Molecular analysis of the F4 progenies obtained through pollen selection for heat tolerance in maize (Zea mays)


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Authors

  • SURESH H ANTRE University of Agricultural Sciences, Gandhi Krishi Vignana Kendra, Bengaluru, Karnataka 560 065, India
  • ASHUTOSH SINGH University of Agricultural Sciences, Gandhi Krishi Vignana Kendra, Bengaluru, Karnataka 560 065, India
  • R L RAVIKUMAR University of Agricultural Sciences, Gandhi Krishi Vignana Kendra, Bengaluru, Karnataka 560 065, India

https://doi.org/10.56093/ijas.v93i2.122767

Keywords:

Heat stress, Maize, Pollen selection, SSRs

Abstract

In the present study, three sets of F4 progeny lines developed through different cycles of pollen selection for heat tolerance were studied for the genetic differences using 16 SSR markers during 2017–20 at Department of Plant Biotechnology, University of Agricultural Sciences, Gandhi Krishi Vignana Kendra, Bengaluru, Karnataka. Three groups of F4 progenies used for the study are GGG (pollen selection for heat tolerance in F1, F2 and F3 generation); GCG (pollen selection for heat tolerance only in F1 and F3 generation); CCC (no pollen selection for heat tolerance in F1, F2 and F3 generation). Five randomly selected F4 lines of the cross of heat stress susceptible BTM4 and heat tolerant BTM6 represented each group. The three groups differed significantly for the number of male parent alleles as evidenced by SSR markers. The F4 (GGG) progenies had significantly more number of male parent type alleles compared to F4 (GCG) and F4 (CCC) lines. The F4 (CCC) lines recorded more number of female alleles compared to other F4 (GGG and GCG) lines. The effectiveness of pollen selection for heat tolerance towards increasing the frequency of male parent alleles and their transmission to the succeeding progenies has been demonstrated in the present study.

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References

Babu D R and Ravikumar R L. 2009. Genetic evidence for resistance to fusarium wilt of pollen grains in chickpea (Cicer arietinum L.). Current Science 811–15.

Cattivelli L, Rizza, F, Badeck F W, Mazzucotelli E, Mastrangelo A M, Francia E and Stanca A. M. 2008. Drought tolerance improvement in crop plants: an integrated view from breeding to genomics. Field Crops Research 105(1–2): 1–14. DOI: https://doi.org/10.1016/j.fcr.2007.07.004

Doyle J J and Doyle J L. 1987. A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochemistry Bulletin 19: 11–15.

Fahad S, Bajwa A A, Nazir U, Anjum S A, Farooq A, Zohaib A, Sadia S, Nasim W, Adkins S, Saud S and Ihsan M Z. 2017. Crop production under drought and heat stress: plant responses and management options. Frontiers in Plant Science 1147. DOI: https://doi.org/10.3389/fpls.2017.01147

Frascaroli E and Songstad D D. 2001. Pollen genotype selection for a simply inherited qualitative factor determining resistance to chlorsulfuron in maize. Theoretical and Applied Genetics 102(2): 342–46. DOI: https://doi.org/10.1007/s001220051651

Lizaso J I, Ruiz-Ramosa M, Rodrigueza L, Gabaldon-Lealb C, Oliveirac J A and Loriteb I J. 2018. Impact of high temperatures in maize: phenology and yield components. Field Crops Research 216: 129–40. DOI: https://doi.org/10.1016/j.fcr.2017.11.013

Lohani N, Singh M B and Bhalla P L. 2020. High temperature susceptibility of sexual reproduction in crop plants. Journal of Experimental Botany 71: 555–68. DOI: https://doi.org/10.1093/jxb/erz426

Mohapatra U, Singh A and Ravikumar R L. 2020. Effect of gamete selection in improving of heat tolerance as demonstrated by shift in allele frequency in maize (Zea mays L.). Euphytica 216(5): 1–10. DOI: https://doi.org/10.1007/s10681-020-02603-z

Ottaviano E, Sari-Gorla M and Villa M. 1988. Pollen competitive ability in maize: Within population variability and response to selection. Theoretical and Applied Genetics 76: 601–08. DOI: https://doi.org/10.1007/BF00260915

Pacini E and Dolferus R. 2019. Pollen developmental arrest: maintaining pollen fertility in a world with a changing climate. Frontiers in Plant Science 679. DOI: https://doi.org/10.3389/fpls.2019.00679

Patil B S, Ravikumar R L and Salimath P M. 2006. Effect of pollen selection for moisture stress tolerance on progeny performance in Sorghum. Journal of Food Agriculture and Environment 4(1): 201–04.

