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PMID: 11278713 Published · ppublish English Journal Article

Plasminogen activator inhibitor type 2 contains mRNA instability elements within exon 4 of the coding region. Sequence homology to coding region instability determinants in other mRNAs.

The Journal of biological chemistry ·Vol. 276 ·No. 17 ·2001-04-27 ·Pages 13675-84

Tierney MJ, Medcalf RL

Abstract

Plasminogen activator inhibitor type 2 (PAI-2) is a serine protease inhibitor that inhibits urokinase. Constitutive and regulated PAI-2 gene expression involves post-transcriptional events, and an AU-rich mRNA instability motif within the 3'-untranslated region of PAI-2 mRNA is required for this process (Maurer, F., Tierney, M., and Medcalf, R. L. (1999) Nucleic Acids Res. 27, 1664-1673). Here we show that instability determinants are present within various exons of the PAI-2 coding region, most notably within exon 4. Deletion of exon 4 from the full-length PAI-2 cDNA results in a doubling in the half-life of PAI-2 mRNA, whereas a 28-nucleotide region within exon 4 contains binding sites for cytoplasmic proteins. Inducible stabilization of PAI-2 mRNA in HT-1080 cells treated with phorbol ester and tumor necrosis factor does not alter the binding of proteins to the exon 4 instability determinant, but resulted in a transient increase in the binding of factors to the AU-rich RNA instability element. Hence, PAI-2 mRNA stability is influenced by elements located within both the coding region and the 3'-untranslated region and that cytoplasmic mRNA binding factors may influence steady state and inducible PAI-2 mRNA expression. Finally a 10-nucleotide region flanking the exon 4 protein-binding site is homologous to instability elements within five other transcripts, suggesting that a common coding region determinant may exist.

MeSH Terms
3' Untranslated Regions/metabolism 3T3 Cells Animals Base Sequence Binding Sites Blotting, Northern Blotting, Western Carcinogens Cell Line Cytoplasm/metabolism DNA, Antisense/metabolism DNA, Complementary/metabolism Electrophoresis, Polyacrylamide Gel Exons Gene Deletion Genes, Reporter Human Growth Hormone/genetics,metabolism Humans Mice Models, Genetic Molecular Sequence Data Mutagenesis Phorbol Esters Plasmids/metabolism Plasminogen Activator Inhibitor 2/chemistry,genetics Promoter Regions, Genetic Protein Binding/drug effects Proto-Oncogene Proteins c-fos/genetics,metabolism RNA Processing, Post-Transcriptional RNA, Messenger/metabolism Time Factors Transcription, Genetic Transfection Tumor Necrosis Factor-alpha/metabolism Ultraviolet Rays
Chemicals
3' Untranslated Regions Carcinogens DNA, Antisense DNA, Complementary Phorbol Esters Plasminogen Activator Inhibitor 2 Proto-Oncogene Proteins c-fos RNA, Messenger Tumor Necrosis Factor-alpha Human Growth Hormone
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tierney M J
Department of Medicine, Monash University, Box Hill Hospital, Box Hill 3128, Victoria, Australia.
Medcalf R L
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2001-04-27
Epub
2001-00-26
Pages
13675-84
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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