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Juxtaposition of N-myc and Ig kappa through a reciprocal t(6;12) translocation in a mouse plasmacytoma

Axelson, H (author)
Karolinska Institutet,Lund University,Lunds universitet,Avdelningen för translationell cancerforskning,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Translational Cancer Research,Department of Laboratory Medicine,Faculty of Medicine
Wang, Y (author)
Silva, S (author)
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Mattei, M G (author)
Klein, G (author)
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 (creator_code:org_t)
1994
1994
English.
In: Genes, Chromosomes and Cancer. - 1045-2257. ; 11:2, s. 85-90
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Nearly all mouse plasmacytomas (MPCs) carry an Ig/myc translocation. Any one of the three Ig loci may participate, while the myc contribution has been limited to c-myc, excluding other members of the myc gene family. The same is true for the other two known Ig/myc translocation-carrying tumors, Burkitt's lymphoma and rat immunocytoma. It is believed that the Ig/myc juxtaposition plays a decisive, rate limiting role in the genesis of the three tumors, acting through the constitutive activation of myc that makes it refractory to normal regulation. Here we describe the molecular analysis of a unique t(6;12)(CI;B) translocation that we previously identified in an exceptional MPC that expressed N-myc but not c-myc. We now show that the translocation led to the juxtaposition of N-myc and Ig kappa. This is the first case of an Ig/myc-carrying tumor that involves N-myc rather than c-myc. These findings suggest that the translocation may already have occurred at the pro- or pre-B cell stage at which N-myc is open for transcription. According to this interpretation, constitutive activation of N-myc would suppress the expression of c-myc, but would not interfere with the differentiation of the pro-B cell into a fully mature plasma cell. Its tumorigenic influence would become manifest only at the time when the cell would normally be programmed to leave the cycling compartment, in connection with its terminal differentiation.

Keyword

Animals
Base Sequence
Chromosome Mapping
Cloning, Molecular
DNA Probes
Genes, myc
Immunoglobulin kappa-Chains
Mice
Molecular Sequence Data
Plasmacytoma
RNA Probes
Translocation, Genetic

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Axelson, H
Wang, Y
Silva, S
Mattei, M G
Klein, G
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Genes, Chromosom ...
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Lund University

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