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Home › Dataset Library › Expression Profiling of Early Myogenesis - Affymetrix Dataset

Dataset: Expression Profiling of Early Myogenesis - Affymetrix Dataset

Analysis of Early Myogenesis Reveals an Extensive Set of Transcriptional Regulators Whose Knock-down Can Inhibit Differentiation...

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Analysis of Early Myogenesis Reveals an Extensive Set of Transcriptional Regulators Whose Knock-down Can Inhibit Differentiation Myogenesis is a tightly controlled process involving the transcriptional activation and repression of thousands of genes. Although many components of the transcriptional network are known for the later phases of myogenesis, relatively little work has described the transcriptional landscape within the first 24 hours, when myoblasts commit to differentiate. Through dense temporal sampling of differentiating C2C12 myoblasts, we identify 266 transcriptional regulators (TRs) whose expression is altered within the first 12 hours of myogenesis. A high-content shRNA screen of 76 TRs involving 427 stable lines identified 48 genes whose knockdown significantly inhibits differentiation of C2C12 myoblasts. These include known regulators of myogenesis (Myod1, Myog and Myf5), as well as 26 regulators not previously associated with the process. Of the TRs differentially expressed within the first 24 hours, two-thirds inhibited differentiation when knocked down. Surprisingly, a similar proportion (67%) of shRNAs targeting TRs whose expression did not change during differentiation also inhibited myogenesis, suggesting that both stably and differentially expressed TRs are essential for this complex differentiation program. This implies that microarray-based approaches that concentrate functional validation studies on differentially-expressed genes will fail to identify many genes that are critically implicated in complex biological processes. C2C12 myoblasts were differentiated into myotubes and sampled at various timepoints for gene expression measurement on MOE-430v2 chips. Cells grown in separate plates were harvested at 14 different timepoints: t_-24h, t_0h, t_0.5h, t_1h, t_1.5h, t_2h, t_3h, t_6h, t_9h, t_12h, t_24h, t_48h, t_96h, t_144h. Cells were also pre-treated with 50uM cycloheximide 1 hour prior to inducing differentiation and harvested at two timepoints: t_chx_1h, t_chx_3h. All harvests were performed in triplicate using growths from successive passages.

Species:
mouse

Samples:
48

Source:
E-GEOD-16992

PubMed:
22147266

Updated:
Dec.12, 2014

Registered:
Nov.11, 2014


Factors: (via ArrayExpress)
Sample REPLICATE TIME
GSM425337 1 -24hr_ctrl
GSM425338 2 -24hr_ctrl
GSM425339 3 -24hr_ctrl
GSM425340 1 0hr_ctrl
GSM42534 2 0hr_ctrl
GSM425342 3 0hr_ctrl
GSM425343 1 0.5hr_differentiation
GSM425344 2 0.5hr_differentiation
GSM425345 3 0.5hr_differentiation
GSM425346 1 1hr_differentiation
GSM425347 2 1hr_differentiation
GSM425348 3 1hr_differentiation
GSM425349 1 1.5hr_differentiation
GSM425350 2 1.5hr_differentiation
GSM42535 3 1.5hr_differentiation
GSM425352 1 2hr_differentiation
GSM425353 2 2hr_differentiation
GSM425354 3 2hr_differentiation
GSM425355 1 3hr_differentiation
GSM425356 2 3hr_differentiation
GSM425357 3 3hr_differentiation
GSM425358 1 6hr_differentiation
GSM425359 2 6hr_differentiation
GSM425360 3 6hr_differentiation
GSM42536 1 9hr_differentiation
GSM425362 2 9hr_differentiation
GSM425363 3 9hr_differentiation
GSM425364 1 12hr_differentiation
GSM425365 2 12hr_differentiation
GSM425366 3 12hr_differentiation
GSM425367 1 24hr_differentiation
GSM425368 2 24hr_differentiation
GSM425369 3 24hr_differentiation
GSM425370 1 48hr_differentiation
GSM42537 2 48hr_differentiation
GSM425372 3 48hr_differentiation
GSM425373 1 96hr_differentiation
GSM425374 2 96hr_differentiation
GSM425375 3 96hr_differentiation
GSM425376 1 144hr_differentiation
GSM425377 2 144hr_differentiation
GSM425378 3 144hr_differentiation
GSM425379 1 1hr_CHX
GSM425380 2 1hr_CHX
GSM42538 3 1hr_CHX
GSM425382 1 3hr_CHX
GSM425383 2 3hr_CHX
GSM425384 3 3hr_CHX

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