Chromosome polymorphism in Holochilus venezuelae (Rodentia: Cricetidae): C- and G-bands

Genome ◽  
1991 ◽  
Vol 34 (1) ◽  
pp. 13-18 ◽  
Author(s):  
N. Sangines ◽  
M. Aguilera

Karyological analysis of C- and G-banding patterns of 44 specimens of Holochilus venezuelae revealed six distinct karyomorphs, which were designated as follows: I (2n = 44; fundamental number (FN) = 56); II (2n = 45; FN = 58); IV (2n = 43; FN = 56);V(2n = 44; FN = 58); IV-a(2n = 42; FN = 56); and V-a (2n = 44; FN = 58). This chromosomal polymorphism is interpreted as the result of (i) one or two Robertsonian changes of the centric-fusion type, originating from one member of chromosome pair 10 and one of pair 11 (in karyotypes IV and V) and two metacentric chromosomes from pairs 10 and 11 (in karyotype IV-a); (ii) one pericentric inversion (in karyotype V-a) forming one submetacentric chromosome from the metacentric fusion product described above; and (iii) the presence of B chromosomes, which are almost completely heterochromatic and do not pair with any member of group A. The pattern of C-banding reveals that the first five pairs of metacentric chromosomes contain very little centromeric heterochromatin, while pair 6 and the fusion chromosomes (10/11 F) present a thick band. Extensive homology was found between G-banding patterns of Holochilus brasiliensis from Brazil and H. venezuelae. These facts support the hypothesis of a karyotypic evolution via centric fusions previously proposed for this genus.Key words: accessory chromosome, C- and G-banding, polymorphism, Holochilus venezuelae.

Hereditas ◽  
2004 ◽  
Vol 127 (3) ◽  
pp. 255-262 ◽  
Author(s):  
Katia Cristina Machado Pellegrino ◽  
Sanae Kasahara ◽  
Miguel Trefaut Rodrigues ◽  
Yatiyo Yonenaga-Yassuda

Hereditas ◽  
2008 ◽  
Vol 106 (1) ◽  
pp. 73-81 ◽  
Author(s):  
LEOPOLDO IANNUZZI ◽  
DINO DI BERARDINO ◽  
INGEMAR GUSTAVSSON ◽  
LINO FERRARA ◽  
GIULIA PIA DI MEO

1978 ◽  
Vol 29 (3) ◽  
pp. 196-205 ◽  
Author(s):  
M. García ◽  
R. Miró ◽  
L. Freitas ◽  
J. Egozcue

Genome ◽  
1993 ◽  
Vol 36 (4) ◽  
pp. 672-675 ◽  
Author(s):  
A. Amores ◽  
G. Martinez ◽  
J. Reina ◽  
M. C. Alvarez

A karyotype analysis was carried out in nine specimens of the Sparid species Diplodus bellottii using conventional staining, as well as C-banding and Ag-NOR banding techniques, showing, respectively, 2n = 46 and fundamental number (FN) = 54, and scarce heterochromatic areas irregularly distributed and up to four NOR active regions that were C positive. When compared with the karyotypes of other related species, one centric fusion giving rise to a large metacentric pair and several pericentric inversions seem to have been involved in the karyotype evolution. An intra-individual polymorphism was detected in one specimen, resulting in two karyotypic forms in roughly identical proportion, owing to a larger C-band by the NOR regions, appearing either in a terminal position of the short arms of pair 2 or in telomeric position of pair 3. These findings suggest that the extra heterochromatic segment responsible for the heteromorphism apparently only involves associated heterochromatin and not the NORs themselves. This C-positive block seems to have eventually been transferred between heterologous NOR chromosomes by a somatic event, facilitated by the physical proximity of NOR pairs in the nucleolus.Key words: Sparidae, karyotype, heterochromatin, nucleolus organizers, chromosome polymorphism.


Zootaxa ◽  
2018 ◽  
Vol 4377 (2) ◽  
pp. 280 ◽  
Author(s):  
MATÚŠ KÚDELA ◽  
PETER H. ADLER ◽  
TATIANA KÚDELOVÁ

The black fly Prosimulium italicum Rivosecchi, distributed in the Apennines and Sicily, was described as a subspecies of Prosimulium hirtipes (Fries), based on a few morphological details. It subsequently was considered conspecific with P. hirtipes and the name was synonymized. Analyses of polytene chromosome banding patterns and sequences of mitochondrial DNA (COI and COII) revealed deep genetic divergence between P. italicum from Italy and P. hirtipes from northern and central Europe and confirmed the species status of P. italicum. Populations of P. italicum either lack chromosomal inversion IS-9 or carry it as an X-chromosome polymorphism, whereas all analyzed populations of P. hirtipes (Slovakia, Sweden, England, and Scotland) are fixed for IS-9. The average K2P genetic distance was 3.7% between P. italicum and P. hirtipes from northern Europe (Sweden) and 4.3 % between P. italicum and P. hirtipes from central Europe (Slovakia). Cytogenetic analysis showed the presence of two cytoforms of P. hirtipes (‘A’ in Sweden and Slovakia and ‘B’ in England and Scotland) and two cytoforms of P. italicum (‘A’ in Sicily and ‘B’ in Campania and Basilicata), all of which differ in their sex chromosomes and autosomal polymorphisms, suggesting that P. hirtipes and P. italicum might each be a complex of cryptic species. 


