Tsai Jyh-Ming, Wang Han-Ching, Leu Jiann-Horng, Hsiao He-Hsuan, Wang Andrew H-J, Kou Guang-Hsiung, Lo Chu-Fang
Graduate Institute of Zoology, National Taiwan University, Taipei 106, Taiwan R.O.C.
J Virol. 2004 Oct;78(20):11360-70. doi: 10.1128/JVI.78.20.11360-11370.2004.
White spot syndrome virus (WSSV) virions were purified from the hemolymph of experimentally infected crayfish Procambarus clarkii, and their proteins were separated by 8 to 18% gradient sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) to give a protein profile. The visible bands were then excised from the gel, and following trypsin digestion of the reduced and alkylated WSSV proteins in the bands, the peptide sequence of each fragment was determined by liquid chromatography-nano-electrospray ionization tandem mass spectrometry (LC-nanoESI-MS/MS) using a quadrupole/time-of-flight mass spectrometer. Comparison of the resulting peptide sequence data against the nonredundant database at the National Center for Biotechnology Information identified 33 WSSV structural genes, 20 of which are reported here for the first time. Since there were six other known WSSV structural proteins that could not be identified from the SDS-PAGE bands, there must therefore be a total of at least 39 (33 + 6) WSSV structural protein genes. Only 61.5% of the WSSV structural genes have a polyadenylation signal, and preliminary analysis by 3' rapid amplification of cDNA ends suggested that some structural protein genes produced mRNA without a poly(A) tail. Microarray analysis showed that gene expression started at 2, 6, 8, 12, 18, 24, and 36 hpi for 7, 1, 4, 12, 9, 5, and 1 of the genes, respectively. Based on similarities in their time course expression patterns, a clustering algorithm was used to group the WSSV structural genes into four clusters. Genes that putatively had common or similar roles in the viral infection cycle tended to appear in the same cluster.
从实验感染的克氏原螯虾血淋巴中纯化白斑综合征病毒(WSSV)病毒粒子,其蛋白质通过8%至18%梯度十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)进行分离以获得蛋白质图谱。然后从凝胶中切下可见条带,对条带中还原和烷基化的WSSV蛋白质进行胰蛋白酶消化后,使用四极杆/飞行时间质谱仪通过液相色谱-纳升电喷雾电离串联质谱(LC-nanoESI-MS/MS)测定每个片段的肽序列。将所得肽序列数据与美国国立生物技术信息中心的非冗余数据库进行比较,鉴定出33个WSSV结构基因,其中20个在此首次报道。由于从SDS-PAGE条带中无法鉴定出其他6种已知的WSSV结构蛋白,因此WSSV结构蛋白基因总数至少为39个(33 + 6)。只有61.5%的WSSV结构基因具有聚腺苷酸化信号,通过3' cDNA末端快速扩增的初步分析表明,一些结构蛋白基因产生的mRNA没有poly(A)尾。微阵列分析显示,在感染后2、6、8、12、18、24和36小时,分别有7、1、4、12、9、5和1个基因开始表达。基于它们在时间进程表达模式上的相似性,使用聚类算法将WSSV结构基因分为四个簇。在病毒感染周期中假定具有共同或相似作用的基因往往出现在同一簇中。