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腺病毒2型晚期非结构33K蛋白的多肽结构及编码位置

Polypeptide structure and encoding location of the adenovirus serotype 2 late, nonstructural 33K protein.

作者信息

Oosterom-Dragon E A, Anderson C W

出版信息

J Virol. 1983 Jan;45(1):251-63. doi: 10.1128/JVI.45.1.251-263.1983.

Abstract

Radiochemical microsequence analysis of selected tryptic peptides of the adenovirus type 2 33K nonstructural protein has revealed the precise region of the genomic nucleotide sequence that encodes this protein. The initiation codon for the 33K protein lies 606 nucleotides to the right of the EcoRI restriction site at 70.7 map units and 281 nucleotides to the left of the postulated carboxyterminal codon of the adenovirus 100K protein. The coding regions for these two proteins thus overlap; however, the 33K protein is derived from the +1 frame with respect to the postulated 100K reading frame. Our results contradict an earlier published report suggesting that these two proteins share extensive amino acid sequence homology (N. Axelrod, Virology 87:366-383, 1978). The published nucleotide sequence of the Ad2 EcoRI-F fragment (70.7 to 75.9 map units) cannot accommodate in a single reading frame the peptide sequences of the 33K protein that we have determined. Sequence analysis of DNA fragments derived from virus has confirmed the published nucleotide sequence in all critical regions with respect to the coding region for the 33K protein. Consequently, our data are only consistent with the existence of an mRNA splice within the coding region for 33K. Consensus donor and acceptor splice sequences have been located that would predict the removal of 202 nucleotides from the transcripts for the 33K protein. Removal of these nucleotides would explain the structure of a peptide that cannot otherwise be directly encoded by the EcoRI-F fragment. Identification of the precise splice points by peptide sequencing has permitted a prediction of the complete amino acid sequence for the 33K protein.

摘要

对腺病毒2型33K非结构蛋白的选定胰蛋白酶肽段进行放射化学微序列分析,已揭示出编码该蛋白的基因组核苷酸序列的精确区域。33K蛋白的起始密码子位于EcoRI限制位点右侧606个核苷酸处,位于70.7图谱单位,且在腺病毒100K蛋白假定的羧基末端密码子左侧281个核苷酸处。因此,这两种蛋白的编码区域重叠;然而,相对于假定的100K阅读框,33K蛋白来自+1框架。我们的结果与早期发表的一份报告相矛盾,该报告表明这两种蛋白具有广泛的氨基酸序列同源性(N. 阿克塞尔罗德,《病毒学》87:366 - 383,1978)。已发表的Ad2 EcoRI - F片段(70.7至75.9图谱单位)的核苷酸序列无法在单一阅读框中容纳我们所确定的33K蛋白的肽段序列。对源自病毒的DNA片段进行的序列分析已证实,在与33K蛋白编码区域相关的所有关键区域中,已发表的核苷酸序列是正确的。因此,我们的数据仅与33K编码区域内存在mRNA剪接相一致。已定位了共有供体和受体剪接序列,这些序列可预测从33K蛋白的转录本中去除202个核苷酸。去除这些核苷酸将解释一个肽段的结构,否则该肽段无法由EcoRI - F片段直接编码。通过肽段测序鉴定精确的剪接位点,使得能够预测33K蛋白的完整氨基酸序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4295/256408/23f8acb20cc7/jvirol00148-0270-a.jpg

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