Identification of deletion mutations and three new genes at the familial polyposis locus

Autor: E. Wolff, Jeff Stevens, John J. Wasmuth, Andrew Thliveris, Lisa Spirio, Janet A. Warrington, M. Carlson, Leslie Sargeant, Ray White, John Douglas Mcpherson, Hadi Abderrahim, Daniel Cohen, Lawrence Gelbert, Denis Le Paslier, Hans Albertsen, Mark Leppert, Geoff Joslyn, Karen Krapcho, Randall W. Burt, Joanna Groden, John P. Hughes, Wade S. Samowitz, Margaret Robertson
Přispěvatelé: Centre d'Etude du Polymorphisme Humain (CEPH), Fondation Jean Dausset-Institut Universitaire d'Hématologie (IUH), Université Paris Diderot - Paris 7 (UPD7)-Université Paris Diderot - Paris 7 (UPD7)
Rok vydání: 1991
Předmět:
Zdroj: Cell
Cell, Elsevier, 1991, 66 (3), pp.601-613. ⟨10.1016/0092-8674(81)90022-2⟩
ISSN: 0092-8674
1097-4172
DOI: 10.1016/0092-8674(81)90022-2⟩
Popis: Small (100-260 kb), nested deletions were characterized in DNA from two unrelated patients with familial adenomatous polyposis coli (APC). Three candidate genes located within the deleted region were ascertained and a previous candidate gene, MCC, was shown to be located outside the deleted region. One of the new genes contained sequence identical to SRP19, the gene coding for the 19 kd component of the ribosomal signal recognition particle. The second, provisionally designated DP1 (deleted in polyposis 1), was found to be transcribed in the same orientation as MCC. Two other cDNAs, DP2 and DP3, were found to overlap, forming a single gene, DP2.5, that is transcribed in the same orientation as SRP19.
Databáze: OpenAIRE