2006
DOI: 10.1111/j.1471-8286.2006.01508.x
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Development of 21 microsatellite loci for puma (Puma concolor) ecology and forensics

Abstract: We developed 21 microsatellite (13 dinucleotide and 8 tetranucleotide) primers specifically for pumas ( Puma concolor ). The primers were tested across 243 individuals from California and Nevada, and displayed an average of 5.5 alleles per locus. Previously, domestic cat ( Felis catus ) primers have been adapted for puma genetic studies. Puma-specific loci may reduce concerns associated with ascertainment bias, improve genetic structure resolution and provide additional tetranucleotide loci valuable for forens… Show more

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Cited by 27 publications
(24 citation statements)
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“…We optimized conditions for microsatellite DNA primers, six of which were developed from the domestic cat (Felis catus) genome (Culver et al 2000;Menotti-Raymond et al 2005) and six developed from the mountain lion genome (Kurushima et al 2006;Rodzen et al 2007). The six F. catus loci used were Fca-43, Fca-57, Fca-82, Fca-90, Fca-96, and Fca-166.…”
Section: Pcr Amplification and Genotypingmentioning
confidence: 99%
See 1 more Smart Citation
“…We optimized conditions for microsatellite DNA primers, six of which were developed from the domestic cat (Felis catus) genome (Culver et al 2000;Menotti-Raymond et al 2005) and six developed from the mountain lion genome (Kurushima et al 2006;Rodzen et al 2007). The six F. catus loci used were Fca-43, Fca-57, Fca-82, Fca-90, Fca-96, and Fca-166.…”
Section: Pcr Amplification and Genotypingmentioning
confidence: 99%
“…The six P. concolor loci used were Pco-A2, Pco-B105, Pco-B010, Pco-D8, Pco-D301, and Pco-D329. The universal M13 primer was added at the 5′ end of the forward primers to allow fluorescent labeling of the amplicons (Schuelke 2000;Kurushima et al 2006), and reverse primers were designed with a "pig-tail" at the 5′ end to reduce variability in adenylation of amplification products (Brownstein et al 1996). Conditions for PCR amplification were 1× PCR buffer, 0.2 μM each dNTP, 0.05% bovine serum albumin, 0.1 μM M13 universal labeled primer, 0.01 μM M13-tailed forward primer, 0.1 μM pig-tailed reverse primer, and 0.25 U of Taq Polymerase enzyme (Qiagen), in a total volume of 10 μl.…”
Section: Pcr Amplification and Genotypingmentioning
confidence: 99%
“…To individualize each fecal sample, we amplified seven microsatellites loci (PcoA208, PcoC108, PcoB003, PcoB010, PcoB210, PcoA339 and PcoA216) described by Kurushima et al [31], following the PCR protocol described in Miotto et al [17]. The PCR products were genotyped in MegaBACE ET-550R Size Standard sequencer (Amersham Biosciences, Little Chalfont, UK).…”
Section: Microsatellite Genotyping Fecal Samples Individualization mentioning
confidence: 99%
“…To individualize each fecal sample, we amplified a set of 12 species-specific microsatellite loci with primers developed by Kurushima et al (2006): Pco C209, Pco D217, Pco D103, Pco C217, Pco C112, Pco C108, all tetranucleotide-repeat microsatellite loci; and Pco B010, Pco B210, Pco A339, Pco A208, Pco A216, Pco B003, dinucleotide-repeat microsatellite loci. Primers were marked with universal fluorescent M13 tails according to Schuelke (2000).…”
Section: Fecal Samples Individualization and Genetic Analysismentioning
confidence: 99%