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1.
Cytogenet Genome Res ; 135(2): 126-34, 2011.
Article in English | MEDLINE | ID: mdl-21934291

ABSTRACT

Deltamys Thomas 1917 is a poorly studied and rarely collected taxon of Akodontini (Sigmodontinae). The single described species, Deltamys kempi (DKE), has a basic karyotype with a diploid number of 2n = 37 in males and 2n = 38 in females, a fundamental number FN = 38 for both sexes, and an X(1)X(1)X(2)X(2)/X(1)X(2)Y sex determination system. Herein, a new allopatric form, Deltamys sp. (DSP), is reported, based on specimens from southern Brazil, with 2n = 40, FN = 40 and XX/XY sex chromosomes. We describe the karyotype and mechanism of chromosomal differentiation between both Deltamys complements. Phylogenetic analyses, based on the complete sequence (1,140 bp) of the mitochondrial cytochrome b gene, grouped Deltamys sp. as sister species to D. kempi, with up to 12% genetic divergence between them. The GTG-banding patterns show complete autosomal correspondence between D. kempi and Deltamys sp. and identify a tandem rearrangement involving DSP7, DSP19 and DKE4 that is responsible for the differences in 2n and FN. Chromosome painting with Akodon paranaensis chromosome 21 (a small metacentric akodont marker) paint revealed total homology with the smallest acrocentric Deltamys sp. chromosome, DSP19. This suggests the occurrence of a pericentric inversion or centromeric shift when compared to other akodontines, with a posterior tandem rearrangement giving rise to DKE4. In DKE, large blocks of pericentromeric constitutive heterochromatin are present on the autosomes and the X, and the Y/autosome has an entirely heterochromatic short arm. In DSP, small heterochromatic blocks are observed on autosomes and X, and the Y is a very small, mostly heterochromatic acrocentric. The cytogenetic analyses suggest that the Deltamys sp. karyotype is ancestral, with the derived condition resulting from a tandem fusion (DSP7 + DSP19) and the Y/autosome translocation giving rise to the multiple sex chromosome system. The autosomal rearrangements, the differences in CBG-banding patterns and Ag-NOR localization, as well as the presence of X(1)X(1)X(2)X(2)/X(1)X(2)Y and XX/XY sex determination mechanisms, possibly acting as a reproductive barrier, and the phylogenetic position within the Deltamys genus, with high genetic divergence, call for a taxonomic review of the genus.


Subject(s)
Chromosomes, Mammalian/genetics , Cytochromes b/genetics , Phylogeny , Sigmodontinae/genetics , Animals , Brazil , Chromosome Banding , Chromosome Painting , Diploidy , Evolution, Molecular , Female , Geography , Karyotype , Karyotyping , Male , Sex Chromosomes/genetics , Sigmodontinae/classification , Species Specificity
2.
Braz. j. biol ; 67(4): 619-625, Nov. 2007. tab
Article in English | LILACS | ID: lil-474184

ABSTRACT

We inventoried terrestrial small mammals in an agricultural area in southern Brazil by using trapping and prey consumed by Barn Owls (Tyto alba) and White-tailed Kites (Elanus leucurus). Small mammals were trapped in three habitat types: corn fields, uncultivated fields ("capoeiras"), and native forest fragments. A total of 1,975 small mammal specimens were trapped, another 2,062 identified from the diet of Barn Owls, and 2,066 from the diet of White-tailed Kites. Both trapping and prey in the predators' diet yielded 18 small mammal species: three marsupials (Didelphis albiventris, Gracilinanus agilis, and Monodelphis dimidiata) and 15 rodents (Akodon paranaensis, Bruceppatersonius iheringi, Calomys sp., Cavia aperea, Euryzygomatomys spinosus, Holochilus brasiliensis, Mus musculus, Necromys lasiurus, Nectomys squamipes, Oligoryzomys nigripes, Oryzomys angouya, Oxymycterus sp.1, Oxymycterus sp.2, Rattus norvegicus, and Rattus rattus (Linnaeus, 1758)). The greatest richness was found in the uncultivated habitat. We concluded that the three methods studied for inventorying small mammals (prey in the diet of Barn Owls, White-tailed Kites, and trapping) were complementary, since together, rather than separately, they produced a better picture of local richness.


