TY - JOUR
T1 - Somatic Apc mutations are selected upon their capacity to inactivate the β-catenin downregulating activity
AU - Smits, Ron
AU - Hofland, Nandy
AU - Edelmann, Winfried
AU - Geugien, Marjan
AU - Jagmohan-Changur, Shantie
AU - Albuquerque, Cristina
AU - Breukel, Cor
AU - Kucherlapati, Raju
AU - Kielman, Menno F.
AU - Fodde, Riccardo
PY - 2000
Y1 - 2000
N2 - The APC gene, originally identified as the gene for familial adenomatous polyposis (FAP), is now considered as the true 'gatekeeper' of colonic epithelial proliferation. Its main tumor suppressing activity seems to reside in the capacity to properly regulate intracellular β-catenin signaling. Most somatic APC mutations are detected between codons 1286 and 1513, the mutation cluster region (MCR). This clustering can be explained either by the presence of mutation-prone sequences within the MCR, or by the selective advantage provided by the resulting truncated polypeptides. Here, a Msh2-deficient mouse model (Msh2(Δ7N)) was generated and bred with Apc(1638N) and Apc(Min) that allowed the comparison of the somatic mutation spectra along the Apc gene in the different allelic combinations. Mutations identified in Msh2(Δ7N/Δ7N) tumors are predominantly dinucleotide deletions at simple sequence repeats leading to truncated Apc polypeptides that partially retain the 20 a.a. β-catenin downregulating motifs. In contrast, the somatic mutations identified in the wild type Apc allele of Msh2(Δ7N/Δ7N/Apc(+/1638N) and Msh2(Δ7N/Δ7N)/Apc(+Min) tumors are clustered more to the 5' end, thereby completely inactivating the β-catenin downregulating activity of APC. These results indicate that somatic Apc mutations are selected during intestinal tumorigenesis and that inactivation of the β-catenin downregulating function of APC is likely to represent the main selective factor. (C) 2000 Wiley-Liss, Inc.
AB - The APC gene, originally identified as the gene for familial adenomatous polyposis (FAP), is now considered as the true 'gatekeeper' of colonic epithelial proliferation. Its main tumor suppressing activity seems to reside in the capacity to properly regulate intracellular β-catenin signaling. Most somatic APC mutations are detected between codons 1286 and 1513, the mutation cluster region (MCR). This clustering can be explained either by the presence of mutation-prone sequences within the MCR, or by the selective advantage provided by the resulting truncated polypeptides. Here, a Msh2-deficient mouse model (Msh2(Δ7N)) was generated and bred with Apc(1638N) and Apc(Min) that allowed the comparison of the somatic mutation spectra along the Apc gene in the different allelic combinations. Mutations identified in Msh2(Δ7N/Δ7N) tumors are predominantly dinucleotide deletions at simple sequence repeats leading to truncated Apc polypeptides that partially retain the 20 a.a. β-catenin downregulating motifs. In contrast, the somatic mutations identified in the wild type Apc allele of Msh2(Δ7N/Δ7N/Apc(+/1638N) and Msh2(Δ7N/Δ7N)/Apc(+Min) tumors are clustered more to the 5' end, thereby completely inactivating the β-catenin downregulating activity of APC. These results indicate that somatic Apc mutations are selected during intestinal tumorigenesis and that inactivation of the β-catenin downregulating function of APC is likely to represent the main selective factor. (C) 2000 Wiley-Liss, Inc.
UR - http://www.scopus.com/inward/record.url?scp=0033804719&partnerID=8YFLogxK
U2 - 10.1002/1098-2264(2000)9999:9999<::AID-GCC1033>3.0.CO;2-R
DO - 10.1002/1098-2264(2000)9999:9999<::AID-GCC1033>3.0.CO;2-R
M3 - Article
C2 - 10992298
AN - SCOPUS:0033804719
SN - 1045-2257
VL - 29
SP - 229
EP - 239
JO - Genes Chromosomes and Cancer
JF - Genes Chromosomes and Cancer
IS - 3
ER -