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result(s) for
"Shearn, Rylan"
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Evolutionary stasis of the pseudoautosomal boundary in strepsirrhine primates
by
Marais, Gabriel AB
,
Wright, Alison E
,
Lecompte, Emilie
in
Animals
,
Evolution, Molecular
,
Evolutionary Biology
2020
Sex chromosomes are typically comprised of a non-recombining region and a recombining pseudoautosomal region. Accurately quantifying the relative size of these regions is critical for sex-chromosome biology both from a functional and evolutionary perspective. The evolution of the pseudoautosomal boundary (PAB) is well documented in haplorrhines (apes and monkeys) but not in strepsirrhines (lemurs and lorises). Here, we studied the PAB of seven species representing the main strepsirrhine lineages by sequencing a male and a female genome in each species and using sex differences in coverage to identify the PAB. We found that during primate evolution, the PAB has remained unchanged in strepsirrhines whereas several recombination suppression events moved the PAB and shortened the pseudoautosomal region in haplorrhines. Strepsirrhines are well known to have much lower sexual dimorphism than haplorrhines. We suggest that mutations with antagonistic effects between males and females have driven recombination suppression and PAB evolution in haplorrhines
Journal Article
Relationship between antibiotic resistance genes and metals in residential soil samples from Western Australia
2017
Increasing drug-resistant infections have drawn research interest towards examining environmental bacteria and the discovery that many factors, including elevated metal conditions, contribute to proliferation of antibiotic resistance (AR). This study examined 90 garden soils from Western Australia to evaluate predictions of antibiotic resistance genes from total metal conditions by comparing the concentrations of 12 metals and 13 genes related to tetracycline, beta-lactam and sulphonamide resistance. Relationships existed between metals and genes, but trends varied. All metals, except Se and Co, were related to at least one AR gene in terms of absolute gene numbers, but only Al, Mn and Pb were associated with a higher percentage of soil bacteria exhibiting resistance, which is a possible indicator of population selection. Correlations improved when multiple factors were considered simultaneously in a multiple linear regression model, suggesting the possibility of additive effects occurring. Soil-metal concentrations must be considered when determining risks of AR in the environment and the proliferation of resistance.
Journal Article
Age and origin of Australian Bennelongia (Crustacea, Ostracoda)
by
Halse, Stuart
,
Shearn, Rylan
,
Martens, Koen
in
Aquatic ecology
,
Biodiversity
,
Biodiversity hot spots
2015
South-western Australia holds an exceptional number of endemic taxa and has been recognized as a biodiversity hotspot at a global scale. We report a much higher diversity in the genus
Bennelongia
(Ostracoda) in Western than in eastern Australia. Using mitochondrial COI sequence data for phylogenies, relative age estimates, lineage-through-time plots, and reconstructions of ancestral distributions, we test four hypotheses that might explain the higher diversity and endemicity in Western Australia. (1) We find no evidence for ancient relictualism as most
Bennelongia
species are probably of Miocene age. (2) There are also no apparent links to vicariant events: speciation has mostly taken place in Western Australia and has been ongoing through the evolutionary history of
Bennelongia
. (3) Dispersal has apparently not negatively affected Western Australian
Bennelongia
endemicity although these ostracods produce drought-resistant eggs. We report one case of recent long distance dispersal in
B. dedeckkeri
with genetically identical populations occurring more than 2,000 km apart. (4) Since speciation has been ongoing, there is no evidence of recent explosive speciation through genetic isolation. The underlying mechanisms of
Bennelongia
speciation thus remain elusive, although speciation has mostly occurred during a period of increasing aridification of Australia.
Journal Article
Evolutionary stasis of the pseudoautosomal boundary in strepsirrhine primates
by
Wright, Alison E
,
Lecompte, Emilie
,
Lemaitre, Jean-François
in
Chromosomes
,
Degeneration
,
Evolution
2020
Abstract Sex chromosomes are typically comprised of a non-recombining region and a recombining pseudoautosomal region. Accurately quantifying the relative size of these regions is critical for sex chromosome biology both from a functional (i.e. number of sex-linked genes) and evolutionary perspective (i.e. extent of Y degeneration and X-Y heteromorphy). The evolution of the pseudoautosomal boundary (PAB) - the limit between the recombining and the non-recombining regions of the sex chromosomes - is well documented in haplorrhines (apes and monkeys) but not in strepsirrhines (lemurs and lorises), which represent almost 30% of all primates. Here we studied the PAB of seven species representing the main strepsirrhine lineages by sequencing a male and a female genome in each species and using sex differences in coverage to identify the PAB. We found that during primate evolution, the PAB has remained unchanged in strepsirrhines whereas several recombination suppression events moved the PAB and shortened the pseudoautosomal region in haplorrhines. Strepsirrhines are well known to have much lower sexual dimorphism than haplorrhines. We suggest that mutations with antagonistic effects between males and females have driven recombination suppression and PAB evolution in haplorrhines. Our work supports the view that sexually antagonistic mutations have influenced the evolution of sex chromosomes in primates. Competing Interest Statement The authors have declared no competing interest. Footnotes * Cite as: Shearn, R., Wright, A. E., Mousset, S., Régis, C., Penel, S., Lemaitre, J.-F., Douay, G., Crouau-Roy, B., Lecompte, E. and Marais, G. A. B. (2020) Evolutionary stasis of the pseudoautosomal boundary in strepsirrhine primates. bioRxiv, 445072, ver. 6 peer-reviewed and recommended by PCI Evolutionary Biology, https://doi.org/10.1101/445072 * Version 6 of this preprint has been peer-reviewed and recommended by Peer Community In Evolutionary Biology (https://doi.org/10.24072/pci.evolbiol.100108)