Cells from murine plasmacytomas (MPC) consistently exhibit either the 12;15 or the 6;15 translocation. Recently, we found that cells from 2 MPC (ABPC 45 and ABPC 26) did not exhibit any known translocation. However, these MPC contained one chromosome 15 (15q-) that was shorter than its normal homolo
Ig/myc translocations of the plasmacytoma-prone BALB/c strain occur independently of the genetic and parental origin of the affected chromosomes 6, 12, and 15
โ Scribed by Santiago Silva; Magdalena Babonits; George Klein
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 548 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1045-2257
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โฆ Synopsis
Virtually all murine plasmacytomas (MPCs) carry chromosomal translocations that juxtapose rnyc on chromosome I 5 (chr IS) t o one of the three immunoglobulin loci carrying chr 6, 12, or 16. Only some mouse strains are susceptible t o MPC induction, however, with BALB/c as the outstanding example. Most other strains are resistant. Our earlier studies with reciprocal BALB/cc*DBA/2 chimeras suggested that part of this susceptibility is determined at the level of the target cell itself (DBA/2 is MPC resistant). The probability of the Iglrnyc translocation is one of the possibly relevant variables. Because MPC resistance is dominant over susceptibility, it is conceivable that the translocations prevail due t o some deficiency of the lg rearrangement or Ig-associated repair mechanisms in BALB/c cells. This could be determined at the level of the chromosomes that participate in the translocation o r by genes on other chromosomes. Here, we show that the substitution of the BALB/c-derived chr 12, 6, and 15, which carry IgH, K, and rnyc, respectively, with their homologs derived from MPC-resistant mice, did not affect MPC Susceptibility. The use of Robertsonian 4. I 2 and 6. I 5 chromosomes in this study has also provided us with the opportunity t o
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