A cellular protein specifically binds to the 3' -terminal sequences of hepatitis C virus intermediate negative-strand RNA

被引:0
|
作者
王巍
邓庆丽
黄开红
段朝晖
邵静
黄志清
黄志明
机构
[1] Medical Research Center
[2] Sun Yat-sen Memorial Hospital of Medical Sciences
[3] Guangzhou 510120
[4] China
关键词
hepatitis C virus·replication complex·UV cross-linking;
D O I
暂无
中图分类号
R346 [];
学科分类号
1001 ;
摘要
Objective To study the mechanism of the cellular proteins involved in the process of replication of hepatitis C virus (HCV) negative-strand RNA.Methods Ultraviolet (UV) cross-linking was used to identify the cellular proteins that would bind to the 3’ -end of HCV negative-strand RNA. Competition experiment was used to confirm the specificity of this binding, in which excess nonhomologous protein and RNA transcripts were used as competitors. The required binding sequence was determined by mapping, then the binding site was predicted through secondary structure analysis.Results A cellular protein of 45 kD (p45) was found to bind specifically to the 3’ -end of HCV negative-strand RNA by UV cross-linking, nhomologous proteins and RNA transcripts could not compete out this binding, whereas the unlabeled 3’ -end of HCV negative-strand RNA could. Mapping of the protein-binding site suggested that the 3’ -end 131-278nt of HCV negative-strand RNA was the possible protein-binding region. Analysis of RNA secondary
引用
收藏
页码:134 / 138
页数:5
相关论文
共 50 条
  • [41] Identification of a cellular protein interacting with RNA polymerase of hepatitis C virus
    Park, KJ
    Choi, SH
    Koh, MS
    Kim, SW
    Hwang, SB
    JOURNAL OF BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2000, 33 (01): : 59 - 62
  • [42] Negative-strand hepatitis C virus (HCV) RNA in peripheral blood mononuclear cells from anti-HCV-positive/HIV-infected women
    Laskus, Tomasz
    Operskalski, Eva A.
    Radkowski, Marek
    Wilkinson, Jeffrey
    Mack, Wendy J.
    deGiacomo, Marina
    Al-Harthi, Lena
    Chen, Zhi
    Xu, Jiaao
    Kovacs, Andrea
    JOURNAL OF INFECTIOUS DISEASES, 2007, 195 (01): : 124 - 133
  • [43] Infectious bronchitis virus nucleocapsid protein binds RNA sequences in the 3' terminus of the genome
    Zhou, ML
    Williams, AK
    Chung, SI
    Wang, L
    Collisson, EW
    VIROLOGY, 1996, 217 (01) : 191 - 199
  • [44] Secondary structure and hybridization accessibility of the hepatitis C virus negative strand RNA 5′-terminus
    Smith, RM
    Wu, GY
    JOURNAL OF VIRAL HEPATITIS, 2004, 11 (02) : 115 - 123
  • [45] Two cis-acting elements in negative RNA strand of hepatitis C virus involved in synthesis of positive RNA strand in vitro
    Ye, L
    Timani, KA
    Ye, L
    Kong, L
    Yang, X
    Liao, Q
    Wu, J
    ACTA VIROLOGICA, 2005, 49 (02) : 83 - 90
  • [46] Failure to detect hepatitis C virus negative strand RNA in serum in patients with chronic hepatitis C using a sensitive strand-specific assay
    González-Peralta, RP
    Qian, KP
    Guo, G
    Lau, JYN
    HEPATOLOGY, 1998, 28 (04) : 569A - 569A
  • [47] The 3′ end of hepatitis E virus (HEV) genome binds specifically to the viral RNA-dependent RNA polymerase (RdRp)
    Agrawal, S
    Gupta, D
    Panda, SK
    VIROLOGY, 2001, 282 (01) : 87 - 101
  • [48] A 68-nucleotide sequence within the 3′ noncoding region of simian hemorrhagic fever virus negative-strand RNA binds to four MA104 cell proteins
    Hwang, YK
    Brinton, MA
    JOURNAL OF VIROLOGY, 1998, 72 (05) : 4341 - 4351
  • [49] Secondary structure and hybridization accessibility of hepatitis C virus 3′-terminal sequences
    Smith, RM
    Walton, CM
    Wu, CH
    Wu, GY
    JOURNAL OF VIROLOGY, 2002, 76 (19) : 9563 - 9574
  • [50] THE PHYSICAL STATE OF THE NEGATIVE STRAND OF HEPATITIS-C VIRUS-RNA IN SERUM OF PATIENTS WITH CHRONIC HEPATITIS-C
    SHINDO, M
    DIBISCEGLIE, AM
    AKATSUKA, T
    FONG, TL
    SCAGLIONE, L
    DONETS, M
    HOOFNAGLE, JH
    FEINSTONE, SM
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (18) : 8719 - 8723