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Título: 
Physical mapping of 18S rDNA and heterochromatin in species of family Lygaeidae (Hemiptera: Heteroptera)
Autor(es): 
Instituição: 
  • Universidade Estadual de Londrina (UEL)
  • Universidade Estadual Paulista (UNESP)
  • Univ Fed Para
ISSN: 
1676-5680
Financiador: 
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
Resumo: 
Analyses conducted using repetitive DNAs have contributed to better understanding the chromosome structure and evolution of several species of insects. There are few data on the organization, localization, and evolutionary behavior of repetitive DNA in the family Lygaeidae, especially in Brazilian species. To elucidate the physical mapping and evolutionary events that involve these sequences, we cytogenetically analyzed three species of Lygaeidae and found 2n (male) = 18 (16 + XY) for Oncopeltus femoralis; 2n (male) = 14 (12 + XY) for Ochrimnus sagax; and 2n (male) = 12 (10 + XY) for Lygaeus peruvianus. Each species showed different quantities of heterochromatin, which also showed variation in their molecular composition by fluorochrome staining. Amplification of the 18S rDNA generated a fragment of approximately 787 bp. The alignment of the consensus sequence with sequences from other species of Heteroptera deposited in the GenBank revealed a similarity of 98% with small differences. Fluorescent in situ hybridization with the 18S rDNA fragment revealed that this ribosomal gene was located in 1 autosomal pair at different positions in the three species. No cytogenetic data are available for these Brazilian species. The basal number and the possible chromosomal changes that occurred among the different species, as well as the evolution of these DNA sequences, are discussed.
Data de publicação: 
1-Jan-2014
Citação: 
Genetics And Molecular Research. Ribeirao Preto: Funpec-editora, v. 13, n. 1, p. 2186-2199, 2014.
Duração: 
2186-2199
Publicador: 
Funpec-editora
Palavras-chaves: 
  • Chromosome structure
  • Fluorescence in situ hybridization
  • Heterochromatin
  • Ribosomal genes
Fonte: 
http://dx.doi.org/10.4238/2014.March.26.7
Endereço permanente: 
Direitos de acesso: 
Acesso aberto
Tipo: 
outro
Fonte completa:
http://repositorio.unesp.br/handle/11449/112846
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