期刊文献+

慢性乙肝患者HBV核心蛋白启动子变异的初步研究

The primary study on variation in the basic core promoter of the hepatitis B virus on the patients with chronic hepatitis B
暂未订购
导出
摘要 目的 通过对乙型肝炎病毒 (HBV)基本核心基因启动子 (BCP)变异的研究 ,阐明HBV准种在慢性感染者中存在的意义。方法 以中国株HBV基因序列为依据 ,设计特异性多聚酶链反应 (PCR)引物 ,自 4 0例慢性HBV感染患者血清中扩增HBV的BCP基因 ,采用聚丙烯酰胺凝胶电泳 (PAGE)技术展示缺失突变 ,DNA测序确定病毒的变异程度。结果 聚丙烯酰胺凝胶电泳结果发现 ,6 0 % (2 4 / 4 0 )患者血清中可见 2~ 3条扩增条带 ;测序结果发现BCP区存在多种突变形式 :点突变中以 14 0nt(T→C)最为常见 ,缺失突变多见于TA1,TA2及TA3,多表现为 8bp和 2 0bp的缺失。 结论 HBVBCP区内有一缺失高变区 ,并在患者体内存有多种变异形式 ;TA1,TA2和TA3的变异可能影响e抗原的表达。 Objective To investigate the variation of the basic core promoter(BCP) of HBV and clarify the significance of HBV quasispecies groups in the patients with chronic HBV. Methods A set of specific primers was synthesized according to HBV DNA sequence of Chinese strain. The BCP was amplified by PCR from the sample serum of 40 patients with chronic HBV, and the PCR products of 5 patients were subcloned into pGEM Teasy vectors. Polyacrylamide gel electrophoresis(PAGE) was employed to display the deletion variant, clones with different length were selected for sequencing. Sequencing results were analyzed. Results 2~3 bands were displayed by PAGE in 60% patients. The results of sequence analysis showed there were some kinds of variation in BCP region. The substitution always occurs in TATA like boxes, especially from T to C on nt140 site. The deletion variations were detected in TA1, TA2 and TA3. The 8?bp, 20?bp deletion variations frequently happened. Conclusion There is a hot deletion region in BCP. The deletion and the substitution in the TATA like box may influence the expression of pre C/C protein. The sequencing results imply that there are HBV quasispecies groups in patients with chronic HBV infection.
出处 《西安交通大学学报(医学版)》 CAS CSCD 北大核心 2003年第3期199-201,214,共4页 Journal of Xi’an Jiaotong University(Medical Sciences)
基金 陕西省自然科学基金资助项目 (No .2 0 0 1sm64 )
关键词 慢性乙型肝炎病毒 基本核心蛋白启动子 聚丙烯酰胺凝胶电泳 基因突变 基因序列 hepatitis B virus basic core promoter variation polyacrylamide gel electrophoresis quasispecies
  • 相关文献

参考文献8

  • 1甘人宝 储美瑾 等.克隆的adr亚型乙型肝炎病毒(pADR-1)DNA的全序列[J].中国科学:B辑,1986,1:55-55.
  • 2董菁,成军,王勤环,刘友昭,王刚,施双双,夏小兵,邵清,斯崇文.慢性乙型肝炎患者体内乙型肝炎病毒准种特点的初步研究[J].中华内科杂志,2000,39(12):838-839. 被引量:36
  • 3董菁,施双双,皇甫竞坤,成军,王勤环,李莉,斯崇文.乙型肝炎病毒X基因准种特点的研究[J].中国病毒学,2002,17(1):22-25. 被引量:39
  • 4Blum HE. Hepatitis B virus :Significance of naturally occurring mutants [J]. Intervirology, 1993,35 (1 - 4) :40 - 50.
  • 5Carman W, Thomas H, Domingo E. Viral genetic variation: Hepatitis B virus as a clinical example [J]. Lancet, 1993,341: 349 - 353.
  • 6Kramvis, Kew MC. The core promoter of hepatitis B virus [J].J Viral Hepatitis, 1999,6:415 - 427.
  • 7Victor EB , Zhichang XU , Min CH , et al . Effects of a naturally occurring mutation in the hepatitis B virus basal core promoter on precore gene expression and viral replication [J]. J Virol, 1996,70: 5845 - 5851.
  • 8Andears E , Ulf R , Dirk B , et al . Mutations of the core promoter and response to interferon treatment in chronic replicative hepatitis B [J]. Hepatology, 2000,31:716 - 725.

二级参考文献7

  • 1甘人宝 储美瑾 等.克隆的adr亚型乙型肝炎病毒(pADR-1)DNA的序列[J].中国科学:B辑,1986,1:55-65.
  • 2Rho HM,Kim K,Hyun SW,et al.The nucleotide sequence and reading frames of a mutant hepatitis B virus subtype adr[].Nucleic Acids Research.1989
  • 3Mukaide M,Kumazawa T,Hoshi A et al.The complete nucleotide sequence of hepatitis B virus, subtype adr (SRADR) and phylogenetic analysis[].Nucleic Acids Research.1992
  • 4Monkongdee P,Boonchird C,Balachadra K,et al.Cloning and sequence analysis of hepatitis B virus genome of adr subtype isolated in Thailand[].Journal of The Science Society of Thailand.1998
  • 5Gan RB,Chu MJ,Shen LP,et al.The complete nucleotide sequence of the cloned DNA of hepatitis B virus subtype adr in pADR-1[].Scientia Sinica.1987
  • 6Carman WF,Thomas H,Domingo E.Viral genetic variation: hepatitis B virus as a clinical example[].The Lancet.1993
  • 7董菁,成军,王勤环,刘友昭,王刚,施双双,夏小兵,邵清,斯崇文.慢性乙型肝炎患者体内乙型肝炎病毒准种特点的初步研究[J].中华内科杂志,2000,39(12):838-839. 被引量:36

共引文献66

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部