## Abstract Studying the molecular basis of familial renal cell carcinoma (RCC) has allowed identification of novel RCC genes involved in the pathogenesis of both inherited and sporadic RCC. We describe a constitutional balanced t(3;8)(p14;q24.1) translocation found in a brother and sister with bil
An (8;14)(q24;q11) translocation involving the T-cell receptor α-chain gene and the MYC oncogene 3′ region in a B-cell lymphoma
✍ Scribed by James K. Park; Timothy W. McKeithan; Michelle M. le Beau; Mitchell A. Bitter; Wilbur A. Franklin; Janet D. Rowley; Dr. Manuel O. Diaz
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 796 KB
- Volume
- 1
- Category
- Article
- ISSN
- 1045-2257
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✦ Synopsis
We describe a t(8; I4)(q24;q I I) involving the T-cell receptor a-chain gene (TCRA) and the 3' region of the MYC protooncogene in a B-cell lymphoma. The 6-cell origin of this tumor was determined by its histological architecture, by immunophenotypic analysis, and by Southern analysis of immunoglobulin gene rearrangements. An identical fragment encompassing the translocation breakpoint junction was detected through Southern analysis using both a TCRA J and a MYCprobe. The other alleles at the TCRA J and MYC loci were in the germline configuration. Restriction enzyme and nucleotide sequencing analyses revealed that the breakpoint junction on chromosome 8 lies approximately 700 base pairs (bp) downstream of the 3' end of the third MYC exon; on chromosome 14, the break is located 12.6 kilobases (kb) downstream of the 3' end of the C6 fourth exon. A heptamer-like consensus sequence on chromosome I 4 adjacent t o the translocation breakpoint implies the involvement of recombinase activity. However, no consensus sequences were found on chromosome 8 within 140 bp in either direction from the breakpoint. It is possible that this translocation involving MYC occurred during an attempt at an inappropriate rearrangement of the TCRA locus in a cell of B-cell lineage.
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