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酵母Ty元件的核苷酸序列:基因表达异常机制的证据。

Nucleotide sequence of a yeast Ty element: evidence for an unusual mechanism of gene expression.

作者信息

Clare J, Farabaugh P

出版信息

Proc Natl Acad Sci U S A. 1985 May;82(9):2829-33. doi: 10.1073/pnas.82.9.2829.

Abstract

We have determined the DNA sequence of the transposable element Ty912 of yeast. The 5918-base-pair element encodes two genes, tya912 and tyb912, which specify proteins similar to sequence-specific DNA-binding proteins of Escherichia coli and retroviral reverse transcriptases, respectively. The tyb912 gene is atypical of eukaryotic genes since (i) it begins 1336 nucleotides into the Ty912 mRNA (i.e., downstream of the tya912 gene) and (ii) the first in-frame AUG is 921 nucleotides into the coding frame. Protein blot analysis of Ty-lacZ fusions shows that the tyb912 gene is translated starting at the 5' end of the tya912 gene and that the primary translational product is a tya912::tyb912 fusion protein. We have shown that synthesis of this fusion protein probably does not occur by RNA splicing. The data are consistent with a mechanism of translational frameshifting occurring within the region of overlap between the 3' end of tya912 and the 5' end of tyb912.

摘要

我们已经确定了酵母转座元件Ty912的DNA序列。这个5918个碱基对的元件编码两个基因,tya912和tyb912,它们分别编码与大肠杆菌序列特异性DNA结合蛋白和逆转录病毒逆转录酶相似的蛋白质。tyb912基因在真核基因中是不典型的,因为(i)它起始于Ty912 mRNA的第1336个核苷酸处(即tya912基因的下游),并且(ii)第一个符合读码框的AUG在编码框的第921个核苷酸处。对Ty-lacZ融合体的蛋白质印迹分析表明,tyb912基因从tya912基因的5'端开始翻译,并且初级翻译产物是一个tya912::tyb912融合蛋白。我们已经表明,这种融合蛋白的合成可能不是通过RNA剪接发生的。这些数据与在tya912的3'端和tyb912的5'端重叠区域内发生翻译移码的机制一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee8d/397659/c4dbdcd6c6a1/pnas00349-0287-a.jpg

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