A necessary considering factor for breeding: growth-defense tradeoff in plants

Hong Zhang, Yuanming Liu, Xiangyu Zhang, Wanquan Ji, Zhensheng Kang

Stress Biology ›› 2023, Vol. 3 ›› Issue (1) : 6. DOI: 10.1007/s44154-023-00086-1
Review

A necessary considering factor for breeding: growth-defense tradeoff in plants

Author information +
History +

Abstract

Crop diseases cause enormous yield losses and threaten global food security. Deployment of resistant cultivars can effectively control the disease and to minimize crop losses. However, high level of genetic immunity to disease was often accompanied by an undesired reduction in crop growth and yield. Recently, literatures have been rapidly emerged in understanding the mechanism of disease resistance and development genes in crop plants. To determine how and why the costs and the likely benefit of resistance genes caused in crop varieties, we re-summarized the present knowledge about the crosstalk between plant development and disease resistance caused by those genes that function as plasma membrane residents, MAPK cassette, nuclear envelope (NE) channels components and pleiotropic regulators. Considering the growth-defense tradeoffs on the basis of current advances, finally, we try to understand and suggest that a reasonable balancing strategies based on the interplay between immunity with growth should be considered to enhance immunity capacity without yield penalty in future crop breeding.

Keywords

Crops / Growth-defense / Reasonable cell death / Yield penalty

Cite this article

Download citation ▾
Hong Zhang, Yuanming Liu, Xiangyu Zhang, Wanquan Ji, Zhensheng Kang. A necessary considering factor for breeding: growth-defense tradeoff in plants. Stress Biology, 2023, 3(1): 6 https://doi.org/10.1007/s44154-023-00086-1

