Functional validation of AaCaM3 response to high temperature stress in Amorphophallus albus.
Amorphophallus Albus
AaCaM3
Heat stress
Promoter-protein interaction
Journal
BMC plant biology
ISSN: 1471-2229
Titre abrégé: BMC Plant Biol
Pays: England
ID NLM: 100967807
Informations de publication
Date de publication:
28 Jun 2024
28 Jun 2024
Historique:
received:
03
04
2024
accepted:
10
06
2024
medline:
28
6
2024
pubmed:
28
6
2024
entrez:
27
6
2024
Statut:
epublish
Résumé
Amorphophallus is a perennial monocotyledonous herbaceous plant native to the southwestern region of China, widely used in various fields such as food processing, biomedicine and chemical agriculture. However, Amorphophallus is a typical thermolabile plant, and the continuous high temperature in summer have seriously affected the growth, development and economic yield of Amorphophallus in recent years. Calmodulin (CaM), a Ca
Identifiants
pubmed: 38937722
doi: 10.1186/s12870-024-05283-2
pii: 10.1186/s12870-024-05283-2
doi:
Substances chimiques
Calmodulin
0
Plant Proteins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
615Subventions
Organisme : Shuangcheng cooperative agreement research grant of Yibin
ID : No. YBYJY20220602
Organisme : Sichuan Special Project
ID : No. 2022ZYD02
Organisme : Fundamental Research Funds for the Central Universities
ID : SWU-KQ22070
Informations de copyright
© 2024. The Author(s).
Références
Behera SS, Ray RC. Konjac Glucomannan, a promising polysaccharide of Amorphophallus konjac K. Koch in health care. Int J Biol Macromol. 2016;92:942–56. https://doi.org/10.1016/j.ijbiomac.2016.07.098
doi: 10.1016/j.ijbiomac.2016.07.098
pubmed: 27481345
Wang K, Niu Y, Wang QJ, Liu HL, Jin Y, Zhang SL. Cloning and evaluation of reference genes for quantitative real-time PCR analysis in Amorphophallus. PeerJ. 2017;5(4). https://doi.org/10.7717/peerj.3260 . e3260.
Gao Y, Zhang YN, Chen F, Chu HL, Feng C, Wang HB, WU LF, Yin S, Liu C, Chen HH, LI ZM, Zou ZR, Tang LZ. A chromosome-level genome assembly of Amorphophallus konjac provides insights into konjac glucomannan biosynthesis. Comput Struct Biotechnol J. 2022;20:1002–11. https://doi.org/10.1016/j.csbj.2022.02.009
doi: 10.1016/j.csbj.2022.02.009
pubmed: 35242290
pmcid: 8860920
Behera SS, Ray RC. Nutritional and potential health benefits of Konjac Glucomannan, a promising polysaccharide of elephant foot yam, Amorphophallus konjac K. Koch: a review. Food Reviews Int. 2017;33:22–43. https://doi.org/10.1080/87559129.2015.1137310
doi: 10.1080/87559129.2015.1137310
Zhu F. Modifications of Konjac Glucomannan for diverse applications. Food Chem. 2018;256:419–26. https://doi.org/10.1016/j.foodchem.2018.02.151
doi: 10.1016/j.foodchem.2018.02.151
pubmed: 29606469
Ye SX, Zongo AW, Shah BR, Li J, Li B. Konjac Glucomannan (KGM), deacetylated KGM (Da-KGM), and degraded KGM derivatives: a special focus on Colloidal Nutrition. J Agric Food Chem. 2021;69:44, 12921–32. https://doi.org/10.1021/acs.jafc.1c03647
doi: 10.1021/acs.jafc.1c03647
pubmed: 34713703
Tilman D, Balzer C, Hill J, Befort BL. Global food demand and the sustainable intensification of agriculture. Proc Natl Acad Sci USA. 2011;108(50):20260–4. https://doi.org/10.1073/pnas.1116437108
doi: 10.1073/pnas.1116437108
pubmed: 22106295
pmcid: 3250154
Teixeira EI, Fischer G, Velthuizen HV, Walter C, Ewert F. Global hot-spots of heat stress on agricultural crops due to climate change. Agric for Meteorol. 2013;170:206–15. https://doi.org/10.1016/j.agrformet.2011.09.002
doi: 10.1016/j.agrformet.2011.09.002
Zhang H, Zhao Y, Zhu JK. Thriving under stress: how plants Balance Growth and the stress response. Dev Cell. 2020;55(5):529–43. https://doi.org/10.1016/j.devcel.2020.10.012
doi: 10.1016/j.devcel.2020.10.012
pubmed: 33290694
Su YJ, Zhang MZ, Chang CH, Li JH, Sun YY, Cai YD, Xiong W, Gu LP, Yang YJ. The effect of citric-acid treatment on the physicochemical and gel properties of Konjac Glucomannan from Amorphophallus bulbifer. Int J Biol Macromol. 2022;216:95–104.
