Gene pyramiding improved cell membrane stability under heat stress in cotton (Gossypium hirsutum L.).


Journal

BMC plant biology
ISSN: 1471-2229
Titre abrégé: BMC Plant Biol
Pays: England
ID NLM: 100967807

Informations de publication

Date de publication:
28 Sep 2024
Historique:
received: 02 06 2023
accepted: 19 09 2024
medline: 29 9 2024
pubmed: 29 9 2024
entrez: 28 9 2024
Statut: epublish

Résumé

Climate change has been drastically affecting cotton not only in Pakistan but also all over the world. Normally cotton is known as heat tolerant when compared with other crops, but if the high temperature occurs during flowering period the yield decreases significantly. Marker assisted gene pyramiding provides a sustainable solution to improve heat tolerance. A total of seven genotypes were developed by a series of crossing seven tolerant genotypes over the period of three years. Tolerant genotypes were selected by screening for important transcription factors (GHSP26, HSP3, HSFA2, DREB1A, HSP101, DREB2A, GhNAC2, HSPCB, GhWRKY41, TPS, GbMYB5, ANNAT8, GhMPK17, GhMKK1, GhMKK3, GhMPK2, HSC70, APX1 and GhPP2A1). The seven genotypes were evaluated under normal and heat stress in a multi-year trial. The traits related to heat tolerance, such as cell membrane stability, relative water content, excised leaf water loss, plant height, number of nodes, internodal length, number of buds, number of bolls and leaf area was observed under normal and heat stress conditions. The developed genotypes showed improvement in cell membrane stability and relative water content under heat stress. The genotypes [(VH-305×MNH-886)×MNH-1035)×NIAB-78)], [(MNH-1035×MNH-886)×MNH-886)×SM-431] and [(MNH-1035×MNH-886)×MNH-886)×SS-32] depicted heat tolerance and could be used as heat tolerant material for variety development in breeding programs.

Identifiants

pubmed: 39342117
doi: 10.1186/s12870-024-05610-7
pii: 10.1186/s12870-024-05610-7
doi:

Substances chimiques

Plant Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

886

Informations de copyright

© 2024. The Author(s).

