The karyotypes of 85 specimens of Oligoryzomys nigripes (Rodentia, Sigmodontinae) collected in the Cerrado and Atlantic Forest of seven states of Brazil were analyzed. Eighty four specimens presented a karyotype with 2n = 62 and one individual had 2n = 61 due to a monosomy of the X chromosome. High levels of intra-and inter-population karyotypic variability, due to sex chromosomes heteromorphisms and pericentric inversions in four autosomes (pairs 2, 3, 4 and 8), led to a variation of the autosomal arm numbers (fundamental number, FN) from 78 to 82. Synaptonemal complex analyses revealed normal meiosis in males heterozygous for pericentric inversions. We found 39 different cytotypes, 27 of which are herein described for the first time. A literature survey revealed 46 described karyotypes for O. nigripes. We tested the hypothesis that chromosomal variants frequencies are dependent on geographical distribution and we propose a model for the karyotypical evolution of Oligoryzomys nigripes with 2n = 62/FN = 78-82.

(2004) An undescribed karyotype for Thaptomys (2n = 50) and the mechanism of differentiation from Thaptomysnigrita (2n = 52) evidenced by FISH and Ag-NORs,

Comparative cytogenetics studies based on conventional staining, CBG, GTG, RBG-banding, Ag-NOR staining, fluorescence in situ hybridization (FISH) using telomere probes, length measurements, and meiotic data were performed on two related but previously undescribed cricetid species referred to as Oligoryzomys sp. 1 and Oligoryzomys sp. 2, respectively, from Pico das Almas (Bahia: Brazil) and Serra do Cipó (Minas Gerais: Brazil). Oligoryzomys sp. 1 had 2n = 46 and Oligoryzomys sp. 2 had 2n = 44, 44/45. Our banding data and measurements as well as FISH results support the hypothesis that the difference between the diploid numbers occurred by centric fusion events. The karyotypes had conspicuous and distinguishable macro- and micro-chromosomes, and we suppose that the largest pairs (1, 2, and 3) have evolved from a higher diploid number because of successive tandem fusion mechanisms.

Fluorescence in situ hybridization (FISH) using telomeric and ribosomal sequences was performed in four species of toad genus Chaunus: C. ictericus, C. jimi, C. rubescens and C. schneideri. Analyses based on conventional, C-banding and Ag-NOR staining were also carried out. The four species present a 2n = 22 karyotype, composed by metacentric and submetacentric chromosomes, which were indistinguishable either after conventional staining or banding techniques. Constitutive heterochromatin was predominantly located at pericentromeric regions, and telomeric sequences (TTAGGG)(n) were restricted to the end of all chromosomes. Silver staining revealed Ag-NORs located at the short arm of pair 7, and heteromorphism in size of NOR signals was also observed. By contrast, FISH with ribosomal probes clearly demonstrated absence of any heteromorphism in size of rDNA sequences, suggesting that the difference observed after Ag-staining should be attributed to differences in chromosomal condensation and/or gene activity rather than to the number of ribosomal cistrons.

The distribution of the telomeric sequence (TTAGGG)n was studied in chromosomes of Micoureus demerarae (2n = 14), a South American marsupial, by fluorescence in-situ hybridization (FISH). The telomeric repeat sequence was present at both ends of all chromosomes, but also various interstitial telomeric sequences (ITS) were detected in the pericentromeric heterochromatic regions. Intraspecific differences in the number of ITS (2 to 8) were observed without intraindividual variation. The presence of telomere-like sequences in the same regions of constitutive heterochromatin suggest that these segments are not necessarily remnants of true telomeres resulting from chromosome rearrangements but could be part of the satellite DNA.