A functional human Poly(A) site requires only a potent DSE and an A-rich upstream sequence.

Journal article

We have analysed the sequences required for cleavage and polyadenylation in the intronless melanocortin 4 receptor (MC4R) pre-mRNA. Unlike other intronless genes, 3'end processing of the MC4R primary transcript is independent of any auxiliary sequence elements and only requires the core poly(A) sequences. Mutation of the AUUAAA hexamer had little effect on MC4R 3'end processing but small changes in the short DSE severely reduced cleavage efficiency. The MC4R poly(A) site requires only the DSE and an A-rich upstream sequence to direct efficient cleavage and polyadenylation. Our observation may be highly relevant for the understanding of how human noncanonical poly(A) sites are recognised. This is supported by a genome-wide analysis of over 10 000 poly(A) sites where we show that many human noncanonical poly(A) signals contain A-rich upstream sequences and tend to have a higher frequency of U and GU nucleotides in their DSE compared with canonical poly(A) signals. The importance of A-rich elements for noncanonical poly(A) site recognition was confirmed by mutational analysis of the human JUNB gene, which contains an A-rich noncanonical poly(A) signal.

Authors: Nunes, N; Li, W; Tian, B; Furger, A

• Publication status: Published
• Journal: EMBO journal
• Volume: 29
• Issue: 9
• Pages: 1523-1536
• Publication date: 2010-05-01
• DOI: 10.1038/emboj.2010.42
• EISSN: 1460-2075
• ISSN: 0261-4189
• Language: English
• Keywords: Mutation; Humans; Proto-Oncogene Proteins c-jun; Molecular Sequence Data; Uridine; RNA Precursors; Cell Line; Adenosine; Neoplasm Proteins; DNA-Binding Proteins; 3' Flanking Region; Poly A; Base Sequence; Antigens, Neoplasm; 3' Untranslated Regions; Receptor, Melanocortin, Type 4