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Research Article Free access | 10.1172/JCI116274

Two preproendothelin 1 mRNAs transcribed by alternative promoters.

L Benatti, L Bonecchi, L Cozzi, and P Sarmientos

Department of Biotechnology, Farmitalia Carlo Erba, Nerviano, Italy.

Find articles by Benatti, L. in: PubMed | Google Scholar

Department of Biotechnology, Farmitalia Carlo Erba, Nerviano, Italy.

Find articles by Bonecchi, L. in: PubMed | Google Scholar

Department of Biotechnology, Farmitalia Carlo Erba, Nerviano, Italy.

Find articles by Cozzi, L. in: PubMed | Google Scholar

Department of Biotechnology, Farmitalia Carlo Erba, Nerviano, Italy.

Find articles by Sarmientos, P. in: PubMed | Google Scholar

Published March 1, 1993 - More info

Published in Volume 91, Issue 3 on March 1, 1993
J Clin Invest. 1993;91(3):1149–1156. https://doi.org/10.1172/JCI116274.
© 1993 The American Society for Clinical Investigation
Published March 1, 1993 - Version history
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Abstract

Endothelin-1, initially identified as potent vasoconstrictor secreted by vascular endothelial cells, was subsequently found to have many effects on both vascular and nonvascular tissues. We have identified from a human placenta cDNA library a clone (cDNA-2) which corresponds to a novel 5'-extended preproendothelin 1 (preproET-1) mRNA. Comparison with the known preproET-1 mRNA (cDNA-1), showed that the two molecules share the same coding sequence but differ in the 5'-untranslated region. Interestingly, cDNA-2 extends upstream of promoter regions previously shown to be essential for full preproET-1 expression. Primer extension and PCR analysis of human placenta RNA demonstrated the presence of additional transcription initiation sites located upstream of the previously identified preproET-1 CAP site. Moreover, the two mRNAs show different pattern of expression. To elucidate the mechanisms controlling the production of alternative transcripts we transfected COS-1 cells with a series of preproET-1 promoter deletion mutants. This analysis revealed that the human preproET-1 gene can be transcribed from a proximal and a distal promoter element which has hitherto been undetected. In addition, we demonstrate the presence of a region in the down-epithelial specific expression.

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