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Activation of picornaviral IRESs by PTB shows differential dependence on each PTB RNA-binding domain

机译:PTB对picornaviral IRES的激活显示出对每个PTB RNA结合域的不同依赖性

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摘要

Polypyrimidine tract binding protein (PTB) is an RNA-binding protein with four RNA-binding domains (RBDs). It is a major regulator of alternative splicing and also stimulates translation initiation at picornavirus IRESs (internal ribosome entry sites). The sites of interaction of each RBD with two picornaviral IRESs have previously been mapped. To establish which RBD–IRES interactions are essential for IRES activation, point mutations were introduced into the RNA-binding surface of each RBD. Three such mutations were sufficient to inactivate RNA-binding by any one RBD, but the sites of the other three RBD–IRES interactions remained unperturbed. Poliovirus IRES activation was abrogated by inactivation of RBD1, 2, or 4, but the RBD3-IRES interaction was superfluous. Stimulation of the encephalomyocarditis virus IRES was reduced by inactivation of RBD1, 3, or 4, and abrogated by mutation of RBD2, or both RBDs 3 and 4. Surprisingly, therefore, the binding of PTB in its normal orientation does not guarantee IRES activation; three native RBDs are sufficient for correct binding but not for activation if the missing RBD–IRES interaction is critical.
机译:聚嘧啶束结合蛋白(PTB)是具有四个RNA结合域(RBD)的RNA结合蛋白。它是替代剪接的主要调节剂,也刺激微小RNA病毒IRES(内部核糖体进入位点)的翻译起始。每个RBD与两个微核病毒IRES的相互作用位点先前已作图。为了确定哪些RBD-IRES相互作用对于IRES激活必不可少,将点突变引入每个RBD的RNA结合表面。三个这样的突变足以使任何一个RBD的RNA结合失活,但是其他三个RBD-IRES相互作用的位点仍然不受干扰。脊髓灰质炎病毒IRES激活被RBD1、2或4灭活所废除,但RBD3-IRES相互作用是多余的。通过使RBD1、3或4失活来减少脑心肌炎病毒IRES的刺激,并由于RBD2或RBD 3和4的突变而废除。因此,令人惊讶的是,以正常方向结合PTB不能保证IRES的激活。如果缺少RBD-IRES相互作用至关重要,则三个本机RBD足以进行正确的绑定,但不足以激活。

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