Sequence and insertion sites of murine melanoma-associated retrovirus

被引:44
作者
Li, MF
Huang, XJ
Zhu, ZY
Gorelik, E
机构
[1] Univ Pittsburgh, Inst Canc, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Pathol, Pittsburgh, PA 15213 USA
关键词
D O I
10.1128/JVI.73.11.9178-9186.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We previously showed that B16 melanoma cells produce ecotropic melanoma-associated retrovirus (MelARV) which encodes a melanoma-associated antigen recognized by MM2-9B6 monoclonal antibody. The biological significance of MelARV in melanoma formation remains unknown, We found that infection of normal melanocytes with MelARV resulted in malignant transformation. It is likely that MelARV emerged from the defective Emv-2 provirus, a single copy of ecotropic provirus existing in the genome of C57BL/6 mice. In the present study, me cloned and sequenced the full-length MelARV genome and its insertion sites and we completed sequencing of the Emv-2 provirus, Our data show that MelARV has a typical full-length retroviral genome with high homology (98.54%) to Emv-2, indicating a close relationship between both viruses. MelARV probably emerged as a result of recombination between Emv-2 and an endogenous nonecotropic provirus. Some observed differences in the gag and pol regions of MelARV might account for the restoration of productivity and infectivity of a novel retrovirus that somatically emerged during melanoma formation. MelARV does not contain any oncogene and therefore might induce transformation by insertional mutagenesis. We sequenced two insertion sites of MelARV. The first insertion site represents the 3' coding region of the c-maf proto-oncogene at 67.0 centimorgans (cM) on chromosome 8, The c-maf proto-oncogene encodes a basic leucine zipper protein homologous to c-fos and c-jun. Insertion of MelARV in BL6 melanoma cells resulted in the up-regulation of c-maf, It is noteworthy that the Emv-2 provirus is also inserted into a noncoding region at 61.0 cM on the same chromosome 8. The second insertion site is the 3' noncoding region of the DNA polymerase gamma (PolG) gene on chromosome 7, The expression of PolG was not affected by the MelARV insertion. Further investigation of the biological significance of MelARV in melanoma formation is being undertaken.
引用
收藏
页码:9178 / 9186
页数:9
相关论文
共 41 条
[1]  
ASKEW DS, 1993, HEMATOL PATHOL, V7, P1
[2]   A LINE OF NONTUMORIGENIC MOUSE MELANOCYTES, SYNGENEIC WITH THE B-16 MELANOMA AND REQUIRING A TUMOR PROMOTER FOR GROWTH [J].
BENNETT, DC ;
COOPER, PJ ;
HART, IR .
INTERNATIONAL JOURNAL OF CANCER, 1987, 39 (03) :414-418
[3]   IDENTIFICATION OF ECOTROPIC PROVIRAL SEQUENCES IN INBRED MOUSE STRAINS WITH A CLONED SUBGENOMIC DNA FRAGMENT [J].
CHAN, HW ;
BRYAN, T ;
MOORE, JL ;
STAAL, SP ;
ROWE, WP ;
MARTIN, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (10) :5779-5783
[4]   STRUCTURE OF ENDOGENOUS MURINE LEUKEMIA-VIRUS DNA IN MOUSE GENOMES [J].
CHATTOPADHYAY, SK ;
LANDER, MR ;
RANDS, E ;
LOWY, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (10) :5774-5778
[5]   Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma [J].
Chesi, M ;
Bergsagel, PL ;
Shonukan, OO ;
Martelli, ML ;
Brents, LA ;
Chen, T ;
Schröck, E ;
Ried, T ;
Kuehl, VM .
BLOOD, 1998, 91 (12) :4457-4463
[6]   A GENETIC-LINKAGE MAP OF THE MOUSE - CURRENT APPLICATIONS AND FUTURE-PROSPECTS [J].
COPELAND, NG ;
JENKINS, NA ;
GILBERT, DJ ;
EPPIG, JT ;
MALTAIS, LJ ;
MILLER, JC ;
DIETRICH, WF ;
WEAVER, A ;
LINCOLN, SE ;
STEEN, RG ;
STEIN, LD ;
NADEAU, JH ;
LANDER, ES .
SCIENCE, 1993, 262 (5130) :57-66
[7]  
EISENTHAL A, 1987, CANCER RES, V47, P2771
[8]  
GORELIK E, 1991, CANCER RES, V51, P5212
[9]  
GORELIK E, 1985, CANCER RES, V45, P5341
[10]  
HART IR, 1979, AM J PATHOL, V97, P587