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The conserved WRPW motif of Hes6 mediates proteasomal degradation

Authors :
Kang, Seon Ah
Seol, Jae Hong
Kim, Jaesang
Source :
Biochemical & Biophysical Research Communications. Jun2005, Vol. 332 Issue 1, p33-36. 4p.
Publication Year :
2005

Abstract

Abstract: Hes6 belongs to a subfamily of basic helix–loop–helix transcription factors that includes Drosophila Hairy and Enhancer of split genes. Like other members of the family, Hes6 features the WRPW motif which is consisted just of four amino acids at its C-terminus. Here, we show that WRPW motif deletion mutant protein is substantially stabilized in comparison to the full length protein and that the enhanced stability is due to its resistance to proteasomal degradation. The WRPW motif also appears to be sufficient for acceleration of proteolysis as its fusion to two heterologous proteins, the green fluorescent protein (GFP) of Aequoria victoria and Gal4 DNA binding domain of Saccharomyces cerevisiae, significantly destabilized the proteins. These findings demonstrate a novel function of this conserved motif as a degradation signal and raise the possibility of utilizing it for controlling the level of ectopically expressed gene products. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
0006291X
Volume :
332
Issue :
1
Database :
Academic Search Index
Journal :
Biochemical & Biophysical Research Communications
Publication Type :
Academic Journal
Accession number :
17827168
Full Text :
https://doi.org/10.1016/j.bbrc.2005.04.089