Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

Dataset Information

Identification of genes that elicit disuse muscle atrophy via the transcription factors p50 and Bcl-3


ABSTRACT: Skeletal muscle atrophy is a debilitating condition associated with weakness, fatigue, and reduced functional capacity. Nuclear factor-kappaB (NF-κB) transcription factors play a critical role in atrophy. Knockout of genes encoding p50 or the NF-κB co-transactivator, Bcl-3, abolish disuse atrophy and thus they are NF-κB factors required for disuse atrophy. We do not know however, the genes targeted by NF-κB that produce the atrophied phenotype. Here we identify the genes required to produce disuse atrophy using gene expression profiling in wild type compared to Nfkb1 (gene encodes p50) and Bcl-3 deficient mice. There were 185 and 240 genes upregulated in wild type mice due to unloading, that were not upregulated in Nfkb1-/- and Bcl-3-/- mice, respectively, and so these genes were consi

ORGANISM(S): Mus musculus

SUBMITTER: Chia-Ling Wu 

PROVIDER: E-GEOD-23497 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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