Alternative splicing modulation by G-quadruplexes

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作者
Ilias Georgakopoulos-Soares
Guillermo E. Parada
Hei Yuen Wong
Ragini Medhi
Giulia Furlan
Roberto Munita
Eric A. Miska
Chun Kit Kwok
Martin Hemberg
机构
[1] Wellcome Sanger Institute,Wellcome Cancer Research UK Gurdon Institute
[2] Wellcome Genome Campus,Department of Genetics
[3] Department of Bioengineering and Therapeutic Sciences,Department of Chemistry and State Key Laboratory of Marine Pollution
[4] University of California San Francisco,Division of Molecular Hematology, Department of Laboratory Medicine
[5] University of Cambridge,Donnelly Centre for Cellular and Biomolecular Research
[6] University of Cambridge,Department of Molecular Genetics
[7] City University of Hong Kong,undefined
[8] Kowloon Tong,undefined
[9] Lund Stem Cell Center,undefined
[10] Faculty of Medicine,undefined
[11] Lund University,undefined
[12] Shenzhen Research Institute of City University of Hong Kong,undefined
[13] University of Toronto,undefined
[14] University of Toronto,undefined
[15] Evergrande Center for Immunologic Diseases,undefined
[16] Harvard Medical School and Brigham and Women’s Hospital,undefined
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摘要
Alternative splicing is central to metazoan gene regulation, but the regulatory mechanisms are incompletely understood. Here, we show that G-quadruplex (G4) motifs are enriched ~3-fold near splice junctions. The importance of G4s in RNA is emphasised by a higher enrichment for the non-template strand. RNA-seq data from mouse and human neurons reveals an enrichment of G4s at exons that were skipped following depolarisation induced by potassium chloride. We validate the formation of stable RNA G4s for three candidate splice sites by circular dichroism spectroscopy, UV-melting and fluorescence measurements. Moreover, we find that sQTLs are enriched at G4s, and a minigene experiment provides further support for their role in promoting exon inclusion. Analysis of >1,800 high-throughput experiments reveals multiple RNA binding proteins associated with G4s. Finally, exploration of G4 motifs across eleven species shows strong enrichment at splice sites in mammals and birds, suggesting an evolutionary conserved splice regulatory mechanism.
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