doi: 10.1016/j.ijbiomac.2022.06.199
pubmed: 35793743
Yue ZY, Wang YH, Zhang N, Zhang B. Expression of the Amorphophallus Albus heat stress transcription factor AaHsfA1 enhances tolerance to environmental stresses in Arabidopsis. Ind Crops Prod. 2021;174:114231. https://doi.org/10.1016/j.indcrop.2021.114231
doi: 10.1016/j.indcrop.2021.114231
Liu HC, Charng YY. Common and distinct functions of Arabidopsis class A1 and A2 heat shock factors in diverse abiotic stress responses and development. Plant Physiol. 2013;163(1):276–90. https://doi.org/10.1104/pp.113.221168
doi: 10.1104/pp.113.221168
pubmed: 23832625
pmcid: 3762648
Ohama N, Sato H, Shinozaki K, Shinozaki YK. Transcriptional Regulatory Network of Plant Heat Stress Response. Trends Plant Sci. 2017;22(1):53–65. https://doi.org/10.1016/j.tplants.2016.08.015
doi: 10.1016/j.tplants.2016.08.015
pubmed: 27666516
Zhang XX, Wang XY, Zhuang LL, Gao YL, Huang BR. Abscisic acid mediation of drought priming-enhanced heat tolerance in tall fescue (Festuca arundinacea) and Arabidopsis. Physiol Plant. 2019;167(4):488–501. https://doi.org/10.1111/ppl.12975
doi: 10.1111/ppl.12975
pubmed: 30977137
Xu HX, Heath MC. Role of calcium in signal transduction during the hypersensitive response caused by basidiospore-derived infection of the cowpea rust fungus. Plant Cell. 1998;10(4):585–97. https://doi.org/10.1105/tpc.10.4.585
doi: 10.1105/tpc.10.4.585
pubmed: 9548984
pmcid: 144015
Tong T, Li Q, Jiang W, Chen G, Xue DW, Deng FL, Zeng FR, Chen ZH. Molecular evolution of calcium signaling and transport in plant adaptation to abiotic stress. Int J Mol Sci. 2021;22(22):12308. https://doi.org/10.3390/ijms222212308
doi: 10.3390/ijms222212308
pubmed: 34830190
pmcid: 8618852
Dong QY, Wallrad L, Almutairi BO, Kudla J. Ca2 + signaling in plant responses to abiotic stresses. J Integr Plant Biol. 2022;64(2):287–300. https://doi.org/10.1111/jipb.13228
doi: 10.1111/jipb.13228
pubmed: 35048537
Ghosh S, Bheri M, Bisht D, Pandey GK. Calcium signaling and transport machinery: potential for development of stress tolerance in plants. Curr Plant Biology. 2022;29:100235. https://doi.org/10.1016/j.cpb.2022.100235
doi: 10.1016/j.cpb.2022.100235
Tuteja N, Mahajan S. Calcium Signaling Network in plants. Plant Signal Behav. 2007;2(2):79–85. https://doi.org/10.4161/psb.2.2.4176
doi: 10.4161/psb.2.2.4176
pubmed: 19516972
pmcid: 2633903
Dodd AN, Kudla J, Sanders D. The language of calcium signaling. Annu Rev Plant Biol. 2010;61:593–620. https://doi.org/10.1146/annurev-arplant-070109-104628
doi: 10.1146/annurev-arplant-070109-104628
pubmed: 20192754
Zhu JK. Abiotic stress signaling and responses in plants. Cell. 2016;167(2):313–24. https://doi.org/10.1016/j.cell.2016.08.029
doi: 10.1016/j.cell.2016.08.029
pubmed: 27716505
pmcid: 5104190
Mohanta TK, Yadav D, Khan AL, Hashem A, Abd_Allah EF, Al-Harrasi A. Molecular players of EF-hand containing calcium signaling event in plants. Int J Mol Sci. 2019;20(6):1476. https://doi.org/10.3390/ijms20061476
