|Title||Mutations in the first exon are associated with altered transcription of c-myc in Burkitt lymphoma.|
|Publication Type||Journal Article|
|Year of Publication||1987|
|Authors||Cesarman E, Dalla-Favera R, Bentley D, Groudine M|
|Date Published||1987 Nov 27|
|Keywords||Burkitt Lymphoma, Cell Line, Chromosomes, Human, Pair 14, Chromosomes, Human, Pair 2, Chromosomes, Human, Pair 22, Chromosomes, Human, Pair 8, Exons, Humans, Mutation, Proto-Oncogenes, Transcription, Genetic, Translocation, Genetic|
The c-myc proto-oncogene is involved in chromosomal translocations that are specifically and consistently found in Burkitt lymphoma. Although these translocations are thought to lead to a deregulation of c-myc expression, the structural and functional basis of this phenomenon has not been identified. Mutations in a specific region spanning approximately 70 base pairs and located at the 3' border of the first exon of translocated c-myc alleles were consistently detected in Burkitt lymphoma cells carrying classic (8:14) as well as variant (8:22 and 2:8) translocations. These structural alterations were accompanied by an altered pattern of c-myc transcription, namely, the removal of a block to transcriptional elongation that has been mapped to the same region. Thus, specific c-myc mutations leading to the alleviation of this block to transcriptional elongation may represent a general mechanism causing c-myc activation in Burkitt lymphoma.
|Grant List||NCI 28151 / CI / NCPDCID CDC HHS / United States |
NCI 37165 / CI / NCPDCID CDC HHS / United States
NCI 37195 / CI / NCPDCID CDC HHS / United States
Ethel Cesarman, M.D., Ph.D.