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登革4型病毒的核苷酸序列:编码非结构蛋白的基因分析。

The nucleotide sequence of dengue type 4 virus: analysis of genes coding for nonstructural proteins.

作者信息

Mackow E, Makino Y, Zhao B T, Zhang Y M, Markoff L, Buckler-White A, Guiler M, Chanock R, Lai C J

出版信息

Virology. 1987 Aug;159(2):217-28. doi: 10.1016/0042-6822(87)90458-2.

Abstract

We recently cloned a full-length DNA copy of the dengue type 4 virus genome. Analysis of the 5' terminal nucleotide sequence suggested that the three-virion structural proteins are synthesized by proteolytic cleavage of a polyprotein precursor which is encoded in one open reading frame. We now present the remaining sequence of the dengue type 4 virus genome which codes for the nonstructural proteins. The entire genome, which is 10,644 nucleotides in length, contains one long open reading frame which codes for a single large polyprotein 3386 amino acids in length. Alignment of the dengue nonstructural protein sequence with that of other flaviviruses, including yellow fever and West Nile viruses, revealed that significant homology exists throughout the entire nonstructural region of the dengue genome and this allowed tentative assignment of individual nonstructural proteins in the following order: NS1, NS2a, NS2b, NS3, NS4a, NS4b, and NS5-COOH. Processing of the nonstructural proteins appears to involve two types of proteolytic cleavage: the first occurs after a long hydrophobic signal sequence and the second occurs at a junction between two basic amino acids and a small polar amino acid. A notable exception is the cleavage at the N-terminus of the dengue NS3 which may take place at the junction between Gln-Arg and Ser. Comparative analysis suggests that dengue NS3 and NS5 may be involved in enzymatic activities related to viral replication and/or transcription. Putative nonstructural proteins NS2a, NS2b, NS4a, and NS4b are extremely hydrophobic, suggesting that these proteins are most likely associated with cellular membranes.

摘要

我们最近克隆了登革4型病毒基因组的全长DNA拷贝。对5'末端核苷酸序列的分析表明,三种病毒体结构蛋白是由一个开放阅读框编码的多蛋白前体经蛋白水解切割合成的。我们现在展示登革4型病毒基因组中编码非结构蛋白的其余序列。整个基因组长度为10644个核苷酸,包含一个长开放阅读框,该阅读框编码一个长度为3386个氨基酸的单一大型多蛋白。将登革非结构蛋白序列与其他黄病毒(包括黄热病和西尼罗河病毒)的序列进行比对,发现登革基因组的整个非结构区域都存在显著的同源性,这使得可以按以下顺序初步确定各个非结构蛋白:NS1、NS2a、NS2b、NS3、NS4a、NS4b和NS5-COOH。非结构蛋白的加工似乎涉及两种类型的蛋白水解切割:第一种发生在一个长的疏水信号序列之后,第二种发生在两个碱性氨基酸和一个小极性氨基酸之间的连接处。一个显著的例外是登革NS3 N端的切割,可能发生在Gln-Arg和Ser之间的连接处。比较分析表明,登革NS3和NS5可能参与与病毒复制和/或转录相关的酶活性。推定的非结构蛋白NS2a、NS2b、NS4a和NS4b具有极强的疏水性,表明这些蛋白很可能与细胞膜相关。

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