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NAC1, a POZ/BTB protein that functions as a corepressor.
Korutla, Laxminarayana; Wang, Peijie; Jackson, Trevor G; Mackler, Scott A.
Afiliação
  • Korutla L; Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia, USA.
Neurochem Int ; 54(3-4): 245-52, 2009.
Article em En | MEDLINE | ID: mdl-19121354
ABSTRACT
We now demonstrate that NAC1 acts as a corepressor for other POZ/BTB proteins. NAC1 is a POZ/BTB motif containing transcriptional repressor protein. In a mammalian two hybrid assay in neuronal (N2A) cells and non-neuronal (HEK 293T) cells, VP16 activation domain tagged NAC1 resulted in significant reversal of transcriptional inhibition with the Gal4-ZID, Gal4-BCL6, Gal4-ZF5, and kelch proteins Gal4-MAYVEN and Gal4-NRP/B fusion proteins. We also observed similar results with another corepressor, BCoR Gal4 fusion protein. NAC1 potentiated ZF5 mediated repression in Gal4-DBD fusion transient assays. GST pulldown assays further confirmed protein-protein interactions between these proteins and NAC1. Both the NAC1 isoforms demonstrated selective interaction through the POZ/BTB domain but not with the non-POZ/BTB region. Endogenous NAC1 and BCL6 physically associated in CNS regions. Strikingly, NAC1 did not interact with the pro-myelocytic leukemia zinc finger protein (PLZF), another POZ/BTB protein that is not found in the adult brain. Therefore, we conclude that NAC1 functions as a corepressor for POZ/BTB proteins expressed in the mature CNS.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Transcrição Gênica / Sistema Nervoso Central / Proteínas de Neoplasias Limite: Animals / Humans Idioma: En Revista: Neurochem Int Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Transcrição Gênica / Sistema Nervoso Central / Proteínas de Neoplasias Limite: Animals / Humans Idioma: En Revista: Neurochem Int Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Estados Unidos