Data Brief. 2016 Feb 24;7:349-53. doi: 10.1016/j.dib.2016.02.031. eCollection 2016 Jun.
Data in brief
Marija Mihailovich, Tiziana Bonaldi
PMID: 26977435 PMCID: PMC4781929 DOI: 10.1016/j.dib.2016.02.031
Micro RNAs (miRNAs) are small non-coding RNAs, which dampen gene expression by repressing translation and/or inducing degradation of target-mRNAs. Although the role of miR-17-19b (a truncated version of miR-17-92 cluster) is well documented in MYC-driven B cell lymphomagenesis, little is known about the function of the cluster in the maintenance of full-blown lymphomas. We employed SILAC-based quantitative proteomics to identify miR-17-19b targets upon a mild overexpression of the cluster in B cell lymphomas, established from λ-MYC transgenic mice. The proteomics data described in detail in this study, whose follow up analysis with MaxQuant algorithm is part of the recent publication (Mihailovich et al., 2015) [1], are deposited to the ProteomeXchange Consortium via the PRIDE partner repository, with the accession code PRIDE: PXD002810.
Keywords: B cell lymphoma; MYC; Mass spectrometry; MiR-17-92; MiRNA targets; Quantitative proteomics; SILAC