Yamniuk AP, Vogel HJ. Structural investigation into the differential target enzyme regulation displayed by plant calmodulin isoforms. Biochemistry. 2005;44(8):3101–11. https://doi.org/10.1021/bi047770y
doi: 10.1021/bi047770y
pubmed: 15723555
Al-Quraan NA, Locy RD, Singh NK. Expression of calmodulin genes in wild type and calmodulin mutants of Arabidopsis thaliana under heat stress. Plant Physiol Biochem. 2010;48(8):697–702. https://doi.org/10.1016/j.plaphy.2010.04.011
doi: 10.1016/j.plaphy.2010.04.011
pubmed: 20554213
Verma S, Negi PN, Narwal P, Kumari P, Kisku AV, Gahlot P, Mittal N, Kumar D. Calcium signaling in coordinating plant development, circadian oscillations and environmental stress responses in plants. Environ Exp Bot. 2022;201:104935. https://doi.org/10.1016/j.envexpbot.2022.104935
doi: 10.1016/j.envexpbot.2022.104935
Li B, Liu HT, Sun DY, Zhou RG. Ca2 + and calmodulin modulate DNA-Binding activity of Maize Heat shock transcription factor in Vitro. Plant Cell Physiol. 2004;45(5):627–34. https://doi.org/10.1093/pcp/pch074
doi: 10.1093/pcp/pch074
pubmed: 15169945
Zheng HY, Wang WL, Xu K, Xu Y, Ji DH, Chen CS, Xie CT. Ca
doi: 10.1016/j.aquaculture.2019.734618
Ding LP, Wu Z, Teng RD, Xu SJ, Cao X, Yuan GZ, Zhang DH, Tan NJ. LlWRKY39 is involved in thermotolerance by activating LlMBF1c and interacting with LlCaM3 in lily (Lilium longiflorum). Hortic Res. 2021;8:36. https://doi.org/10.1038/s41438-021-00473-7
doi: 10.1038/s41438-021-00473-7
pubmed: 33542226
pmcid: 7862462
Liu HT, Sun DY, Zhou RG. Ca2 + and AtCaM3 are involved in the expression of heat shock protein gene in Arabidopsis. Plant Cell Environ. 2005;28:1276–84. https://doi.org/10.1111/j.1365-3040.2005.01365.x
doi: 10.1111/j.1365-3040.2005.01365.x
Zhang W, Zhou RG, Gao YJ, Zheng SZ, Xu P, Zhang SQ, Sun DY. Molecular and genetic evidence for the Key Role of AtCaM3 in Heat-Shock Signal Transduction in Arabidopsis. Plant Physiol. 2009;149(4):1773–84. https://doi.org/10.1104/pp.108.133744
doi: 10.1104/pp.108.133744
pubmed: 19211698
pmcid: 2663753
Xuan Y, Zhou S, Wang L, Cheng YD, Zhao LQ. Nitric oxide functions as a signal and acts upstream of AtCaM3 in thermotolerance in Arabidopsis seedlings. Plant Physiol. 2010;153(4):1895–906. https://doi.org/10.1104/pp.110.160424
doi: 10.1104/pp.110.160424
pubmed: 20576787
pmcid: 2923878
Zheng Y, Xu Y, Ji DH, Xu K, Chen CS, Wang WL, Xie CT. Calcium-calmodulin-involved heat shock response of Neoporphyra haitanensis. Front Mar Sci. 2022;9:875308. https://doi.org/10.3389/fmars.2022.875308
doi: 10.3389/fmars.2022.875308
Wu HC, Jinn TL. Oscillation regulation of Ca
doi: 10.4161/psb.21124
pubmed: 22899079
pmcid: 3489625
Wang Z, Ye SF, Li JJ, Zheng B, Bao MZ, Ning GG. Fusion primer and nested integrated PCR (FPNI-PCR): a new high-efficiency strategy for rapid chromosome walking or flanking sequence cloning. BMC Biotechnol. 2011;11:109. https://doi.org/10.1186/1472-6750-11-109
