Quantification of Cellular NEMO Content and Its Impact on NF-[kappa]B Activation by Genotoxic Stress

NF-[kappa]B essential modulator, NEMO, plays a key role in canonical NF-[kappa]B signaling induced by a variety of stimuli, including cytokines and genotoxic agents. To dissect the different biochemical and functional roles of NEMO in NF-[kappa]B signaling, various mutant forms of NEMO have been pre...

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Bibliographic Details
Published in:PloS one 2015-03, Vol.10 (3)
Main Authors: Hwang, Byounghoon, Phan, Funita P, McCool, Kevin, Choi, Eun Young, You, Jinsam, Johnson, Adam, Audhya, Anjon, Miyamoto, Shigeki
Format: Article
Language:English
Subjects:
DNA damage
Genetic research
Genetic toxicology
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Summary:NF-[kappa]B essential modulator, NEMO, plays a key role in canonical NF-[kappa]B signaling induced by a variety of stimuli, including cytokines and genotoxic agents. To dissect the different biochemical and functional roles of NEMO in NF-[kappa]B signaling, various mutant forms of NEMO have been previously analyzed. However, transient or stable overexpression of wild-type NEMO can significantly inhibit NF-[kappa]B activation, thereby confounding the analysis of NEMO mutant phenotypes. What levels of NEMO overexpression lead to such an artifact and what levels are tolerated with no significant impact on NEMO function in NF-[kappa]B activation are currently unknown. Here we purified full-length recombinant human NEMO protein and used it as a standard to quantify the average number of NEMO molecules per cell in a 1.3E2 NEMO-deficient murine pre-B cell clone stably reconstituted with full-length human NEMO (C5). We determined that the C5 cell clone has an average of 4 x 10.sup.5 molecules of NEMO per cell. Stable reconstitution of 1.3E2 cells with different numbers of NEMO molecules per cell has demonstrated that a 10-fold range of NEMO expression (0.6--6x10.sup.5 molecules per cell) yields statistically equivalent NF-[kappa]B activation in response to the DNA damaging agent etoposide. Using the C5 cell line, we also quantified the number of NEMO molecules per cell in several commonly employed human cell lines. These results establish baseline numbers of endogenous NEMO per cell and highlight surprisingly normal functionality of NEMO in the DNA damage pathway over a wide range of expression levels that can provide a guideline for future NEMO reconstitution studies.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0116374