Document Detail


Splicing is required for rapid and efficient mRNA export in metazoans.
MedLine Citation:
PMID:  10611316     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Pre-mRNA splicing is among the last known nuclear events before export of mature mRNA to the cytoplasm. At present, it is not known whether splicing and mRNA export are biochemically coupled processes. In this study, we have injected pre-mRNAs containing a single intron or the same mRNAs lacking an intron (Deltai-mRNAs) into Xenopus oocyte nuclei. We find that the spliced mRNAs are exported much more rapidly and efficiently than the identical Deltai-mRNAs. Moreover, competition studies using excess Deltai-mRNA indicate that different factor(s) are involved in the inefficient export of Deltai-mRNA vs. the efficient export of spliced mRNA. Consistent with this conclusion, spliced mRNA and Deltai-mRNA, though identical in sequence, are assembled into different messenger ribonucleoprotein particles (mRNP) in vitro. Strikingly, the mRNA in the spliced mRNP, but not in the Deltai-mRNP, is exported rapidly and efficiently. We conclude that splicing generates a specific nucleoprotein complex that targets mRNA for export. Our results, revealing a link between splicing and efficient mRNA export, may explain the reports that an intron is required for efficient expression of many protein-coding genes in metazoans.
Authors:
M J Luo; R Reed
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Proceedings of the National Academy of Sciences of the United States of America     Volume:  96     ISSN:  0027-8424     ISO Abbreviation:  Proc. Natl. Acad. Sci. U.S.A.     Publication Date:  1999 Dec 
Date Detail:
Created Date:  2000-01-27     Completed Date:  2000-01-27     Revised Date:  2013-04-17    
Medline Journal Info:
Nlm Unique ID:  7505876     Medline TA:  Proc Natl Acad Sci U S A     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  14937-42     Citation Subset:  IM    
Affiliation:
Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Biological Transport
Cell Nucleus / metabolism*
DNA-Binding Proteins / genetics
Fushi Tarazu Transcription Factors
HeLa Cells
Homeodomain Proteins / genetics
Humans
Introns
Microinjections
Nucleoproteins / metabolism
Oocytes
RNA Precursors / metabolism*
RNA Splicing*
RNA, Messenger / metabolism*
Transcription Factors / genetics
Viral Proteins
Xenopus
Chemical
Reg. No./Substance:
0/DNA-Binding Proteins; 0/Fushi Tarazu Transcription Factors; 0/Homeodomain Proteins; 0/MLTF protein, adenovirus; 0/Nucleoproteins; 0/RNA Precursors; 0/RNA, Messenger; 0/Transcription Factors; 0/Viral Proteins
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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