Abstract
Mammalian homeobox genes are widely expressed in the developing central nervous system and are postulated to control developmental processes by regulating gene expression at the transcriptional level. In vitro studies have identified consensus DNA sequences that contain an ATTA core as sites for interaction with homeodomain proteins. Such elements have been found in the upstream regulatory region of the gene encoding beta-amyloid precursor protein, which is associated with the neurological disorder Alzheimer disease. As the beta-amyloid precursor protein gene is also expressed in the developing central nervous system and appears to play a role in cellular regulatory processes, we have examined the possibility that a homeobox gene product can regulate its transcription. We demonstrate by Northern blot analyses and transfection experiments that the expression of the beta-amyloid precursor protein gene is decreased in cultured cells expressing the mouse homeobox gene Hox-3.1.
Dates
Type | When |
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Created | 19 years, 2 months ago (May 31, 2006, 8:21 a.m.) |
Deposited | 3 years, 4 months ago (April 13, 2022, 1:35 p.m.) |
Indexed | 4 months ago (April 19, 2025, 2:24 a.m.) |
Issued | 33 years, 3 months ago (May 1, 1992) |
Published | 33 years, 3 months ago (May 1, 1992) |
Published Online | 33 years, 3 months ago (May 1, 1992) |
Published Print | 33 years, 3 months ago (May 1, 1992) |
@article{Violette_1992, title={Repression of the beta-amyloid gene in a Hox-3.1-producing cell line.}, volume={89}, ISSN={1091-6490}, url={http://dx.doi.org/10.1073/pnas.89.9.3805}, DOI={10.1073/pnas.89.9.3805}, number={9}, journal={Proceedings of the National Academy of Sciences}, publisher={Proceedings of the National Academy of Sciences}, author={Violette, S M and Shashikant, C S and Salbaum, J M and Belting, H G and Wang, J C and Ruddle, F H}, year={1992}, month=may, pages={3805–3809} }