The dcc gene: Structural analysis and mutations in colorectal carcinomas

Kathleen R. Cho, Jonathan D. Oliner, Jonathan W. Simons, Lora Hedrick, Eric R. Fearon, Antonette C. Preisinger, Philip Hedge, Gary A. Silverman, Bert Vogelstein

Research output: Contribution to journalArticlepeer-review

Abstract

DCC is a candidate tumor-suppressor gene encoding a protein with sequence similarity to cell adhesion molecules such as N-CAM. A set of overlapping YAC clones that contains the entire DCC coding region was isolated. Studies of this YAC contig showed that the DCC gene spans approximately 1.4 Mb. For elucidation of exon-intron structure, lambda phage clones containing all known coding sequences were isolated from a genomic library. These clones were used to demonstrate the existence of 29 DCC exons, and the sequences of the exon-intron boundaries were determined for each. Twenty-three polymorphic markers from chromosome 18 were then studied in a panel of primary colorectal tumors that had lost some, but not all, of chromosome 18. In most of these tumors, the region that was lost included DCC. Finally, Southern blot and PCR-based approaches were used to search for subtle mutations in several DCC exons. One tumor that had a point mutation in exon 28 was found, resulting in a proline to histidine substitution. A second tumor with a point mutation in intron 13 was also found. The regional map and genomic structure of DCC should provide the means to more extensively study DCC gene alterations and protein function in normal and neoplastic cells.

Original languageEnglish (US)
Pages (from-to)525-531
Number of pages7
JournalGenomics
Volume19
Issue number3
DOIs
StatePublished - Feb 1994

ASJC Scopus subject areas

  • Genetics

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