Alexeeva E V, Shpanchenko O V, Dontsova O A, Bogdanov A A, Nierhaus K H
Max-Planck-Institut für Molekulare Genetik, Berlin, Germany.
Nucleic Acids Res. 1996 Jun 15;24(12):2228-35. doi: 10.1093/nar/24.12.2228.
The contacts of phosphate groups in mRNAs with ribosomes were studied. Two mRNAs were used: one mRNA contained in the middle two defined codons to construct the pre- and the post-translocational states, the other was a sequence around the initiation site of the natural cro-mRNA. Phosphorothioate nucleotides were randomly incorporated at a few A, G, U or C positions during in vitro transcription. Iodine can cleave the thioated positions if they are not shielded by ribosomal components. Only a few minor differences in iodine cleavage of ribosome bound and non-bound mRNA were observed: the nucleotide two positions upstream of the decoding codons (i.e. those codons involved in codon-anticodon interactions) showed a reduced accessibility for iodine and the nucleotide immediately following the decoding codons an enhanced accessibility in both elongating states. In initiating ribosomes where the mRNA contained a strong Shine-Dalgarno sequence, at least five phosphates were additionally slightly protected covering the Shine-Dalgarno sequence and nucleotides downstream including the initiator AUG in the P site (Al, G3, G-2, G-5 and A-7). The low contact levels of the phosphates in the mRNA with the elongating ribosome strikingly contrast with the pronounced contact patterns previously described for tRNAs. The data obtained in this study, as well as results of previous studies, suggest that mRNA regions downstream and upstream of decoding codons form only weak contacts with ribosomal components and that the mRNA thus is mainly fixed by codon-anticodon interaction on the elongating ribosome.
对信使核糖核酸(mRNA)中磷酸基团与核糖体的接触情况进行了研究。使用了两种mRNA:一种mRNA在中间包含两个确定的密码子,用于构建转位前和转位后的状态,另一种是天然cro - mRNA起始位点周围的序列。在体外转录过程中,硫代磷酸核苷酸被随机掺入到一些A、G、U或C位置。如果硫代化位置未被核糖体成分屏蔽,碘可以切割这些位置。在核糖体结合和未结合的mRNA的碘切割中仅观察到一些微小差异:解码密码子上游两个位置的核苷酸(即那些参与密码子 - 反密码子相互作用的密码子)对碘的可及性降低,而在两种延伸状态下,解码密码子之后紧邻的核苷酸的可及性增强。在起始核糖体中,若mRNA包含强的Shine - Dalgarno序列,至少有五个磷酸基团会额外受到轻微保护,覆盖Shine - Dalgarno序列及下游核苷酸,包括P位点的起始密码子AUG(A1、G3、G - 2、G - 5和A - 7)。mRNA中磷酸基团与延伸核糖体的低接触水平与先前描述的转运核糖核酸(tRNA)明显的接触模式形成鲜明对比。本研究获得的数据以及先前研究的结果表明,解码密码子下游和上游的mRNA区域与核糖体成分仅形成弱接触,因此mRNA在延伸核糖体上主要通过密码子 - 反密码子相互作用固定。