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人1型副流感病毒核蛋白基因的序列分析与表达

Sequence analysis and expression of the human parainfluenza type 1 virus nucleoprotein gene.

作者信息

Matsuoka Y, Ray R

机构信息

Secretech Inc., Birmingham, Alabama 35205.

出版信息

Virology. 1991 Mar;181(1):403-7. doi: 10.1016/0042-6822(91)90514-c.

Abstract

The nucleotide sequence of the human parainfluenza type 1 (Pl1) virus nucleoprotein (NP) gene was determined from cDNA clones of the mRNA. A cDNA clone, 4-31, containing a 1.7-kb insert, was identified as a Pl1 NP-specific clone by partial nucleotide sequence analysis and sequence comparison with Sendai virus (SV) NP. Using a vaccinia virus transient expression system, a polypeptide with electrophoretic mobility similar to that of Pl1 NP was synthesized from this clone, which reacted specifically with both polyclonal and monoclonal antibodies against Pl1 virus and Pl1 NP, respectively. The complete nucleotide sequence of this clone was determined and was found to contain a single open reading frame that can encode a protein of 524 amino acids with a predicted molecular weight of 57,547. Comparison of the amino acid sequence of Pl1 NP with that of other paramyxoviruses showed that two conserved amino acid sequences found within other paramyxoviruses are also present in Pl1 NP. Although Pl1 and SV showed a high sequence homology, approximately 100 amino acids at the C-terminal region were highly divergent as found also among other paramyxoviruses.

摘要

从人1型副流感病毒(P11)信使核糖核酸(mRNA)的互补脱氧核糖核酸(cDNA)克隆中确定了该病毒核蛋白(NP)基因的核苷酸序列。通过部分核苷酸序列分析以及与仙台病毒(SV)NP进行序列比较,鉴定出一个包含1.7千碱基对(kb)插入片段的cDNA克隆4 - 31,它是P11 NP特异性克隆。利用痘苗病毒瞬时表达系统,从该克隆中合成了一种电泳迁移率与P11 NP相似的多肽,该多肽分别与针对P11病毒和P11 NP的多克隆抗体及单克隆抗体发生特异性反应。测定了该克隆的完整核苷酸序列,发现其包含一个单一的开放阅读框,可编码一个由524个氨基酸组成、预测分子量为57,547的蛋白质。将P11 NP的氨基酸序列与其他副粘病毒的氨基酸序列进行比较,结果表明在其他副粘病毒中发现的两个保守氨基酸序列在P11 NP中也存在。尽管P11与SV显示出高度的序列同源性,但正如在其他副粘病毒中也发现的那样,其C末端区域约100个氨基酸高度不同。

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