A novel human c-sis mRNA species is transcribed from a promoter in c-sis intron 1 and contains the code for an alternative PDGF B-like protein

The human platelet-derived growth factor (PDGF) B chain precursor is usually translated from a 3.5 kb c-sis/PDGF B gene transcript. The first exon of the c-sis gene contains the code for the signal peptide of the PDGF B chain precursor, preceded by a 1 kb long untranslated sequence with potent trans...

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Published inNucleic acids research Vol. 23; no. 15; pp. 2815 - 2822
Main Authors Dirks, Ron P.H., Onnekink, Carla, Jansen, Hans J., de Jong, Aard, Bloemers, Henri P.J.
Format Journal Article
LanguageEnglish
Published England Oxford University Press 11.08.1995
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Summary:The human platelet-derived growth factor (PDGF) B chain precursor is usually translated from a 3.5 kb c-sis/PDGF B gene transcript. The first exon of the c-sis gene contains the code for the signal peptide of the PDGF B chain precursor, preceded by a 1 kb long untranslated sequence with potent translation Inhibitory activity. In this paper we show that a novel 2.6 kb c-sis mRNA present in the human choriocarcinoma cell line JEG-3 initiates at an alternative exon 1, which we refer to as exon 1a. The 90 bp long exon 1a is located in the center of the first intron of the gene. It coincides with a very pronounced DNase-hhypersensitive site and is preceded by a functional promoter. Of the three ATG codons present in exon 1 a, the third one perfectly matches the criteria of a consensus start codon. It Initiates an open reading frame that is continuous with the code for the PDGF B chain precursor but lacks the code for a signal peptide. We conclude that this novel 2.6 kb c-sis mRNA species lacks the strong translation inhibitory potential of the regular exon 1 and contains the code for a PDGF B-IIke protein that may be targeted to the cell nucleus.
Bibliography:istex:EE0AA8F4561409E3A9B98EC9419D761E64E180AB
ark:/67375/HXZ-MHBP187D-T
To whom correspondence should be addressed at present address: Department of Molecular Biology, University of Nijmegen, Toernooiveld , 6525 ED Nijmegen, The Netherlands
ArticleID:23.15.2815
ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
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ISSN:0305-1048
1362-4962
DOI:10.1093/nar/23.15.2815