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Functional Genomics Analysis of Singapore Grouper Iridovirus: Complete Sequence Determination and Proteomic Analysis

机译:新加坡石斑鱼虹膜病毒的功能基因组学分析:完整序列确定和蛋白质组学分析。

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摘要

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.
机译:在这里,我们报告新加坡石斑鱼iridovirus(SGIV)的完整基因组序列。随机shot弹枪和限制性核酸内切酶基因组文库的测序表明,整个SGIV基因组由140,131个核苷酸bp组成。鉴定了来自有义和反义DNA链的一百六十二个开放阅读框(ORF),其编码的长度范围为41至1,268个氨基酸。推导的氨基酸序列的计算机辅助分析表明,77个ORF与已知病毒基因表现出同源性,其中23个与功能性虹膜病毒蛋白匹配。在国家生物技术信息CD-Search数据库和PROSITE数据库中检测到42个假定的保守域或签名。鉴定了涉及DNA复制,转录,核苷酸代谢,细胞信号传导等的多种酶活性。在源自石斑鱼石斑鱼石斑鱼胚卵的细胞系上培养病毒,分离并通过蔗糖梯度超速离心纯化。通过聚丙烯酰胺凝胶电泳,然后在凝胶中消化蛋白条带,分析了纯化病毒体的蛋白提取物。基质辅助激光解吸电离飞行时间质谱和数据库搜索可鉴定出26种蛋白质。这些基因中有20个代表新的或以前未鉴定的基因,通过逆转录PCR(RT-PCR)和它们各自的RT-PCR产物的DNA测序进一步证实了这些基因。

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