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Purity Testing Method for Maize Hybrids Using SSR Markers

Tan Zhen-xin

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Abstract

In this study, (1)two sets of DNA samples were extracted from ground dry seeds and seedlings respectively and compared for their qualities and suitability for PCR amplification; (2)non-denaturing polyacrylamide gel electrophoresis (PAGE) was evaluated for its usefulness in separating maize SSR amplification fragments; (3)9 SSR primer pairs were screened to search for the SSR loci that are suitable for testing the purities of 4 maize hybrids that lack a reliable laboratory method for purity testing. The results are as follows: (1)DNA samples extracted from ground dry seeds are comparable in quality to those from seedlings and amplified no differently from the later; (2)non-denaturing PAGE can detect a large proportion of variation in SSR allele sizes and thus is useful in hybrid purity testing; (3)Polymorphic SSR loci have been found that could be applied to purity testing of these 4 hybrids. A procedure featuring inexpensive equipment and ease of use has been set up for testing maize hybrid purity using SSR marker.

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In this study, (1)two sets of DNA samples were extracted from ground dry seeds and seedlings respectively and compared for their qualities and suitability for PCR amplification; (2)non-denaturing polyacrylamide gel electrophoresis (PAGE) was evaluated for its usefulness in separating maize SSR amplification fragments; (3)9 SSR primer pairs were screened to search for the SSR loci that are suitable for testing the purities of 4 maize hybrids that lack a reliable laboratory method for purity testing. The results are as follows: (1)DNA samples extracted from ground dry seeds are comparable in quality to those from seedlings and amplified no differently from the later; (2)non-denaturing PAGE can detect a large proportion of variation in SSR allele sizes and thus is useful in hybrid purity testing; (3)Polymorphic SSR loci have been found that could be applied to purity testing of these 4 hybrids. A procedure featuring inexpensive equipment and ease of use has been set up for testing maize hybrid purity using SSR marker.

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Available abstract

In this study, (1)two sets of DNA samples were extracted from ground dry seeds and seedlings respectively and compared for their qualities and suitability for PCR amplification; (2)non-denaturing polyacrylamide gel electrophoresis (PAGE) was evaluated for its usefulness in separating maize SSR amplification fragments; (3)9 SSR primer pairs were screened to search for the SSR loci that are suitable for testing the purities of 4 maize hybrids that lack a reliable laboratory method for purity testing. The results are as follows: (1)DNA samples extracted from ground dry seeds are comparable in quality to those from seedlings and amplified no differently from the later; (2)non-denaturing PAGE can detect a large proportion of variation in SSR allele sizes and thus is useful in hybrid purity testing; (3)Polymorphic SSR loci have been found that could be applied to purity testing of these 4 hybrids. A procedure featuring inexpensive equipment and ease of use has been set up for testing maize hybrid purity using SSR marker.

Key concepts: Hybrid, Primer (cosmetics), Biology, Microsatellite, Polyacrylamide gel electrophoresis, Allele, Chromatography, Genetics

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