Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
Comparative analysis of the expression and oncogenic activities of Xenopus c-, N-, and L-myc homologs.
Schreiber-Agus N
,
Torres R
,
Horner J
,
Lau A
,
Jamrich M
,
DePinho RA
.
???displayArticle.abstract???
A polymerase chain reaction-based cloning strategy allowed for the isolation of two distinct Xenopus L-myc genes, as well as previously isolated xc- and xN-myc genes, thus demonstrating that these three well-defined members of the mammalian myc gene family are present in lower vertebrates as well. Comparison of the Xenopus and mammalian Myc families revealed a high degree of structural relatedness at the gene and protein levels; this homology was consistent with the ability of the xc-myc1 and xN-myc1 genes to function as oncogenes in primary mammalian cells. In contrast, the xL-myc1 gene was found to be incapable of transforming rat embryofibroblast cells, and this inactivity may relate to localized but significant differences in its putative transactivation domain. Analysis of xc-, xN-, and xL-myc gene expression demonstrated that (i) all three genes were highly expressed during oogenesis and their transcripts accumulated as abundant maternal mRNAs, (ii) each gene exhibited a distinctive pattern of expression during embryogenesis and in adult tissues, and (iii) the xL-myc1 and xL-myc2 genes were coordinately expressed in the maternal and zygotic genomes. The markedly high expression of the Xenopus myc gene family in differentiated tissues, such as the central nervous system and kidney, contrasts sharply with the low levels observed in mammalian adult tissues. These differences may reflect unique functions of the Myc family proteins in processes specific to amphibians, such as tissue regeneration.
Andersson,
A defined subgenomic fragment of in vitro synthesized Moloney sarcoma virus DNA can induce cell transformation upon transfection.
1979, Pubmed
Andersson,
A defined subgenomic fragment of in vitro synthesized Moloney sarcoma virus DNA can induce cell transformation upon transfection.
1979,
Pubmed
Auffray,
Purification of mouse immunoglobulin heavy-chain messenger RNAs from total myeloma tumor RNA.
1980,
Pubmed
Birrer,
L-myc cooperates with ras to transform primary rat embryo fibroblasts.
1988,
Pubmed
Bisbee,
Albumin phylogeny for clawed frogs (Xenopus).
1977,
Pubmed
,
Xenbase
Blackwood,
Max: a helix-loop-helix zipper protein that forms a sequence-specific DNA-binding complex with Myc.
1991,
Pubmed
Cabada,
Differential accumulation of two size classes of poly(A) associated with messenger RNA during oogenesis in Xenopus laevis.
1977,
Pubmed
,
Xenbase
DePinho,
Structure and expression of the murine N-myc gene.
1986,
Pubmed
DePinho,
The human myc gene family: structure and activity of L-myc and an L-myc pseudogene.
1987,
Pubmed
DePinho,
myc family oncogenes in the development of normal and neoplastic cells.
1991,
Pubmed
Devereux,
A comprehensive set of sequence analysis programs for the VAX.
1984,
Pubmed
Downs,
Contrasting patterns of myc and N-myc expression during gastrulation of the mouse embryo.
1989,
Pubmed
Dumont,
Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals.
1972,
Pubmed
,
Xenbase
Fasano,
Sequence and structure of the coding region of the human H-ras-1 gene from T24 bladder carcinoma cells.
1983,
Pubmed
Frykberg,
The transforming activity of the chicken c-myc gene can be potentiated by mutations.
1987,
Pubmed
Géraudie,
Enhanced c-myc gene expression during forelimb regenerative outgrowth in the young Xenopus laevis.
1990,
Pubmed
,
Xenbase
Godeau,
C-myc expression is dissociated from DNA synthesis and cell division in Xenopus oocyte and early embryonic development.
1986,
Pubmed
,
Xenbase
Golden,
Accumulation of individual pA+ RNAs during oogenesis of Xenopus laevis.
1980,
Pubmed
,
Xenbase
Grady,
Expression of N-myc and c-src during the development of fetal human brain.
