Dave B J, Pickering D L, Hess M M, Weisenburger D D, Armitage J O, Sanger W G
Munroe Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha 68198-5440, USA.
Cancer Genet Cytogenet. 1999 Jan 15;108(2):120-6. doi: 10.1016/s0165-4608(98)00138-1.
Our laboratories have documented a significantly high occurrence of chromosome 1p36 rearrangements in non-Hodgkin lymphoma (NHL). The cell division cycle 2-like 1(CDC2L1) (also known as TP58 or PITSLRE) gene, a protein kinase implicated in apoptotic signaling, is located at the very distal region of chromosome 1p36 and is likely to be disrupted by structural rearrangements involving 1p36. To determine the molecular consequences of the recurrent involvement of the 1p36 region, we examined metaphases containing 1p36 abnormalities from 31 specimens derived from 26 patients for the possible deletion of CDC2L1 by fluorescence in situ hybridization (FISH) using the TP58clk-1 DNA probe. Twenty-three cases exhibited the loss of CDC2L1 from the abnormal chromosome 1. In 2 of 26 cases, the gene locus was translocated to the partner chromosome, and in four specimens, all derived from one case, CDC2L1 was not deleted. This pilot investigation suggests that 1p36 rearrangements, and consequently the loss of the CDC2L1 gene locus, is important in NHL. This work also opens avenues for further molecular studies and prognostic correlations.
我们的实验室已记录到非霍奇金淋巴瘤(NHL)中1p36染色体重排的发生率显著偏高。细胞分裂周期2样1(CDC2L1)(也称为TP58或PITSLRE)基因是一种参与凋亡信号传导的蛋白激酶,位于1p36染色体的最远端区域,很可能因涉及1p36的结构重排而被破坏。为了确定1p36区域反复受累的分子后果,我们使用TP58clk-1 DNA探针,通过荧光原位杂交(FISH)检测了来自26例患者的31个标本中含有1p36异常的中期细胞,以确定CDC2L1是否可能缺失。23例病例显示异常的1号染色体上CDC2L1缺失。在26例病例中的2例中,该基因位点易位至配对染色体,在4个均来自同一病例的标本中,CDC2L1未缺失。这项初步研究表明,1p36重排以及随之而来的CDC2L1基因位点缺失在NHL中具有重要意义。这项工作也为进一步的分子研究和预后相关性研究开辟了道路。