NF-
B determines the degradation pathway of I
B
. (A) NF-
B protects I
B
from proteasomal degradation in vitro. Top: purified 20S proteasome and I
B
were incubated at 37°C, with or without purified p65. (I) represents the proteasome inhibitor MG132. (B) I
B
is highly stable in vivo in the presence of NF-
B. Left panel: WB showing WT, IKK phosphorylation and ubiquitination-defective mutants introduced into ikba-/-, where all NF-
B subunits are present. Cells were treated with cycloheximide (CHX) for different lengths of time (up to 24 h) and the protein levels were visualized by WB. Right panel: this experiment was repeated twice and is represented graphically with error bars signifying
s.e.m. (
) Transgenic WT I
B
, (
) K21, 22R I
B
, (
) KR9 I
B
and (
) S32, 36A I
B
. (C) A model of NF-
B repression by I
B
in pre-stimulated cells. There are two processes that control I
B
degradation. In the resting cell, basal IKK activity phosphorylates bound I
B
and targets it for ubiquitin-dependent degradation. In addition, free I
B
is continuously synthesized and degraded in an IKK- and Ub-independent mechanism. This keeps NF-
B from being activated in the resting cell.
Corrigendum
- The EMBO Journal (2008) 27, 1421
- doi:10.1038/emboj.2008.91
NF-
B dictates the degradation pathway of I
B
Erika Mathes, Ellen L O'Dea, Alexander Hoffmann and Gourisankar Ghosh
Abstract
Correction to:The EMBO Journal, advance online publication 10 April 2008; doi:10.1038/emboj.2008.73
Introduction
Since the publication of this paper, the authors have noticed an error in Figure 2B. The X-axis should have been labelled in hours and not minutes.
Figure 1.
The correct Figure 2 is shown below.
The authors apologize for any inconvenience caused.
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