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Specific G-quadruplex ligands modulate the alternative splicing of Bcl-X

机译:特定的G四联体配体调节Bcl-X的选择性剪接

摘要

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.
机译:在哺乳动物内含子中,特别是在5'剪接位点(5'SS)附近,具有形成RNA G-四链体(G4s)潜力的序列是常见的。然而,很难证明G4s在功能条件下在前mRNA中形成,意味着对它们的作用或作用机理知之甚少。先前我们已经证明在Bcl-X pre-mRNA中形成了两个G4,一个接近两个替代5'SS的每一个。如果这些G4影响剪接,但与其他RNA结构或RNA结合蛋白竞争,那么稳定它们的配体将增加其中一个或两个G4形成的Bcl-X pre-mRNA分子的比例,从而改变Bcl-X剪接。我们在这里表明,一组受限制的G4配体确实会影响剪接,它们的活性和特异性强烈取决于它们的结构,并且它们在两个剪接位点独立发挥作用。配体之一玫瑰树碱GQC-05拮抗表达Bcl-X抗凋亡同工型的主要5'SS,并激活表达促凋亡同工型的替代5'SS。我们提出的机制,将解释这些跷跷板效应,并建议这些效应有助于GQC-05诱导细胞凋亡的能力。

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