Références

FAO. 2020. The state of food and agriculture: overcoming water challenges in agriculture.
Ali A, Erenstein O. Assessing farmer use of climate change adaptation practices and impacts on food security and poverty in Pakistan. Clim Risk Manage. 2017;1:16:183–94.
doi: 10.1016/j.crm.2016.12.001
Amin A, Nasim W, Fahad S, Ali S, Ahmad S, Rasool A, Saleem N, Hammad HM, Sultana SR, Mubeen M, Bakhat HF. Evaluation and analysis of temperature for historical (1996–2015) and projected (2030–2060) climates in Pakistan using SimCLIM climate model: ensemble application. Atmos Res. 2018;15:213:422–36.
doi: 10.1016/j.atmosres.2018.06.021
Han W, Liu S, Lei Y, Zhang Y, Han Y, Wang G, Feng L, Li X, Li Y, Wang Z. Climate warming accelerates cotton growth while cultivar shifts extend the growth period. Field Crops Res. 2023;15:293:108850.
doi: 10.1016/j.fcr.2023.108850
Khalil SI, El-Bassiouny HM, Hassanein RA, Mostafa HA, El-Khawas SA, El-Monem AA. Antioxidant defense system in heat shocked wheat plants previously treated with arginine or putrescine. Australian J Basic App Sci. 2009;3(3):1517–26.
Wahid A, Gelani S, Ashraf M, Foolad MR. Heat tolerance in plants: an overview. Env. Exp. Bot. 2007; 1;61(3):199–223.
Khan MK, Ditta A, Wang B, Fang L, Anwar Z, Ijaz A, Ahmed SR, Khan SM. The intervention of multi-omics approaches for developing abiotic stress resistance in cotton crop under climate change. InSustainable agriculture in the era of the OMICs revolution. 2023; (pp. 37–82). Cham: Springer Int. Pub.
Goutam U, Kukreja S, Yadav R, Salaria N, Thakur K, Goyal AK. Recent trends and perspectives of molecular markers against fungal diseases in wheat. Front Microbio. 2015;25:6:154636.
Singh M, Mallick N, Chand S, Kumari P, Sharma JB, Sivasamy M, Jayaprakash P, Prabhu KV, Jha SK. Vinod. Marker-assisted pyramiding of Thinopyrum-derived leaf rust resistance genes Lr19 and Lr24 in bread wheat variety HD2733. J Gen. 2017;96:951–7.
doi: 10.1007/s12041-017-0859-7
Lu Q. Partial resistance to Fusarium head blight and powdery mildew in wheat 2011.
Santra D, DeMacon VK, Garland-Campbell K, Kidwell K. Marker assisted backcross breeding for simultaneous introgression of stripe rust resistance genes yr5 and yr15 into spring wheat (Triticum aestivum L.). InProceedings of the International Meeting of ASA-CSSA-SSSA, Salt Lake City, UT. 2006; 13 (pp. 74–75).
Cox TS, Raupp WJ, Gill BS. Leaf rust-resistance genes Lr41, Lr42, and Lr43 transferred from Triticum tauschii to common wheat. Crop Sci. 1994;34(2):339–43.
doi: 10.2135/cropsci1994.0011183X003400020005x
Song S, Tian D, Zhang Z, Hu S, Yu J. Rice genomics: over the past two decades and into the future. Genomics Prot Bioinf. 2018;16(6):397–404.
doi: 10.1016/j.gpb.2019.01.001
Ramalingam J, Basharat HS, Zhang G. STS and microsatellite marker-assisted selection for bacterial blight resistance and waxy genes in rice, Oryza sativa L. Euphytica. 2002;127:255–60.
doi: 10.1023/A:1020267000418
Kim YS, Kim IS, Shin SY, Park TH, Park HM, Kim YH, Lee GS, Kang HG, Lee SH, Yoon HS. Overexpression of dehydroascorbate reductase confers enhanced tolerance to salt stress in rice plants (Oryza sativa L. Japonica). J Agr Crop Sci. 2014;200(6):444–56.
doi: 10.1111/jac.12078
Hittalmani S, Parco A, Mew TV, Zeigler RS, Huang N. Fine mapping and DNA marker-assisted pyramiding of the three major genes for blast resistance in rice. Theo App Gen. 2000;100:1121–8.
doi: 10.1007/s001220051395
Narayanan NN, Baisakh N, Vera Cruz CM, Gnanamanickam SS, Datta KB, Datta SK. Molecular breeding for the development of blast and bacterial blight resistance in rice cv. IR50. Crop Sci. 2002;42(6):2072–9.
doi: 10.2135/cropsci2002.2072
Gahan LJ, Ma YT, MacgregorCoble ML, Gould F, Moar WJ, Heckel DG. Genetic basis of resistance to Cry1Ac and Cry2Aa in Heliothis virescens (Lepidoptera: Noctuidae). J Eco Ento. 2005;98(4):1357–68.
doi: 10.1603/0022-0493-98.4.1357
Jing QI, Peng GA, Zhang XX, LU MX, DU YZ. Characterization of two novel heat shock protein 70s and their transcriptional expression patterns in response to thermal stress in adult of Frankliniella occidentalis (Thysanoptera: Thripidae). J Integ Agri. 2018;17(5):1023–31.
doi: 10.1016/S2095-3119(17)61725-8
Lee JH, Hübel A, Schöffl F. Derepression of the activity of genetically engineered heat shock factor causes constitutive synthesis of heat shock proteins and increased thermotolerance in transgenic Arabidopsis. Plant J. 1995;8(4):603–12.
pubmed: 7496404 doi: 10.1046/j.1365-313X.1995.8040603.x
