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将p16基因(CDKN2)作为9号染色体黑色素瘤易感位点的候选基因进行分析。

Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus.

作者信息

Kamb A, Shattuck-Eidens D, Eeles R, Liu Q, Gruis N A, Ding W, Hussey C, Tran T, Miki Y, Weaver-Feldhaus J

机构信息

Myriad Genetics, Inc., Salt Lake City, Utah 84108.

出版信息

Nat Genet. 1994 Sep;8(1):23-6. doi: 10.1038/ng0994-22.

Abstract

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.

摘要

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。

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