Genome-wide analysis of TIAR RNA ligands in mouse macrophages before and after LPS stimulation

• Main Authors: Yacine Kharraz, Anne Lefort, Frédérick Libert, Christopher J. Mann, Cyril Gueydan, Véronique Kruys
• Format: Article
• Language: English
• Published: Elsevier 2016-03-01
• Series: Genomics Data
• Online Access: http://www.sciencedirect.com/science/article/pii/S2213596016300265

TIA-1 related protein (TIAR) is a RNA-binding protein involved in several steps of gene expression such as RNA splicing Aznarez et al. (2008) [1] and translation Piecyk et al. (2000) [2]. TIAR contains three RNA recognition motifs (RRMs) allowing its interaction with specific sequences localized in the untranslated regions (UTRs) of several mRNAs. In myeloid cells, TIAR has been shown to bind and regulate the translation and stability of various mRNA-encoding proteins important for the inflammatory response, such as TNFα Piecyk et al. (2000), Gueydan et al. (1999) [2,3], Cox-2 Cok et al. (2003) [4] or IL-8 Suswam et al. (2005) [5]. Here, we generated two macrophage-like RAW 264.7 cell lines expressing either a tagged full-length TIAR protein or a RRM2-truncated mutant unable to bind RNA with high affinity Dember et al. (1996), Kim et al. (2013) . By a combination of RNA-IP and microarray analysis (RIP-chip), we identified mRNAs specifically bound by the full-length protein both in basal conditions and in response to LPS (GSE77577). Keywords: RIP-chip, AU-rich element, TIAR, Translation repression, LPS