Nós inventariamos a fauna de pequenos mamíferos terrestres numa área agrícola no sul do Brasil utilizando armadilhas e presas consumidas pela coruja suindara (Tyto alba) e pelo gavião-peneira (Elanus leucurus). Os pequenos mamíferos foram amostrados em três tipos de habitat: cultivos de milho, capoeiras e fragmentos de floresta nativa. Ao todo, 1975 espécimes de pequenos mamíferos foram capturados com armadilhas, 2062 identificados a partir da dieta da suindara e 2066 da dieta do gavião-peneira. Juntas, as capturas com armadilhas e presas identificadas na dieta de ambos os predadores revelaram 18 espécies de pequenos mamíferos: três marsupiais (Didelphis albiventris, Gracilinanus -agilis e Monodelphis dimidiata) e 15 roedores (Akodon paranaensis, Bruceppatersonius iheringi, Calomys sp., Cavia -aperea, Euryzygomatomys spinosus, Holochilus brasiliensis, Mus musculus, Necromys lasiurus, Nectomys squamipes, Oligoryzomys nigripes, Oryzomys angouya, Oxymycterus sp.1, Oxymycterus sp.2, Rattus norvegicus e Rattus rattus). A maior riqueza de espécies foi encontrada nas capoeiras. Nós concluímos que os três métodos estudados para inventariar a fauna de pequenos mamíferos (presas na dieta da suindara, do gavião-peneira e capturas com armadilhas) foram complementares, pois juntos forneceram uma idéia melhor da riqueza local do que individualmente.


Subject(s)
Animals , Biodiversity , Marsupialia/classification , Predatory Behavior , Rodentia/classification , Strigiformes/physiology , Brazil
3.
Braz J Biol ; 67(4): 619-25, 2007 Nov.
Article in English | MEDLINE | ID: mdl-18278312

ABSTRACT

We inventoried terrestrial small mammals in an agricultural area in southern Brazil by using trapping and prey consumed by Barn Owls (Tyto alba) and White-tailed Kites (Elanus leucurus). Small mammals were trapped in three habitat types: corn fields, uncultivated fields ("capoeiras"), and native forest fragments. A total of 1,975 small mammal specimens were trapped, another 2,062 identified from the diet of Barn Owls, and 2,066 from the diet of White-tailed Kites. Both trapping and prey in the predators' diet yielded 18 small mammal species: three marsupials (Didelphis albiventris, Gracilinanus agilis, and Monodelphis dimidiata) and 15 rodents (Akodon paranaensis, Bruceppatersonius iheringi, Calomys sp., Cavia aperea, Euryzygomatomys spinosus, Holochilus brasiliensis, Mus musculus, Necromys lasiurus, Nectomys squamipes, Oligoryzomys nigripes, Oryzomys angouya, Oxymycterus sp.1, Oxymycterus sp.2, Rattus norvegicus, and Rattus rattus (Linnaeus, 1758)). The greatest richness was found in the uncultivated habitat. We concluded that the three methods studied for inventorying small mammals (prey in the diet of Barn Owls, White-tailed Kites, and trapping) were complementary, since together, rather than separately, they produced a better picture of local richness.


Subject(s)
Biodiversity , Marsupialia/classification , Predatory Behavior , Rodentia/classification , Strigiformes/physiology , Animals , Brazil
4.
Cytogenet Genome Res ; 115(2): 169-75, 2006.
Article in English | MEDLINE | ID: mdl-17065799

ABSTRACT

Comparative studies among four species--Akodonazarae (2n = 38), A. lindberghi (2n = 42), A. paranaensis (2n = 44) and A. serrensis (2n = 46)--employing classic cytogenetics (C- and G-bands) and fluorescence in situ hybridization with telomeric (TTAGGG)n sequencesare reported here. Non-telomeric signals in addition to the regular telomeric sites were detected in three species:A. azarae, A. lindberghi and A. serrensis. One interstitial telomeric site (ITS) was observed proximally at the long arm of chromosome 1 of A. azarae. The comparison of G-banding patterns among the species indicated that the ITS was due to a tandem fusion/fission rearrangement. Non-telomeric signals of A. lindberghi and A. serrensis were not related to chromosomal rearrangements; instead, the sequences co-localized with (i) heterochromatic regions of all chromosomes in A. serrensis; (ii) some heterochromatic regions in A. lindberghi, and (iii) both euchromatic and heterochromatic regions in the metacentric pair of A. lindberghi. These exceptional findings revealed that ITS in Akodon can be related to chromosomal rearrangements and repetitive sequences in the constitutive heterochromatin and that the richness of TTAGGG-like sequences in the euchromatin could be hypothesized to be a result of amplification of the referred sequence along the chromosome arms.