Genes ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 165
Author(s):  
David Javier Galindo ◽  
Gabriela Siqueira Martins ◽  
Miluse Vozdova ◽  
Halina Cernohorska ◽  
Svatava Kubickova ◽  
...  

Chromosomal polymorphism plays a major role in speciation processes in mammals with high rates of karyotypic evolution, as observed in the family Cervidae. One remarkable example is the genus Mazama that comprises wide inter- and intra-specific chromosomal variability. To evaluate the impact of chromosomal polymorphisms as reproductive barriers within the genus Mazama, inter-specific hybrids between Mazama gouazoubira and Mazama nemorivaga (MGO × MNE) and intra-specific hybrids between cytotypes of Mazama americana (MAM) differing by a tandem (TF) or centric fusion (Robertsonian translocations—RT) were evaluated. MGO × MNE hybrid fertility was evaluated by the seminal quality and testicular histology. MAM hybrids estimation of the meiotic segregation products was performed by sperm-FISH analysis. MGO × MNE hybrids analyses showed different degrees of fertility reduction, from severe subfertility to complete sterility. Regarding MAM, RT, and TF carriers showed a mean value for alternate segregation rate of 97.74%, and 67.23%, and adjacent segregation rate of 1.80%, and 29.07%, respectively. Our results suggested an efficient post-zygotic barrier represented by severe fertility reduction for MGO × MNE and MAM with heterozygous TF. Nevertheless, RT did not show a severe effect on the reproductive fitness in MAM. Our data support the validity of MGO and MNE as different species and reveals cryptic species within MAM.


1968 ◽  
Vol 32 (2) ◽  
pp. 191-193 ◽  
Author(s):  
A. DE CAPOA ◽  
W. R. BREG ◽  
T. KUSHNICK ◽  
O. J. MILLER
Keyword(s):  

2000 ◽  
Vol 68 (6) ◽  
pp. 3523-3534 ◽  
Author(s):  
Sonia Chatellier ◽  
Nahla Ihendyane ◽  
Rita G. Kansal ◽  
Farukh Khambaty ◽  
Hesham Basma ◽  
...  

ABSTRACT The relatedness of group A streptococcal (GAS) strains isolated from 35 Canadian patients with invasive disease of different severity was investigated by a variety of molecular methods. All patients were infected with M1T1 strains and, based on clinical criteria, were classified as severe (n = 21) and nonsevere (n = 14) invasive GAS infection cases. All the M1 strains studied had the emm1.0 allele and the same streptococcal pyrogenic exotoxin (Spe) genotype,speA+ speB+ speC speF+speG+ speH smeZ+ ssa. All isolates had the same speA allotype, speA2. The randomly amplified polymorphic DNA banding pattern with two different primers was identical for all strains, and pulsed field gel electrophoresis analysis showed that 33 and 30 isolates had identical banding patterns after DNA digestion with SfiI or SmaI, respectively; the nonidentical isolates differed from the main pattern by only one band. A relatively high degree of polymorphism in specific regions of the sic gene was observed among isolates; however, this polymorphism was not associated with disease severity. Likewise, although the phenotypic expression of SpeA, SpeB, and SpeF proteins varied among the M1T1 isolates, there was no correlation between the amount of Spe expressed and disease severity. Importantly, mitogenic and cytokine responses induced by partially purified bacterial culture supernatants containing a mixture of expressed superantigens were very similar for isolates from severe and nonsevere cases (P > 0.1). Together, the data indicate that highly related invasive M1T1 isolates, some indistinguishable, can cause disease of varying severity in different individuals. These findings underscore the contribution of host factors to the outcome of invasive GAS infections.


Genome ◽  
1989 ◽  
Vol 32 (6) ◽  
pp. 935-940 ◽  
Author(s):  
M. D. B. Eldridge ◽  
P. G. Johnston ◽  
R. L. Close ◽  
P. S. Lowry

Chromosomal rearrangements in the two currently recognised races of Petrogale godmani were examined using C- and G-banding. The nominate race P. godmani godmani (2n = 20) was found to possess an inverted chromosome 5 and an acrocentric 6–10 fusion, which can be derived from a 6–10 centric fusion by a centromeric transposition. The Cape York race (2n = 22) was found to retain the ancestral submetacentric chromosome 4 and the ancestral chromosome 5. Thus despite their genie similarity, the two races clearly have major chromosomal differences and should be regarded as separate species. Petrogale g. godmani shares two derived chromosomes with another Queensland taxon, the assimilis race of P. assimilis, indicating recent common ancestry. The Cape York race retains characteristics of an ancestral stock of Petrogale and its genic similarity with P. g. godmani could therefore be the result of extensive introgression.Key words: chromosomal rearrangements, G-banding, Marsupialia, Petrogale.


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