2008
DOI: 10.1590/s1415-47572008000400020
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Genetic diversity in Brazilian sweet potato (Ipomoea batatas (L.) Lam., Solanales, Convolvulaceae) landraces assessed with microsatellite markers

Abstract: We used simple sequence repeat (SSR) markers to investigate the genetic diversity of 78 sweet potato (Ipomoea batatas) accessions (58 landraces and 20 putative clones) from traditional agricultural households from 19 local communities in the Vale do Ribeira, São Paulo, Brazil. Eight SSR loci were assessed using 6% (w/v) polyacrylamide gels stained with silver nitrate and the accessions genotyped considering the presence or absence of bands. The results were subjected to analysis of molecular variance (AMOVA), … Show more

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Cited by 64 publications
(46 citation statements)
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“…Dilutions of 1 ng µL -1 of DNA were used for PCR amplification. Eight primer pairs: Ib-316, Ib-318, Ib-242, Ib-248, Ib-255F1, Ib-255, Ib-286 and Ib-297 (Buteler et al, 1999;Veasey et al, 2008) were applied for SSR assessment. PCR reactions were performed in a final volume of 11 μL, containing 1 ng of genomic DNA and following reagents with starting concentrations of: 10 × PCR buffer (Biotools, Madrid, Spain), 10 mM of each dNTP's, 50 mM MgCl2 (Biotools), 10 µM of each primer, 10 µM 5' fluorescently labelled universal primer (6-FAM, NED, HEX) and 0.5 U of Taq DNA polymerase (Biotools).…”
Section: Genetic Analysismentioning
confidence: 99%
See 2 more Smart Citations
“…Dilutions of 1 ng µL -1 of DNA were used for PCR amplification. Eight primer pairs: Ib-316, Ib-318, Ib-242, Ib-248, Ib-255F1, Ib-255, Ib-286 and Ib-297 (Buteler et al, 1999;Veasey et al, 2008) were applied for SSR assessment. PCR reactions were performed in a final volume of 11 μL, containing 1 ng of genomic DNA and following reagents with starting concentrations of: 10 × PCR buffer (Biotools, Madrid, Spain), 10 mM of each dNTP's, 50 mM MgCl2 (Biotools), 10 µM of each primer, 10 µM 5' fluorescently labelled universal primer (6-FAM, NED, HEX) and 0.5 U of Taq DNA polymerase (Biotools).…”
Section: Genetic Analysismentioning
confidence: 99%
“…Application of short sequence repeats (SSR markers) in genetic diversity studies of different agro-economically important species represents informative, effective and reliable marker system (Rusjan et al, 2012(Rusjan et al, , 2015Pipan et al, 2011Pipan et al, , 2013Pipan et al, , 2016Maras et al, 2015;Derlink et al, 2014) for distinguishing among different genetic resources. For sweet potato, which is a hexaploid (2n=6x=90) plant species with an out-crossing mating system (Veasey et al, 2008), SSR marker system is highly applicable due its codominant nature (Pipan et al, 2016).…”
Section: Introductionmentioning
confidence: 99%
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“…It was also observed that 56% of the farmers cultivate only one variety of D. trifida, unlike other species of vegetative propagation, such as cassava (Manihot esculenta), potato (Solanum tuberosum), sweet potato (Ipomoea batatas) (Brush et al, 1981;Salick et al, 1997;Sambatti et al, 2001;Emperaire and Peroni, 2007;Amorozo, 2008;Veasey et al, 2008), where it is customary to keep two or more varieties in the same farm. This decrease in the number of yam varieties maintained by farmers is worrisome because it is directly related to the loss of genetic resources and the process of genetic erosion.…”
Section: Distribution and Socioeconomic Aspectsmentioning
confidence: 99%
“…Although over 1600 EST-based SSR markers have been identified for sweetpotato (Schafleitner et al, 2010), only a limited number of SSR markers have been tested and used in diversity analysis of sweetpotato by various authors (Zhang et al, 1999;Hwang et al, 2002;Gichuru et al, 2005;Elameen et al, 2008;Veasey et al, 2008;Karuri et al, 2010;Tumwegamire et al, 2011;Gwandu et al, 2012).…”
Section: Introductionmentioning
confidence: 99%