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Publication : Regulatory roles of AP-2 transcription factors in vertebrate development, apoptosis and cell-cycle control.

First Author  Hilger-Eversheim K Year  2000
Journal  Gene Volume  260
Issue  1-2 Pages  1-12
PubMed ID  11137286 Mgi Jnum  J:66547
Mgi Id  MGI:1928608 Doi  10.1016/s0378-1119(00)00454-6
Citation  Hilger-Eversheim K, et al. (2000) Regulatory roles of AP-2 transcription factors in vertebrate development, apoptosis and cell-cycle control. Gene 260(1-2):1-12
abstractText  AP-2 transcription factors represent a family of three closely related and evolutionarily conserved sequence-specific DNA-binding proteins, AP-2alpha, -beta and -gamma. Subsequent studies have identified spatially and temporally regulated embryonic expression patterns in a number of different tissues including neural crest derivatives, neural, epidermal and urogenital tissues. Here, we review the current understanding of developmental defects in AP-2-deficient mice and consider regulatory functions of AP-2 in control of apoptosis, cell cycle, and gene expression. Recently, the first inherited human disorder, Char syndrome, was identified to be caused by AP-2beta missense mutations. In light of the manifold and essential functions of AP-2 proteins in cell growth, differentiation and programmed death, mutations or changes in precisely programmed expression patterns are likely to contribute to other congenital malformations or neoplastic diseases.
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