GSBS Student Publications

Title

The nuclear experience of CPEB: implications for RNA processing and translational control.

Student Author(s)

Chien-Ling Lin

UMMS Affiliation

Program in Molecular Medicine

Date

2-1-2010

Document Type

Article

Medical Subject Headings

Active Transport, Cell Nucleus; Alternative Splicing; Amino Acid Sequence; Animals; Cell Line; Cell Nucleus; Female; Humans; Mice; Models, Biological; Molecular Sequence Data; NIH 3T3 Cells; Oocytes; Protein Biosynthesis; RNA Processing, Post-Transcriptional; RNA, Messenger; RNA-Binding Proteins; Recombinant Proteins; Sequence Homology, Amino Acid; Transcription Factors; Xenopus; Xenopus Proteins; mRNA Cleavage and Polyadenylation Factors

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

CPEB is a sequence-specific RNA binding protein that promotes polyadenylation-induced translation in early development, during cell cycle progression and cellular senescence, and following neuronal synapse stimulation. It controls polyadenylation and translation through other interacting molecules, most notably the poly(A) polymerase Gld2, the deadenylating enzyme PARN, and the eIF4E-binding protein Maskin. Here, we report that CPEB shuttles between the nucleus and cytoplasm and that its export occurs via the CRM1-dependent pathway. In the nucleus of Xenopus oocytes, CPEB associates with lampbrush chromosomes and several proteins involved in nuclear RNA processing. CPEB also interacts with Maskin in the nucleus as well as with CPE-containing mRNAs. Although the CPE does not regulate mRNA export, it influences the degree to which mRNAs are translationally repressed in the cytoplasm. Moreover, CPEB directly or indirectly mediates the alternative splicing of at least one pre-mRNA in mouse embryo fibroblasts as well as certain mouse tissues. We propose that CPEB, together with Maskin, binds mRNA in the nucleus to ensure tight translational repression upon export to the cytoplasm. In addition, we propose that nuclear CPEB regulates specific pre-mRNA alternative splicing.

Rights and Permissions

Citation: RNA. 2010 Feb;16(2):338-48. Epub 2009 Dec 29.

Related Resources

Link to article in PubMed

Journal Title

RNA (New York, N.Y.)

PubMed ID

20040591