Comparative cytogenetics in three species of Wood-Warblers (Aves: Passeriformes: Parulidae) reveal divergent banding patterns and chromatic heterogeneity for the W chromosome

Chromosomal rearrangements are an important process in the evolution of species. It is assumed that these rearrangements occur near repetitive sequences and heterochromatic regions. Avian karyotypes have diverse chromosomal band patterns and have been used as the parameters for phylogenetic studies. Although the group has a high diversity of species, no more than 12% has been analyzed cytogenetically, and the Parulidae family are extremely underrepresented in these studies. The aim of this study was to detect independent or simultaneous chromosomal rearrangements, and also to analyze chromosomal banding convergences and divergences of three Wood-Warblers species (Myiothlypis leucoblephara, Basileuterus culicivorus, and Setophaga pitiayumi). Our CBG-band results reveal an unusual W sex chromosome in the three studied species, containing a telomeric euchromatic region. The GTG and RBG bands identify specific regions in the macrochromosomes involved in the rearrangements. Cytogenetic data confirm the identification of speciation processes at the karyotypic of this group.

Identification of the Sibling Species of the Blackfly, Simulium damnosum Complex Using their Polytene Chromosomal Banding Patterns in Oji River System, Enugu State, Nigeria

Identification of the sibling species of the blackfly, S. damnosum complex using their polytene chromosomal banding patterns in Oji river system was carried out with the aim of accurately identifying the particular sibling species of S. damnosum complex involved in the transmission of onchocerciasis in Oji-river LGA and environ. Simulium damnosum complex larvae were collected monthly in forty eight (48) breeding sites in four sampling units for three years in the Oji river system in wet and dry seasons. Collected larvae were preserved in cold Carnoy’s solution prior to processing. Salivary gland chromosomes were extracted, processed and analyzed microscopically for polytene chromosomal banding patterns. Three sibling species of Simulium damnosum complex that breed in the Oji river system were identified in varying degrees. They included S. squamosum, S. yahense and S. damnosum sensu stricto (s.s.). Variation in the occurrence of the sibling species was statistically significant. Dry and wet season catches for all the sibling species in the sampling units were found to differ statistically. The identified sibling species of S. damnosum complex are known to be vectors of Onchocerca volvulus, the causative agent of onchocerciasis, a disease highly prevalent in Oji-river LGA and environ.

Chromosomal relationships among the native rodents (Cricetidae: Oryzomyini) of the Galápagos Islands, Ecuador

Although the Galápagos Islands are recognized for their contribution to our understanding of evolutionary theory and have received the attention of scientists for over 185 years, our understanding of the native rodents there has been minimal relative to many other groups of organisms. Much of what we knew through most of the 20th century was based solely on species descriptions. Chromosome data has been limited to only Nesoryzomys narboroughi (2n = 32, FN (number of autosomal arms) = 50) and Aegialomys galapagoensis (2n = 56; FN = 58). We present the karyotypes of the only remaining extant species in the genus, N. swarthi (2n = 56; FN = 54) and N. fernandinae (2n = 44; FN = 54). Chromosomal banding reveals that extensive rearrangement has occurred within Nesoryzomys, including Robertsonian fusion and tandem fusion events but these alone cannot account for the diverse diploid numbers found within the genus. We propose that 1) N. swarthi represents the ancestral karyotype for the genus, similar to A. galapagoensis, 2) N. swarthi and N. fernandinae share the same fundamental number, suggesting divergence by Robertsonian fusions, and 3) N. narboroughi has the most derived karyotype, based on banding morphology and low diploid number.

