3'-UTR SIRF: A database for identifying clusters of short interspersed repeats in 3' untranslated regions
- Equal contributors
1 Bioinformatics Program, Boston University, Boston, MA, USA
2 Department of Biology, Boston University, Boston, MA, USA
3 Department of Computer Science, Boston University, Boston, MA, USA
BMC Bioinformatics 2007, 8:274 doi:10.1186/1471-2105-8-274Published: 30 July 2007
Short (~5 nucleotides) interspersed repeats regulate several aspects of post-transcriptional gene expression. Previously we developed an algorithm (REPFIND) that assigns P-values to all repeated motifs in a given nucleic acid sequence and reliably identifies clusters of short CAC-containing motifs required for mRNA localization in Xenopus oocytes.
In order to facilitate the identification of genes possessing clusters of repeats
that regulate post-transcriptional aspects of gene expression in mammalian genes,
we used REPFIND to create a database of all repeated motifs in the 3' untranslated
regions (UTR) of genes from the Mammalian Gene Collection (MGC). The MGC database
includes seven vertebrate species: human, cow, rat, mouse and three non-mammalian
vertebrate species. A web-based application was developed to search this database
of repeated motifs to generate species-specific lists of genes containing specific
classes of repeats in their 3'-UTRs. This computational tool is called 3'-UTR SIRF
Finder), and it reveals that hundreds of human genes contain an abundance of short
CAC-rich and CAG-rich repeats in their 3'-UTRs that are similar to those found in
mRNAs localized to the neurites of neurons. We tested four candidate mRNAs for localization
in rat hippocampal neurons by in situ hybridization. Our results show that two candidate CAC-rich (Syntaxin 1B and Tubulin β4) and two candidate CAG-rich (Sec61α and Syntaxin 1A) mRNAs are localized to distal neurites, whereas two control mRNAs lacking repeated
motifs in their 3'-UTR remain primarily in the cell body.
Computational data generated with 3'-UTR SIRF indicate that hundreds of mammalian genes have an abundance of short CA-containing motifs that may direct mRNA localization in neurons. In situ hybridization shows that four candidate mRNAs are localized to distal neurites of cultured hippocampal neurons. These data suggest that short CA-containing motifs may be part of a widely utilized genetic code that regulates mRNA localization in vertebrate cells. The use of 3'-UTR SIRF to search for new classes of motifs that regulate other aspects of gene expression should yield important information in future studies addressing cis-regulatory information located in 3'-UTRs.