Nelson M A, Ariza M E, Yang J M, Thompson F H, Taetle R, Trent J M, Wymer J, Massey-Brown K, Broome-Powell M, Easton J, Lahti J M, Kidd V J
Arizona Cancer Center, Tucson 85724, USA.
Cancer Genet Cytogenet. 1999 Jan 15;108(2):91-9. doi: 10.1016/s0165-4608(98)00122-8.
The two genes encoding the PITSLRE protein kinase isoforms, CDC2L1 and CDC2L2, are localized to human chromosome band 1p36. The PITSLRE protein kinases are a part of the p34cdc2 supergene family. Several protein products of the CDC2L locus may be effector(s) in apoptotic signaling. The larger PITSLRE p110 isoforms appear to regulate some aspect of RNA splicing/transcription during the cell cycle. One or more of these genes may function as tumor suppressor genes in melanoma. Using fluorescence in situ hybridization, one allele of the CDC2L gene complex on chromosome 1 was either deleted or translocated in 8 of 14 different melanoma cell lines. We also observed mutations in the 5' promoter region of the CDC2L1 gene in four different cell lines relative to normal melanocytes using PCR-SSCP analysis and direct DNA sequencing. Western blot analysis revealed decreased level of PITSLRE protein expression in several cell lines, as well as in four surgical malignant melanoma specimens relative to normal melanocytes. Thus, the decreased PITSLRE protein expression appears to result from deletion of the CDC2L alleles and possibly by mutations within the 5' promoter region. We propose that aberrations in the CDC2L genes may contribute to the pathogenesis or progression of melanoma.
编码PITSLRE蛋白激酶同工型的两个基因CDC2L1和CDC2L2定位于人类染色体1p36带。PITSLRE蛋白激酶是p34cdc2超基因家族的一部分。CDC2L基因座的几种蛋白质产物可能是凋亡信号传导中的效应器。较大的PITSLRE p110同工型似乎在细胞周期中调节RNA剪接/转录的某些方面。这些基因中的一个或多个可能在黑色素瘤中作为肿瘤抑制基因发挥作用。使用荧光原位杂交技术,在14种不同的黑色素瘤细胞系中的8种中,1号染色体上的CDC2L基因复合体的一个等位基因被缺失或易位。我们还使用PCR-SSCP分析和直接DNA测序观察到,相对于正常黑素细胞,四种不同细胞系中CDC2L1基因的5'启动子区域存在突变。蛋白质印迹分析显示,相对于正常黑素细胞,几种细胞系以及四个手术切除的恶性黑色素瘤标本中PITSLRE蛋白表达水平降低。因此,PITSLRE蛋白表达降低似乎是由于CDC2L等位基因的缺失以及可能由于5'启动子区域内的突变所致。我们提出,CDC2L基因的异常可能导致黑色素瘤的发病机制或进展。