doi: 10.1186/1472-6750-11-109
pubmed: 22093809
pmcid: 3239319
Cai KF, Kuang LH, Yue WH, Xie SG, Xia X, Zhang GP, Wang JM. Calmodulin and calmodulin-like gene family in barley: identification, characterization and expression analyses. Front Plant Sci. 2022;13:964888. https://doi.org/10.3389/fpls.2022.964888
doi: 10.3389/fpls.2022.964888
pubmed: 36061813
pmcid: 9439640
Cao X, Yi J, Wu Z, Luo X, Zhong XH, Wu J, Khan MA, Zhao Y, Yi MF. Involvement of Ca
doi: 10.1007/s11105-013-0587-y
Li JT, Yu G, Sun XH, Jia CG, Du Q, Li QY, Pan HY. Modification of vectors for functional genomic analysis in plants. Genet Mol Res. 2014;13(3):7815–25. https://doi.org/10.4238/2014.september.26.20
doi: 10.4238/2014.september.26.20
pubmed: 25299096
Grossmann G, Krebs M, Maizel A, Stahl Y, Vermeer JE, Ott T. Green light for quantitative live-cell imaging in plants. J Cell Sci. 2018;131(2):jcs209270. https://doi.org/10.1242/jcs.209270
doi: 10.1242/jcs.209270
pubmed: 29361538
Sharma M, Klösgen RB, Bennewitz B. Fluorescent protein-based approaches for subcellular protein localization in plants. Methods Mol Biol. 2022;2564:203–11. https://doi.org/10.1007/978-1-0716-2667-2_9
doi: 10.1007/978-1-0716-2667-2_9
Zhang K, Yue DY, Wei W, Hu Y, Feng JY, Zou ZR. Characterization and functional analysis of Calmodulin and Calmodulin-Like genes in Fragaria vesca. Front Plant Sci. 2016;7(01820). https://doi.org/10.3389/fpls.2016.01820
Fasani E, DalCorso G, Varotto C, Li MG, Visioli G, Mattarozzi M, Furini A. The MTP1 promoters from Arabidopsis Halleri reveal cis-regulating elements for the evolution of metal tolerance. New Phytol. 2017;214(4):1614–30. https://doi.org/10.1111/nph.14529
doi: 10.1111/nph.14529
pubmed: 28332702
Zhu YF, Zhu GT, Xu R, Jiao ZX, Yang JW, Lin T, Wang Z, Huang SW, Zhang LL, Zhu JK. A natural promoter variation of SlBBX31 confers enhanced cold tolerance during tomato domestication. Plant Biotechnol J. 2023;21(5):1033–43. https://doi.org/10.1111/pbi.14016
doi: 10.1111/pbi.14016
pubmed: 36704926
pmcid: 10106858
Ponjavic J, Lenhard B, Kai C, Kawai J, Carninci P, Hayashizaki Y, Sandelin A. Transcriptional and structural impact of TATA-initiation site spacing in mammalian core promoters. Genome Biol. 2006;7:R78. https://doi.org/10.1186/gb-2006-7-8-r78
doi: 10.1186/gb-2006-7-8-r78
pubmed: 16916456
pmcid: 1779604
Reddy PS, Mahanty S, Kaul T, Nair S, Sopory SK, Reddy MK. A high-throughput genome-walking method and its use for cloning unknown flanking sequences. Anal Biochem. 2008;381(2):248–53. https://doi.org/10.1016/j.ab.2008.07.012
doi: 10.1016/j.ab.2008.07.012
pubmed: 18674512
Wu Z, Li T, Cao X, Zhang DH, Teng NJ. Lily WRKY factor LlWRKY22 promotes thermotolerance through autoactivation and activation of LlDREB2B. Hortic Res. 2022;9:uhac186. https://doi.org/10.1093/hr/uhac186
doi: 10.1093/hr/uhac186
pubmed: 36338843
pmcid: 9627522