| Literature DB >> 25120199 |
Jingwei Xie1, Guennadi Kozlov1, Kalle Gehring2.
Abstract
The cytoplasmic poly(A) binding protein 1 (PABPC1) is an essential eukaryotic translational initiation factor first described over 40 years ago. Most studies of PABPC1 have focused on its N-terminal RRM domains, which bind the mRNA 3' poly(A) tail and 5' translation complex eIF4F via eIF4G; however, the protein also contains a C-terminal MLLE domain that binds a peptide motif, termed PAM2, found in many proteins involved in translation regulation and mRNA metabolism. Studies over the past decade have revealed additional functions of PAM2-containing proteins (PACs) in neurodegenerative diseases, circadian rhythms, innate defense, and ubiquitin-mediated protein degradation. Here, we summarize functional and structural studies of the MLLE/PAM2 interaction and discuss the diverse roles of PACs.Entities:
Keywords: Polyadenylation; RNA binding protein; Structural biology; Translational control; mRNA decay; mRNA translation
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Year: 2014 PMID: 25120199 DOI: 10.1016/j.bbagrm.2014.08.001
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002