Human endogenous retrovirus HERV-K113 is capable of producing intact viral particles

被引:103
作者
Boller, Klaus [1 ]
Schoenfeld, Kurt [1 ]
Lischer, Stefanie [1 ]
Fischer, Nicole [1 ]
Hoffmann, Andreas [1 ]
Kurth, Reinhard [2 ]
Tonjes, Ralf R. [1 ]
机构
[1] Paul Ehrlich Inst, D-63225 Langen, Germany
[2] Robert Koch Inst, D-13353 Berlin, Germany
关键词
TERATOCARCINOMA CELL-LINES; HERV-K; HUMAN GENOME; EXPRESSION; IDENTIFICATION; PROTEIN; RETROELEMENTS; ANTIBODIES; ENVELOPE; ASSAY;
D O I
10.1099/vir.0.83534-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Of all human endogenous retroviruses; known today, HERV-K is the only one that has been shown to produce viral particles. While the first of the approximately 30 HERV-K sequences integrated into the human genome more than 40 million years ago, evidence is accumulating that HERV-K was active more recently, provinus HERV-K113 being the youngest sequence found. However, it is unclear which HERV-K sequences code for the viral particles that are produced by human germ-cell tumours or melanomas. Here, we show that the provirus HERV-K113, cloned into a baculovirus expression vector, is capable of producing intact particles of retroviral morphology, exhibiting the typical structure of those particles that were characterized in cell lines derived from human germ-cell tumours. Thus, the HERV-K113 sequence is a candidate for particle production in vivo and for an active human endogenous retrovirus of today.
引用
收藏
页码:567 / 572
页数:6
相关论文
共 26 条
[1]   Retroelements and the human genome: New perspectives on an old relation [J].
Bannert, N ;
Kurth, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 :14572-14579
[2]   Long-term reinfection of the human genome by endogenous retroviruses [J].
Belshaw, R ;
Pereira, V ;
Katzourakis, A ;
Talbot, G ;
Paces, J ;
Burt, A ;
Tristem, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :4894-4899
[3]   Phenotypic heterogeneity of human endogenous retrovirus particles produced by teratocarcinoma cell lines [J].
Bieda, K ;
Hoffmann, A ;
Boller, K .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :591-596
[4]   Characterization of the antibody response specific for the human endogenous retrovirus HTDV/HERV-K [J].
Boller, K ;
Janssen, O ;
Schuldes, H ;
Tonjes, RR ;
Kurth, R .
JOURNAL OF VIROLOGY, 1997, 71 (06) :4581-4588
[5]   STRUCTURAL ORGANIZATION OF UNIQUE RETROVIRUS-LIKE PARTICLES BUDDING FROM HUMAN TERATOCARCINOMA CELL-LINES [J].
BOLLER, K ;
FRANK, H ;
LOWER, J ;
LOWER, R ;
KURTH, R .
JOURNAL OF GENERAL VIROLOGY, 1983, 64 (DEC) :2549-2559
[6]   EVIDENCE THAT HERV-K IS THE ENDOGENOUS RETROVIRUS SEQUENCE THAT CODES FOR THE HUMAN TERATOCARCINOMA-DERIVED RETROVIRUS HTDV [J].
BOLLER, K ;
KONIG, H ;
SAUTER, M ;
MUELLERLANTZSCH, N ;
LOWER, R ;
LOWER, J ;
KURTH, R .
VIROLOGY, 1993, 196 (01) :349-353
[7]  
Büscher K, 2006, MELANOMA RES, V16, P223
[8]   Identification of a functional envelope protein from the HERV-K family of human endogenous retroviruses [J].
Dewannieux, M ;
Blaise, S ;
Heidmann, T .
JOURNAL OF VIROLOGY, 2005, 79 (24) :15573-15577
[9]   Identification of an infectious progenitor for the multiple-copy HERV-K human endogenous retroelements [J].
Dewannieux, Marie ;
Harper, Francis ;
Richaud, Aurelien ;
Letzelter, Claire ;
Ribet, David ;
Pierron, Gerard ;
Heidmann, Thierry .
GENOME RESEARCH, 2006, 16 (12) :1548-1556
[10]   A BACULOVIRUS VECTOR CAN EXPRESS INTRON-CONTAINING GENES [J].
JEANG, KT ;
HOLMGRENKONIG, M ;
KHOURY, G .
JOURNAL OF VIROLOGY, 1987, 61 (05) :1761-1764