Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
J Proteomics ; 111: 184-97, 2014 Dec 05.
Artigo em Inglês | MEDLINE | ID: mdl-25108200

RESUMO

The human papillomavirus type 16 (HPV-16) E6/E7 spliced transcripts are heterogeneously expressed in cervical carcinoma. The heterogeneity of the E6/E7 splicing profile might be in part due to the intrinsic variation of splicing factors in tumor cells. However, the splicing factors that bind the E6/E7 intron 1 (In-1) have not been defined. Therefore, we aimed to identify these factors; we used HeLa nuclear extracts (NE) for in vitro spliceosome assembly. The proteins were allowed to bind to an RNA/DNA hybrid formed by the In-1 transcript and a 5'-biotinylated DNA oligonucleotide complementary to the upstream exon sequence, which prevented interference in protein binding to the intron. The hybrid probes bound with the nuclear proteins were coupled to streptavidin magnetic beads for chromatography affinity purification. Proteins were eluted and identified by mass spectrometry (MS). Approximately 170 proteins were identified by MS, 80% of which were RNA binding proteins, including canonical spliceosome core components, helicases and regulatory splicing factors. The canonical factors were identified as components of the spliceosomal B-complex. Although 35-40 of the identified factors were cognate splicing factors or helicases, they have not been previously detected in spliceosome complexes that were assembled using in vivo or in vitro models.


Assuntos
Papillomavirus Humano 16/química , Íntrons , Proteoma , Spliceossomos/metabolismo , Processamento Alternativo , Sequência de Bases , Núcleo Celular/metabolismo , Cromatografia Líquida , DNA Helicases/metabolismo , Éxons , Células HeLa , Humanos , Dados de Sequência Molecular , Proteínas Oncogênicas Virais/química , Proteínas E7 de Papillomavirus/química , Proteômica , Splicing de RNA , Proteínas de Ligação a RNA/química , Proteínas Repressoras/química , Espectrometria de Massas em Tandem
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA