Complete Nucleotide Sequence of Mouse Mammary Tumor Virus from JYG Chinese Wild Mice: Absence of Bacterial Insertion Sequences in the Cloned Viral gag Gene.

Détails

ID Serval
serval:BIB_7F46A6DABB14
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Complete Nucleotide Sequence of Mouse Mammary Tumor Virus from JYG Chinese Wild Mice: Absence of Bacterial Insertion Sequences in the Cloned Viral gag Gene.
Périodique
Breast Cancer
Auteur⸱e⸱s
Nishio M., Xu L., Sasaki M., Haga S., Okumoto M., Mori N., Sarkar N.H., Acha-Orbea H., Enami J., Imai S.
ISSN
1880-4233 (Electronic)
ISSN-L
1340-6868
Statut éditorial
Publié
Date de publication
1994
Volume
1
Numéro
2
Pages
89-94
Langue
anglais
Résumé
Mammary tumors of a newly isolated strain of Chinese wild mouse (JYG mouse) harbor exogenous mouse mammary tumor virus (MMTV). The complete nucleotide sequence of exogenous JYG-MMTV was determined on the proviral 5' long terminal repeat (LTR)(partial)-gag-pol-env-3' LTR (partial) fragment cloned into a plasmid vector and the cDNA sequence from JYG-MMTV producing cells. Similarly to the other MMTV species the LTR of JYG-MMTV contains an open reading frame (ORF). The amino acid sequence of the JYG-MMTV ORF resembles that of SW-MMTV (92% identity) and endogenous Mtv-7 (93% identity) especially at the C-terminal region. Thus, a functional similarity in T-cell receptor V beta recognition as a superantigen is implicated among these MMTV species. Analysis of the viral gag nucleotide sequence revealed that this gene is not disrupted by the bacterial insertion sequence IS1 or IS2, which have been reported to be present in the majority of the plasmids containing the gag region. Comparison of amino acid sequences of JYG-MMTV with those of BR6-MMTV showed that over 96% of the amino acids of gag, pol, protease and env products are identical. These results suggest the intact nature of the nucleotide sequence of the near full-length MMTV genome cloned in the plasmid.
Pubmed
Création de la notice
24/01/2008 14:48
Dernière modification de la notice
20/08/2019 14:40
Données d'usage