Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Mechanisms of Lin28-mediated miRNA and mRNA regulation : a structural and functional perspective

[img] PDF - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
3MB

Item Type:Review
Title:Mechanisms of Lin28-mediated miRNA and mRNA regulation : a structural and functional perspective
Creators Name:Mayr, F. and Heinemann, U.
Abstract:Lin28 is an essential RNA-binding protein that is ubiquitously expressed in embryonic stem cells. Its physiological function has been linked to the regulation of differentiation, development, and oncogenesis as well as glucose metabolism. Lin28 mediates these pleiotropic functions by inhibiting let-7 miRNA biogenesis and by modulating the translation of target mRNAs. Both activities strongly depend on Lin28's RNA-binding domains (RBDs), an N-terminal cold-shock domain (CSD) and a C-terminal Zn-knuckle domain (ZKD). Recent biochemical and structural studies revealed the mechanisms of how Lin28 controls let-7 biogenesis. Lin28 binds to the terminal loop of pri- and pre-let-7 miRNA and represses their processing by Drosha and Dicer. Several biochemical and structural studies showed that the specificity of this interaction is mainly mediated by the ZKD with a conserved GGAGA or GGAGA-like motif. Further RNA crosslinking and immunoprecipitation coupled to high-throughput sequencing (CLIP-seq) studies confirmed this binding motif and uncovered a large number of new mRNA binding sites. Here we review exciting recent progress in our understanding of how Lin28 binds structurally diverse RNAs and fulfills its pleiotropic functions.
Keywords:Lin28, let-7 miRNA, miRNA Processing, RNA-Binding Protein, Cold-Shock Domain, Zinc-Knuckle Domain, TUTase, Oncogene, Stem Cell, Animals
Source:International Journal of Molecular Sciences
ISSN:1422-0067
Publisher:MDPI (Switzerland)
Volume:14
Number:8
Page Range:16532-16553
Date:9 August 2013
Official Publication:https://doi.org/10.3390/ijms140816532
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library