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与一小串非最优密码子相反,5'-二级结构的形成会抑制酵母中丙酮酸激酶mRNA的翻译。

5'-secondary structure formation, in contrast to a short string of non-preferred codons, inhibits the translation of the pyruvate kinase mRNA in yeast.

作者信息

Bettany A J, Moore P A, Cafferkey R, Bell L D, Goodey A R, Carter B L, Brown A J

机构信息

Biotechnology Unit, University of Glasgow, U.K.

出版信息

Yeast. 1989 May-Jun;5(3):187-98. doi: 10.1002/yea.320050308.

DOI:10.1002/yea.320050308
PMID:2660464
Abstract

The effects of poor codon bias and secondary structure formation upon the translation of the pyruvate kinase (PYK1) mRNA have been investigated in Saccharomyces cerevisiae. Following insertion mutagenesis at the 5'-end of the PYK1 coding region, the gene was transformed into yeast, and translation assessed directly in vivo by determining the distribution of the modified PYK1 mRNAs across polysomes fractionated by sucrose density gradient centrifugation. The chromosomally-encoded (wild-type) PYK1 mRNA, and the actin, ribosomal protein L3 and glyceraldehyde-3-phosphate dehydrogenase mRNAs were used to control for minor differences between polysome preparations. An insertion containing 13 non-preferred codons at the 5'-end of the coding region was found to have no significant effect upon PYK1 mRNA translation. In contrast, translation was inhibited by an insertion which increased the formation of secondary structures at the 5'-end of the mRNA (overall delta G = -36.6 kcal/mol). Control insertions were also analysed to exclude the possibility that alterations to the amino acid sequence of pyruvate kinase affect the translation of its mRNA. These insertions, which introduced preferred codons or restored wild-type levels of secondary structure formation, did not significantly influence PYK1 mRNA translation.

摘要

已在酿酒酵母中研究了密码子偏好性差和二级结构形成对丙酮酸激酶(PYK1)mRNA翻译的影响。在PYK1编码区5'端进行插入诱变后,将该基因转化到酵母中,并通过确定经蔗糖密度梯度离心分级分离的多聚核糖体上修饰的PYK1 mRNA的分布,直接在体内评估翻译情况。使用染色体编码的(野生型)PYK1 mRNA以及肌动蛋白、核糖体蛋白L3和甘油醛-3-磷酸脱氢酶mRNA来控制多聚核糖体制剂之间的微小差异。发现在编码区5'端含有13个非偏好密码子的插入对PYK1 mRNA翻译没有显著影响。相反,一个增加mRNA 5'端二级结构形成的插入(总体ΔG = -36.6千卡/摩尔)抑制了翻译。还分析了对照插入,以排除丙酮酸激酶氨基酸序列的改变影响其mRNA翻译的可能性。这些引入偏好密码子或恢复二级结构形成野生型水平的插入,对PYK1 mRNA翻译没有显著影响。

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