References

[1]
BaceteL, MelidaH, MiedesE, MolinaA. Plant cell wall-mediated immunity: cell wall changes trigger disease resistance responses. Plant J, 2018, 93(4):614-636
CrossRef Google scholar
[2]
BaiX, ZhanG, TianS, PengH, CuiX, IslamMA, GoherF, MaY, KangZ, XuZS, GuoJ. Transcription factor BZR2 activates chitinase Cht20.2 transcription to confer resistance to wheat stripe rust. Plant Physiol, 2021, 187(4):2749-2762
CrossRef Google scholar
[3]
Balint-KurtiP. The plant hypersensitive response: concepts, control and consequences. Mol Plant Pathol, 2019, 20(8):1163-1178
CrossRef Google scholar
[4]
BartelsS, AndersonJC, Gonzalez BesteiroMA, CarreriA, HirtH, BuchalaA, MetrauxJP, PeckSC, UlmR. MAP kinase phosphatase1 and protein tyrosine phosphatase1 are repressors of salicylic acid synthesis and SNC1-mediated responses in Arabidopsis. Plant Cell, 2009, 21(9):2884-2897
CrossRef Google scholar
[5]
BrownJK. Yield penalties of disease resistance in crops. Curr Opin Plant Biol, 2002, 5(4):339-344
CrossRef Google scholar
[6]
BrutusA, SiciliaF, MaconeA, CervoneF, De LorenzoG. A domain swap approach reveals a role of the plant wall-associated kinase 1 (WAK1) as a receptor of oligogalacturonides. Proc Natl Acad Sci U S A, 2010, 107(20):9452-9457
CrossRef Google scholar
[7]
ChinchillaD, ZipfelC, RobatzekS, KemmerlingB, NurnbergerT, JonesJD, FelixG, BollerT. A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence. Nature, 2007, 448(7152):497-500
CrossRef Google scholar
[8]
ChoudharySP, YuJQ, Yamaguchi-ShinozakiK, ShinozakiK, TranLS. Benefits of brassinosteroid crosstalk. Trends Plant Sci, 2012, 17(10):594-605
CrossRef Google scholar
[9]
ChoudhuryS, MansiMuthusamy SK, PadariaJC, DalalM. Genome-wide identification of Ran GTPase family genes from wheat (T. aestivum) and their expression profile during developmental stages and abiotic stress conditions. Funct Integr Genomics, 2021, 21(2):239-250
CrossRef Google scholar
[10]
de OliveiraMV, XuG, LiB, de SouzaVL, MengX, ChenX, YuX, de SouzaSA, IntorneAC, de AMAM, Musinsky AL, Koiwa H, de Souza Filho GA, Shan L, He P, . Specific control of Arabidopsis BAK1/SERK4-regulated cell death by protein glycosylation. Nat Plants, 2016, 2: 15218
CrossRef Google scholar
[11]
DengY, ZhaiK, XieZ, YangD, ZhuX, LiuJ, WangX, QinP, YangY, ZhangG, LiQ, ZhangJ, WuS, MilazzoJ, MaoB, WangE, XieH, TharreauD, HeZ. Epigenetic regulation of antagonistic receptors confers rice blast resistance with yield balance. Science, 2017, 355(6328):962-965
CrossRef Google scholar
[12]
DongX. NPR1, all things considered. Curr Opin Plant Biol, 2004, 7(5):547-552
CrossRef Google scholar
[13]
DuJ, GaoY, ZhanY, ZhangS, WuY, XiaoY, ZouB, HeK, GouX, LiG, LinH, LiJ. Nucleocytoplasmic trafficking is essential for BAK1- and BKK1-mediated cell-death control. Plant J, 2016, 85(4):520-531
CrossRef Google scholar
[14]
EichC, ManzoC, de KeijzerS, BakkerGJ, Reinieren-BeerenI, Garcia-ParajoMF, CambiA. Changes in membrane sphingolipid composition modulate dynamics and adhesion of integrin nanoclusters. Sci Rep, 2016, 6: 20693
CrossRef Google scholar
[15]
EkanayakeG, LaMontagneED, HeeseA. Never walk alone: Clathrin-Coated Vesicle (CCV) components in plant immunity. Annu Rev Phytopathol, 2019, 57: 387-409
CrossRef Google scholar
[16]
FanJ, BaiP, NingY, WangJ, ShiX, XiongY, ZhangK, HeF, ZhangC, WangR, MengX, ZhouJ, WangM, ShirsekarG, ParkCH, BellizziM, LiuW, JeonJS, XiaY, ShanL, WangGL. The monocot-specific receptor-like kinase SDS2 controls cell death and immunity in rice. Cell Host Microbe, 2018, 23(4):498-510 e495
CrossRef Google scholar
[17]
FeherA, LajkoDB. Signals fly when kinases meet Rho-of-plants (ROP) small G-proteins. Plant Sci, 2015, 237: 93-107
CrossRef Google scholar
[18]
