Methods

Ab initio identification of functionally interacting pairs of cis-regulatory elements

    • 1 Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA;
    • 2 Department of Mathematics, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA;
    • 3 Division of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA
    • 4 Present address: Department of Molecular and Cellular Biology, Harvard University, 7 Divinity Avenue, Cambridge, MA 02138, USA;
    • 5 Friedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, 4058 Basel, Switzerland.
    • 6 Corresponding authors. E-mail [email protected]; fax (617) 495-3537. E-mail [email protected]; fax (617) 452-2936.
Published September 17, 2008. Vol 18 Issue 10, pp. 1643-1651. https://doi.org/10.1101/gr.080085.108
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Abstract

Cooperatively acting pairs of cis-regulatory elements play important roles in many biological processes. Here, we describe a statistical approach, compositionally orthogonalized co-occurrence analysis (coCOA) that detects pairs of oligonucleotides that preferentially co-occur in pairs of sequence regions, controlling for correlations between the compositions of the analyzed regions. coCOA identified three clusters of oligonucleotide pairs that frequently co-occur at 5′ and 3′ ends of human and mouse introns. The largest cluster involved GC-rich sequences at the 5′ ends of introns that co-occur and are co-conserved with specific AU-rich sequences near intron 3′ ends. These motifs are preferentially conserved when they occur together, as measured by a new co-conservation measure, supporting common in vivo function. These motif pairs are also enriched in introns flanking alternative “cassette” exons, suggesting a role in silencing of intervening exons, and we showed that these motifs can cooperatively silence splicing of an intervening exon in a splicing reporter assay. This approach can be easily generalized to problems beyond RNA splicing.

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