Identification, phylogeny, and evolution of retroviral elements based on their envelope genes

被引:116
作者
Bénit, L
Dessen, P
Heidmann, T
机构
[1] Inst Gustave Roussy, Unite Retrovirus Endogenes & Elements Retroides E, CNRS, UMR 1573, F-94805 Villejuif, France
[2] INFOBIOGEN, Serv Bioinformat, CNRS,UMS 825, INSERM,SC13, F-94801 Villejuif, France
关键词
D O I
10.1128/JVI.75.23.11709-11719.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Phylogenetic analyses of retroviral elements, including endogenous retroviruses, have relied essentially on the retroviral pol gene expressing the highly conserved reverse transcriptase. This enzyme is essential for the life cycle of all retroid elements, but other genes are also endowed with conserved essential functions. Among them, the transmembrane (TM) subunit of the envelope gene is involved in virus entry through membrane fusion. It has also been reported to contain a domain, named the immunosuppressive domain, that has immunosuppressive properties most probably essential for virus spread within the host. This domain is conserved among a large series of retroviral elements, and we have therefore attempted to generate phylogenetic links between retroviral elements identified from databases following tentative alignments of the immunosuppressive domain and adjacent sequences. This allowed us to unravel a conserved organization among TM domains, also found in the Ebola and Marburg filoviruses, and to identify a large number of human endogenous retroviruses (HERVs) from sequence databases. The latter elements are part of previously identified families of HERVs, and some of them define new families. A general phylogenetic analysis based on the TM proteins of retroelements, and including those with no clearly identified immunosuppressive domain, could then be derived and compared with pol-based phylogenetic trees, providing a comprehensive survey of retroelements and definitive evidence for recombination events in the generation of both the endogenous and the present-day infectious retroviruses.
引用
收藏
页码:11709 / 11719
页数:11
相关论文
共 53 条
  • [1] Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
    Altschul, SF
    Madden, TL
    Schaffer, AA
    Zhang, JH
    Zhang, Z
    Miller, W
    Lipman, DJ
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (17) : 3389 - 3402
  • [2] Envelope gene of the human endogenous retrovirus HERV-W encodes a functional retrovirus envelope
    An, DS
    Xie, YM
    Chen, ISY
    [J]. JOURNAL OF VIROLOGY, 2001, 75 (07) : 3488 - 3489
  • [3] Identification of a cellular cofactor required for infection by feline leukemia virus
    Anderson, MM
    Lauring, AS
    Burns, CC
    Overbaugh, J
    [J]. SCIENCE, 2000, 287 (5459) : 1828 - 1830
  • [4] Bénit L, 1999, J VIROL, V73, P3301
  • [5] Positional cloning of the mouse retrovirus restriction gene Fv1
    Best, S
    LeTissier, P
    Towers, G
    Stoye, JP
    [J]. NATURE, 1996, 382 (6594) : 826 - 829
  • [6] The envelope of Mason-Pfizer monkey virus has immunosuppressive properties
    Blaise, S
    Mangeney, M
    Heidmann, T
    [J]. JOURNAL OF GENERAL VIROLOGY, 2001, 82 : 1597 - 1600
  • [7] An envelope glycoprotein of the human endogenous retrovirus HERV-W is expressed in the human placenta and fuses cells expressing the type D mammalian retrovirus receptor
    Blond, JL
    Lavillette, D
    Cheynet, V
    Bouton, O
    Oriol, G
    Chapel-Fernandes, S
    Mandrand, B
    Mallet, F
    Cosset, FL
    [J]. JOURNAL OF VIROLOGY, 2000, 74 (07) : 3321 - 3329
  • [8] THE GP-PROTEIN OF MARBURG VIRUS CONTAINS THE REGION SIMILAR TO THE IMMUNOSUPPRESSIVE DOMAIN OF ONCOGENIC RETROVIRUS P15E PROTEINS
    BUKREYEV, AA
    VOLCHKOV, VE
    BLINOV, VM
    NETESOV, SV
    [J]. FEBS LETTERS, 1993, 323 (1-2) : 183 - 187
  • [9] HEPTAD REPEAT SEQUENCES ARE LOCATED ADJACENT TO HYDROPHOBIC REGIONS IN SEVERAL TYPES OF VIRUS FUSION GLYCOPROTEINS
    CHAMBERS, P
    PRINGLE, CR
    EASTON, AJ
    [J]. JOURNAL OF GENERAL VIROLOGY, 1990, 71 : 3075 - 3080
  • [10] Core structure of gp41 from the HIV envelope glycoprotein
    Chan, DC
    Fass, D
    Berger, JM
    Kim, PS
    [J]. CELL, 1997, 89 (02) : 263 - 273