Abstract

3'-Untranslated regions (UTRs) of genes often contain key regulatory elements involved in gene expression control. A high degree of evolutionary conservation in regions of the 3'-UTR suggests important, conserved elements. In particular, we are interested in those elements involved in regulation of 3' end formation. In addition to canonical sequence elements, auxiliary sequences likely play an important role in determining the polyadenylation efficiency of mammalian pre-mRNAs. We identified highly conserved sequence elements upstream of the AAUAAA in three human collagen genes, COL1A1, COL1A2, and COL2A1, and demonstrate that these upstream sequence elements (USEs) influence polyadenylation efficiency. Mutation of the USEs decreases polyadenylation efficiency both in vitro and in vivo, and inclusion of competitor oligoribonucleotides representing the USEs specifically inhibit polyadenylation. We have also shown that insertion of a USE into a weak polyadenylation signal can enhance 3' end formation. Close inspection of the COL1A2 3'-UTR reveals an unusual feature of two closely spaced, competing polyadenylation signals. Taken together, these data demonstrate that USEs are important auxiliary polyadenylation elements in mammalian genes.

Highlights

  • Poly(A) tails are found on the 3Ј end of nearly every fully processed eukaryotic mRNA

  • Upstream elements (USEs) Can Stimulate in Vitro 3Ј End Processing of a Weak Polyadenylation Signal—Previously, auxiliary polyadenylation elements known as upstream efficiency elements (USEs) have been described and characterized in the SV40 late polyadenylation signal [21]

  • In this study we have identified auxiliary 3Ј end processing elements in highly conserved regions of the 3Ј-Untranslated regions (UTRs) of human collagen genes

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Summary

Introduction

Poly(A) tails are found on the 3Ј end of nearly every fully processed eukaryotic mRNA. These downstream elements (DSEs) can be characterized as a block containing 4 of 5 uracil (U) residues. These two sequence elements recruit cleavage and polyadenylation specificity factor (CPSF) and cleavage stimulatory factor (CstF), respectively, to define the cleavage site; mutations within these sequences abolish polyadenylation. 19 and 20 and references therein) have been identified as auxiliary cis-acting polyadenylation efficiency elements Such elements may play an important role in modulating the overall processing efficiency. Studies on human immunodeficiency virus suggest that definition of the polyadenylation site involves the recognition of multiple sequence elements, including the USE, in the context of the AAUAAA [27]

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