| Literature DB >> 22387028 |
Eun Kyung Lee1, Wook Kim, Kumiko Tominaga, Jennifer L Martindale, Xiaoling Yang, Sarah S Subaran, Olga D Carlson, Evi M Mercken, Rohit N Kulkarni, Wado Akamatsu, Hideyuki Okano, Nora I Perrone-Bizzozero, Rafael de Cabo, Josephine M Egan, Myriam Gorospe.
Abstract
Although expression of the mammalian RNA-binding protein HuD was considered to be restricted to neurons, we report that HuD is present in pancreatic β cells, where its levels are controlled by the insulin receptor pathway. We found that HuD associated with a 22-nucleotide segment of the 5' untranslated region (UTR) of preproinsulin (Ins2) mRNA. Modulating HuD abundance did not alter Ins2 mRNA levels, but HuD overexpression decreased Ins2 mRNA translation and insulin production, and conversely, HuD silencing enhanced Ins2 mRNA translation and insulin production. Following treatment with glucose, HuD rapidly dissociated from Ins2 mRNA and enabled insulin biosynthesis. Importantly, HuD-knockout mice displayed higher insulin levels in pancreatic islets, while HuD-overexpressing mice exhibited lower insulin levels in islets and in plasma. In sum, our results identify HuD as a pivotal regulator of insulin translation in pancreatic β cells.Entities:
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Year: 2012 PMID: 22387028 PMCID: PMC3319250 DOI: 10.1016/j.molcel.2012.01.016
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970