Deletion of Alu sequences in the fifth c-sis intron in individuals with meningiomas.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 2212004.
- Also identified by PMC identifier 296844.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
An abnormality in the c-sis protooncogene was identified in leukocyte DNA from members of a family predisposed to the development of meningioma, and was found to be associated with the development of the tumor in those individuals. Molecular analysis of this abnormality demonstrated a deletion within the fifth intron of the c-sis gene. The normal c-sis gene has an Alu sequence in this region which includes two perfect 130 nucleotide repeated sequences separated by 5 bp. The deleted c-sis allele is missing precisely one copy of the 130 bp repeat and the intervening 5 bp. An identical deletion was also found in DNA from 1 of 13 sporadic meningiomas.
Medical subject headings
- Chromosome Deletion
- Introns
- Meningeal Neoplasms
- Meningioma
- Platelet-Derived Growth Factor
- Proto-Oncogene Proteins
- Proto-Oncogenes
- Repetitive Sequences, Nucleic Acid