SL3-3 ENHANCER FACTOR-I TRANSCRIPTIONAL ACTIVATORS ARE REQUIRED FOR TUMOR-FORMATION BY SL3-3 MURINE LEUKEMIA-VIRUS

被引:70
作者
HALLBERG, B
SCHMIDT, J
LUZ, A
PEDERSEN, FS
GRUNDSTROM, T
机构
[1] UMEA UNIV, DEPT APPL CELL & MOLEC BIOL, S-90187 UMEA, SWEDEN
[2] AARHUS UNIV, DEPT MOLEC BIOL & PLANT PHYSIOL, DK-8000 AARHUS, DENMARK
[3] GESELL STRAHLEN & UMWELTFORSCH MBH, MOLEK ZELLPATHOL ABT, W-8042 NEUHERBERG, GERMANY
[4] GESELL STRAHLEN & UMWELTFORSCH MBH, INST PATHOL, W-8042 NEUHERBERG, GERMANY
关键词
D O I
10.1128/JVI.65.8.4177-4181.1991
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The transcriptional enhancers of retroviruses that lack an oncogene are important determinants of their oncogenicity. However, no specific cellular transcriptional activator has yet been found to determine the oncogenicity for any of these viruses. The SL3-3 enhancer factor 1 (SEF1) cellular transcriptional activators are expressed preferentially in T lymphocytes. In the SL3-3 murine leukemia virus enhancer, two different sequences can bind SEF1 activators. We show that mutation of the SEF1 binding sites disrupts the disease potential of SL3-3 murine leukemia virus, implying that SEF1 transcriptional activators are required for tumor induction by SL3-3. The SEF1 site mutations did not appear to affect the pathogenicity of SL3-3 by impairment of virus multiplication, but rather by a specific defect in the ability of neoplastic transformation.
引用
收藏
页码:4177 / 4181
页数:5
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