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真核生物和原核生物mRNA翻译起始区域的潜在二级结构。

Potential secondary structure at the translational start domain of eukaryotic and prokaryotic mRNAs.

作者信息

Ganoza M C, Louis B G

机构信息

Banting and Best Department of Medical Research, University of Toronto, Ontario, Canada.

出版信息

Biochimie. 1994;76(5):428-39. doi: 10.1016/0300-9084(94)90120-1.

Abstract

In order to identify conserved potential secondary structures within translational start sites, mRNA sequences derived from different species were studied with programs able to depict such features. The potential secondary structure of 71 bases around the initiator AUG or AUGs in the coding sequences of 290 eukaryotic mRNAs was first examined and compared to 290 similarly analyzed regions derived from prokaryotic mRNA sequences (Nucleic Acids Res (1987) 15, 345-360). In both sets of sequences the initiator codon was often found to be in an open potential structure whereas a denser region characterized by nearly-periodic spacings defined the coding regions. Randomization of the sequences obliterated the observed patterns suggesting that the structure of the mRNA may determine these differences. Three sets of eukaryotic and prokaryotic mRNAs of approximately equal length were analyzed and found to preserve an open unpaired non-coding region 5' to the start codon. The start codon was found free of potential secondary structure in over 80% of all the sequences analyzed. These data, and study of mutants that restrict the accessibility of the start codon to the ribosomal initiation complex, suggest that both the prokaryotic and eukaryotic mRNA start sites must occur free of potential secondary structure for efficient initiation. A striking difference of the eukaryotic mRNA sequences analyzed was the high propensity of the coding region vicinal to the start codon to form secondary structures. Certain translation-defective mutants exhibit impaired formation of these secondary structures suggesting that the structure of the coding regions adjacent to the start codons of eukaryotic mRNAs may be an important, thus far unexamined, determinant of initiation. We propose that, for all genes studied, the transition in secondary structure between the coding and non-coding regions may be an important determinant of initiation.

摘要

为了识别翻译起始位点内保守的潜在二级结构,利用能够描绘此类特征的程序对来自不同物种的mRNA序列进行了研究。首先检查了290个真核mRNA编码序列中起始AUG或多个AUG周围71个碱基的潜在二级结构,并与290个来自原核mRNA序列的类似分析区域进行了比较(《核酸研究》(1987年)15卷,345 - 360页)。在这两组序列中,起始密码子常常处于开放的潜在结构中,而以近乎周期性间隔为特征的更密集区域界定了编码区。序列随机化消除了观察到的模式,这表明mRNA的结构可能决定了这些差异。分析了三组长度大致相等的真核和原核mRNA,发现起始密码子5'端存在一个开放的未配对非编码区。在所分析的所有序列中,超过80%的起始密码子没有潜在二级结构。这些数据以及对限制起始密码子与核糖体起始复合物结合能力的突变体的研究表明,原核和真核mRNA起始位点都必须不存在潜在二级结构才能有效起始。所分析的真核mRNA序列的一个显著差异是起始密码子附近编码区形成二级结构的倾向很高。某些翻译缺陷型突变体表现出这些二级结构形成受损,这表明真核mRNA起始密码子相邻编码区的结构可能是一个重要的、但迄今未被研究的起始决定因素。我们提出,对于所有研究的基因,编码区与非编码区之间二级结构的转变可能是起始的一个重要决定因素。

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