2016
DOI: 10.3844/ajabssp.2016.13.18
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SSR Analysis of Maternal and Paternal Lines Selected in the Don Region (Russia)

Abstract: Evaluation of DNA polymorphisms of breeding material of sunflower from L.A. Zhdanov Don Experimental Station of oil Crops of V.S. Pustovoit All-Russian Research Institute of Oil Crops represented by 17 maternal (CMS) lines and 12 paternal (Rf) lines was conducted. There were identified 35 allelic variants of CMS lines and 42 allelic variants of Rf lines with use of 11 SSR markers. It is shown that the level of genetic diversity of microsatellite loci of CMS lines is 1.2 times lower than that of Rf lines. The a… Show more

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Cited by 3 publications
(3 citation statements)
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“…Using sunflower map from NCBI database (https://www.ncbi.nlm.nih.gov/projects/mapview/map_sear ch.cgi?taxid=4232&query=Helianthus), we selected 52 SSR markers, with localization on all the 17 linkage groups (chromosomes) of the sunflower genome (Table 2). Genomic DNA was isolated from sunflower leaf tissue, with our modifications (Markin et al, 2016). PCR The PCR was carried out in 25 μL reaction mixture of the following composition: 67 mm Tris-HCl buffer, pH 8.8, 16 mM (NH4)2SO4, 2.5 mM MgSO4, 0.1 mM mercaptoethanol, 0.25 mM of each dNTP (dATP, dCTP, dTTP and dGTP), 400 nM primers, 2.5 units of Taq polymerase and 15 ng of DNA template.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Using sunflower map from NCBI database (https://www.ncbi.nlm.nih.gov/projects/mapview/map_sear ch.cgi?taxid=4232&query=Helianthus), we selected 52 SSR markers, with localization on all the 17 linkage groups (chromosomes) of the sunflower genome (Table 2). Genomic DNA was isolated from sunflower leaf tissue, with our modifications (Markin et al, 2016). PCR The PCR was carried out in 25 μL reaction mixture of the following composition: 67 mm Tris-HCl buffer, pH 8.8, 16 mM (NH4)2SO4, 2.5 mM MgSO4, 0.1 mM mercaptoethanol, 0.25 mM of each dNTP (dATP, dCTP, dTTP and dGTP), 400 nM primers, 2.5 units of Taq polymerase and 15 ng of DNA template.…”
Section: Methodsmentioning
confidence: 99%
“…The most effective and simplest molecular methods for assessing genetic polymorphism are PCR-based techniques. Among such techniques, the Random Amplified Polymorphic DNA (RAPD) and Simple Sequence Repeats (SSR) markers are widely used, allowing rapid detection of the variability of a large number of genome loci (Sivolap and Solodenko, 1998;Sossey-Alaoui et al, 1998;1999;Markin et al, 2016;Suresha et al, 2017;Yang et al, 2018;Uma et al, 2018). The spectra of DNA fragments, obtained as a result of their amplification, can be used as genetic markers for species identification and barcoding, as well as for determining taxonomic differences between species.…”
Section: Introductionmentioning
confidence: 99%
“…Total DNA isolation and PCR were carried out as it was described earlier (Markin et al 2016). Primers designed by Horn (Horn et al 2003) were used for the amplification of SCAR markers (HRG01 and HRG02)…”
Section: Researchmentioning
confidence: 99%