FukuokaS, SakaN, KogaH, OnoK, ShimizuT, EbanaK, HayashiN, TakahashiA, HirochikaH, OkunoK, YanoM. Loss of function of a proline-containing protein confers durable disease resistance in rice. Science, 2009, 325(5943):998-1001
CrossRef Google scholar
[19]
GaoM, WangX, WangD, XuF, DingX, ZhangZ, BiD, ChengYT, ChenS, LiX, ZhangY. Regulation of cell death and innate immunity by two receptor-like kinases in Arabidopsis. Cell Host Microbe, 2009, 6(1):34-44
CrossRef Google scholar
[20]
GotoS, Sasakura-ShimodaF, SuetsuguM, SelvarajMG, HayashiN, YamazakiM, IshitaniM, ShimonoM, SuganoS, MatsushitaA, TanabataT, TakatsujiH. Development of disease-resistant rice by optimized expression of WRKY45. Plant Biotechnol J, 2015, 13(6):753-765
CrossRef Google scholar
[21]
GraumannK, VanrobaysE, TutoisS, ProbstAV, EvansDE, TatoutC. Characterization of two distinct subfamilies of SUN-domain proteins in Arabidopsis and their interactions with the novel KASH-domain protein AtTIK. J Exp Bot, 2014, 65(22):6499-6512
CrossRef Google scholar
[22]
Graumann K, Evans DE (2017), The nuclear envelope - structure and protein interactions. In: Annual plant reviews online, edited, pp. 19–56, https://doi.org/10.1002/9781119312994.apr0498.
[23]
GuY, ZebellSG, LiangZ, WangS, KangBH, DongX. Nuclear pore permeabilization is a convergent signaling event in effector-triggered immunity. Cell, 2016, 166(6):1526-1538 e1511
CrossRef Google scholar
[24]
GuoT, ChenK, DongNQ, ShiCL, YeWW, GaoJP, ShanJX, LinHX. GRAIN SIZE AND NUMBER1 negatively regulates the OsMKKK10-OsMKK4-OsMPK6 cascade to coordinate the trade-off between grain number per panicle and grain size in rice. Plant Cell, 2018, 30(4):871-888
CrossRef Google scholar
[25]
Guo F, Wu T, Xu G, Qi H, Zhu X, Zhang Z (2021) TaWAK2A-800, a wall-associated kinase, participates positively in resistance to fusarium head blight and sharp eyespot in wheat. Int J Mol Sci 22(21). https://doi.org/10.3390/ijms222111493.
[26]
HarkenriderM, SharmaR, De VleesschauwerD, TsaoL, ZhangX, ChernM, CanlasP, ZuoS, RonaldPC. Overexpression of Rice Wall-Associated Kinase 25 (OsWAK25) Alters Resistance to Bacterial and Fungal Pathogens. PLoS One, 2016, 11(1):e0147310
CrossRef Google scholar
[27]
HeM, DingNZ. Plant unsaturated fatty acids: multiple roles in stress response. Front Plant Sci, 2020, 11: 562785
CrossRef Google scholar
[28]
HeK, GouX, YuanT, LinH, AsamiT, YoshidaS, RussellSD, LiJ. BAK1 and BKK1 regulate brassinosteroid-dependent growth and brassinosteroid-independent cell-death pathways. Curr Biol, 2007, 17(13):1109-1115
CrossRef Google scholar
[29]
HeZH, XiaXC, ChenXM, ZhuangQS. Progress of wheat breeding in China and the future perspective. Acta Agron Sin, 2011, 37(2):202-215
CrossRef Google scholar
[30]
HeZ, WebsterS, HeSY. Growth-defense trade-offs in plants. Curr Biol, 2022, 32(12):R634-R639
CrossRef Google scholar
[31]
He Y, Zhu M, Li Z, Jiang S, He Z, Xu S, Chen X, Hu Z, Zhang Z (2021) IPA1 negatively regulates early rice seedling development by interfering with starch metabolism via the GA and WRKY pathways. Int J Mol Sci 22(12). https://doi.org/10.3390/ijms22126605.
[32]
HematyK, CherkC, SomervilleS. Host-pathogen warfare at the plant cell wall. Curr Opin Plant Biol, 2009, 12(4):406-413
CrossRef Google scholar
[33]
HewittT, ZhangJ, HuangL, UpadhyayaN, LiJ, ParkR, HoxhaS, McIntoshR, LagudahE, ZhangP. Wheat leaf rust resistance gene Lr13 is a specific Ne2 allele for hybrid necrosis. Mol Plant, 2021, 14(7):1025-1028
CrossRef Google scholar
[34]
HowardAF, KoenraadtCJ, FarenhorstM, KnolsBG, TakkenW. Pyrethroid resistance in Anopheles gambiae leads to increased susceptibility to the entomopathogenic fungi Metarhizium anisopliae and Beauveria bassiana. Malar J, 2010, 9: 168
CrossRef Google scholar
[35]
