Literature DB >> 6579544

Avian carcinoma virus MH2 contains a transformation-specific sequence, mht, and shares the myc sequence with MC29, CMII, and OK10 viruses.

N C Kan, C S Flordellis, C F Garon, P H Duesberg, T S Papas.   

Abstract

Avian carcinoma virus MH2 has been grouped together with MC29, CMII, and OK10, because all of these viruses share a transformation-specific sequence termed myc. A 5.2-kilobase (kb) DNA provirus of MH2 has been molecularly cloned. The complete genetic structure of MH2 is 5'-delta gag(1.9-kb)-mht(1.2-kb)-myc(1.3-kb)-delta env(?) and noncoding c-region (0.2-kb)-3'. delta gag, delta env, and c are genetic elements shared with nondefective retroviruses, whereas mht is a unique, possibly MH2 transformation-specific, sequence. Hybridizations with normal chicken DNA and cloned chicken c-myc DNA indicate that the mht sequence probably derives from a normal cellular gene that is distinct from the c-myc gene. The genetic structure of MH2 suggests that the delta gag and mht sequences function as a hybrid gene that encodes the p100 putative transforming protein. The myc sequence of MH2 appears to encode a second transforming function. Therefore, it seems that MH2 contains two genes with possible oncogenic function, whereas MC29, CMII, and OK10 each carries a single hybrid delta gag-myc transforming gene. It is remarkable that, despite these fundamental differences in their primary structures and mechanisms of gene expression, MH2 and MC29 have very similar oncogenic properties.

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Year:  1983        PMID: 6579544      PMCID: PMC390394          DOI: 10.1073/pnas.80.21.6566

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  20 in total

1.  Avian acute leukemia virus MC29: conserved and variable RNA sequences and recombination with helper virus.

Authors:  P H Duesberg; K Bister; C Moscovici
Journal:  Virology       Date:  1979-11       Impact factor: 3.616

2.  Three new types of viral oncogene of cellular origin specific for haematopoietic cell transformation.

Authors:  M Roussel; S Saule; C Lagrou; C Rommens; H Beug; T Graf; D Stehelin
Journal:  Nature       Date:  1979-10-11       Impact factor: 49.962

3.  The defectiveness of Mill Hill 2, a carcinoma-inducing avian oncovirus.

Authors:  S S Hu; C Moscovici; P K Vogt
Journal:  Virology       Date:  1978-08       Impact factor: 3.616

4.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

5.  Avian oncovirus Mill Hill No. 2: pathogenicity in chickens.

Authors:  R W Alexander; C Moscovici; P K Vogt
Journal:  J Natl Cancer Inst       Date:  1979-02       Impact factor: 13.506

6.  Specific RNA sequences and gene products of MC29 avian acute leukemia virus.

Authors:  P Mellon; A Pawson; K Bister; G S Martin; P H Duesberg
Journal:  Proc Natl Acad Sci U S A       Date:  1978-12       Impact factor: 11.205

7.  Electron microscopy of nucleic acids.

Authors:  C F Garon
Journal:  Gene Amplif Anal       Date:  1981

8.  Molecular cloning of avian myelocytomatosis virus (MC29) transforming sequences.

Authors:  J A Lautenberger; R A Schulz; C F Garon; P N Tsichlis; T S Papas
Journal:  Proc Natl Acad Sci U S A       Date:  1981-03       Impact factor: 11.205

9.  Genetic structure of avian acute leukemia viruses.

Authors:  K Bister; P H Duesberg
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1980

10.  Heterogeneity of genetic loci in chickens: analysis of endogenous viral and nonviral genes by cleavage of DNA with restriction endonucleases.

Authors:  S H Hughes; F Payvar; D Spector; R T Schimke; H L Robinson; G S Payne; J M Bishop; H E Varmus
Journal:  Cell       Date:  1979-10       Impact factor: 41.582

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  32 in total

1.  Transformed and tumorigenic phenotypes induced by avian retroviruses containing the v-mil oncogene.

Authors:  C Béchade; G Dambrine; T David-Pfeuty; E Esnault; G Calothy
Journal:  J Virol       Date:  1988-04       Impact factor: 5.103

2.  Molecular cloning of proviral DNA and structural analysis of the transduced myc oncogene of avian oncovirus CMII.

Authors:  N Walther; R Lurz; T Patschinsky; H W Jansen; K Bister
Journal:  J Virol       Date:  1985-05       Impact factor: 5.103

3.  Long terminal repeat sequences impart hematopoietic transformation properties to the myeloproliferative sarcoma virus.

Authors:  C Stocking; R Kollek; U Bergholz; W Ostertag
Journal:  Proc Natl Acad Sci U S A       Date:  1985-09       Impact factor: 11.205

4.  Isolation of an MH2 retrovirus mutant temperature sensitive for macrophage but not fibroblast transformation.

Authors:  S Palmieri
Journal:  J Virol       Date:  1986-04       Impact factor: 5.103

5.  Dispersed chromosomal localization of the proto-oncogenes transduced into the genome of Mill Hill 2 or E26 leukemia virus.

Authors:  G Symonds; N Quintrell; E Stubblefield; J M Bishop
Journal:  J Virol       Date:  1986-07       Impact factor: 5.103

6.  FH3, a v-myc avian retrovirus with limited transforming ability.

Authors:  C Chen; B J Biegalke; R N Eisenman; M L Linial
Journal:  J Virol       Date:  1989-12       Impact factor: 5.103

7.  Protein product of proto-oncogene c-mil.

Authors:  T Patschinsky; B Schroeer; K Bister
Journal:  Mol Cell Biol       Date:  1986-02       Impact factor: 4.272

8.  Nucleotide sequence of avian carcinoma virus MH2: two potential onc genes, one related to avian virus MC29 and the other related to murine sarcoma virus 3611.

Authors:  N C Kan; C S Flordellis; G E Mark; P H Duesberg; T S Papas
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

9.  Cellular myc (c-myc) in fish (rainbow trout): its relationship to other vertebrate myc genes and to the transforming genes of the MC29 family of viruses.

Authors:  R J Van Beneden; D K Watson; T T Chen; J A Lautenberger; T S Papas
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

10.  Cellular homologs of the avian erythroblastosis virus erb-A and erb-B genes are syntenic in mouse but asyntenic in man.

Authors:  B U Zabel; R E Fournier; P A Lalley; S L Naylor; A Y Sakaguchi
Journal:  Proc Natl Acad Sci U S A       Date:  1984-08       Impact factor: 11.205

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