2000
DOI: 10.1111/j.0014-3820.2000.tb01253.x
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Mitochondrial Dna Phylogeography of the Polytypic North American Rat Snake (Elaphe Obsoleta): A Critique of the Subspecies Concept

Abstract: Subspecies have been considered artificial subdivisions of species, pattern classes, or incipient species. However, with more data and modern phylogenetic techniques, some subspecies may be found to represent true species. Mitochondrial DNA analysis of the polytypic snake, Elaphe obsoleta, yields well-supported clades that do not conform to any of the currently accepted subspecies. Complete nucleotide sequences of the cytochrome b gene and the mitochondrial control region produced robust maximum-parsimony and … Show more

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Cited by 423 publications
(291 citation statements)
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“…The polymerase chain reaction (PCR) was used for amplification of both the cyt b and c-mos genes. For amplification of the cyt b gene, the forward primer was L14910 (5′-GAC CTG TGA TMT GAA AAA CCA YCG TTG T-3′) according to de Queiroz et al (2002), and the reverse primer was H16064 (5′-CTT TGG TTT ACA AGA ACA ATG CTT TA-3′) according to Burbrink et al (2000). For amplification of the c-mos gene segment, the primers S77 (5′-CAT GGA CTG GGA TCAGTT ATG-3′) and S78 (5′-CCT TGGGTG TGA TTT TCT CAC CT-3′) (Slowinski & Lawson 2002) were used.…”
Section: Methodsmentioning
confidence: 99%
“…The polymerase chain reaction (PCR) was used for amplification of both the cyt b and c-mos genes. For amplification of the cyt b gene, the forward primer was L14910 (5′-GAC CTG TGA TMT GAA AAA CCA YCG TTG T-3′) according to de Queiroz et al (2002), and the reverse primer was H16064 (5′-CTT TGG TTT ACA AGA ACA ATG CTT TA-3′) according to Burbrink et al (2000). For amplification of the c-mos gene segment, the primers S77 (5′-CAT GGA CTG GGA TCAGTT ATG-3′) and S78 (5′-CCT TGGGTG TGA TTT TCT CAC CT-3′) (Slowinski & Lawson 2002) were used.…”
Section: Methodsmentioning
confidence: 99%
“…In North America, some studies have uncovered reduced levels of genetic variation in northern populations supporting expansions from southern refugia (7)(8)(9). However, phylogeographic surveys of the central U.S. are incomplete, and recolonization scenarios have not been adequately tested (10,11).…”
mentioning
confidence: 99%
“…For this study, we targeted Cytb because there are comparable data in GenBank. We amplified partial sequences of the Cytb gene using the primers L14910 and H16064 [25]. DNA was amplified using a SimpliAmp Thermal Cycler (Life Technologies, Carlsbad, CA, USA) in 25 μl reaction volumes, consisting of 10 ng of template DNA, 1.25 U of ELPIS rTaq DNA polymerase (ELPIS, Daejeon, South Korea), 2.5 μl of 10x PCR buffer, 2 μl of 10 mM dNTP mix (2.5 mM each) and 0.5 μl of each primer (10 pmol).…”
Section: Methodsmentioning
confidence: 99%
“…DNA was amplified using a SimpliAmp Thermal Cycler (Life Technologies, Carlsbad, CA, USA) in 25 μl reaction volumes, consisting of 10 ng of template DNA, 1.25 U of ELPIS rTaq DNA polymerase (ELPIS, Daejeon, South Korea), 2.5 μl of 10x PCR buffer, 2 μl of 10 mM dNTP mix (2.5 mM each) and 0.5 μl of each primer (10 pmol). The cycling conditions for PCR were as follows: 94°C for 4 min, followed by 35 cycles at 94°C for 30 s, 57°C for 30 s and 72°C for 1 min with a final extension step of 72°C for 7 min [25]. We verified PCR products by electrophoresis on 1.5% agarose gels, and purified products using an AccuPrep ® PCR Purification Kit (Bioneer, Daejeon, South Korea).…”
Section: Methodsmentioning
confidence: 99%