HuL, YeM, LiR, ZhangT, ZhouG, WangQ, LuJ, LouY. The rice transcription factor WRKY53 suppresses herbivore-induced defenses by acting as a negative feedback modulator of mitogen-activated protein kinase activity. Plant Physiol, 2015, 169(4):2907-2921
CrossRef Google scholar
[36]
HuotB, YaoJ, MontgomeryBL, HeSY. Growth-defense tradeoffs in plants: a balancing act to optimize fitness. Mol Plant, 2014, 7(8):1267-1287
CrossRef Google scholar
[37]
InoueH, HayashiN, MatsushitaA, XinqiongL, NakayamaA, SuganoS, JiangCJ, TakatsujiH. Blast resistance of CC-NB-LRR protein Pb1 is mediated by WRKY45 through protein-protein interaction. Proc Natl Acad Sci U S A, 2013, 110(23):9577-9582
CrossRef Google scholar
[38]
JeongSY, RoseA, JosephJ, DassoM, MeierI. Plant-specific mitotic targeting of RanGAP requires a functional WPP domain. Plant J, 2005, 42(2):270-282
CrossRef Google scholar
[39]
JiangL, ChenY, LuoL, PeckSC. Central roles and regulatory mechanisms of dual-specificity MAPK phosphatases in developmental and stress signaling. Front Plant Sci, 2018, 9: 1697
CrossRef Google scholar
[40]
Jones JD, Vance RE, Dangl JL (2016) Intracellular innate immune surveillance devices in plants and animals. Science 354(6316). https://doi.org/10.1126/science.aaf6395.
[41]
KangY, ZhouM, MerryA, BarryK. Mechanisms of powdery mildew resistance of wheat – a review of molecular breeding. Plant Pathol, 2020, 69(4):601-617
CrossRef Google scholar
[42]
KarasovTL, ChaeE, HermanJJ, BergelsonJ. Mechanisms to mitigate the trade-off between growth and defense. Plant Cell, 2017, 29(4):666-680
CrossRef Google scholar
[43]
KassianidouE, KalitaJ, LimRYH. The role of nucleocytoplasmic transport in mechanotransduction. Exp Cell Res, 2019, 377(1–2):86-93
CrossRef Google scholar
[44]
KelleyJB, PaschalBM. Fluorescence-based quantification of nucleocytoplasmic transport. Methods, 2019, 157: 106-114
CrossRef Google scholar
[45]
KohornBD, KohornSL. The cell wall-associated kinases, WAKs, as pectin receptors. Front Plant Sci, 2012, 3: 88
CrossRef Google scholar
[46]
KohornBD, JohansenS, ShishidoA, TodorovaT, MartinezR, DefeoE, ObregonP. Pectin activation of MAP kinase and gene expression is WAK2 dependent. Plant J, 2009, 60(6):974-982
CrossRef Google scholar
[47]
KohornBD, KohornSL, TodorovaT, BaptisteG, StanskyK, McCulloughM. A dominant allele of Arabidopsis pectin-binding wall-associated kinase induces a stress response suppressed by MPK6 but not MPK3 mutations. Mol Plant, 2012, 5(4):841-851
CrossRef Google scholar
[48]
LaMontagneED, HeeseA. Trans-Golgi network/early endosome: a central sorting station for cargo proteins in plant immunity. Curr Opin Plant Biol, 2017, 40: 114-121
CrossRef Google scholar
[49]
LiH, ZhouSY, ZhaoWS, SuSC, PengYL. A novel wall-associated receptor-like protein kinase gene, OsWAK1, plays important roles in rice blast disease resistance. Plant Mol Biol, 2009, 69(3):337-346
CrossRef Google scholar
[50]
LiX, YangDL, SunL, LiQ, MaoB, HeZ. The systemic acquired resistance regulator OsNPR1 attenuates growth by repressing auxin signaling through promoting IAA-Amido synthase expression. Plant Physiol, 2016, 172(1):546-558
CrossRef Google scholar
[51]
LiW, ZhuZ, ChernM, YinJ, YangC, RanL, ChengM, HeM, WangK, WangJ, ZhouX, ZhuX, ChenZ, WangJ, ZhaoW, MaB, QinP, ChenW, WangY, LiuJ, WangW, WuX, LiP, WangJ, ZhuL, LiS, ChenX. A natural allele of a transcription factor in rice confers broad-spectrum blast resistance. Cell, 2017, 170(1):114-126 e115
CrossRef Google scholar
[52]
LiW, ChernM, YinJ, WangJ, ChenX. Recent advances in broad-spectrum resistance to the rice blast disease. Curr Opin Plant Biol, 2019, 50: 114-120
CrossRef Google scholar
[53]
LiS, LinD, ZhangY, DengM, ChenY, LvB, LiB, LeiY, WangY, ZhaoL, LiangY, LiuJ, ChenK, LiuZ, XiaoJ, QiuJ-L, GaoC. Genome-edited powdery mildew resistance in wheat without growth penalties. Nature, 2022
CrossRef Google scholar
[54]