CHROMOSOMAL ANALYSIS OF PEROMYSCUS GRATUS (CRICETIDAE) OF TECAMACHALCO, PUEBLA, MEXICO

<p>The description was made of the karyotype of <em>Peromyscus gratus</em> (Cricetidae) in the municipality of Tecamachalco, Puebla. Performing the technique of bone marrow extraction, in the obtention of chromosome, G bands was used Trypsin and for C bands a Barium Hydroxide solution was employed. <em>P</em>. <em>gratus</em> presents a diploid number of 2n = 48 and a fundamental number of NF = 54, the autosomes correspond to one metacentric, one submetacentric, two subtelocentric and 19 pairs telocentric from large to small. The sex chromosome X was subtelocentric and the Y was submetacentric unlike other populations of the species. The chromosomal banding pattern G was obtained. As for chromosome C banding, it was found that the constitutive heterochromatin was in the centromeric regions of the chromosomes.</p>

Treatments Principles in Malignant Homeopathies

Aim of this study is to present the latest researches in the field of molecular medicine, in terms of treatments in malignant hemopathies, emerged from the P53 gene deletion in human lymphoma genome. Method: In recent years proved that the best techniques in the investigation of malignant lymphocytes are the Flow Cytometry, Elisa, ICT and Fluorescence in situ hybridization (FISH). This method is used as an alternative to chromosomal banding, a conventional application in molecular medicine. Discussion: Recent, endogenous somatic gene therapy research is a basic of trial clinical and therapeutic trial. The DNA is used to treat a disease arising as a result of mutations in chromosomal regions. In the past few years, this method has been included in the treatment of CLL, acute lymphocytic leukemia, [ALL], or multiple myeloma [MM]. Conclusion: The frequencies of P53 gene mutations and deletion in CLL can be categorized as individual biomarkers in proteomic and genomic profile for this type of leukemia that can be implemented in targeted patient treatment of personalized medicine.

Allopatric chromosomal variation in Nematocharax venustus Weitzman, Menezes & Britski, 1986 (Actinopterygii: Characiformes) based on mapping of repetitive sequences

ABSTRACT Characiformes is the most cytogenetically studied group of freshwater Actinopterygii, but karyotypical data of several taxa remain unknown. This is the case of Nematocharax , regarded as a monotypic genus and characterized by marked sexual dimorphism. Therefore, we provide the first cytogenetic report of allopatric populations of Nematocharax venustus based on distinct methods of chromosomal banding and fluorescence in situ hybridization (FISH) with repetitive DNA probes (18S and 5S rDNA). The karyotype macrostructure was conserved in all specimens and populations, independently on sex, since they shared a diploid number (2n) of 50 chromosomes divided into 8m+26sm+14st+2a. The heterochromatin was mainly distributed at pericentromeric regions and base-specific fluorochrome staining revealed a single pair bearing GC-rich sites, coincident with nucleolar organizer regions (NORs). On the other hand, interpopulation variation in both number and position of repetitive sequences was observed, particularly in relation to 5S rDNA. Apparently, the short life cycles and restricted dispersal of small characins, such as N. venustus , might have favored the divergence of repetitive DNA among populations, indicating that this species might encompass populations with distinct evolutionary histories, which has important implications for conservation measures.

C-heterochromatin and NORs distribution in karyotypes of three vespertilionid bat species from Turkey

The chromosomal banding analysis of the karyotypes of Turkish populations of Eptesicus serotinus, Nyctalus lasiopterus and Barbastellus barbastellus was performed with the use of C-banding and Ag-NOR staining. The results obtained in E. serotinus and N. lasiopterus were congruent with previous data reported from other regions. The karyotype of E. serotinus (2n = 50, NF = 52) contained a moderate amount of centromeric C-heterochromatin and a single NOR was localized in an acrocentric autosomal pairs. The karyotype of N. lasiopterus (2n = 42, NF = 54) contained a higher amount of centromeric C-heterochromatin and the NORs were localized in two autosomal pairs. The karyotype of B. barbastellus was standard in its general characteristics (2n = 32, NF = 54, low amount of C-heterochromatin) but the NOR was localized in only one acrocentric autosomal pair. In studies from other regions, the NORs were recognized in all five acrocentric autosomal pairs of the complement of B. barbastellus.