Subject(s)
Chromosomes/genetics , Muridae/genetics , Repetitive Sequences, Nucleic Acid/genetics , Animals , Biological Evolution , Brazil , Chromosomes/ultrastructure , Euchromatin/genetics , Euchromatin/ultrastructure , Heterochromatin/genetics , Heterochromatin/ultrastructure , In Situ Hybridization, Fluorescence , Karyotyping/veterinary , Muridae/classification , Species Specificity , Telomere/genetics , Telomere/ultrastructure
5.
Cytogenet Cell Genet ; 88(1-2): 124-9, 2000.
Article in English | MEDLINE | ID: mdl-10773685

ABSTRACT

In a Brazilian population of the neotropical rodent Akodon montensis we found five sex-reversed XY females. These animals were cytogenetically analyzed by chromosome painting using species-specific DNA probes from the Y chromosome, generated by chromosomal microdissection and subsequent use of the degenerate oligonucleotide-primed polymerase chain reaction (DOP-PCR). The results showed a chromosome complement with an apparently normal Y chromosome and an X chromosome carrying a translocation that encompasses a large portion of the Y chromosome (seemingly the entire Y). Ovarian histology suggested that these females are fertile. Amplification of the SRY HMG box sequence by PCR shows that at least one copy of the Sry gene is present in the A. montensis XY females. Based on our findings, we suggest that the breakpoint of the X;Y translocation probably altered an X-linked sex-determining locus (or loci), blocking testicular organogenesis in the XY females. Further studies are necessary to determine the precise location and role of this putative sex-determining chromosomal region. Genetic mechanisms of XY sex reversal in A. montensis populations are discussed.


Subject(s)
Chromosome Painting , Fertility/genetics , Muridae/genetics , Nuclear Proteins , Transcription Factors , Translocation, Genetic/genetics , X Chromosome/genetics , Y Chromosome/genetics , Amino Acid Motifs , Animals , Brazil , Chromosome Banding , Chromosome Breakage/genetics , DNA Probes/genetics , DNA-Binding Proteins/chemistry , DNA-Binding Proteins/genetics , Diploidy , Disorders of Sex Development , Female , Gene Dosage , Heterochromatin/genetics , Karyotyping , Male , Ovary/pathology , Polymerase Chain Reaction , Sex Determination Processes , Sex-Determining Region Y Protein
6.
Hereditas ; 129(3): 263-74, 1998.
Article in English | MEDLINE | ID: mdl-10319722

ABSTRACT

All available published cytogenetic data show the presence of 28 different karyotypes in 311 specimens of A. cursor as an exceptional example of high karyotype variability in a single species. Our present sample of 116 animals collected in the rain forest of the Atlantic coast of the states of São Paulo and Bahia, Brazil, show 25 karyotype constitutions. The diploid number (2n) ranged from 16 to 14, and the number of autosomal arms (NF) from 26 to 18, because of centric fusion and pericentric inversions involving two autosome pairs, pericentric inversions in three other chromosome pairs, trisomy in the pair 7 and the presence of two XO females. Synaptonemal complex analysis, associated with data from experimental cross-breeding, suggested that heterozygous individuals for pericentric inversions have normal fertility. In this paper, we have reviewed the chromosomal data of this species, and have thus standardized the karyotype description and chromosome numbering. We discuss about karyotype evolution of Akodon cursor based on the frequency and constitution of karyotypes of all different geographical samples described so far in the literature.


Subject(s)
Polymorphism, Genetic , Sigmodontinae/genetics , Animals , Brazil , Chromosome Banding , Crosses, Genetic , Female , Karyotyping , Male , Pedigree , Synaptonemal Complex
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