Journals / Turkish Journal of Botany / 2015 / Cilt: 39 - Sayı: 6

Estimating genetic diversity among selected cotton genotypes and the identificationof DNA markers associated with resistance to cotton leaf curl disease

Pages
1033–1041
Publication Date
2015-12-04
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

These preliminary results set the stage for initiating in-depth marker-trait association studies, which will be instrumental for initiating marker-assisted breeding in cotton.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:To the extent of our knowledge, applications of DNA markers in marker-assisted breeding of cotton are handicapped due to low genetic diversity in cotton germplasm.
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Key Findings & Data:Based upon 2 years of disease-screening field experiments, a total of 10 cotton genotypes (five highly tolerant, four highly susceptible, and one immune) of diverse origin were selected from the available cotton germplasm (~1200 accessions) of the National Institute for Biotechnology and Genetic Engineering, Faisalabad, Pakistan.
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Conclusion & Impact:These preliminary results set the stage for initiating in-depth marker-trait association studies, which will be instrumental for initiating marker-assisted breeding in cotton.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Gossypium · simple sequence repeats · tetraploid cotton

Abstract

To the extent of our knowledge, applications of DNA markers in marker-assisted breeding of cotton are handicapped due to low genetic diversity in cotton germplasm. Cotton leaf curl disease, a disease of viral origin, has substantially depressed cotton production in Pakistan, and this disease is also an emerging threat to the neighboring cotton-growing countries like China and India. The present study was designed to identify DNA markers, predominately simple sequence repeats (SSRs), associated with tolerance and/or resistance to the disease. Based upon 2 years of disease-screening field experiments, a total of 10 cotton genotypes (five highly tolerant, four highly susceptible, and one immune) of diverse origin were selected from the available cotton germplasm (~1200 accessions) of the National Institute for Biotechnology and Genetic Engineering, Faisalabad, Pakistan. In total, 322 SSRs derived from bacterial artificial chromosome end sequences of Gossypium raimondii (one of the progenitor species of cultivated tetraploid cotton) were screened. Out of these, 65 primer pairs were found polymorphic, and the extent of genetic similarity was in the range of 81.7% to 98.7%. A similarity matrix was used for studying their phylogenetic relationship using unweighted pair-group method with arithmetic means (UPGMA) analysis. The dendrogram showed the grouping of the genotypes into two distinct clusters comprising tolerant and susceptible genotypes, respectively. Out of the polymorphic markers, two SSR markers, PR-91 and CM-43, that were amplified only in tolerant genotypes showed significant association with resistance to the disease. These preliminary results set the stage for initiating in-depth marker-trait association studies, which will be instrumental for initiating marker-assisted breeding in cotton.

Özet

To the extent of our knowledge, applications of DNA markers in marker-assisted breeding of cotton are handicapped due to low genetic diversity in cotton germplasm. Cotton leaf curl disease, a disease of viral origin, has substantially depressed cotton production in Pakistan, and this disease is also an emerging threat to the neighboring cotton-growing countries like China and India. The present study was designed to identify DNA markers, predominately simple sequence repeats (SSRs), associated with tolerance and/or resistance to the disease. Based upon 2 years of disease-screening field experiments, a total of 10 cotton genotypes (five highly tolerant, four highly susceptible, and one immune) of diverse origin were selected from the available cotton germplasm (~1200 accessions) of the National Institute for Biotechnology and Genetic Engineering, Faisalabad, Pakistan. In total, 322 SSRs derived from bacterial artificial chromosome end sequences of Gossypium raimondii (one of the progenitor species of cultivated tetraploid cotton) were screened. Out of these, 65 primer pairs were found polymorphic, and the extent of genetic similarity was in the range of 81.7% to 98.7%. A similarity matrix was used for studying their phylogenetic relationship using unweighted pair-group method with arithmetic means (UPGMA) analysis. The dendrogram showed the grouping of the genotypes into two distinct clusters comprising tolerant and susceptible genotypes, respectively. Out of the polymorphic markers, two SSR markers, PR-91 and CM-43, that were amplified only in tolerant genotypes showed significant association with resistance to the disease. These preliminary results set the stage for initiating in-depth marker-trait association studies, which will be instrumental for initiating marker-assisted breeding in cotton.

