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鼻咽癌中EB病毒LMP1基因的序列变异
引用本文:Lin SX,Zong YS,Zhang M,Han AJ,Zhong BL,Liang YJ. 鼻咽癌中EB病毒LMP1基因的序列变异[J]. 中华病理学杂志, 2005, 34(12): 791-795
作者姓名:Lin SX  Zong YS  Zhang M  Han AJ  Zhong BL  Liang YJ
作者单位:1. 510060,广州,中山大学附属肿瘤医院病理科
2. 中山大学中山医学院病理学教研室
3. 广东省第二人民医院病理科
基金项目:国家自然科学基金资助项目(39730200-Ⅱ)
摘    要:目的 检测广州地区鼻咽癌中EB病毒LMP1基因N-和C-末端区序列变异的热点,并探讨其产生的机制。方法 收集中山大学肿瘤医院未经治疗的鼻咽癌患者鼻咽新鲜活检标本63例。采用巢式聚合酶链反应(PCR)扩增EB病毒LMP1基因N-和C-末端区,用XhoⅠ对N-末端区扩增产物进行酶切分析,并检测C-末端区扩增产物30bp缺失的情况。采用四色荧光末端终止法对4例患者N-和C-末端区的8份扩增产物进行序列分析。结果 63例鼻咽癌组织EB病毒LMP1基因N-和C-末端区有4种序列变异类型:wt-XhoⅠ/wt-LMP1(4例,6.3%)、wt-XhoⅠ&XhoⅠ-loss/del-LMP1(4例,6.3%)、wt-XhoⅠ/del-LMP1(5例,7.9%)和XhoⅠ-loss/del-LMP1(50例,79.5%)。序列分析显示:与B95-8细胞相比较,所有检测的鼻咽癌组织中EB病毒LMP1基因均发生了错义点突变和无义点突变。错义点突变数与无义点突变数之间的比值为2.25(9/4)。结论 广州地区鼻咽癌中EB病毒LMP1基因的序列变异类型以XhoⅠ-loss/del-LMP1占主导。LMP1基因N-末端区XhoⅠ酶切位点的丢失很可能是在C-末端区30bp缺失的基础上发生的。LMP1基因的4种序列变异类型可能代表了鼻咽癌变过程中EB病毒在宿主内演变的4个时相。

关 键 词:鼻咽肿瘤 疱疹病毒4型 膜蛋白类 基因序列 EB病毒
收稿时间:2005-04-26
修稿时间:2005-04-26

Study of sequence variations of Epstein-Barr virus LMP1 gene in nasopharyngeal carcinoma
Lin Su-xia,Zong Yong-sheng,Zhang Min,Han An-jia,Zhong Bi-ling,Liang Ying-jie. Study of sequence variations of Epstein-Barr virus LMP1 gene in nasopharyngeal carcinoma[J]. Chinese Journal of Pathology, 2005, 34(12): 791-795
Authors:Lin Su-xia  Zong Yong-sheng  Zhang Min  Han An-jia  Zhong Bi-ling  Liang Ying-jie
Affiliation:Department of Pathology, Affiliated Tumor Hospital of Sun Yat-sen University, Guangzhou 510060, China
Abstract:OBJECTIVE: To detect the sequence variations frequently found within the N- and C-terminal regions of Epstein-Barr virus (EBV) LMP1 gene in nasopharyngeal carcinoma (NPC) and to study the underlying mechanisms. METHODS: Fresh tumor tissues were sampled from 63 patients with untreated NPC encountered in Affiliated Tumor Hospital of Sun Yat-sen University, Guangzhou. The N-terminal region of EBV LMP1 gene was amplified with nested polymerase chain reaction (PCR), followed by XhoI enzyme digestion. Nested PCR was also employed to detect the 30 base pairs deletion within the C-terminal region. Four-colored fluorescence terminator sequencing method was applied for bi-directional solid-phase sequencing of the 8 representative PCR products in 4 cases of NPC. The DNA sequence within the N- and C-terminal regions of LMP1 gene was then analyzed. RESULTS: There were 4 patterns of sequence variations, namely, wt-XhoI/wt-LMP1 (4 cases, 6.3%), wt-XhoI and XhoI-loss/del-LMP1 (4 cases, 6.3%), wt-XhoI/del-LMP1 (5 cases, 7.9%) and XhoI-loss/del-LMP1 (50 cases, 79.5%), detected in the 63 studied cases. Sequence analysis showed that the EBV LMP1 gene had underwent non-synonymous and synonymous substitutions, as compared with the prototype of B95-8 cells. The ratio of non-synonymous to synonymous substitutions was 2.25. CONCLUSIONS: XhoI-loss/del-LMP1 is the predominant sequence variation pattern of EBV LMP1 gene in NPC from Guangzhou. The XhoI-loss variation seems to develop on top of del-LMP1. When compared with the EBV LMP1 gene in peripheral blood B-lymphocytes of virus carriers and in preinvasive epithelial lesions (reported previously), it is likely that the sequence variation patterns of LMP1 gene may represent 4 different phases of intrahost evolution of EBV during nasopharyngeal carcinogenesis.
Keywords:Nasopharyngeal neoplasms   Herpesvirus 4, human   Membrane proteins
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