Liu Ai-Ling, Liu Chang-Jun, Zhang Yan-Ping, Li Jing-Mei, Shi Wei-Song, Yan Fu-Hai, Zhang Feng, Cheng Zhi-Wei
Division of Avian Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150001, China.
Bing Du Xue Bao. 2009 Sep;25(5):368-75.
Recently, much work has been devoted to study MD-induced oncogenesis and the genes involved in this process. Among many genes in the MDV genome, several genes such as Meq, RLORF4, RLORF12, and 132bpr have been considered recently associated with virulence of MDV. In this paper, primers of Meq, RLORF4, RLORF12 and 132bpr genes were designed and synthesized, based on the published whole genome sequence of MDV strain GA. The genes of Meq, RLORF4 and RLORF12 from four Chinese epidemic MDV strains highly passaged on chicken embryo fibroblast (CEF), i. e. L-SYp85C, L-MSp75C, L-CZp75C, and L-ZYp75C, as well as their corresponding parent strains, i. e. L-SY, L-MS, L-CZ, and L-ZY, the reference virulent strain J-1 and the vaccine strain 814 were amplified by PCR respectively. Then the PCR products of interest were cloned and sequenced respectively. The results of sequence comparison and analysis of Meq genes in the study indicated that Meq genes from the two strains L-ZYp75C and L-CZp75C contained single nucleotide insertion and deletion. The Meq gene from strain L-ZYp75C contained an extra cytidine (C) insertion at nucleotide position 529 and a single thymidine (T) deletion at nucleotide position 602, resulting in a frameshift mutation. And this frameshift mutation could lead to changes in deduced amino acid sequence from position 177 to 200 of Meq gene. The extra C insertion at nucleotide position 625 in Meq gene of strain L-CZp75C was also predicted to cause frameshift mutation in three overlapping genes (Meq, RLORF6 and 23KD genes). The comparison of nucleotide sequences of RLORF4 genes in the study revealed that the RLORF4 gene of strain L-SYp85C contained a fragment deletion in Open Reading Frame (ORF) from nucleotide position 215 to 265, resulting in 17 amino acids deletions, which were not found in other sequenced strains. Comparison of nucleotide sequences of RLORF12 genes in the study revealed several mutations. The RLORF12 gene of strain L-MSp75C contained a single T deletion at nucleotide position 67 and of 814 vaccine strain a large fragment deletion from nucleotide position 18 to 86, both of the deletions located in Origin of replication site (Ori) of MDV genome. But strain L-ZYp75C possessed an unique "TGTTGGG" deletion in its RLORF12 gene. When the four Chinese epidemic MDV strains were serially passaged on CEF, the number of copies of the 132bp repeats increased from 2 to more than 10 copies. All of above results indicated that deletion and/or insertion mutation occurred in Meq, RLORF4, RLORF12 and 132bpr after serial passage of these four Chinese epidemic MDV strains on CEF.
近年来,许多工作致力于研究马立克氏病病毒(MDV)诱导的肿瘤发生以及参与该过程的基因。在MDV基因组的众多基因中,诸如Meq、RLORF4、RLORF12和132bpr等几个基因最近被认为与MDV的毒力有关。本文基于已发表的MDV GA株全基因组序列,设计并合成了Meq、RLORF4、RLORF12和132bpr基因的引物。分别从鸡胚成纤维细胞(CEF)上高度传代的4株中国流行MDV毒株,即L - SYp85C、L - MSp75C、L - CZp75C和L - ZYp75C,以及它们相应的亲本毒株,即L - SY、L - MS、L - CZ和L - ZY,参考强毒株J - 1和疫苗株814中扩增出Meq、RLORF4和RLORF12基因。然后分别对感兴趣的PCR产物进行克隆和测序。该研究中Meq基因的序列比较和分析结果表明,L - ZYp75C和L - CZp75C这两个毒株的Meq基因存在单核苷酸插入和缺失。L - ZYp75C毒株的Meq基因在核苷酸位置529处有一个额外的胞嘧啶(C)插入,在核苷酸位置602处有一个胸腺嘧啶(T)单碱基缺失,导致移码突变。这种移码突变可导致Meq基因从第177位到200位的推导氨基酸序列发生变化。L - CZp75C毒株Meq基因在核苷酸位置625处的额外C插入也预计会导致三个重叠基因(Meq、RLORF6和23KD基因)发生移码突变。该研究中RLORF4基因核苷酸序列比较显示,L - SYp85C毒株的RLORF4基因在开放阅读框(ORF)中从核苷酸位置215到265处存在一个片段缺失,导致17个氨基酸缺失,这在其他测序毒株中未发现。该研究中RLORF12基因核苷酸序列比较发现了几个突变。L - MSp75C毒株的RLORF12基因在核苷酸位置67处有一个T单碱基缺失,814疫苗株在核苷酸位置18到86处有一个大片段缺失,这两个缺失均位于MDV基因组的复制起始位点(Ori)。但L - ZYp75C毒株在其RLORF12基因中存在一个独特的“TGTTGGG”缺失。当这4株中国流行MDV毒株在CEF上连续传代时,132bp重复序列的拷贝数从2增加到超过10个拷贝。上述所有结果表明,这4株中国流行MDV毒株在CEF上连续传代后,Meq、RLORF4、RLORF12和132bpr基因发生了缺失和/或插入突变。