Calcitonin exon sequences influence alternative RNA processing

Gilbert J. Cote, Irene N. Nguyen, Susan M. Berget, Robert F. Gagel

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

The pre-mRNA encoding calcitonin (CT) and CT gene-related peptide (CGRP) is differentially processed in a tissue-specific fashion to include exon 4 (which encodes CT) or exclude this exon and splice to exon 5 (which encodes CGRP). We have used a CT-specific in vitro RNA-processing system to identify cis-acting sequences required to prevent splicing to exon 5. Deletion mapping demonstrated the presence of an element within the first 45 nucleotides of the CT-specific exon 4 that was required to suppress splicing to the CGRP-specific exon 5. This element was able to function in a completely heterologous system to suppress splicing when the CGRP exon was replaced with a constitutive viral exon. The element was unable to suppress splicing in the absence of a proximal CT-specific 3′ splice site. Our results suggest that CT-specific splicing requires assisted recognition of its 3′ splice site.

Original languageEnglish (US)
Pages (from-to)1744-1749
Number of pages6
JournalMolecular Endocrinology
Volume4
Issue number11
StatePublished - 1990

ASJC Scopus subject areas

  • Molecular Biology
  • Endocrinology

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