Research Article

Selection of high heterozygosity popcorn varieties in Brazil based on SSR markers

Published: July 19, 2012
Genet. Mol. Res. 11 (3) : 1851-1860 DOI: https://doi.org/10.4238/2012.July.19.5
Cite this Article:
I.B.O. Eloi, C.A. Mangolin, C.A. Scapim, C.S. Gonçalves, M.F.P.S. Machado (2012). Selection of high heterozygosity popcorn varieties in Brazil based on SSR markers. Genet. Mol. Res. 11(3): 1851-1860. https://doi.org/10.4238/2012.July.19.5
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Abstract

We analyzed genetic structure and diversity among eight populations of popcorn, using SSR loci as genetic markers. Our objectives were to select SSR loci that could be used to estimate genetic diversity within popcorn populations, and to analyze the genetic structure of promising populations with high levels of heterozygosity that could be used in breeding programs. Fifty-seven alleles (3.7 alleles per locus) were detected; the highest effective number of alleles (4.21) and the highest gene diversity (0.763) were found for the Umc2226 locus. A very high level of population differentiation was found (FST = 0.3664), with FST for each locus ranging from 0.1029 (Umc1664) to 0.6010 (Umc2350). This analysis allowed us to identify SSR loci with high levels of heterozygosity and heterozygous varieties, which could be selected for production of inbred lines and for developing new cultivars.

We analyzed genetic structure and diversity among eight populations of popcorn, using SSR loci as genetic markers. Our objectives were to select SSR loci that could be used to estimate genetic diversity within popcorn populations, and to analyze the genetic structure of promising populations with high levels of heterozygosity that could be used in breeding programs. Fifty-seven alleles (3.7 alleles per locus) were detected; the highest effective number of alleles (4.21) and the highest gene diversity (0.763) were found for the Umc2226 locus. A very high level of population differentiation was found (FST = 0.3664), with FST for each locus ranging from 0.1029 (Umc1664) to 0.6010 (Umc2350). This analysis allowed us to identify SSR loci with high levels of heterozygosity and heterozygous varieties, which could be selected for production of inbred lines and for developing new cultivars.