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对48个澳大利亚黑色素瘤家族的CDKN2A、CDKN2B和CDK4基因进行分析。

Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds.

作者信息

Flores J F, Pollock P M, Walker G J, Glendening J M, Lin A H, Palmer J M, Walters M K, Hayward N K, Fountain J W

机构信息

University of Southern California, Institute for Genetic Medical, Department of Biochemistry and Molecular Biology, Los Angeles 90033, USA.

出版信息

Oncogene. 1997 Dec 11;15(24):2999-3005. doi: 10.1038/sj.onc.1201470.

Abstract

Germline mutations within the cyclin-dependent kinase inhibitor 2A (CDKN2A) gene and one of its targets, the cyclin dependent kinase 4 (CDK4) gene, have been identified in a proportion of melanoma kindreds. In the case of CDK4, only one specific mutation, resulting in the substitution of a cysteine for an arginine at codon 24 (R24C), has been found to be associated with melanoma. We have previously reported the identification of germline CDKN2A mutations in 7/18 Australian melanoma kindreds and the absence of the R24C CDK4 mutation in 21 families lacking evidence of a CDKN2A mutation. The current study represents an expansion of these efforts and includes a total of 48 melanoma families from Australia. All of these families have now been screened for mutations within CDKN2A and CDK4, as well as for mutations within the CDKN2A homolog and 9p21 neighbor, the CDKN2B gene, and the alternative exon 1 (E1beta) of CDKN2A. Families lacking CDKN2A mutations, but positive for a polymorphism(s) within this gene, were further evaluated to determine if their disease was associated with transcriptional silencing of one CDKN2A allele. Overall, CDKN2A mutations were detected in 3/30 (10%) of the new kindreds. Two of these mutations have been observed previously: a 24 bp duplication at the 5' end of the gene and a G to C transversion in exon 2 resulting in an M531 substitution. A novel G to A transition in exon 2, resulting in a D108N substitution was also detected. Combined with our previous findings, we have now detected germline CDKN2A mutations in 10/48 (21%) of our melanoma kindreds. In none of the 'CDKN2A-negative' families was melanoma found to segregate with either an untranscribed CDKN2A allele, an R24C CDK4 mutation, a CDKN2B mutation, or an E1beta mutation. The last three observations suggest that these other cell cycle control genes (or alternative gene products) are either not involved at all, or to any great extent, in melanoma predisposition.

摘要

在一部分黑色素瘤家族中,已发现细胞周期蛋白依赖性激酶抑制剂2A(CDKN2A)基因及其一个靶点——细胞周期蛋白依赖性激酶4(CDK4)基因存在种系突变。就CDK4而言,仅发现一种特定突变与黑色素瘤相关,该突变导致第24密码子处的精氨酸被半胱氨酸取代(R24C)。我们之前报道过在18个澳大利亚黑色素瘤家族中的7个家族鉴定出种系CDKN2A突变,并且在21个缺乏CDKN2A突变证据的家族中未发现R24C CDK4突变。当前研究是这些工作的扩展,共纳入了来自澳大利亚的48个黑色素瘤家族。现在对所有这些家族进行了CDKN2A和CDK4内的突变筛查,以及CDKN2A同源物和9p21邻域内的CDKN2B基因和CDKN2A的可变外显子1(E1beta)的突变筛查。对缺乏CDKN2A突变但该基因内存在多态性的家族进行了进一步评估,以确定其疾病是否与一个CDKN2A等位基因的转录沉默相关。总体而言,在30个新家族中的3个(10%)检测到CDKN2A突变。其中两个突变先前已被观察到:基因5'端的24 bp重复以及外显子2中的G到C颠换导致M531取代。还检测到外显子2中一个新的G到A转换,导致D108N取代。结合我们之前的发现,现在我们在48个黑色素瘤家族中的10个(21%)检测到种系CDKN2A突变。在任何一个“CDKN2A阴性”家族中,均未发现黑色素瘤与未转录的CDKN2A等位基因、R24C CDK4突变、CDKN2B突变或E1beta突变共分离。后三项观察结果表明,这些其他细胞周期调控基因(或替代基因产物)要么根本不参与,要么在很大程度上不参与黑色素瘤易感性。

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