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新加坡石斑鱼虹彩病毒的功能基因组学分析:全序列测定与蛋白质组学分析

Functional genomics analysis of Singapore grouper iridovirus: complete sequence determination and proteomic analysis.

作者信息

Song Wen Jun, Qin Qi Wei, Qiu Jin, Huang Can Hua, Wang Fan, Hew Choy Leong

机构信息

Department of Biological Sciences, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260, Singapore.

出版信息

J Virol. 2004 Nov;78(22):12576-90. doi: 10.1128/JVI.78.22.12576-12590.2004.

Abstract

Here we report the complete genome sequence of Singapore grouper iridovirus (SGIV). Sequencing of the random shotgun and restriction endonuclease genomic libraries showed that the entire SGIV genome consists of 140,131 nucleotide bp. One hundred sixty-two open reading frames (ORFs) from the sense and antisense DNA strands, coding for lengths varying from 41 to 1,268 amino acids, were identified. Computer-assisted analyses of the deduced amino acid sequences revealed that 77 of the ORFs exhibited homologies to known virus genes, 23 of which matched functional iridovirus proteins. Forty-two putative conserved domains or signatures were detected in the National Center for Biotechnology Information CD-Search database and PROSITE database. An assortment of enzyme activities involved in DNA replication, transcription, nucleotide metabolism, cell signaling, etc., were identified. Viruses were cultured on a cell line derived from the embryonated egg of the grouper Epinephelus tauvina, isolated, and purified by sucrose gradient ultracentrifugation. The protein extract from the purified virions was analyzed by polyacrylamide gel electrophoresis followed by in-gel digestion of protein bands. Matrix-assisted laser desorption ionization-time of flight mass spectrometry and database searching led to identification of 26 proteins. Twenty of these represented novel or previously unidentified genes, which were further confirmed by reverse transcription-PCR (RT-PCR) and DNA sequencing of their respective RT-PCR products.

摘要

在此,我们报道新加坡石斑鱼虹彩病毒(SGIV)的全基因组序列。对随机鸟枪法和限制性内切酶基因组文库的测序表明,SGIV的整个基因组由140,131个核苷酸碱基对组成。从正义和反义DNA链中鉴定出162个开放阅读框(ORF),其编码的氨基酸长度从41到1268个不等。对推导的氨基酸序列进行计算机辅助分析显示,其中77个ORF与已知病毒基因具有同源性,其中23个与功能性虹彩病毒蛋白匹配。在国家生物技术信息中心的CD-Search数据库和PROSITE数据库中检测到42个假定的保守结构域或特征序列。鉴定出了一系列参与DNA复制、转录、核苷酸代谢、细胞信号传导等的酶活性。病毒在源自巨石斑鱼胚胎卵的细胞系上培养,通过蔗糖梯度超速离心进行分离和纯化。对纯化病毒粒子的蛋白质提取物进行聚丙烯酰胺凝胶电泳分析,随后对蛋白条带进行胶内消化。基质辅助激光解吸电离飞行时间质谱分析和数据库搜索鉴定出26种蛋白质。其中20种代表新的或以前未鉴定的基因,通过逆转录PCR(RT-PCR)及其各自RT-PCR产物的DNA测序进一步得到证实。

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