TY - JOUR
T1 - Specific G-quadruplex ligands modulate the alternative splicing of Bcl-X
AU - Weldon, Carika
AU - Dacanay, Justine G.
AU - Gokhale, Vijay
AU - Boddupally, Peda Venkat L.
AU - Behm-Ansmant, Isabelle
AU - Burley, Glenn A.
AU - Branlant, Christiane
AU - Hurley, Laurence H.
AU - Dominguez, Cyril
AU - Eperon, Ian C.
N1 - Publisher Copyright:
© The Author(s) 2017.
PY - 2018/1/25
Y1 - 2018/1/25
N2 - Sequences with the potential to form RNA G-quadruplexes (G4s) are common in mammalian introns, especially in the proximity of the 5 splice site (5’SS). However, the difficulty of demonstrating that G4s form in pre-mRNA in functional conditions has meant that little is known about their effects or mechanisms of action. We have shown previously that two G4s form in Bcl-X pre-mRNA, one close to each of the two alternative 5’SS. If these G4s affect splicing but are in competition with other RNA structures or RNA binding proteins, then ligands that stabilize them would increase the proportion of Bcl-X pre-mRNA molecules in which either or both G4s had formed, shifting Bcl-X splicing. We show here that a restricted set of G4 ligands do affect splicing, that their activity and specificity are strongly dependent on their structures and that they act independently at the two splice sites. One of the ligands, the ellipticine GQC-05, antagonizes the major 5’SS that expresses the anti-apoptotic isoform of Bcl-X and activates the alternative 5’SS that expresses a pro-apoptotic isoform. We propose mechanisms that would account for these see-saw effects and suggest that these effects contribute to the ability of GQC-05 to induce apoptosis.
AB - Sequences with the potential to form RNA G-quadruplexes (G4s) are common in mammalian introns, especially in the proximity of the 5 splice site (5’SS). However, the difficulty of demonstrating that G4s form in pre-mRNA in functional conditions has meant that little is known about their effects or mechanisms of action. We have shown previously that two G4s form in Bcl-X pre-mRNA, one close to each of the two alternative 5’SS. If these G4s affect splicing but are in competition with other RNA structures or RNA binding proteins, then ligands that stabilize them would increase the proportion of Bcl-X pre-mRNA molecules in which either or both G4s had formed, shifting Bcl-X splicing. We show here that a restricted set of G4 ligands do affect splicing, that their activity and specificity are strongly dependent on their structures and that they act independently at the two splice sites. One of the ligands, the ellipticine GQC-05, antagonizes the major 5’SS that expresses the anti-apoptotic isoform of Bcl-X and activates the alternative 5’SS that expresses a pro-apoptotic isoform. We propose mechanisms that would account for these see-saw effects and suggest that these effects contribute to the ability of GQC-05 to induce apoptosis.
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U2 - 10.1093/nar/gkx1122
DO - 10.1093/nar/gkx1122
M3 - Article
C2 - 29156002
AN - SCOPUS:85044622931
SN - 0305-1048
VL - 46
SP - 886
EP - 896
JO - Nucleic acids research
JF - Nucleic acids research
IS - 2
ER -