2005
DOI: 10.1111/j.1471-8286.2005.01136.x
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Isolation and characterization of 12 tetra‐repeated microsatellite loci from the Formosan grass lizard (Takydromus formosanus)

Abstract: Twelve tetra‐repeated microsatellite loci were developed for the island‐endemic grass lizard Takydromus formosanus (Squamata: Lacertidae). We characterized these loci by genotyping 51 individuals sampled from six localities. The number of alleles per locus ranged between 12 and 23, whereas the observed heterozygosity ranged between 0.686 and 0.941. None of these loci showed gametic disequilibrium or sex linkage. With such high polymorphism, we believe that these loci should be suitable for fine‐scaled analysis… Show more

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Cited by 4 publications
(5 citation statements)
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“…The result supported that the Platyplacopus merged into Takydromus and negated the validity of Platyplacopus . It is also consistent with the opinions of Arnold et al 21, 22 and Lin et al 8, 23, whom supported the combination of subgenera Platyplacopus and Takydromus into Takydromus .…”
Section: Discussionsupporting
confidence: 92%
See 1 more Smart Citation
“…The result supported that the Platyplacopus merged into Takydromus and negated the validity of Platyplacopus . It is also consistent with the opinions of Arnold et al 21, 22 and Lin et al 8, 23, whom supported the combination of subgenera Platyplacopus and Takydromus into Takydromus .…”
Section: Discussionsupporting
confidence: 92%
“…However, after comparing representative specimens of Platyplacopus and Takydromus , Zhao et al, argued for the validity of Platyplacopus as a full genus on the basis of its distinctness in toe structure from Takydromus 7. Based on molecular data, Lin et al and Ota et al inferred phylogenetic relationships of the genus Takydromus , and negated the validity of Platyplacopus at any taxonomic level 8, 9. Our previous analyses of 12S rRNA sequences from 14 Takydromus spp.…”
Section: Introductionmentioning
confidence: 76%
“…Ten microsatellite loci [37] were evaluated to estimate individual heterozygosity (Table S2). The polymerase chain reactions (PCRs) were set up in a volume of 10 µl containing 50–100 ng genomic DNA, 1× PCR buffer (PROMEGA), 0.15–0.2 µM each forward and reverse primers, 2.5 mM MgCl 2 , 0.2 mM dNTP, and 0.25 U Taq DNA polymerase (PROMEGA).…”
Section: Methodsmentioning
confidence: 99%
“…The polymerase chain reactions (PCRs) were set up in a volume of 10 µl containing 50–100 ng genomic DNA, 1× PCR buffer (PROMEGA), 0.15–0.2 µM each forward and reverse primers, 2.5 mM MgCl 2 , 0.2 mM dNTP, and 0.25 U Taq DNA polymerase (PROMEGA). PCR was carried out under standard conditions, with modifications for each locus [37]. The PCR products were electrophoresed in a MegaBASE™ 1000 autosequencer (Amersham Bioscience, New Jersey, USA) with size marker ET-400 (Amersham Bioscience New Jersey, USA).…”
Section: Methodsmentioning
confidence: 99%
“… 2002 ; Lin et al. 2006 ). In recent years, with the development of mitochondrial DNA (mtDNA) molecular marker technology, the complete mitochondrial genome of T. wolteri and T. sexlineatus is sequenced (Yu & Ji 2013 ; Qin et al.…”
mentioning
confidence: 99%