Park CJ, Seo YS. Heat shock proteins: a review of the molecular chaperones for plant immunity. Plant Path J. 2015;31(4):323.
doi: 10.5423/PPJ.RW.08.2015.0150
Rasheed A, Zhao L, Raza A, Mahmood A, Xing H, Lv X, Saeed H, Alqahtani FM, Hashem M, Hassan MU, Gillani SF. Role of molecular breeding tools in enhancing the breeding of Drought-resilient cotton genotypes: an updated review. Water. 2023;15(7):1377.
doi: 10.3390/w15071377
Clarke JM, Townley-Smith TF. Heritability and relationship to yield of excised‐Leaf Water Retention in Durum Wheat 1. Crop Sci. 1986;26(2):289–92.
doi: 10.2135/cropsci1986.0011183X002600020016x
CLARKE JM, McCAIG TN. Excised-leaf water retention capability as an indicator of drought resistance of Triticum genotypes. Can J Plant Sci. 1982;62(3):571–8.
doi: 10.4141/cjps82-086
Blum A, Ebercon A. Cell membrane stability as a measure of drought and heat tolerance in wheat 1. Crop Sci. 1981;21(1):43–7.
doi: 10.2135/cropsci1981.0011183X002100010013x
JJ D. Isolation of plant DNA from plant tissue. Focus. 1990;12:13–5.
Saleem MA, Qayyum A, Malik W, Amjid MW. Molecular breeding of cotton for drought stress tolerance. Cotton Production and Uses: Agronomy, Crop Protection, and Postharvest Technologies. 2020:495–508.
Steel RG, Torrie JH, Dickey DA. Principles and procedures of statistics: a biometrical approach. 1997.
Dewey DR, Lu K. A correlation and path-coefficient analysis of components of crested wheatgrass seed production 1. Agr J. 1959;51(9):515–8.
doi: 10.2134/agronj1959.00021962005100090002x
Zlatev Z, Lidon FC. An overview on drought induced changes in plant growth, water relationsand photosynthesis. Emirates J Food Agri. 2012;57–72.
Sapeta H, Costa JM, Lourenco T, Maroco J, Van der Linde P, Oliveira MM. Drought stress response in Jatropha curcas: growth and physiology. Envi Exp Bot. 2013;85:76–84.
doi: 10.1016/j.envexpbot.2012.08.012
Petrović S, Zvezdanović J, Marković D. Chlorophyll degradation in aqueous mediums induced by light and UV-B irradiation: an UHPLC-ESI-MS study. Rad Phy Chem. 2017;141:8–16.
doi: 10.1016/j.radphyschem.2017.05.024
Hadacek F. Secondary metabolites as plant traits: current assessment and future perspectives. Crit Rev Plant Sci. 2002;21(4):273–322.
doi: 10.1080/0735-260291044269
ur Rahman H, Malik SA, Saleem M. Heat tolerance of upland cotton during the fruiting stage evaluated using cellular membrane thermostability. Field Crops Res. 2004;85(2–3):149–58.
doi: 10.1016/S0378-4290(03)00159-X
Jamil A, Khan SJ, Ullah K. Genetic diversity for cell membrane thermostability, yield and quality attributes in cotton (Gossypium hirsutum L). Gen Res Crop Evo. 202;67(6):1405–14.
Haq SU, Khan A, Ali M, Gai WX, Zhang HX, Yu QH, Yang SB, Wei AM, Gong ZH. Knockdown of CaHSP60-6 confers enhanced sensitivity to heat stress in pepper (Capsicum annuum L). Planta. 2019;250:2127–45.
pubmed: 31606756 doi: 10.1007/s00425-019-03290-4
Saleem MA, Malik W, Qayyum A, Ul-Allah S, Ahmad MQ, Afzal H, Amjid MW, Ateeq MF, Zia ZU. Impact of heat stress responsive factors on growth and physiology of cotton (Gossypium hirsutum L). Mol Bio Rep. 2021;48:1069–79.
doi: 10.1007/s11033-021-06217-z
Yang L, Duan J, Liu Y, Hu W, Liu X, Wang Y, Zhou Z, Zhao W. Changes in carbohydrate distribution of cotton and increase in boll weight reduced yield loss under high temperature. J Exp Bot. 2024:erae122.
Rehman M, Bakhsh A, Zubair M, Rehmani MI, Shahzad A, Nayab S, Khan M, Anum W, Akhtar R, Kanwal N, Manzoor N. Effects of water stress on cotton (Gossypium spp.) plants and productivity. Egypt J Agron. 2021;43(3):307–15.
Mubeen M, Khaliq T, Ahmad A, Ali A, Rasul F, Hussain J. Quantification of seed cotton yield and water use efficiency of cotton under variable irrigation schedules. Crop Environ. 2012;3(1–2):54–7.
Farooq M, Wahid A, Kobayashi NS, Fujita DB, Basra SM. Plant drought stress: effects, mechanisms and management. Sustainable agriculture. 2009:153 – 88.
Colom MR, Vazzana C. Photosynthesis and PSII functionality of drought-resistant and drought-sensitive weeping lovegrass plants. Env Exp Bot. 2003;49(2):135–44.
doi: 10.1016/S0098-8472(02)00065-5
Silva MD, Jifon JL, Da Silva JA, Sharma V. Use of physiological parameters as fast tools to screen for drought tolerance in sugarcane. Braz J Plant Physio. 2007;19:193–201.
doi: 10.1590/S1677-04202007000300003
Rahman S, Shaheen MS, Rahman M, Malik TA. Evaluation of excised leaf water loss and relative water content as screening techniques for breeding drought resistant wheat. Pak J Biol Sci. 2000;3(4):663–5.