1987,
Pubmed
Gurdon,
The use of Xenopus oocytes for the expression of cloned genes.
1983,
Pubmed
,
Xenbase
Gusse,
Translocation of a store of maternal cytoplasmic c-myc protein into nuclei during early development.
1989,
Pubmed
,
Xenbase
Henikoff,
Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing.
1984,
Pubmed
Jakobovits,
Expression of N-myc in teratocarcinoma stem cells and mouse embryos.
,
Pubmed
Kato,
An amino-terminal c-myc domain required for neoplastic transformation activates transcription.
1990,
Pubmed
King,
Expression of the c-myc proto-oncogene during development of Xenopus laevis.
1986,
Pubmed
,
Xenbase
Kyte,
A simple method for displaying the hydropathic character of a protein.
1982,
Pubmed
Land,
Tumorigenic conversion of primary embryo fibroblasts requires at least two cooperating oncogenes.
,
Pubmed
Legouy,
Structure and expression of the murine L-myc gene.
1987,
Pubmed
Maxam,
Sequencing end-labeled DNA with base-specific chemical cleavages.
1980,
Pubmed
Mugrauer,
Contrasting expression patterns of three members of the myc family of protooncogenes in the developing and adult mouse kidney.
1991,
Pubmed
Mugrauer,
N-myc proto-oncogene expression during organogenesis in the developing mouse as revealed by in situ hybridization.
1988,
Pubmed
Mukherjee,
Myc family oncoproteins function through a common pathway to transform normal cells in culture: cross-interference by Max and trans-acting dominant mutants.
1992,
Pubmed
Newport,
A major developmental transition in early Xenopus embryos: II. Control of the onset of transcription.
1982,
Pubmed
,
Xenbase
Newport,
A major developmental transition in early Xenopus embryos: I. characterization and timing of cellular changes at the midblastula stage.
1982,
Pubmed
,
Xenbase
Nishikura,
Expression of c-myc proto-oncogene during the early development of Xenopus laevis.
1987,
Pubmed
,
Xenbase
Pfeifer-Ohlsson,
Cell-type-specific pattern of myc protooncogene expression in developing human embryos.
1985,
Pubmed
Prendergast,
Association of Myn, the murine homolog of max, with c-Myc stimulates methylation-sensitive DNA binding and ras cotransformation.
1991,
Pubmed
Principaud,
Xenopus laevis c-myc I and II genes: molecular structure and developmental expression.
1991,
Pubmed
,
Xenbase
Schmid,
Dynamic expression pattern of the myc protooncogene in midgestation mouse embryos.
1989,
Pubmed
Schwab,
Human N-myc gene contributes to neoplastic transformation of mammalian cells in culture.
,
Pubmed
Shaw,
A conserved AU sequence from the 3' untranslated region of GM-CSF mRNA mediates selective mRNA degradation.
1986,
Pubmed
Stone,
Definition of regions in human c-myc that are involved in transformation and nuclear localization.
1987,
Pubmed
Symonds,
Transformation of murine myelomonocytic cells by myc: point mutations in v-myc contribute synergistically to transforming potential.
1989,
Pubmed
Tabor,
DNA sequence analysis with a modified bacteriophage T7 DNA polymerase.
1987,
Pubmed
Taylor,
Xenopus myc proto-oncogene during development: expression as a stable maternal mRNA uncoupled from cell division.
1986,
Pubmed
,
Xenbase
Torres,
Myc and Max: a putative transcriptional complex in search of a cellular target.
1992,
Pubmed
Vize,
Expression of the N-myc proto-oncogene during the early development of Xenopus laevis.
1990,
Pubmed
,
Xenbase
Vriz,
Differential expression of two Xenopus c-myc proto-oncogenes during development.
1989,
Pubmed
,
Xenbase
Yancopoulos,
N-myc can cooperate with ras to transform normal cells in culture.
1985,
Pubmed
Yasuda,
Temporal regulation in the early embryo: is MBT too good to be true?
1992,
Pubmed
,
Xenbase
Zimmerman,
Differential expression of myc family genes during murine development.
,
Pubmed