HOPS: a novel cAMP-dependent shuttling protein involved in protein synthesis regulation.
The liver has the ability to autonomously regulate growth and mass. Following partial hepatectomy, hormones, growth factors, cytokines and their coupled signal transduction pathways have been implicated in hepatocyte proliferation. To understand the mechanisms responsible for the proliferative response, we studied liver regeneration by characterization of novel genes that are ... activated in residual hepatocytes. A regenerating liver cDNA library screening was performed with cDNA-subtracted probes derived from regenerating and normal liver. Here, we describe the biology of Hops (for hepatocyte odd protein shuttling). HOPS is a novel shuttling protein that contains an ubiquitin-like domain, a putative NES and a proline-rich region. HOPS is rapidly exported from the nucleus and is overexpressed during liver regeneration. Evidence shows that cAMP governs HOPS export in hepatocytes of normal and regenerating liver and is mediated via CRM-1. We demonstrate that HOPS binds to elongation factor eEF-1A and interferes in protein synthesis. HOPS overexpression in H-35-hepatoma and 3T3-NIH cells strongly reduces proliferation.
Mesh Terms:
Amino Acid Sequence, Animals, COS Cells, Carrier Proteins, Cell Growth Processes, Cercopithecus aethiops, Cloning, Molecular, Cyclic AMP, DNA, Complementary, Hepatocytes, Liver, Liver Regeneration, Male, Mice, Molecular Sequence Data, NIH 3T3 Cells, Nuclear Proteins, Peptide Elongation Factor 1, Protein Biosynthesis, RNA, Messenger, Rats, Rats, Sprague-Dawley, Substrate Specificity
Amino Acid Sequence, Animals, COS Cells, Carrier Proteins, Cell Growth Processes, Cercopithecus aethiops, Cloning, Molecular, Cyclic AMP, DNA, Complementary, Hepatocytes, Liver, Liver Regeneration, Male, Mice, Molecular Sequence Data, NIH 3T3 Cells, Nuclear Proteins, Peptide Elongation Factor 1, Protein Biosynthesis, RNA, Messenger, Rats, Rats, Sprague-Dawley, Substrate Specificity
J. Cell. Sci.
Date: Jul. 15, 2005
PubMed ID: 16014383
View in: Pubmed Google Scholar
Download Curated Data For This Publication
165883
Switch View:
- Interactions 2