LitricoI, ViolleC. Diversity in plant breeding: a new conceptual framework. Trends Plant Sci, 2015, 20(10):604-613
CrossRef Google scholar
[55]
LiuS, HuaL, DongS, ChenH, ZhuX, JiangJ, ZhangF, LiY, FangX, ChenF. OsMAPK6, a mitogen-activated protein kinase, influences rice grain size and biomass production. Plant J, 2015, 84(4):672-681
CrossRef Google scholar
[56]
LiuX, InoueH, HayashiN, JiangC-J, TakatsujiH. CC-NBS-LRR-Type R proteins for rice blast commonly interact with specific WRKY transcription factors. Plant Mol Bio Rep, 2015, 34(2):533-537
CrossRef Google scholar
[57]
LocatoV, De GaraL. Programmed cell death in plants: an overview. Methods Mol Biol, 2018, 1743: 1-8
CrossRef Google scholar
[58]
Lozano-DuranR, ZipfelC. Trade-off between growth and immunity: role of brassinosteroids. Trends Plant Sci, 2015, 20(1):12-19
CrossRef Google scholar
[59]
Lozano-DuranR, MachoAP, BoutrotF, SegonzacC, SomssichIE, ZipfelC. The transcriptional regulator BZR1 mediates trade-off between plant innate immunity and growth. Elife, 2013, 2: e00983
CrossRef Google scholar
[60]
LuK, ChenX, YaoX, AnY, WangX, QinL, LiX, WangZ, LiuS, SunZ, ZhangL, ChenL, LiB, LiuB, WangW, DingX, YangY, ZhangM, ZouS, DongH. Phosphorylation of a wheat aquaporin at two sites enhances both plant growth and defense. Mol Plant, 2022
CrossRef Google scholar
[61]
MaL, HongZ, ZhangZ. Perinuclear and nuclear envelope localizations of Arabidopsis Ran proteins. Plant Cell Rep, 2007, 26(8):1373-1382
CrossRef Google scholar
[62]
ManWK, TahirbegiB, VrettasMD, PreetS, YingL, VendruscoloM, De SimoneA, FuscoG. The docking of synaptic vesicles on the presynaptic membrane induced by alpha-synuclein is modulated by lipid composition. Nat Commun, 2021, 12(1):927
CrossRef Google scholar
[63]
MaoG, MengX, LiuY, ZhengZ, ChenZ, ZhangS. Phosphorylation of a WRKY transcription factor by two pathogen-responsive MAPKs drives phytoalexin biosynthesis in Arabidopsis. Plant Cell, 2011, 23(4):1639-1653
CrossRef Google scholar
[64]
NejatN, MantriN. Plant immune system: crosstalk between responses to biotic and abiotic stresses the missing link in understanding plant defence. Curr Issues Mol Biol, 2017, 23: 1-16
CrossRef Google scholar
[65]
NelsonR, Wiesner-HanksT, WisserR, Balint-KurtiP. Navigating complexity to breed disease-resistant crops. Nat Rev Genet, 2018, 19(1):21-33
CrossRef Google scholar
[66]
NingY, LiuW, WangGL. Balancing immunity and yield in crop plants. Trends Plant Sci, 2017, 22(12):1069-1079
CrossRef Google scholar
[67]
OffringaR, HuangF. Phosphorylation-dependent trafficking of plasma membrane proteins in animal and plant cells. J Integr Plant Biol, 2013, 55(9):789-808
CrossRef Google scholar
[68]
Pan YH, Gao LJ, Liang YT, Zhao Y, Liang HF, Chen WW, Yang XH, Qing DJ, Gao J, Wu H, Huang J, Zhou WY, Huang CC, Dai GX, Deng GF (2021) OrMKK3 influences morphology and grain size in rice. J Plant Biol: 1–14. https://doi.org/10.1007/s12374-020-09290-2.
[69]
ParryMA, ReynoldsM, SalvucciME, RainesC, AndralojcPJ, ZhuXG, PriceGD, CondonAG, FurbankRT. Raising yield potential of wheat. II. Increasing photosynthetic capacity and efficiency. J Exp Bot, 2011, 62(2):453-467
CrossRef Google scholar
[70]
PengM, LinX, XiangX, RenH, FanX, ChenK. Characterization and evaluation of transgenic rice pyramided with the Pi genes Pib, Pi25 and Pi54. Rice (n y), 2021, 14(1):78
CrossRef Google scholar
[71]
QiG, ChenH, WangD, ZhengH, TangX, GuoZ, ChengJ, ChenJ, WangY, BaiMY, LiuF, WangD, FuZQ. The BZR1-EDS1 module regulates plant growth-defense coordination. Mol Plant, 2021, 14(12):2072-2087
CrossRef Google scholar
[72]
Qiu JL, Fiil BK, Petersen K, Nielsen HB, Botanga CJ, Thorgrimsen S, Palma K, Suarez-Rodriguez MC, Sandbech-Clausen S, Lichota J, Brodersen P, Grasser KD, Mattsson O, Glazebrook J, Mundy J, Petersen M (2008) Arabidopsis MAP kinase 4 regulates gene expression through transcription factor release in the nucleus. EMBO J 27(16):2214–2221. https://doi.org/10.1038/emboj.2008.147
