Abel Frida, Sjöberg Rose-Marie, Krona Cecilia, Nilsson Staffan, Martinsson Tommy
Department of Clinical Genetics, Gothenburg University, Sahlgrenska University Hospital/East, S-416 85 Gothenburg, Sweden.
Int J Oncol. 2004 Nov;25(5):1297-302.
DFF45 has essential functions in the final stage of apoptosis by acting both as a folding chaperone and a DNase inhibitor of DFF40. The gene encoding DFF45 (DFFA) maps to the consensus deleted region in primary neuroblastoma (NB; 1p36.2-3) and within the homozygously deleted region in an NB cell line (1p36.2). DFF45 is therefore an attractive candidate NB tumor suppressor. In a previous study we found a rare allele variant, causing a non-polar to a polar amino acid exchange (Ile69Thr) in a preserved hydrophobic patch of DFF45, and we also found DFFA to be preferentially expressed in favorable NB tumors. We have extended the previous study and performed mutation analyses in another 56 NB tumors (100 in total) as well as a set of other tumors for coding mutations in DFFA. We have also performed studies of the DFFA expression in tumors using real-time PCR. We found a missense mutation (Ile15Met) in the remaining allele of a teratoma with heterozygous deletion of 1p, and a three base-pair deletion in an NB of unknown stage causing a deletion of amino acid 37 in DFF45. The one-base substitution detected in the teratoma was not present in the patients constitutional DNA, i.e. it is a true mutation present in the tumor DNA only. In conclusion, three different coding alterations have been found in the region encoding the N-terminal regulatory domain of DFF45, responsible for binding and achieving its chaperone and inhibitor functions on other proteins. Moreover, by real-time RT-PCR expression study, we found the mRNA level of DFFA to be significantly (p=0.038) reduced by a factor of 1.7 times in NB tumors of unfavorable outcome.
DFF45在细胞凋亡的最后阶段发挥着重要作用,它既是一种折叠伴侣蛋白,也是DFF40的DNA酶抑制剂。编码DFF45的基因(DFFA)定位于原发性神经母细胞瘤(NB;1p36.2 - 3)的共有缺失区域以及一个NB细胞系(1p36.2)的纯合缺失区域内。因此,DFF45是一个有吸引力的NB肿瘤抑制候选基因。在之前的一项研究中,我们发现了一个罕见的等位基因变体,它导致DFF45保守疏水区域内的一个非极性氨基酸替换为极性氨基酸(Ile69Thr),并且我们还发现DFFA在预后良好的NB肿瘤中优先表达。我们扩展了之前的研究,对另外56个NB肿瘤(总共100个)以及一组其他肿瘤进行了DFFA编码突变的分析。我们还使用实时PCR对肿瘤中的DFFA表达进行了研究。我们在一个1p杂合缺失的畸胎瘤的剩余等位基因中发现了一个错义突变(Ile15Met),在一个分期不明的NB中发现了一个三碱基对缺失,导致DFF45中的氨基酸37缺失。在畸胎瘤中检测到的单碱基替换在患者的基因组DNA中不存在,即它是仅存在于肿瘤DNA中的一个真正突变。总之,在编码DFF45 N端调节域的区域中发现了三种不同的编码改变,该区域负责与其他蛋白质结合并发挥其伴侣蛋白和抑制剂功能。此外,通过实时RT-PCR表达研究,我们发现DFFA的mRNA水平在预后不良的NB肿瘤中显著降低(p = 0.038),降低了1.7倍。