Heterochromatin and chromosome evolution: a FISH probe of Cebus apella paraguayanus (Primate: Platyrrhini) developed by chromosome microdissection.

Neotropical Primate karyotypes are highly variable, particularly in the heterochromatic regions, not only regarding the amount of heterochromatin, but also the composition. G and C banding and FISH techniques provide useful information to characterize interspecific relationships. We used chromosome...

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Detalles Bibliográficos
Autor principal: Nieves, M.
Otros Autores: Mühlmann, M., Mudry, M.D
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2005
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
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024 7 |2 cas  |a Heterochromatin 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
100 1 |a Nieves, M. 
245 1 0 |a Heterochromatin and chromosome evolution: a FISH probe of Cebus apella paraguayanus (Primate: Platyrrhini) developed by chromosome microdissection. 
260 |c 2005 
270 1 0 |m Nieves, M.email: maenieves@yahoo.com 
506 |2 openaire  |e Política editorial 
520 3 |a Neotropical Primate karyotypes are highly variable, particularly in the heterochromatic regions, not only regarding the amount of heterochromatin, but also the composition. G and C banding and FISH techniques provide useful information to characterize interspecific relationships. We used chromosome microdissection to develop a FISH probe of the chromosome 11 heterochromatic block (11qHe+) of Cebus apella paraguayanus (CAPp). Fragments of the 11qHe+ microdissected from fibroblast cell culture were collected in a PCR tube, amplified by degenerate oligonucleotide primer-PCR and subsequently labeled. The specificity of the FISH probe was confirmed in metaphases of some Ceboidea species. Signals were located in the He+ of chromosomes 4, 11, 12, 13, and 19 of CAPp and in the He+ of chromosomes 4, 12 and 13 of C. a. nigritus (CAPn); no signals were observed when other Ceboidea species were analyzed. We propose that the heterochromatin observed in CAPp and CAPn is specific for these species. We consider this C. apella heterochromatin identity as a possible key for the interpretation of chromosomal evolution in these Ceboidea.  |l eng 
593 |a Grupo de Investigación en Biología Evolutiva (GIBE), Dpto. de Ecología, Genética y Evolución, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Argentina 
690 1 0 |a ANIMAL 
690 1 0 |a ARTICLE 
690 1 0 |a CEBIDAE 
690 1 0 |a CHROMOSOME BANDING PATTERN 
690 1 0 |a FEMALE 
690 1 0 |a FLUORESCENCE IN SITU HYBRIDIZATION 
690 1 0 |a GENETICS 
690 1 0 |a HETEROCHROMATIN 
690 1 0 |a MALE 
690 1 0 |a METHODOLOGY 
690 1 0 |a MICRODISSECTION 
690 1 0 |a MOLECULAR EVOLUTION 
690 1 0 |a POLYMERASE CHAIN REACTION 
690 1 0 |a SENSITIVITY AND SPECIFICITY 
690 1 0 |a ANIMALS 
690 1 0 |a CEBUS 
690 1 0 |a CHROMOSOME BANDING 
690 1 0 |a EVOLUTION, MOLECULAR 
690 1 0 |a FEMALE 
690 1 0 |a HETEROCHROMATIN 
690 1 0 |a IN SITU HYBRIDIZATION, FLUORESCENCE 
690 1 0 |a MALE 
690 1 0 |a MICRODISSECTION 
690 1 0 |a POLYMERASE CHAIN REACTION 
690 1 0 |a SENSITIVITY AND SPECIFICITY 
700 1 |a Mühlmann, M. 
700 1 |a Mudry, M.D. 
773 0 |d 2005  |g v. 4  |h pp. 675-683  |k n. 4  |p Genet. Mol. Res.  |x 16765680  |w (AR-BaUEN)CENRE-8446  |t Genetics and molecular research : GMR 
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