scholarly journals Melon Transcriptome Characterization: Simple Sequence Repeats and Single Nucleotide Polymorphisms Discovery for High Throughput Genotyping across the Species

2011 ◽  
Vol 4 (2) ◽  
pp. 118-131 ◽  
Author(s):  
José Miguel Blanca ◽  
Joaquín Cañizares ◽  
Pello Ziarsolo ◽  
Cristina Esteras ◽  
Gisela Mir ◽  
...  
2005 ◽  
Vol 130 (6) ◽  
pp. 912-917 ◽  
Author(s):  
Jernej Jakse ◽  
William Martin ◽  
John McCallum ◽  
Michael J. Havey

The commercial production of onion (Allium cepa L.) inbreds, hybrids, and open-pollinated (OP) cultivars would benefit from a robust set of molecular markers that confidently distinguish among elite germplasms. Large-scale DNA sequencing has revealed that single nucleotide polymorphisms (SNPs), short insertion-deletion (indel) events, and simple sequence repeats (SSRs) are relatively abundant classes of codominant DNA markers. We identified 398 SNPs, indels, and SSRs among 35 elite onion ulations and observed that all populations could be distinguished. Phylogenetic analyses of simple-matching and Jaccard's coefficients for SSRs produced essentially identical trees and relationships were consistent with known pedigrees and previous marker evaluations. The SSRs revealed that elite germplasms from specific companies or breeding programs were often closely related. In contrast, phylogenetic analyses of SNPs and indels did not reveal clear relationships among elite onion populations and there was no agreement among trees generated using SNPs and indels vs. SSRs. This discrepancy was likely due to SNPs and indels occurring among amplicons from duplicated regions (paralogs) of the onion genome. Nevertheless, these PCR-based markers will be useful in the quality control of inbred, hybrid, and OP onion seed lots.


2015 ◽  
Vol 195 ◽  
pp. 124-137 ◽  
Author(s):  
Chandrika Ramadugu ◽  
Manjunath L. Keremane ◽  
Xulan Hu ◽  
David Karp ◽  
Claire T. Federici ◽  
...  

2008 ◽  
Vol 133 (1) ◽  
pp. 42-47 ◽  
Author(s):  
Anil Khar ◽  
Jernej Jakse ◽  
Michael J. Havey

Onion (Allium cepa L.) bulb color is controlled by at least five major loci (I, C, G, L, and R) and seedcoat color by one locus (B). The authors developed families segregating for bulb and seedcoat colors, simple sequence repeats (SSRs), and single nucleotide polymorphisms (SNPs) in genomic amplicons of dihydroflavonol 4-reductase (DFR) and anthocyanidin synthase (ANS). The B and C loci were linked to SSRs on chromosomes 1 and 6 respectively. For all of three families, SNPs in DFR cosegregated with the R locus conditioning red bulb color. In the family from B2246 × B11159, red bulbs versus yellow bulbs were controlled by DFR and a locus (L2) linked at 6.3 cM to ANS. The authors propose that yellow bulb onions have been independently selected numerous times and that yellow populations carry independent mutations in structural or regulatory genes controlling the production of red bulb color in onion.


2012 ◽  
Vol 49 (2) ◽  
pp. 307-315 ◽  
Author(s):  
Yoosook Lee ◽  
Stephanie N. Seifert ◽  
Christen M. Fornadel ◽  
Douglas E. Norris ◽  
Gregory C. Lanzaro

2004 ◽  
Vol 50 (11) ◽  
pp. 2028-2036 ◽  
Author(s):  
Susan Bortolin ◽  
Margot Black ◽  
Hemanshu Modi ◽  
Ihor Boszko ◽  
Daniel Kobler ◽  
...  

Abstract Background: We have developed a novel, microsphere-based universal array platform referred to as the Tag-It™ platform. This platform is suitable for high-throughput clinical genotyping applications and was used for multiplex analysis of a panel of thrombophilia-associated single-nucleotide polymorphisms (SNPs). Methods: Genomic DNA from 132 patients was amplified by multiplex PCR using 6 primer sets, followed by multiplex allele-specific primer extension using 12 universally tagged genotyping primers. The products were then sorted on the Tag-It array and detected by use of the Luminex xMAP™ system. Genotypes were also determined by sequencing. Results: Empirical validation of the universal array showed that the highest nonspecific signal was 3.7% of the specific signal. Patient genotypes showed 100% concordance with direct DNA sequencing data for 736 SNP determinations. Conclusions: The Tag-It microsphere-based universal array platform is a highly accurate, multiplexed, high-throughput SNP-detection platform.


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