scholarly journals Corrigenda: Genomic characterisation of Arachis porphyrocalyx (Valls & C.E. Simpson, 2005) (Leguminosae): multiple origin of Arachis species with x = 9. Comparative Cytogenetics 11(1): 29–43. doi: 10.3897/CompCytogen.v11i1.10339

2017 ◽  
Vol 11 (4) ◽  
pp. 819-820 ◽  
Author(s):  
Silvestri María Celeste ◽  
Alejandra Marcela Ortiz ◽  
Germán Ariel Robledo ◽  
José Francisco Montenegro Valls ◽  
Graciela Inés Lavia
2017 ◽  
Vol 11 (1) ◽  
pp. 29-43
Author(s):  
Graciela Inés Lavia ◽  
Silvestri María Celeste ◽  
Alejandra Marcela Ortiz ◽  
Germán Ariel Robledo ◽  
José Francisco Montenegro Valls

1991 ◽  
Vol 83 (4) ◽  
pp. 560-567 ◽  
Author(s):  
M. B. Peoples ◽  
C. A. Atkins ◽  
J. S. Pate ◽  
K. Chong ◽  
A. W. Faizah ◽  
...  

2021 ◽  
pp. 1-11
Author(s):  
David S. da Silva ◽  
Heriberto F. da Silva Filho ◽  
Marcelo B. Cioffi ◽  
Edivaldo H.C. de Oliveira ◽  
Anderson J.B. Gomes

With 82 species currently described, the genus <i>Leptodactylus</i> is the most diverse and representative one in the family Leptodactylidae. Concerning chromosomal organization, this genus represents an interesting and underexplored group since data from molecular cytogenetics are incipient, and little is known about the organization and distribution of repetitive DNA elements in the karyotypes. In this sense, this study aimed at providing a comparative analysis in 4 <i>Leptodactylus</i> species (<i>L. macrosternum, L. pentadactylus, L. fuscus,</i> and <i>Leptodactylus</i> cf<i>. podicipinus</i>), combining conventional cytogenetics (Giemsa staining, C-banding, and AgNOR staining) and mapping of molecular markers (18S rDNA, telomeric and microsatellite probes), to investigate mechanisms underlying their karyotype differentiation process. The results showed that all species had karyotypes with 2n = 22 and FN = 44, except for <i>Leptodactylus</i> cf. <i>podicipinus</i> which presented FN = 36. The 18S rDNA was observed in pair 8 of all analyzed species (corresponding to pair 4 in <i>L. pentadactylus</i>), coinciding with the secondary constrictions and AgNOR staining. FISH with microsatellite DNA probes demonstrated species-specific patterns, as well as an association of these repetitive sequences with constitutive heterochromatin blocks and ribosomal DNA clusters, revealing the dynamics of microsatellites in the genome of the analyzed species. In summary, our data demonstrate an ongoing process of genomic divergence inside species with almost similar karyotype, driven most likely by a series of pericentric inversions, followed by differential accumulation of repetitive sequences.


Author(s):  
Beatrice Anfuso ◽  
Korri E. El-Khobar ◽  
Caecilia H.C. Sukowati ◽  
Claudio Tiribelli

Author(s):  
Carla Andreia Lorscheider ◽  
Jordana Inácio Nascimento Oliveira ◽  
Thais Aparecida Dulz ◽  
Viviane Nogaroto ◽  
Isabel Cristina Martins-Santos ◽  
...  

PROTOPLASMA ◽  
2019 ◽  
Vol 256 (3) ◽  
pp. 805-814
Author(s):  
Maria Angélica Oliveira Marinho ◽  
Gustavo Souza ◽  
Leonardo P. Felix ◽  
Reginaldo De Carvalho

2021 ◽  
Vol 15 (2) ◽  
pp. 89-99
Author(s):  
Ricardo Firmino de Sousa ◽  
Paulo Cesar Venere ◽  
Karina de Cassia Faria

Dermanura Gervais, 1856 is represented by small frugivorous bats of the Stenodermatinae subfamily. The taxonomy of this group presents controversies and has been subject to changes, especially since the morphological characters evaluated have left gaps that are difficult to fill regarding good species characterization. Previous studies performed in Dermanura cinerea Gervais, 1856 found that the karyotype of this species has a diploid number of chromosomes equal to 30 and 56 autosomal arms. The objective of the present study was to describe, for the first time, the karyotypes of the species Dermanura anderseni (Osgood, 1916) and Dermanura gnoma (Handley, 1987) based on classical cytogenetic markers. For both species, the diploid number found was 2n = 30 and NFa = 56. Two pairs of chromosomes showed markings of the nucleolus organizing regions (AgNORs) in the species D. anderseni and only one pair in D. gnoma, differing from what has already been described for D. cinerea. The two species analyzed here also showed differences in the sex chromosome system, with D. gnoma showing a neo-XY type system while in D. anderseni the classic XY sexual system was observed. In both species, visualization of the constitutive heterochromatin occurred in the pericentromeric region of all chromosomes, as well as in the short arms of the subtelocentric chromosomes. The present work represents an important expansion of karyotypic information for the subfamily Stenodermatinae, bringing chromosomal features that are possible to use in the taxonomic implications of the group.


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