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Cite This Article

ABBAS, A., IQBAL, M. A., RAHMAN, M., PATERSON, A. H. (2015). Estimating genetic diversity among selected cotton genotypes and the identificationof DNA markers associated with resistance to cotton leaf curl disease. Turkish Journal of Botany, Cilt: 39 - Sayı: 6, 1033–1041. https://ajindex.com/articles/183579

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References (12)

  1. Abdurakhmonov IY, Buriev ZT, Saha S, Pepper AE, Musaev JA, Almatov A, Shermatov SE, Kushanov FN, Mavlonov GT, Reddy UK et al. (2007). Microsatellite markers associated with lint percentage trait in cotton, Gossypium hirsutum. Euphytica 156: 141–156.
  2. Bardak A, Bolek Y (2012). Genetic diversity of diploid and tetraploid cottons determined by SSR and ISSR markers. Turk J Field Crops 17: 139–144.
  3. Becerra Lopez-Lavalle L, Matheson B, Brubaker CL (2011). A genetic map of an Australian wild Gossypium C genome and assignment of homoeologies with tetraploid cultivated cotton. Genome 54: 779–794.
  4. Bertini CH, Schuster I, Sediyama T, Barros EGD, Moreira MA (2006). Characterization and genetic diversity analysis of cotton cultivars using microsatellites. Genet Mol Biol 29: 321–329.
  5. Blenda A, Scheffler J, Scheffler B, Palmer M, Lacape JM, Yu JZ, Jesudurai C, Jung S, Muthukumar S, Yellambalase P et al. (2006). CMD: A cotton microsatellite database resource for Gossypium genomics. BMC Genomics 7: 132. Briddon RW (2003). Cotton leaf curl disease, a multicomponent begomovirus complex. Mol Plant Pathol 4: 427–434.
  6. Briddon RW, Markham PG (2000). Cotton leaf curl virus disease. Virus Res 71: 151–159.
  7. Brubaker CL, Wendel JF (1994). Reevaluating the origin of domesticated cotton (Gossypium hirsutum; Malvaceae) using nuclear restriction fragment length polymorphisms (RFLPs). Am J Bot 81: 1309–1326.
  8. Cai C, Ye W, Zhang T, Guo W (2014). Association analysis of fiber quality traits and exploration of elite alleles in Upland cotton cultivars/accessions (Gossypium hirsutum L.). J Integr Plant Biol 56: 51–62.
  9. Cai JH, Xie K, Lin L, Qin BX, Chen BS, Meng JR, Liu YL (2010). Cotton leaf curl Multan virus newly reported to be associated with cotton leaf curl disease in China. Plant Pathol 59: 794–795.
  10. Doğan B, Ünal M, Özgökçe F, Martin E, Kaya A (2011). Phylogenetic relationships between Malcolmia, Strigosella, Zuvanda, and some closely related genera (Brassicaceae) from Turkey revealed by inter-simple sequence repeat amplification. Turk J Bot 35: 17–23.
  11. Farooq A, Farooq J, Mahmood A, Shakeel A, Rehman KA, Batool A, Riaz M, Shahid MTH, Mehboob S (2011). An overview of cotton leaf curl virus disease (CLCuD) a serious threat to cotton productivity. Aust J Crop Sci 5: 1823–1831.
  12. Ghaffari S, Hasnaoui N (2013). Microsatellite amplification in plants: optimization procedure of major PCR components. In: Kantartzi SK, editor. Microsatellites: Methods and Protocols. New York, NY, USA: Humana Press, p