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BORIS/CTCFL is an RNA-binding protein that associates with polysomes.
Ogunkolade, Babatunji W; Jones, Tania A; Aarum, Johan; Szary, Jaroslaw; Owen, Nicholas; Ottaviani, Diego; Mumin, Muhammad A; Patel, Shyam; Pieri, Christopher A; Silver, Andrew R; Sheer, Denise.
Afiliação
  • Sheer D; Centre for Neuroscience and Trauma, Queen Mary University of London, Blizard Institute, Barts and the London School of Medicine and Dentistry, London, E1 2AT, UK. d.sheer@qmul.ac.uk.
BMC Cell Biol ; 14: 52, 2013 Nov 26.
Article em En | MEDLINE | ID: mdl-24279897
ABSTRACT

BACKGROUND:

BORIS (CTCFL), a paralogue of the multifunctional and ubiquitously expressed transcription factor CTCF, is best known for its role in transcriptional regulation. In the nucleus, BORIS is particularly enriched in the nucleolus, a crucial compartment for ribosomal RNA and RNA metabolism. However, little is known about cytoplasmic BORIS, which represents the major pool of BORIS protein.

RESULTS:

We show, firstly, that BORIS has a putative nuclear export signal in the C-terminal domain. Furthermore, BORIS associates with mRNA in both neural stem cells and young neurons. The majority of the BORIS-associated transcripts are different in the two cell types. Finally, by using polysome profiling we show that BORIS is associated with actively translating ribosomes.

CONCLUSION:

We have demonstrated the RNA binding properties of cellular BORIS and its association with actively translating ribosomes. We suggest that BORIS is involved in gene expression at both the transcriptional and post-transcriptional levels.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polirribossomos / RNA Mensageiro / RNA Ribossômico / Nucléolo Celular / Regulação da Expressão Gênica / Citoplasma / Proteínas de Ligação a DNA Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polirribossomos / RNA Mensageiro / RNA Ribossômico / Nucléolo Celular / Regulação da Expressão Gênica / Citoplasma / Proteínas de Ligação a DNA Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2013 Tipo de documento: Article