[73]
QuX, ZhangD, ZhangX, WangS, WangC, WangY, WangY, ChenC, ZhangH, JiW. Cytogenetic and marker assisted identification of a wheat–Psathyrostachys huashanica Keng f. ex P.C.Kuo alien substitution line conferring processing quality and resistance to stripe rust. Genet Resour Crop Evol, 2022, 69(2):687-698
CrossRef Google scholar
[74]
RidleyAJ. Rho GTPases and actin dynamics in membrane protrusions and vesicle trafficking. Trends Cell Biol, 2006, 16(10):522-529
CrossRef Google scholar
[75]
SaccoMA, MansoorS, MoffettP. A RanGAP protein physically interacts with the NB-LRR protein Rx, and is required for Rx-mediated viral resistance. Plant J, 2007, 52(1):82-93
CrossRef Google scholar
[76]
SimkinAJ, FaralliM, RamamoorthyS, LawsonT. Photosynthesis in non-foliar tissues: implications for yield. Plant J, 2020, 101(4):1001-1015
CrossRef Google scholar
[77]
SinghA, BrejaP, KhuranaJP, KhuranaP. Wheat Brassinosteroid-Insensitive1 (TaBRI1) Interacts with Members of TaSERK Gene Family and Cause Early Flowering and Seed Yield Enhancement in Arabidopsis. PLoS One, 2016, 11(6):e0153273
CrossRef Google scholar
[78]
SpitzF, FurlongEE. Transcription factors: from enhancer binding to developmental control. Nat Rev Genet, 2012, 13(9):613-626
CrossRef Google scholar
[79]
StephensC, Hammond-KosackKE, KanyukaK. WAKsing plant immunity, waning diseases. J Exp Bot, 2022, 73(1):22-37
CrossRef Google scholar
[80]
SuganoS, JiangCJ, MiyazawaS, MasumotoC, YazawaK, HayashiN, ShimonoM, NakayamaA, MiyaoM, TakatsujiH. Role of OsNPR1 in rice defense program as revealed by genome-wide expression analysis. Plant Mol Biol, 2010, 74(6):549-562
CrossRef Google scholar
[81]
SunY, HanZ, TangJ, HuZ, ChaiC, ZhouB, ChaiJ. Structure reveals that BAK1 as a co-receptor recognizes the BRI1-bound brassinolide. Cell Res, 2013, 23(11):1326-1329
CrossRef Google scholar
[82]
SunY, LiL, MachoAP, HanZ, HuZ, ZipfelC, ZhouJM, ChaiJ. Structural basis for flg22-induced activation of the Arabidopsis FLS2-BAK1 immune complex. Science, 2013, 342(6158):624-628
CrossRef Google scholar
[83]
SunF, DingL, FengW, CaoY, LuF, YangQ, LiW, LuY, ShabekN, FuF, YuH. Maize transcription factor ZmBES1/BZR1-5 positively regulates kernel size. J Exp Bot, 2021, 72(5):1714-1726
CrossRef Google scholar
[84]
TajG, AgarwalP, GrantM, KumarA. MAPK machinery in plants: recognition and response to different stresses through multiple signal transduction pathways. Plant Signal Behav, 2010, 5(11):1370-1378
CrossRef Google scholar
[85]
TangC, WangX, DuanX, WangX, HuangL, KangZ. Functions of the lethal leaf-spot 1 gene in wheat cell death and disease tolerance to Puccinia striiformis. J Exp Bot, 2013, 64(10):2955-2969
CrossRef Google scholar
[86]
TapleyEC, StarrDA. Connecting the nucleus to the cytoskeleton by SUN-KASH bridges across the nuclear envelope. Curr Opin Cell Biol, 2013, 25(1):57-62
CrossRef Google scholar
[87]
TianX, LiX, ZhouW, RenY, WangZ, LiuZ, TangJ, TongH, FangJ, BuQ. Transcription factor OsWRKY53 positively regulates brassinosteroid signaling and plant architecture. Plant Physiol, 2017, 175(3):1337-1349
CrossRef Google scholar
[88]
UauyC, WulffBBH, DubcovskyJ. Combining traditional mutagenesis with new high-throughput sequencing and genome editing to reveal hidden variation in polyploid wheat. Annu Rev Genet, 2017, 51(1):435-454
CrossRef Google scholar
[89]
Uji Y, Kashihara K, Kiyama H, Mochizuki S, Akimitsu K, Gomi K (2019) Jasmonic acid-induced VQ-motif-containing protein OsVQ13 influences the OsWRKY45 signaling pathway and grain size by associating with OsMPK6 in rice. Int J Mol Sci 20(12). https://doi.org/10.3390/ijms20122917.
[90]
