Negative acting HLH proteins Id1, Id2, Id3, and Id4 are expressed in prostate epithelial cells

Authors

  • Jaideep Chaudhary,

    Corresponding author
    1. Center for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, Washington
    • Center for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, WA 99164-4231.
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  • Michelle Schmidt,

    1. Center for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, Washington
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  • Ingrid Sadler-Riggleman

    1. Center for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, Washington
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Abstract

Background

The four known Id proteins, Id1, Id2, Id3, and Id4 are largely considered as dominant negative helix-loop-helix (HLH) proteins. They can dimerize with basic helix loop proteins (bHLH) but the dimers fail to bind the consensus E box response element (CANNTG). Alternatively, members of the Id family, for example, Id2 can also bind to non-bHLH proteins such as retinoblastoma (Rb) and ETS-TCF to modulate their activities. Consistent with their role as promoters of proliferation, subset of Id genes for example, Id1 and Id2 are expressed in many cancers including that of the prostate. However, their expression and function in the normal prostate is unknown.

Methods

The present study was designed to evaluate the expression profile and functional significance of all Id isoforms in normal rat prostate epithelial cells. The data suggests that all four Id isoforms are expressed in normal cells, albeit at different levels.

Results

Agents that promote growth, for example, serum increase the levels of Id1, Id2, and Id3. The hormones and mitogens such as testosterone and hepatocyte growth factor (HGF) that promote prostate epithelial cell differentiation stimulate Id4 and Id2, respectively.

Conclusions

In prostate epithelial cells, Id1 may be specifically involved in promoting proliferation whereas Id4 and Id2 may have defined roles in regulating differentiated functions in response to androgens and local paracrine factors such as HGF. © 2005 Wiley-Liss, Inc.

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