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    J Cell Biol. 2005 Jul 18;170(2):191-200.

    Huntingtin interacting protein 1 modulates the transcriptional activity of nuclear hormone receptors.

    Mills IG, Gaughan L, Robson C, Ross T, McCracken S, Kelly J, Neal DE.

    Cancer Research UK Uro-Oncology Research Group, Department of Oncology, University of Cambridge, Hutchison/Medical Research Council Cancer Research Centre, Cambridge CB2 2XZ, England, UK. igm23@cam.ac.uk

    Comment in:

    Internalization of activated receptors regulates signaling, and endocytic adaptor proteins are well-characterized in clathrin-mediated uptake. One of these adaptor proteins, huntingtin interacting protein 1 (HIP1), induces cellular transformation and is overexpressed in some prostate cancers. We have discovered that HIP1 associates with the androgen receptor through a central coiled coil domain and is recruited to DNA response elements upon androgen stimulation. HIP1 is a novel androgen receptor regulator, significantly repressing transcription when knocked down using a silencing RNA approach and activating transcription when overexpressed. We have also identified a functional nuclear localization signal at the COOH terminus of HIP1, which contributes to the nuclear translocation of the protein. In conclusion, we have discovered that HIP1 is a nucleocytoplasmic protein capable of associating with membranes and DNA response elements and regulating transcription.

    PMID: 16027218 [PubMed - indexed for MEDLINE]

    PMCID: 2171420

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