2010
DOI: 10.1016/j.ympev.2010.01.032
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Phylogenetic relationships and divergence dates of the whole mitochondrial genome sequences among three gibbon genera

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Cited by 59 publications
(69 citation statements)
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“…In agreement with this scenario we hypothesized that the HyA was heterozygous for variant forms of chromosomes 6, 8, 9, and 18, as reported in Figure 3. Our results are in agreement with the pattern found by Matsudaira and Ishida (2010) who sequenced the full mtDNA of the genera Hylobates, Nomascus, and Syndactylus and with Kim et al (2011), who based their conclusions on 60 kb of sequence data from a panel of 19 gibbons representing nine species from all four genera.…”
Section: Discussionsupporting
confidence: 92%
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“…In agreement with this scenario we hypothesized that the HyA was heterozygous for variant forms of chromosomes 6, 8, 9, and 18, as reported in Figure 3. Our results are in agreement with the pattern found by Matsudaira and Ishida (2010) who sequenced the full mtDNA of the genera Hylobates, Nomascus, and Syndactylus and with Kim et al (2011), who based their conclusions on 60 kb of sequence data from a panel of 19 gibbons representing nine species from all four genera.…”
Section: Discussionsupporting
confidence: 92%
“…The importance of understanding their rapid genome evolution is also provided by their phylogenetic affinity to humans. Gibbons and humans diverged about 17-23 million years ago (Matsudaira and Ishida 2010) and are classified in the same superfamily Hominoidea.…”
mentioning
confidence: 99%
“…Evidence for this comes from evolutionary comparisons of Great Apes to Old World monkeys (e.g., humans have a 30% slower evolutionary rate as compared to baboons) (Kim et al 2006). While generally bigger Decreasing the mutation rate would lead to a Late Miocene speciation time of up to 10 MYA, thus encompassing previous estimates of divergence at 6-8 MYA based on mtDNA (Chan et al 2010;Matsudaira and Ishida 2010;Van Ngoc et al 2010). However, fossil calibration-based estimates such as used in these studies are subject to their own biases (Lukoschek et al 2012), while estimates of demography from a single locus (especially a nonrecombining region of the genome, no matter how well resolved the gene tree) are subject to large evolutionary stochasticity (Rosenberg and Nordborg 2002).…”
mentioning
confidence: 87%
“…Primarily on the basis of their karyotypes, gibbons are now divided into four major genera, with Nomascus, Symphalangus, Hylobates, and Hoolock each possessing 52, 50, 44, and 38 diploid chromosomes, respectively. While many genetic studies have been performed, including a number based on karyotypes (Müller et al 2003), mitochondrial DNA (mtDNA) (Hayashi et al 1995;Takacs et al 2005;Monda et al 2007;Whittaker et al 2007;Matsudaira and Ishida 2010;Van Ngoc et al 2010), Y chromosomes (Chan et al 2012), Arthrobacter luteus (ALU) repeats (Meyer et al 2012), and short stretches of autosomal sequence Wall et al 2013), the phylogenetic relationships among the four gibbon genera remain unresolved, with at least seven different topologies being supported by different data. A recent study examined 1.5 Mb of orthologous autosomal sequence generated by second-generation sequencing from one individual representing each of the four genera .…”
mentioning
confidence: 99%
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