doi: 10.3923/pjbs.2000.663.665
Sibel T, Birol T. Some physiological responses of drought stress in wheat genotypes with different ploidity in Turkey. World J Agric Sci. 2007;3:178–83.
Collado MB, Arturi MJ, Aulicino MB, Molina MC. Identification of salt tolerance in seedling of maize (Zea mays L.) with the cell membrane stability trait. Int Res J Plant Sci. 2010;1(5):126–32.
Arfan M. Genetic Basis of Variation for High Temperature Tolerance in Gossypium Hirsutum L (Doctoral dissertation, University of Agriculture, Faisalabad. 2018.
Amjid MW, Malik TA, Amir Shakeel AS, Abdul Wahid AW. QTL mapping for relative leaf water contents, cell membrane stability and excised leaf water loss under drought by using EST-SSR markers in Gossypium hirsutum. 2015; 779–784.
Aslam S, Hussain SB, Baber M, Shaheen S, Aslam S, Waheed R, Seo H, Azhar MT. Estimation of drought tolerance indices in upland cotton under water deficit conditions. Agronomy. 2023;13(4):984.
doi: 10.3390/agronomy13040984
Fu Y, Dong C, Wang J, Wang Y, Li C. Genome-wide association study reveals the genetic control underlying node of the first fruiting branch and its height in upland cotton (Gossypium hirsutum L). Euphytica. 2019;215(2):35.
doi: 10.1007/s10681-019-2361-1
Guo Y, McCarty JC, Jenkins JN, Saha S. QTLs for node of first fruiting branch in a cross of an upland cotton, Gossypium hirsutum L., cultivar with primitive accession Texas 701. Euphytica. 2008;163:113–22.
doi: 10.1007/s10681-007-9613-1
Low A, Hesketh J, Muramoto H. Some environmental effects on the varietal node number of the first fruiting branch 1969.
Abro S, Rajput MT, Khan MA, Sial MA, Tahir SS. Screening of cotton (Gossypium hirsutum L.) genotypes for heat tolerance. Pak J Bot. 2015;47(6):2085–91.
Batcho AA, Sarwar MB, Rashid B, Hassan S, Husnain T. Heat shock protein gene identified from Agave sisalana (as HSP70) confers heat stress tolerance in transgenic cotton (Gossypium hirsutum). Theo. Experi. Plant Physio. 2021;33(2):141–56.
Anwar M, Saleem MA, Dan M, Malik W, Ul-Allah S, Ahmad MQ, Qayyum A, Amjid MW, Zia ZU, Afzal H, Asif M. Morphological, physiological and molecular assessment of cotton for drought tolerance under field conditions. Saudi J Biol Sci. 2022;29(1):444–52.
pubmed: 35002440 doi: 10.1016/j.sjbs.2021.09.009
Sajid M, Saddique MA, Tahir MH, Matloob A, Ali Z, Ahmad F, Shakil Q, Nisa ZU, Kifayat M. Physiological and molecular response of cotton (Gossypium hirsutum L.) to heat stress at the seedling stage 2022.
Iqbal J, Hanif M, Ahmad NH, Bibi A, Nisa Z, Kanwal S. Estimation of relative cell injury in response to heat stress in Gossypium hirsutum L. Sar J Agri. 2023;39(4):952–6.
Nasimi RA, Khan IA, Iqbal MA, Khan AA. Genetic analysis of drought tolerance with respect to fiber traits in upland cotton. Genet Mol Res. 2016;15(4):1–6.
doi: 10.4238/gmr.15048626
Chen T, Li W, Hu X, Guo J, Liu A, Zhang B. A cotton MYB transcription factor, GbMYB5, is positively involved in plant adaptive response to drought stress. Plant Cell Physio. 2015;56(5):917–29.
doi: 10.1093/pcp/pcv019
Wang C, Lu W, He X, Wang F, Zhou Y, Guo X, Guo X. The cotton mitogen-activated protein kinase kinase 3 functions in drought tolerance by regulating stomatal responses and root growth. Plant Cell Physio. 2016;57(8):1629–42.
doi: 10.1093/pcp/pcw090

Auteurs

Muhammad Asif Saleem (MA)

Department of Plant Breeding and Genetics, B. Z. University Multan, Multan, Pakistan. drasifsaleem@bzu.edu.pk.

Waqas Malik (W)

Department of Plant Breeding and Genetics, B. Z. University Multan, Multan, Pakistan.

Muhammad Qadir Ahmad (MQ)

Department of Plant Breeding and Genetics, B. Z. University Multan, Multan, Pakistan.

Sarmad Farogh Arshad (SF)

Institute of Plant Breeding & Biotechnology (IPBB), Muhammad Nawaz Shareef University of Agriculture, Multan, 60000, Pakistan.

Mirza Muhammad Ahad Baig (MMA)

Department of Plant Breeding and Genetics, B. Z. University Multan, Multan, Pakistan.

Muhammad Asif (M)

Department of Plant Breeding and Genetics, B. Z. University Multan, Multan, Pakistan.

Muhammad Nauman (M)

Department of Plant Breeding and Genetics, B. Z. University Multan, Multan, Pakistan.

Muhammad Anwar (M)

School of Tropical Agriculture and Forestry, School of Agriculture and Rural Affairs, School of Rural Revitalization), Hainan University, Haikou, China. anwar_uaar@yahoo.com.

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