cluster analysis of actin cytoskeletal structures in plant cells: role of actin bundling in stomatal movement during diurnal cycles in Arabidopsis guard cells. Plant J, 2010, 61: 156-165.
doi: 10.1111/tpj.2009.61.issue-1 |
[45] |
Zhao Y, Zhao S, Mao T, Qu X, Cao W, Zhang L, Zhang W, He L, Li S, Ren S, Zhao J, Zhu G, Huang S, Ye K, Yuan M, Guo Y. The plant-specific actin binding protein SCAB1 stabilizes actin filaments and regulates stomatal movement in Arabidopsis. Plant Cell, 2011, 23: 2314-2330.
doi: 10.1105/tpc.111.086546 |
[46] |
Yoo C Y, Pence H E, Jin J B, Miura K, Gosney M J, Hasegawa P M, Mickelbart M V. The Arabidopsis GTL1 transcription factor regulates water use efficiency and drought tolerance by modulating stomatal density via transrepression of SDD1. Plant Cell, 2010, 22: 4128-4141.
doi: 10.1105/tpc.110.078691 |
[47] |
Li X, Han H, Chen M, Yang W, Liu L, Li N, Ding X H. Chu Z H. Overexpression of OsDT11, which encodes a novel cysteine-rich peptide, enhances drought tolerance and increases ABA concentration in rice. Plant Mol Biol, 2016, 93: 21-34.
doi: 10.1007/s11103-016-0544-x |
[48] |
Park J J, Jin P, Yoon J, Yang J I, Jeong H J, Ranathunge K, Schreiber L, Franke R, Lee I J, An G. Mutation in Wilted Dwarf and Lethal 1 (WDL1) causes abnormal cuticle formation and rapid water loss in rice. Plant Mol Biol, 2010, 74: 91-103.
doi: 10.1007/s11103-010-9656-x |
[49] |
Liu J, Zhang F, Zhou J, Chen F, Wang B, Xie X. Phytochrome B control of total leaf area and stomatal density affects drought tolerance in rice. Plant Mol Biol, 2012, 78: 289-300.
doi: 10.1007/s11103-011-9860-3 |
[50] |
Dey A, Samanta M K, Gayen S, Maiti M K. The sucrose non fermenting 1-related kinase 2 gene SAPK9 improves drought tolerance and grain yield in rice by modulating cellular osmotic potential, stomatal closure and stress-responsive gene expression. BMC Plant Biol, 2016, 16: 158.
doi: 10.1186/s12870-016-0845-x |
[51] |
Hetherington A M, Woodward F I. The role of stomata in sensing and driving environmental change. Nature, 2003, 424: 901-908.
doi: 10.1038/nature01843 |
[52] |
Pantin F, Blatt M R. Stomatal response to humidity: blurring the boundary between active and passive movement. Plant Physiol, 2018, 176: 485-488.
doi: 10.1104/pp.17.01699 |
[53] |
Fang Y J, Xiong L Z. General mechanisms of drought response and their application in drought resistance improvement in plants. Cell Mol Life Sci, 2015, 72: 673-689.
doi: 10.1007/s00018-014-1767-0 |
[54] | 刘延波, 项阳, 秦利军, 赵德刚. 转玉米ZmSDD1基因烟草降低气孔密度提高抗旱性. 植物生理学报, 2014, 50: 1889-1898. |
Liu Y B, Xiang Y, Qin L J, Zhao D G. Improvement of drought tolerance in transgenic tobacco expressed maize ZmSDD1 by reducing stomatal density. Plant Physiol J, 2014, 50: 1889-1898 (in Chinese with English abstract). | |
[55] | 陈腾君, 曾丹, 张帆, 周永力, 石英尧, 黎志康. 胁迫相关蛋白激酶OsSAPK9调控水稻对铝胁迫的反应. 植物遗传资源学报, 2018, 19: 1149-1153. |
Chen T J, Zeng D, Zhang F, Zhou Y L, Shi Y Y, Li Z K. Stress-activated protein kinase OsSAPK9 is involved in regulating tolerant response to al stress in rice. J Plant Genet Res, 2018, 19: 1149-1153 (in Chinese with English abstract). | |
[56] |
Zhou W Q, Zhou Y Q, He C Y, Mou B Q, Zhou W. Over- expression of Oshox4 enhances drought and salinity tolerance in rice. Russ J Plant Physiol, 2020, 67: 1152-1162.
doi: 10.1134/S1021443720060205 |
[57] |
Isner J C, Xu Z, Costa J M, Monnet F, Batstone T, Ou X, Deeks M J, Genty B, Jiang K, Hetherington A M. Actin filament reorganization controlled by the SCAR/WAVE complex mediates stomatal response to darkness. New Phytol, 2017, 215: 1059-1067.
doi: 10.1111/nph.2017.215.issue-3 |
[58] |
Xiang Y, Sun X, Bian X, Wei T, Han T, Yan J, Zhang A. The transcription factor ZmNAC49 reduces stomatal density and improves drought tolerance in maize. J Exp Bot, 2021, 72: 1399-1410.
doi: 10.1093/jxb/eraa507 pmid: 33130877 |
[59] |
Zhao B Y, Hu Y F, Li J J, Yao X, Liu K D. BnaABF2, a bZIP transcription factor from rapeseed (Brassica napus L.), enhances drought and salt tolerance in transgenic Arabidopsis. Bot Stud, 2016, 57: 12-24.
doi: 10.1186/s40529-016-0127-9 |
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