Localization of the Gene for MEN 2A

Authors

Jay B. Lichter
Michael Difilippantonio
Jingshi Wu
Diane Miller
David C. Ward
Paul J. Goodfellow
Kenneth K. Kidd

Abstract

The search for the gene that causes the multiple endocrine neoplasia type 2A (MEN 2A) syndrome is entering a new phase. Genetic linkage studies have localized the gene to the pericentromeric region of chromosome 10. The statistical portion of mapping the gene for MEN 2A is nearly complete and now classical molecular biological/gene mapping techniques will be employed. We have used fluorescence in situ hybridization to estimate the size of the MEN2A region to be about 2 to 5 mb, using some liberal assumptions; at worst the region should contain no more than about 10 mb of non-alphoid DNA. Our mapping panels (meiotic recombinant and radiation reduced hybrid) give consistent orders of markers in this small region. We describe our initial attempts to clone the region using yeast artificial chromosomes.

Recommended Citation

Lichter, Jay B.; Difilippantonio, Michael; Wu, Jingshi; Miller, Diane; Ward, David C.; Goodfellow, Paul J.; and Kidd, Kenneth K. (1992) "Localization of the Gene for MEN 2A," Henry Ford Hospital Medical Journal : Vol. 40 : No. 3 , 199-204.
Available at: https://scholarlycommons.henryford.com/hfhmedjournal/vol40/iss3/13