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Wallace, M.R., Marchuk, D.A., Anderson, R., Letcher, R., Odeh, H.M., Saulino, A.M., Fountain, J.W., Bereton, A., Nicholson, J., Mitchell, A.L., Brownstein, B.H. and Collins, F.S. (1990) Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients. Science, 249, 181-186.

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• TITLE: Genetic Variations and Cultivar Purity within the G. hirsutum Cultivars via RAPD Marker

  AUTHORS: Farah Raheel, Muhammad Kauser Nawaz Shah, Muhammad Shahid Iqbal, Ijaz Rasool Noorka, Zareen Sarfraz

  KEYWORDS: Polymerase Chain Reaction (PCR), G. hirsutum, RAPD, Variation within the Cultivars

  JOURNAL NAME: American Journal of Plant Sciences, Vol.6 No.2, February 15, 2015

  ABSTRACT: To assess genetic variation within a cultivar, four commercial varieties with five individual G. hirsutum genotypes and their bulk were assayed with selected forty 10-mer RAPDs per cultivar via PCR. CIM-473 cultivar showed amplification of 321 bands in total per primer with an average of 8 bands. A range of similarity i.e.; 80% - 100% within the cultivar has been observed for minimum and maximum respectively. CIM-448 showed amplification of 300 bands in total per primer with an average of 7.5 bands. Maximum similarity of 95% and minimum similarity of 84% was observed within the cultivar. In CIM-1100 the total numbers of fragments amplified are 304, with the average of 7.6 bands per primer and are 12% - 20% polymorphic. Similarly, in NIAB-78 the total numbers of fragments amplified were 310, with the average of 7.7 bands per primer. The reliability of RAPD technique for finding genetic resemblances is indicated by the mentioned results. Numerous groups within 5 individual genotypes bulk among 4 cultivars of G. hirsutum L. have been through cluster analysis which was by the unweighted pair group method of arithmetic means (UPGMA). Dendrograms have been used for showing cultivar relationship.