2008
DOI: 10.1590/s1415-47572008000100028
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Genetic structure in two northern muriqui populations (Brachyteles hypoxanthus, Primates, Atelidae) as inferred from fecal DNA

Abstract: We assessed the genetic diversity of two northern muriqui (Brachyteles hypoxanthus Primata, Atelidae) populations, the Feliciano Miguel Abdala population (FMA, n = 108) in the Brazilian state of Minas Gerais (19°44' S, 41°49' W) and the Santa Maria de Jetibá population (SMJ, n = 18) in the Brazilian state of Espírito Santo (20°01' S, 40°44' W). Fecal DNA was isolated and PCR-RFLP analysis used to analyze 2160 bp of mitochondrial DNA, made up of an 820 bp segment of the gene cytochrome c oxidase subunit 2 (cox2… Show more

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Cited by 6 publications
(3 citation statements)
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“…Total genomic DNA was extracted using the QIAamp DNA Stool Mini Kit (Qiagen) following the manufacturer’s protocol. PCR amplification using the species-specific primers Mono1 and Mono2 produced an internal section of 366 bp that bears the first hypervariable segment (HVSI) of mtDNA as previously described [37] . The PCR products were purified with the Wizard SV Gel and PCR Clean-Up System (Promega) and then quantified using 2.0% agarose gels with Low DNA Mass Ladder (Invitrogen).…”
Section: Methodsmentioning
confidence: 99%
“…Total genomic DNA was extracted using the QIAamp DNA Stool Mini Kit (Qiagen) following the manufacturer’s protocol. PCR amplification using the species-specific primers Mono1 and Mono2 produced an internal section of 366 bp that bears the first hypervariable segment (HVSI) of mtDNA as previously described [37] . The PCR products were purified with the Wizard SV Gel and PCR Clean-Up System (Promega) and then quantified using 2.0% agarose gels with Low DNA Mass Ladder (Invitrogen).…”
Section: Methodsmentioning
confidence: 99%
“…A 463‐base‐pair (bp) fragment containing the mtDNAs hypervariable region I (HVI) was amplified via the polymerase chain reaction (PCR) using the primers Mono1 and Mono2 (Fagundes et al, ). We used primers specifically designed for Brachyteles and high initial annealing temperature (see below) to reduce the risk of amplifying nuclear DNA insertions ( numts ).…”
Section: Methodsmentioning
confidence: 99%
“…A study of a small number of individuals from 2 isolated populations of the endangered species Brachyteles arachnoides with allozymes showed a level of polymorphism of 34.4% and a mean heterozygosity per locus of 11%, with a highly significant differentiation between localities, suggesting that these remnant populations represented important genetic allele reservoirs [Pope, 1998b]. A more recent study [Fagundes et al, 2008] of 2 populations of the northern Brachyteles population (sp. hypoxanthus ) in the State of Espírito Santo (Brazil), based on 2,160 bp of mtDNA, showed a high overall haplotype and nucleotide diversity albeit low within populations, and a high fixation index, probably resulting from their historical subdivision.…”
Section: Population Genetics Of Selected Neotropical Primatesmentioning
confidence: 99%