Hirose Tetsuro, Sugiura Masahiro
Center for Gene Research, Nagoya University, Nagoya 464-8602, Japan.
Nucleic Acids Res. 2004 Jun 30;32(11):3503-10. doi: 10.1093/nar/gkh682. Print 2004.
The mechanism of translational initiation differs between prokaryotes and eukaryotes. Prokaryotic mRNAs generally contain within their 5'-untranslated region (5'-UTR) a Shine-Dalgarno (SD) sequence that serves as a ribosome-binding site. Chloroplasts possess prokaryotic-like translation machinery, and many chloroplast mRNAs have an SD-like sequence, but its position is variable. Tobacco chloroplast atpB mRNAs contain no SD-like sequence and are U-rich in the 5'-UTR (-20 to -1 with respect to the start codon). In vitro translation assays with mutated mRNAs revealed that an unstructured sequence encompassing the start codon, the AUG codon and its context are required for translation. UV crosslinking experiments showed that a 50 kDa protein (p50) binds to the 5'-UTR. Insertion of an additional initiation region (SD-sequence and AUG) in the 5'-UTR, but not downstream, arrested translation from the authentic site; however, no inhibition was observed by inserting only an AUG triplet. We hypothesize for translational initiation of the atpB mRNA that the ribosome enters an upstream region, slides to the start codon and forms an initiation complex with p50 and other components.
原核生物和真核生物的翻译起始机制有所不同。原核生物的mRNA通常在其5'-非翻译区(5'-UTR)内含有一个作为核糖体结合位点的Shine-Dalgarno(SD)序列。叶绿体具有类似原核生物的翻译机制,许多叶绿体mRNA具有类似SD的序列,但其位置是可变的。烟草叶绿体atpB mRNA不含类似SD的序列,且在5'-UTR(相对于起始密码子为-20至-1)富含尿嘧啶。对突变mRNA进行的体外翻译试验表明,翻译需要一个包含起始密码子、AUG密码子及其上下文的非结构化序列。紫外线交联实验表明,一种50 kDa的蛋白质(p50)与5'-UTR结合。在5'-UTR而非下游插入额外的起始区域(SD序列和AUG)会阻止从真实位点开始的翻译;然而,仅插入一个AUG三联体未观察到抑制作用。我们推测atpB mRNA的翻译起始过程为核糖体进入上游区域,滑动至起始密码子,并与p50和其他成分形成起始复合物。