United Nations DoEaSA, Population Division (2022) World population prospects 2022: summary of results. UN DESA/POP/2022/TR/NO. 3.
[91]
ValandroF, MenguerPK, Cabreira-CagliariC, Margis-PinheiroM, CagliariA. Programmed cell death (PCD) control in plants: New insights from the Arabidopsis thaliana deathosome. Plant Sci, 2020, 299: 110603
CrossRef Google scholar
[92]
ViottiC, BubeckJ, StierhofYD, KrebsM, LanghansM, van den BergW, van DongenW, RichterS, GeldnerN, TakanoJ, JurgensG, de VriesSC, RobinsonDG, SchumacherK. Endocytic and secretory traffic in Arabidopsis merge in the trans-Golgi network/early endosome, an independent and highly dynamic organelle. Plant Cell, 2010, 22(4):1344-1357
CrossRef Google scholar
[93]
Wan J, He M, Hou Q, Zou L, Yang Y, Wei Y, Chen X (2021) Cell wall associated immunity in plants. Stress Biol 1(1). https://doi.org/10.1007/s44154-021-00003-4.
[94]
WangS, GuY, ZebellSG, AndersonLK, WangW, MohanR, DongX. A noncanonical role for the CKI-RB-E2F cell-cycle signaling pathway in plant effector-triggered immunity. Cell Host Microbe, 2014, 16(6):787-794
CrossRef Google scholar
[95]
WangY, ChengX, ShanQ, ZhangY, LiuJ, GaoC, QiuJL. Simultaneous editing of three homoeoalleles in hexaploid bread wheat confers heritable resistance to powdery mildew. Nat Biotechnol, 2014, 32(9):947-951
CrossRef Google scholar
[96]
WangJ, ZhouL, ShiH, ChernM, YuH, YiH, HeM, YinJJ, ZhuXB, LiY, LiWT, LiuJL, WangJC, ChenXQ, QingH, WangYP, LiuGF, WangWM, LiP, WuXJ, ZhuLH, ZhouJM, RonaldPC, LiSG, LiJY, ChenXW. A single transcription factor promotes both yield and immunity in rice. Science, 2018, 361(6406):1026-1028
CrossRef Google scholar
[97]
WangP, ZhouL, JamiesonP, ZhangL, ZhaoZ, BabiloniaK, ShaoW, WuL, MustafaR, AminI, DiomaiutiA, PontiggiaD, FerrariS, HouY, HeP, ShanL. The cotton wall-associated kinase GhWAK7A mediates responses to fungal wilt pathogens by complexing with the chitin sensory receptors. Plant Cell, 2020, 32(12):3978-4001
CrossRef Google scholar
[98]
WangW, FengB, ZhouJM, TangD. Plant immune signaling: advancing on two frontiers. J Integr Plant Biol, 2020, 62(1):2-24
CrossRef Google scholar
[99]
WangX, ZhangH, NyamesortoB, LuoY, MuX, WangF, KangZ, LagudahE, HuangL. A new mode of NPR1 action via an NB-ARC-NPR1 fusion protein negatively regulates the defence response in wheat to stem rust pathogen. New Phytol, 2020, 228(3):959-972
CrossRef Google scholar
[100]
WangY, CaoQ, ZhangJ, WangS, ChenC, WangC, ZhangH, WangY, JiW. Cytogenetic analysis and molecular marker development for a new wheat-thinopyrum ponticum 1J(s) (1D) disomic substitution line with resistance to stripe rust and powdery mildew. Front Plant Sci, 2020, 11: 1282
CrossRef Google scholar
[101]
WangN, TangC, FanX, HeM, GanP, ZhangS, HuZ, WangX, YanT, ShuW, YuL, ZhaoJ, HeJ, LiL, WangJ, HuangX, HuangL, ZhouJM, KangZ, WangX. Inactivation of a wheat protein kinase gene confers broad-spectrum resistance to rust fungi. Cell, 2022, 185(16):2961-2974 e2919
CrossRef Google scholar
[102]
Wang C, Wang G, Wen X, Qu X, Zhang Y, Zhang X, Deng P, Chen C, Ji W, Zhang H (2023) Characteristics and expression analysis of invertase gene family in common wheat (Triticum aestivum L.). Genes (Basel) 14(1). https://doi.org/10.3390/genes14010041.
[103]
WilkinsonSW, MageroyMH, Lopez SanchezA, SmithLM, FurciL, CottonTEA, KrokeneP, TonJ. Surviving in a hostile world: plant strategies to resist pests and diseases. Annu Rev Phytopathol, 2019, 57: 505-529
CrossRef Google scholar
[104]
WolfS. Plant cell wall signalling and receptor-like kinases. Biochem J, 2017, 474(4):471-492
CrossRef Google scholar
[105]
WolfS. Cell wall signaling in plant development and defense. Annu Rev Plant Biol, 2022, 73: 323-353
CrossRef Google scholar
[106]
