2006
DOI: 10.1007/s10592-006-9259-x
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Characterization of 21 microsatellite marker loci in the ring-tailed lemur (Lemur catta)

Abstract: Ring-tailed lemur (Lemur catta) is the only species in the Genus Lemur, distributed in the deciduous and spiny forests of southwestern Madagascar. This species is listed as endangered due to the loss and fragmentation of its natural habitat, a consequence of deforestation. Twenty-one nuclear microsatellite loci were isolated from a genomic DNA derived from a free-ranging ring-tailed lemur population from the Tsimanampetsotsa National Park, Madagascar. We report various parameter estimates and measures to estab… Show more

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Cited by 7 publications
(6 citation statements)
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“…All loci showed high levels of heterozygosity in both populations. Observed heterozygosity for each marker was comparable with—and in many cases greater than—that reported for these markers in other lemur studies, including those on Eulemur fulvus (Jekielek and Strobeck,1999) and captive and wild L. catta (Pastorini et al,2005; Zaonarivelo et al,2007). Additionally, all microsatellites were highly polymorphic, with allele number across loci ranging between 5 and 14 (Table 1).…”
Section: Resultssupporting
confidence: 81%
“…All loci showed high levels of heterozygosity in both populations. Observed heterozygosity for each marker was comparable with—and in many cases greater than—that reported for these markers in other lemur studies, including those on Eulemur fulvus (Jekielek and Strobeck,1999) and captive and wild L. catta (Pastorini et al,2005; Zaonarivelo et al,2007). Additionally, all microsatellites were highly polymorphic, with allele number across loci ranging between 5 and 14 (Table 1).…”
Section: Resultssupporting
confidence: 81%
“…Samples were amplified at up to 6 highly polymorphic loci, Lc5, Lc7 [Pastorini et al, 2005], 69HDZ267 [Zaonarivelo et al, 2007], Efr09 [Jekielek and Strobeck, 1999], L-2 [Merenlender, 1993] and Em12 [Pastorini, in preparation, as cited in Parga et al, 2012] via PCR. The 5 ′ ends of forward primers were fluorescently labeled and DNA was amplified using Qiagen Multiplex kits following Burrell [2009] using annealing temperatures specified in the literature.…”
mentioning
confidence: 99%
“…Eleven microsatellite primers with high variability (Table S2) were selected among those developed by Pastorini, Fernando, Forstner, and Melnick () and Zaonarivelo et al (). PCR conditions for the 11 microsatellite primers were as follows: 10 ng DNA, 200 mM each dNTP, 12.5 pmol of each primer (one of each primer pair was end‐labeled with a fluorescent tag), 1.5 mM MgCl 2 , and 0.5 units of Taq DNA polymerase (hot master Taq 5 Prime).…”
Section: Methodsmentioning
confidence: 99%