Payero J O, Melvin S R, Irmak S and Tarkalson D. 2006. Yield response of corn to deficit irrigation in a semiarid climate. Agricultural Water Management 84(1–2): 101–12. DOI: https://doi.org/10.1016/j.agwat.2006.01.009

Prasad P V, Bheemanahalli R and Jagadish S K. 2017. Field crops and the fear of heat stress-opportunities, challenges and future directions. Field Crops Research 200: 114–21. DOI: https://doi.org/10.1016/j.fcr.2016.09.024

Ravikumar R L, Patil B S and Salimath P M. 2003. Drought tolerance in sorghum by pollen selection using osmotic stress. Euphytica 133(3): 371–76. DOI: https://doi.org/10.1023/A:1025702709095

Ravikumar R L, Patil B S, Soregaon C D and Hegde S G. 2007. Genetic evidence for gametophytic selection of wilt resistant alleles in chickpea. Theoretical and Applied Genetics 114(4): 619–25. DOI: https://doi.org/10.1007/s00122-006-0462-4

Shobha Rani T and Ravikumar R L. 2006. Sporophytic and gametophytic recurrent selection for improvement of partial resistance to Alternaria leaf blight in sunflower (Helianthus annuus L.). Euphytica 147(3): 421–31. DOI: https://doi.org/10.1007/s10681-005-9039-6

Singh A, Antre S H, Ravikumar R L, Kuchanur P H and Lohithaswa H C. 2020. Genetic evidence of pollen selection mediated phenotypic changes in maize conferring transgenerational heat-stress tolerance. Crop Science 60(4): 1907–24. DOI: https://doi.org/10.1002/csc2.20179

Singh A, Kuchanur P H and Ravikumar R L. 2017. Identification of heat tolerant inbred lines using TIR technique and its association with field tolerance. The Bioscan 12(4): 2053–58.

Singh A, Ravikumar R L, Antre S H, Kuchanur P H and Lohithaswa H C. 2022. Consequence of cyclic pollen selection for heat tolerance on the performance of different generations in maize (Zea mays L.). Journal of Genetics 101(2): 1–9. DOI: https://doi.org/10.1007/s12041-022-01373-y

Thakur P, Kumar S, Malik J A, Berger J D and Nayyar H. 2010. Cold stress effects on reproductive development in grain crops: an overview. Environmental and Experimental Botany 67: 429–43. DOI: https://doi.org/10.1016/j.envexpbot.2009.09.004

Touraev A, Fink C S, Stoger E and Heberle-Bors E. 1995. Pollen selection: A transgenic reconstruction approach. Proceedings of the National Academy of Sciences 92: 12165–169. DOI: https://doi.org/10.1073/pnas.92.26.12165

Yumurtaci A, Sipahi H and Zhao L. 2017. Genetic analysis of microsatellite markers for salt stress in two contrasting maize parental lines and their RIL population. Acta Botanica Croatica 76(1): 55–63. DOI: https://doi.org/10.1515/botcro-2016-0042

Zhao C, Liu B, Piao S, Wang X, Lobell D B, Huang Y and Asseng S. 2017. Temperature increase reduces global yields of major crops in four independent estimates. Proceedings of the National Academy of Sciences 114(35): 9326–31. DOI: https://doi.org/10.1073/pnas.1701762114

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Submitted

2022-03-29

Published

2023-02-28

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Short-Communication

How to Cite

ANTRE, S. H., SINGH, A., & RAVIKUMAR, R. L. (2023). Molecular analysis of the F4 progenies obtained through pollen selection for heat tolerance in maize (Zea mays). The Indian Journal of Agricultural Sciences, 93(2), 210–213. https://doi.org/10.56093/ijas.v93i2.122767
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