Pervasive TTP binding but selective target mRNA destabilization in the macrophage transcriptome [RNA-Seq]

ABSTRACT: Precise control of mRNA decay is fundamental for robust yet not exaggerated inflammatory responses to pathogens. Parameters determining the specificity and extent of mRNA degradation within the entire inflammation-associated transcriptome remain incompletely understood. Using transcriptome-wide high resolution occupancy assessment of the mRNA-destabilizing protein TTP, a major inflammation-limiting factor, we qualitatively and quantitatively characterize TTP binding positions and functionally relate them to TTP-dependent mRNA decay in immunostimulated macrophages. We identify pervasive TTP binding with incompletely penetrant linkage to mRNA destabilization. A necessary but not sufficient feature of TTP-mediated mRNA destabilization is binding to 3’ untranslated regions (UTRs). Mapping of

ORGANISM(S): Mus musculus

SUBMITTER: Vitaly Sedlyarov 

PROVIDER: E-GEOD-63467 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress