Human T-cell leukemia virus type 1 pX-I and pX-II open reading frames are dispensable for the immortalization of primary lymphocytes

被引:83
作者
Robek, MD
Wong, FH
Ratner, L
机构
[1] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
关键词
D O I
10.1128/JVI.72.5.4458-4462.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human T-cell leukemia virus type 1 (HTLV-1) infects and transforms CD4(+) T-lymphocytes both in vivo and in vitro. Although the Tax protein of HTLV-1 has been strongly implicated as a transforming agent, other virally encoded proteins may also play a role in the transformation process. In addition to the rex and tax genes, the pX region of the HTLV-1 genome contains two open reading frames (pX-I and pX-II) which encode the putative viral accessory proteins known as p12(I), p30(II), and p13(II), Mutations in the ACH molecular clone of HTLV-1 that are predicted to abrogate the expression of p12(I), p13(II) and p30(II) were constructed. These mutations had no effect on viral replication or the immortalization of primary lymphocytes. Although these proteins are dispensable for viral replication and immortalization in vitro, it remains possible that they alter infection in vivo.
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页码:4458 / 4462
页数:5
相关论文
共 39 条
[1]   ANTISENSE PHOSPHOROTHIOATE OLIGODEOXYNUCLEOTIDES TARGETED TO THE VPR GENE INHIBIT HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REPLICATION IN PRIMARY HUMAN MACROPHAGES [J].
BALOTTA, C ;
LUSSO, P ;
CROWLEY, R ;
GALLO, RC ;
FRANCHINI, G .
JOURNAL OF VIROLOGY, 1993, 67 (07) :4409-4414
[2]   EXPRESSION OF ALTERNATIVELY SPLICED HUMAN T-LYMPHOTROPIC VIRUS TYPE-I PX MESSENGER-RNA IN INFECTED CELL-LINES AND IN PRIMARY UNCULTURED CELLS FROM PATIENTS WITH ADULT T-CELL LEUKEMIA LYMPHOMA AND HEALTHY CARRIERS [J].
BERNEMAN, ZN ;
GARTENHAUS, RB ;
REITZ, MS ;
BLATTNER, WA ;
MANNS, A ;
HANCHARD, B ;
IKEHARA, O ;
GALLO, RC ;
KLOTMAN, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :3005-3009
[3]   IDENTIFICATION OF THE GENE RESPONSIBLE FOR HUMAN T-CELL LEUKEMIA-VIRUS TRANSCRIPTIONAL REGULATION [J].
CANN, AJ ;
ROSENBLATT, JD ;
WACHSMAN, W ;
SHAH, NP ;
CHEN, ISY .
NATURE, 1985, 318 (6046) :571-574
[4]  
CHEN YM, 1997, INT J CANCER, V71, P1
[5]  
CHOU KS, 1995, INT J CANCER, V60, P701
[6]   COMPLEX SPLICING IN THE HUMAN T-CELL LEUKEMIA-VIRUS (HTLV) FAMILY OF RETROVIRUSES - NOVEL MESSENGER-RNAS AND PROTEINS PRODUCED BY HTLV TYPE-I [J].
CIMINALE, V ;
PAVLAKIS, GN ;
DERSE, D ;
CUNNINGHAM, CP ;
FELBER, BK .
JOURNAL OF VIROLOGY, 1992, 66 (03) :1737-1745
[7]   EXPRESSION AND CHARACTERIZATION OF PROTEINS PRODUCED BY MESSENGER-RNAS SPLICED INTO THE X-REGION OF THE HUMAN T-CELL LEUKEMIA LYMPHOTROPIC VIRUS TYPE-II [J].
CIMINALE, V ;
DAGOSTINO, DM ;
ZOTTI, L ;
FRANCHINI, G ;
FELBER, BK ;
CHIECOBIANCHI, L .
VIROLOGY, 1995, 209 (02) :445-456
[8]   A deletion in the proximal untranslated pX region of human T-cell leukemia virus type II decreases viral replication but not infectivity in vivo [J].
Cockerell, GL ;
Rovnak, J ;
Green, PL ;
Chen, ISY .
BLOOD, 1996, 87 (03) :1030-1035
[9]   In vitro CD4(+) lymphocyte transformation and infection in a rabbit model with a molecular clone of human T-cell lymphotropic virus type 1 [J].
Collins, ND ;
Newbound, GC ;
Ratner, L ;
Lairmore, MD .
JOURNAL OF VIROLOGY, 1996, 70 (10) :7241-7246
[10]  
COLLINS ND, 1997, UNPUB