Abstract:Rodents constitute one of the most diversified mammalian orders. Due to the morphological similarity in many of the groups, their taxonomy is controversial. Karyotype information proved to be an important tool for distinguishing some species because some of them are species-specific. Additionally, rodents can be an excellent model for chromosome evolution studies since many rearrangements have been described in this group.This work brings a review of cytogenetic data of Brazilian rodents, with information abou… Show more
“…Species identification was confirmed through comparisons with skulls of A. cursor specimens from the mammalian collections, as well as through microscopic analyses of the chromosomes after Giemsa stain procedure, following the morphological classification proposed by Levan et al (1964). The specimen presented diploid number (2n)=14 and fundamental number (NF)=20, which is in agreement with karyotypic data reported for A. cursor (Di-Nizo et al, 2017). Skull, skin, and tissues of the specimen were deposited into the mammalian collection of "Museu de Zoologia João Moojen da Universidade Federal de Viçosa" (MZUFV 4423), Viçosa, Minas Gerais state, Brazil ( Figure 1A).…”
“…Species identification was confirmed through comparisons with skulls of A. cursor specimens from the mammalian collections, as well as through microscopic analyses of the chromosomes after Giemsa stain procedure, following the morphological classification proposed by Levan et al (1964). The specimen presented diploid number (2n)=14 and fundamental number (NF)=20, which is in agreement with karyotypic data reported for A. cursor (Di-Nizo et al, 2017). Skull, skin, and tissues of the specimen were deposited into the mammalian collection of "Museu de Zoologia João Moojen da Universidade Federal de Viçosa" (MZUFV 4423), Viçosa, Minas Gerais state, Brazil ( Figure 1A).…”
“…5). According to cytogenetic data (Di-Nizo et al, 2017;Oliveira da Silva et al, 2019), the species also ranges southward into Vila Rica in northeastern Mato Grosso state. These records suggest that the species is restricted to the Xingu center of endemism (Silva et al, 2005).…”
Section: Neacomys Marajoara New Speciesmentioning
confidence: 99%
“…(2015), "Neacomys sp. " by Di-Nizo et al (2017) and Brandão et al (2019), and "Neacomys sp. C" by Oliveira da Silva et al (2019).…”
Species of Neacomys are small cricetid rodents that occur in forested habitats of Central and South America, from eastern Panama to central Bolivia and central/western Brazil. In order to assess species diversity of this poorly known genus, we obtained cytochrome b gene sequences from the most comprehensive taxonomic and geographic sampling analyzed to date. We also conducted morphological analyses on a large series of specimens housed in 15 museums, including types of 10 out of 14 nominal taxa. Our analyses of the genetic data recovered 17
“…In attempting to review the cytogenetic data of Oxymycterus, Di-Nizo et al [43] listed 2n = 54 for O. amazonicus; however, the sources cited for this information do not describe the karyotype of this taxon [19,36]. In fact, Bonvicino et al [36] (Table 2), exhibit at least one large submetacentric (pair 1), and range from three to five bi-armed chromosomes.…”
Section: New Cytogenetic Data For Oxymycterus and Blarinomysmentioning
Comparative chromosome-painting analysis among highly rearranged karyotypes of Sigmodontinae rodents (Rodentia, Cricetidae) detects conserved syntenic blocks, which are proposed as chromosomal signatures and can be used as phylogenetic markers. In the Akodontini tribe, the molecular topology (Cytb and/or IRBP) shows five low-supported clades (divisions: “Akodon”, “Bibimys”, “Blarinomys”, “Oxymycterus”, and “Scapteromys”) within two high-supported major clades (clade A: “Akodon”, “Bibimys”, and “Oxymycterus”; clade B: “Blarinomys” and “Scapteromys”). Here, we examine the chromosomal signatures of the Akodontini tribe by using Hylaeamys megacephalus (HME) probes to study the karyotypes of Oxymycterus amazonicus (2n = 54, FN = 64) and Blarinomys breviceps (2n = 28, FN = 50), and compare these data with those from other taxa investigated using the same set of probes. We strategically employ the chromosomal signatures to elucidate phylogenetic relationships among the Akodontini. When we follow the evolution of chromosomal signature states, we find that the cytogenetic data corroborate the current molecular relationships in clade A nodes. We discuss the distinct events that caused karyotypic variability in the Oxymycterus and Blarinomys genera. In addition, we propose that Blarinomys may constitute a species complex, and that the taxonomy should be revised to better delimit the geographical boundaries and their taxonomic status.
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