Your browser doesn't support javascript.
loading
Complete nucleotide sequence of a mouse VL30 retro-element.
Adams, S E; Rathjen, P D; Stanway, C A; Fulton, S M; Malim, M H; Wilson, W; Ogden, J; King, L; Kingsman, S M; Kingsman, A J.
Afiliación
  • Adams SE; Department of Biochemistry, University of Oxford, United Kingdom.
Mol Cell Biol ; 8(8): 2989-98, 1988 Aug.
Article en En | MEDLINE | ID: mdl-2850474
ABSTRACT
The complete nucleotide sequence of a mouse retro-element is presented. The cloned element is composed of 4,834 base pairs (bp) with long terminal repeats of 568 bp separated by an internal region of 3,698 bp. The element did not appear to have any open reading frames that would be capable of encoding the functional proteins that are normally produced by retro-elements. However, some regions of the genome showed some homology to retroviral gag and pol open reading frames. There was no region in VL30 corresponding to a retroviral env gene. This implies that VL30 is related to retrotransposons rather than to retroviruses. The sequence also contained regions that were homologous to known reverse transcriptase priming sites and viral packaging sites. These observations, combined with the known transcriptional capacity of the VL30 promoter, suggest that VL30 relies on protein functions of other retro-elements, such as murine leukemia virus, while maintaining highly conserved cis-active promoter, packaging, and priming sites necessary for its replication and cell-to-cell transmission.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 3_ND Problema de salud: 3_neglected_diseases / 3_zoonosis Asunto principal: Retroviridae / ADN Viral Límite: Animals Idioma: En Revista: Mol Cell Biol Año: 1988 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 3_ND Problema de salud: 3_neglected_diseases / 3_zoonosis Asunto principal: Retroviridae / ADN Viral Límite: Animals Idioma: En Revista: Mol Cell Biol Año: 1988 Tipo del documento: Article País de afiliación: Reino Unido
...