XuXM, MeuliaT, MeierI. Anchorage of plant RanGAP to the nuclear envelope involves novel nuclear-pore-associated proteins. Curr Biol, 2007, 17(13):1157-1163
CrossRef Google scholar
[107]
XuR, DuanP, YuH, ZhouZ, ZhangB, WangR, LiJ, ZhangG, ZhuangS, LyuJ, LiN, ChaiT, TianZ, YaoS, LiY. Control of grain size and weight by the OsMKKK10-OsMKK4-OsMAPK6 signaling pathway in rice. Mol Plant, 2018, 11(6):860-873
CrossRef Google scholar
[108]
XuP, MaW, LiuJ, HuJ, CaiW. Overexpression of a small GTP-binding protein Ran1 in Arabidopsis leads to promoted elongation growth and enhanced disease resistance against P. syringae DC3000. Plant J, 2021, 108(4):977-991
CrossRef Google scholar
[109]
YangZ. Plant growth: a matter of WAK seeing the wall and talking to BRI1. Curr Biol, 2022, 32(12):R564-R566
CrossRef Google scholar
[110]
YangY, WangW, ChuZ, ZhuJK, ZhangH. Roles of nuclear pores and nucleo-cytoplasmic trafficking in plant stress responses. Front Plant Sci, 2017, 8: 574
CrossRef Google scholar
[111]
YuanB, ShenX, LiX, XuC, WangS. Mitogen-activated protein kinase OsMPK6 negatively regulates rice disease resistance to bacterial pathogens. Planta, 2007, 226(4):953-960
CrossRef Google scholar
[112]
ZhangJ, LiW, XiangT, LiuZ, LalukK, DingX, ZouY, GaoM, ZhangX, ChenS, MengisteT, ZhangY, ZhouJ-M. Receptor-like cytoplasmic kinases integrate signaling from multiple plant immune receptors and are targeted by a pseudomonas syringae effector. Cell Host Microbe, 2010, 7(4):290-301
CrossRef Google scholar
[113]
ZhangN, PomboMA, RosliHG, MartinGB. Tomato wall-associated kinase SlWak1 depends on Fls2/Fls3 to promote apoplastic immune responses to pseudomonas syringae. Plant Physiol, 2020, 183(4):1869-1882
CrossRef Google scholar
[114]
ZhangH, XuX, WangM, WangH, DengP, ZhangY, WangY, WangC, WangY, JiW. A dominant spotted leaf gene TaSpl1 activates endocytosis and defense-related genes causing cell death in the absence of dominant inhibitors. Plant Sci, 2021, 310: 110982
CrossRef Google scholar
[115]
ZhangM, LvS, WangY, WangS, ChenC, WangC, WangY, ZhangH, JiW. Fine mapping and distribution analysis of hybrid necrosis genes Ne1 and Ne2 in wheat in China. Theor Appl Genet, 2022, 135(4):1177-1189
CrossRef Google scholar
[116]
ZhangX, WangG, QuX, WangM, GuoH, ZhangL, LiT, WangY, ZhangH, JiW. A truncated CC-NB-ARC gene TaRPP13L1-3D positively regulates powdery mildew resistance in wheat via the RanGAP-WPP complex-mediated nucleocytoplasmic shuttle. Planta, 2022, 255(3):60
CrossRef Google scholar
[117]
Zhang H, Li HP, Zhang XY, Yan WQ, Deng PC, Zhang YN, Peng SL, Wang YJ, Wang CY, Ji WQ (2021a) Wall-associated Receptor Kinase and The Expression Profiles in Wheat Responding to Fungal stress. BioRxiv: 451968. https://doi.org/10.1101/2021.07.11.451968.
[118]
ZhouX, GraumannK, EvansDE, MeierI. Novel plant SUN-KASH bridges are involved in RanGAP anchoring and nuclear shape determination. J Cell Biol, 2012, 196(2):203-211
CrossRef Google scholar
[119]
ZhouX, GraumannK, MeierI. The plant nuclear envelope as a multifunctional platform LINCed by SUN and KASH. J Exp Bot, 2015, 66(6):1649-1659
CrossRef Google scholar
[120]
ZhouX, GrovesNR, MeierI. Plant nuclear shape is independently determined by the SUN-WIP-WIT2-myosin XI-i complex and CRWN1. Nucleus, 2015, 6(2):144-153
CrossRef Google scholar
[121]
ZhuZ, YinJ, ChernM, ZhuX, YangC, HeK, LiuY, HeM, WangJ, SongL, WangL, WeiY, WangJ, LiuJ, QingH, BiY, LiM, HuK, QiT, HouQ, ChenX, LiW. New insights into bsr-d1-mediated broad-spectrum resistance to rice blast. Mol Plant Pathol, 2020, 21(7):951-960
CrossRef Google scholar
[122]
ZhuX, RongW, WangK, GuoW, ZhouM, WuJ, YeX, WeiX, ZhangZ. Overexpression of TaSTT3b-2B improves resistance to sharp eyespot and increases grain weight in wheat. Plant Biotechnol J, 2022, 20(4):777-793
CrossRef Google scholar

Accesses

Citations

Detail

Sections
Recommended

/