Amy D. Roeder
Cardiff University
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Featured researches published by Amy D. Roeder.
Molecular Ecology | 2004
Anthony M. Nsubuga; Martha M. Robbins; Amy D. Roeder; Phillip A. Morin; Christophe Boesch; Linda Vigilant
Genetic analysis using noninvasively collected samples such as faeces continues to pose a formidable challenge because of unpredictable variation in the extent to which usable DNA is obtained. We investigated the influence of multiple variables on the quantity of DNA extracted from faecal samples from wild mountain gorillas and chimpanzees. There was a small negative correlation between temperature at time of collection and the amount of DNA obtained. Storage of samples either in RNAlater solution or dried using silica gel beads produced similar results, but significantly higher amounts of DNA were obtained using a novel protocol that combines a short period of storage in ethanol with subsequent desiccation using silica.
PLOS Biology | 2004
Susan E. Ptak; Amy D. Roeder; Matthew Stephens; Yoav Gilad; Svante Pääbo; Molly Przeworski
Recent experiments using sperm typing have demonstrated that, in several regions of the human genome, recombination does not occur uniformly but instead is concentrated in “hotspots” of 1–2 kb. Moreover, the crossover asymmetry observed in a subset of these has led to the suggestion that hotspots may be short-lived on an evolutionary time scale. To test this possibility, we focused on a region known to contain a recombination hotspot in humans, TAP2, and asked whether chimpanzees, the closest living evolutionary relatives of humans, harbor a hotspot in a similar location. Specifically, we used a new statistical approach to estimate recombination rate variation from patterns of linkage disequilibrium in a sample of 24 western chimpanzees (Pan troglodytes verus). This method has been shown to produce reliable results on simulated data and on human data from the TAP2 region. Strikingly, however, it finds very little support for recombination rate variation at TAP2 in the western chimpanzee data. Moreover, simulations suggest that there should be stronger support if there were a hotspot similar to the one characterized in humans. Thus, it appears that the human TAP2 recombination hotspot is not shared by western chimpanzees. These findings demonstrate that fine-scale recombination rates can change between very closely related species and raise the possibility that rates differ among human populations, with important implications for linkage-disequilibrium based association studies.
Folia Primatologica | 2006
Richard Marvan; Jeroen Stevens; Amy D. Roeder; I. Mazura; Michael William Bruford; J. R. de Ruiter
In the recent past, application of DNA genotyping techniques has enabled researchers to more accurately test relationships between dominance rank (DR), mating success (MS) and reproductive success (RS). Paternity studies often reveal that reproductive outcome does not always correlate with male DR and/or MS and thus open room for discussion and interpretation of alternative reproductive tactics of both sexes. In this study, we analysed male DR, MS and RS in a group of bonobos at Twycross Zoo (UK). Genetic relationships were determined using 8 tetrameric microsatellite loci. Despite clear and asymmetric dominance relationships, analysed using normalised David’s scores based on a dyadic index of dominance among the group’s 3 mature males, we found that the most dominant male did not sire the most offspring. In fact, both infants conceived during the observation period were found to be sired by the lower-ranking males. Although the alpha male had almost exclusive mating access to one of the females during the time she was showing a maximal anogenital swelling, her infant was sired by the lowest-ranking male who mostly mated with her when outside the maximal swelling period. This result suggests that either sperm competition operates and/or ovulation is decoupled from the phase of maximal anogenital swelling which could allow greater female choice.
Folia Primatologica | 2009
Amy D. Roeder; Maxime Bonhomme; Corrine M. C. Heijmans; Michael William Bruford; Brigitte Crouau-Roy; Gaby G. M. Doxiadis; Nel Otting
Many genetic studies on catarrhines use microsatellite markers that were isolated from human DNA. A large number of these markers have been characterized in the great apes, macaques and baboons. However, there are few or no markers available for other members of this group. In this study, an extensive literature search was performed to find microsatellite markers that had been successfully amplified across a range of catarrhine species. These conserved loci can provide a valuable starting point for characterizing loci in other catarrhines. Finally, microsatellite markers were tested in a range of species that are not well represented in the literature.
Folia Primatologica | 2006
Amy D. Roeder; Kathryn Jane Jeffery; Michael William Bruford
DNA profiling with microsatellite markers is a commonly used genetic method of studying the great apes. An efficient method of generating the genetic data is amplification of multiple microsatellites in a single PCR reaction. Here we describe a PCR multiplex in which 9 genetic markers can be amplified simultaneously, thereby saving time, expenses and DNA. This marker system can discriminate between all the great ape species except bonobos and chimpanzees. Furthermore, the cumulative probability of identity values were low for all 4 species tested.
