2002
DOI: 10.1046/j.1471-8286.2002.00294.x
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Characterization of microsatellite loci in Lychnis flos‐cuculi (Caryophyllaceae)

Abstract: We cloned microsatellite repeats from ragged robin Lychnis flos‐cuculi (Caryophyllaceae) and developed 20 primer pairs for microsatellite marker analysis. We used 18 individuals of a large Swiss population to screen microsatellites. Seven loci were polymorphic. Between seven and 11 alleles were found per locus and the observed heterozygosity was between 0.308 and 0.813. Observed heterozygote deficits were significant in five of the seven loci, in line with the mixed mating system of L. flos‐cuculi.

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Cited by 11 publications
(6 citation statements)
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“…DNA was extracted from 10 mg of dry leaf material using the Dneasy 96 Plant Kit (QIAGEN, Hombrechtikon, Switzerland). We used three microsatellite markers developed for L. flos-cuculi (Galeuchet et al, 2002) and three markers developed for Silene latifolia (Moccia et al, 2009), a close relative of L. floscuculi. PCR was carried out as described in Aavik et al (2012).…”
Section: Methodsmentioning
confidence: 99%
“…DNA was extracted from 10 mg of dry leaf material using the Dneasy 96 Plant Kit (QIAGEN, Hombrechtikon, Switzerland). We used three microsatellite markers developed for L. flos-cuculi (Galeuchet et al, 2002) and three markers developed for Silene latifolia (Moccia et al, 2009), a close relative of L. floscuculi. PCR was carried out as described in Aavik et al (2012).…”
Section: Methodsmentioning
confidence: 99%
“…As a measure of herbivory in the field, we used the average number of leaves damaged by herbivores in the field populations during the 3 years 2000–2002 (Galeuchet 2003), including the time when the initial selfing and outcrossing hand‐pollinations (see below) were conducted in 2000 (Perret 2003). Observed heterozygosity of the populations was determined with microsatellite markers based on 9–19 plants from each population (Galeuchet et al. 2002, 2005b).…”
Section: Methodsmentioning
confidence: 99%
“…We screened all plants for variation at seven polymorphic microsatellite loci (Galeuchet et al . 2002b).…”
Section: Microsatellite Analysismentioning
confidence: 99%
“…Polymerase chain reaction (PCR) amplifications were performed in 10-µ L reaction volumes with 25 ng of genomic DNA, 0.5 µ m each of the fluorescence-labelled forward primer and of the reverse primer, and 0.5 units of the HotStar Taq Master Mix (QIAGEN). After a preliminary denaturation step at 95 ° C for 15 min, PCR amplification was performed for 30 cycles of 30 s denaturing at 95 ° C, 30 s of annealing at locus-specific temperatures (Galeuchet et al . 2002b) and 30 s of extension at 72 ° C, with a final 8 minute extension step at 72 ° C. We mixed 2 µ L of the PCR product with 10 µ L of a 75: 1 solution of formamide and GENESCAN-350(ROX) size standard (Applied Biosystems) solution.…”
Section: Microsatellite Analysismentioning
confidence: 99%