From unloaded MedChemExpress DprE1-IN-2 muscle and gray represents the plot from peaks found in the input chromatin from unloaded muscle. The y-axis is the proportion of peaks relative to all genes in the genome. Peaks are plotted every 20 bases from 22500 to +2500 relative to the TSS. doi:10.1371/journal.pone.0051478.gFigure 2. Plot of phylogenomic conservation for the 2,817 Bcl-3 peaks produced by unloading. The peaks and surrounding genome regions (21500 bp to +1500 bp) were compared to a database of 50-14-6 supplier Phastcon alignment scores for 31 placental mammals on the Galaxy/Cistrome server. Phastcon scores are higher for sequence similarity and are weighted higher for species farther removed from mice phylogenetically. A Phastcon score of 1.0 would reflect perfect identity in all 31 species. Conservation is highest at the center of the peaks indicating that the centers share sequence homology between species, a sign that the sites of Bcl-3 binding are important to function. doi:10.1371/journal.pone.0051478.gA Bcl-3 Network Controls Muscle AtrophyFigure 3. Distribution of Bcl-3 peaks by location in genes. (A) ChIPseeqer genomic annotation for the 2,817 peaks of increased Bcl-3 binding found in unloaded compared to control muscle. (B) ChIPseeqer genomic annotation for peaks found in the sequence alignments from the unloaded muscle input chromatin which was sheared and used to create a library without any further manipulation (no immunoprecipitation). The peak finder in ChIPseeqer was set to the same parameters as for the 2,817 Bcl-3 peaks in unloaded muscle and found 1,594 random peaks. doi:10.1371/journal.pone.0051478.gcontribute to unloading atrophy. The pathways regulated by Bcl-3 also include those of the transition from aerobic to glycolytic metabolism in atrophying muscle. We have identified for the first time, gene target networks regulated by a transcription factor (Bcl3) that is required for skeletal muscle atrophy.bearing for 5 days by elastic tail cast as described previously [14]. The use of animals in this study was approved by the Institutional Animal Care and Use Committee of Boston University (protocol number 12-012).ChIP-seq Methods Animals and Hindlimb UnloadingFor the gene expression array and for ChIP-seq, 7-week-old female wild type mice (C57BL/6J) were purchased from the Jackson Laboratory (Bar Harbor, ME). Animals were provided with chow and water ad libitum and housed individually in Boston University Animal Care Facility. After 3 days of acclimation, mice were randomly assigned to weight-bearing (WB) or hind limb unloaded (HU) groups. Mice in the HU group had their hind limbs elevated off the cage floor for 5 days to induce unloading induced muscle atrophy, as described previously [10]. We used published time course data from our microarray study [13] to identify an appropriate time point, when the most genes are differentially regulated, to use in undertaking a ChIP-seq study, and in this way to capture the time during the atrophy process that would best represent the time for binding of NF-kB transcription factors to the gene targets of the NF-kB transcriptional network. For reporter activity measurements, 7-week-old female Wistar rats from Charles River Lab (Wilmington, MA) were used. 40 mg of wild type or mutant MuRF1-promoter reporters were transfected into rat soleus muscle as previously described [14]. Twenty four hours after reporter injection, rats were randomly assigned to either the weight bearing group or the HU group. The HU group o.From unloaded muscle and gray represents the plot from peaks found in the input chromatin from unloaded muscle. The y-axis is the proportion of peaks relative to all genes in the genome. Peaks are plotted every 20 bases from 22500 to +2500 relative to the TSS. doi:10.1371/journal.pone.0051478.gFigure 2. Plot of phylogenomic conservation for the 2,817 Bcl-3 peaks produced by unloading. The peaks and surrounding genome regions (21500 bp to +1500 bp) were compared to a database of Phastcon alignment scores for 31 placental mammals on the Galaxy/Cistrome server. Phastcon scores are higher for sequence similarity and are weighted higher for species farther removed from mice phylogenetically. A Phastcon score of 1.0 would reflect perfect identity in all 31 species. Conservation is highest at the center of the peaks indicating that the centers share sequence homology between species, a sign that the sites of Bcl-3 binding are important to function. doi:10.1371/journal.pone.0051478.gA Bcl-3 Network Controls Muscle AtrophyFigure 3. Distribution of Bcl-3 peaks by location in genes. (A) ChIPseeqer genomic annotation for the 2,817 peaks of increased Bcl-3 binding found in unloaded compared to control muscle. (B) ChIPseeqer genomic annotation for peaks found in the sequence alignments from the unloaded muscle input chromatin which was sheared and used to create a library without any further manipulation (no immunoprecipitation). The peak finder in ChIPseeqer was set to the same parameters as for the 2,817 Bcl-3 peaks in unloaded muscle and found 1,594 random peaks. doi:10.1371/journal.pone.0051478.gcontribute to unloading atrophy. The pathways regulated by Bcl-3 also include those of the transition from aerobic to glycolytic metabolism in atrophying muscle. We have identified for the first time, gene target networks regulated by a transcription factor (Bcl3) that is required for skeletal muscle atrophy.bearing for 5 days by elastic tail cast as described previously [14]. The use of animals in this study was approved by the Institutional Animal Care and Use Committee of Boston University (protocol number 12-012).ChIP-seq Methods Animals and Hindlimb UnloadingFor the gene expression array and for ChIP-seq, 7-week-old female wild type mice (C57BL/6J) were purchased from the Jackson Laboratory (Bar Harbor, ME). Animals were provided with chow and water ad libitum and housed individually in Boston University Animal Care Facility. After 3 days of acclimation, mice were randomly assigned to weight-bearing (WB) or hind limb unloaded (HU) groups. Mice in the HU group had their hind limbs elevated off the cage floor for 5 days to induce unloading induced muscle atrophy, as described previously [10]. We used published time course data from our microarray study [13] to identify an appropriate time point, when the most genes are differentially regulated, to use in undertaking a ChIP-seq study, and in this way to capture the time during the atrophy process that would best represent the time for binding of NF-kB transcription factors to the gene targets of the NF-kB transcriptional network. For reporter activity measurements, 7-week-old female Wistar rats from Charles River Lab (Wilmington, MA) were used. 40 mg of wild type or mutant MuRF1-promoter reporters were transfected into rat soleus muscle as previously described [14]. Twenty four hours after reporter injection, rats were randomly assigned to either the weight bearing group or the HU group. The HU group o.