International Journal of Primatology | 2006
Ann-Charlotte Rönn; Olga Andrés; Michael William Bruford; Brigitte Crouau-Roy; Gaby G. M. Doxiadis; Xavier Domingo-Roura; Amy D. Roeder; Ernst J. Verschoor; Hans Zischler; Ann-Christine Syvänen
We evaluated a whole genome amplification method—multiple displacement amplification (MDA)—as a means to conserve valuable nonhuman primate samples. We tested 148 samples from a variety of species and sample sources, including blood, tissue, cell-lines, plucked hair and noninvasively collected semen. To evaluate genotyping success and accuracy of MDA, we used routine genotyping methods, including short tandem repeat (STR) analysis, denaturing gradient gel electrophoresis (DGGE), Alu repeat analysis, direct sequencing, and nucleotide detection by tag-array minisequencing. We compared genotyping results from MDA products to genotypes generated from the original (non-MD amplified) DNA samples. All genotyping methods showed good results with the MDA products as a DNA template, and for some samples MDA improved genotyping success. We show that the MDA procedure has the potential to provide a long-lasting source of DNA for genetic studies, which would be highly valuable for the primate research field, in which genetic resources are limited and for other species in which similar sampling constraints apply.
International Journal of Primatology | 2011
Sabrina Locatelli; Amy D. Roeder; Michael William Bruford; Ronald Noë; Eric Delaporte; Martine Peeters
It is now well established that the human immunodeficiency viruses, HIV-1 and HIV-2, are the results of cross-species transmissions of simian immunodeficiency viruses (SIV) naturally infecting nonhuman primates in sub-Saharan Africa. SIVs are found in many African primates, and humans continue to be exposed to these viruses by hunting and handling primate bushmeat. Sooty mangabeys (Cercocebus atys) and western red colobus (Piliocolobus badius badius) are infected with SIV at a high rate in the Taï Forest, Côte d’Ivoire. We investigated the SIV infection and prevalence in 6 other monkey species living in the Taï Forest using noninvasive methods. We collected 127 fecal samples from 2 colobus species (Colobus polykomos and Procolobus verus) and 4 guenon species (C. diana, C. campbelli, C. petaurista, and C. nictitans). We tested these samples for HIV cross-reactive antibodies and performed reverse transcriptase-polymerase chain reactions (RT-PCR) targeting the gag, pol, and env regions of the SIV genome. We screened 16 human microsatellites for use in individual discrimination and identified 4–6 informative markers per species. Serological analysis of 112 samples yielded negative (n = 86) or uninterpretable (n = 26) results. PCR analysis on 74 samples confirmed the negative results. These results may reflect either the limited number of individuals sampled or a low prevalence of infection. Further research is needed to improve the sensitivity of noninvasive methods for SIV detection.
Infection, Genetics and Evolution | 2008
Sabrina Locatelli; Florian Liegeois; Bénédicte Lafay; Amy D. Roeder; Michael William Bruford; Pierre Formenty; Ronald Noë; Eric Delaporte; Martine Peeters
Folia Primatol 2008;79:305–401 DOI: 10.1159/000137690 2nd Congress of the European Federation for Primatology Prague, September 3–7, 2007 Editors: Vaclav Vancata and Marina Vancatova, Prague, Czech Republic Do Capuchin Monkeys (Cebus apella) Deal with Tokens as They Do with Real Food? Elsa Addessi a , Alessandra Mancini a, b , Lara Crescimbene a, b , Elisabetta Visalberghi a a Unit of Cognitive Primatology and Primate Centre, Institute of Cognitive Sciences and Technologies, CNR, Rome, b Università La Sapienza, Rome, Italy E-Mail: [email protected]
Archive | 2008
S. Van Coillie; P. Galbusera; Amy D. Roeder; W. Schempp; Jeroen Stevens; Michael William Bruford; Kristin Leus
Folia Primatol 2008;79:305–401 DOI: 10.1159/000137690 2nd Congress of the European Federation for Primatology Prague, September 3–7, 2007 Editors: Vaclav Vancata and Marina Vancatova, Prague, Czech Republic Do Capuchin Monkeys (Cebus apella) Deal with Tokens as They Do with Real Food? Elsa Addessi a , Alessandra Mancini a, b , Lara Crescimbene a, b , Elisabetta Visalberghi a a Unit of Cognitive Primatology and Primate Centre, Institute of Cognitive Sciences and Technologies, CNR, Rome, b Università La Sapienza, Rome, Italy E-Mail: [email protected]
Molecular Ecology Notes | 2004
Amy D. Roeder; Frederick I. Archer; Hendrik N. Poinar; Phillip A. Morin