Kamb A, Shattuck-Eidens D, Eeles R, Liu Q, Gruis N A, Ding W, Hussey C, Tran T, Miki Y, Weaver-Feldhaus J
Myriad Genetics, Inc., Salt Lake City, Utah 84108.
Nat Genet. 1994 Sep;8(1):23-6. doi: 10.1038/ng0994-22.
A locus for familial melanoma, MLM, has been mapped within the same interval on chromosome 9p21 as the gene for a putative cell cycle regulator, p16INK4 (CDKN2) MTS1. This gene is homozygously deleted from many tumour cell lines including melanomas, suggesting that CDKN2 is a good candidate for MLM. We have analysed CDKN2 coding sequences in pedigrees segregating 9p melanoma susceptibility and 38 other melanoma-prone families. In only two families were potential predisposing mutations identified. No evidence was found for heterozygous deletions of CDKN2 in the germline of melanoma-prone individuals. The low frequency of potential predisposing mutations detected suggests that either the majority of mutations fall outside the CDKN2 coding sequence or that CDKN2 is not MLM.
家族性黑素瘤位点(MLM)已被定位于9号染色体短臂21区的同一区间内,该区间与一种假定的细胞周期调节因子p16INK4(CDKN2)MTS1的基因位置相同。在包括黑素瘤在内的许多肿瘤细胞系中,该基因均发生纯合缺失,这表明CDKN2是MLM的一个很好的候选基因。我们分析了9号染色体短臂黑素瘤易感性家系以及其他38个黑素瘤高发家系中的CDKN2编码序列。仅在两个家系中发现了潜在的易感性突变。在黑素瘤高发个体的种系中未发现CDKN2杂合缺失的证据。检测到的潜在易感性突变频率较低,这表明要么大多数突变位于CDKN2编码序列之外,要么CDKN2不是MLM。