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Translation elongation after assembly of ribosomes on the Cricket paralysis virus internal ribosomal entry site without initiation factors or initiator tRNA

机译:在the麻痹病毒内部核糖体进入位点上组装核糖体后翻译起始伸长没有起始因子或起始RNA

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摘要

Reconstitution of translation elongation from purified components confirmed that ribosomes that assembled on the Cricket paralysis virus intercistronic internal ribosomal entry site (IRES) without the involvement of initiation factors or initiator tRNA were active in elongation and are, therefore, true initiation complexes. The first elongation cycle occurred without peptide bond formation on 80S ribosomes that did not contain tRNA in the P site. It required elongation factors 1A and 2 and A site-cognate aminoacylated tRNA. Cycloheximide arrested ribosomes on the IRES only after two cycles of elongation, when the first deacylated tRNA reached the E-site after translocation from the A-site.
机译:从纯化的成分重建翻译伸长,证实在Cri启动瘫痪病毒顺反子内部核糖体进入位点(IRES)上组装的核糖体在伸长中是活跃的,因此是真正的起始复合物,而在核糖体麻痹病毒顺反子内部核糖体进入位点(IRES)上组装。在没有在P位点包含tRNA的80S核糖体上没有形成肽键的情况下发生了第一个延长周期。它需要伸长因子1A和2和A位点同源的氨基酰化tRNA。当第一个脱酰基的tRNA从A位点易位后到达E位点时,环己二酰亚胺仅在两个延长周期后才在IRES上捕获核糖体。

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