Eloy Philippine, Dehainault Catherine, Sefta Meriem, Aerts Isabelle, Doz François, Cassoux Nathalie, Lumbroso le Rouic Livia, Stoppa-Lyonnet Dominique, Radvanyi François, Millot Gaël A, Gauthier-Villars Marion, Houdayer Claude
Service de Génétique, Institut Curie, Paris, France.
CNRS UMR144, centre de recherche de l'Institut Curie, Paris, France.
PLoS Genet. 2016 Feb 29;12(2):e1005888. doi: 10.1371/journal.pgen.1005888. eCollection 2016 Feb.
Retinoblastoma (Rb), the most common pediatric intraocular neoplasm, results from inactivation of both alleles of the RB1 tumor suppressor gene. The second allele is most commonly lost, as demonstrated by loss of heterozygosity studies. RB1 germline carriers usually develop bilateral tumors, but some Rb families display low penetrance and variable expressivity. In order to decipher the underlying mechanisms, 23 unrelated low penetrance pedigrees segregating the common c.1981C>T/p.Arg661Trp mutation and other low penetrance mutations were studied. In families segregating the c.1981C>T mutation, we demonstrated, for the first time, a correlation between the gender of the transmitting carrier and penetrance, as evidenced by Fisher's exact test: the probability of being unaffected is 90.3% and 32.5% when the mutation is inherited from the mother and the father, respectively (p-value = 7.10(-7). Interestingly, a similar correlation was observed in families segregating other low penetrance alleles. Consequently, we investigated the putative involvement of an imprinted, modifier gene in low penetrance Rb. We first ruled out a MED4-driven mechanism by MED4 methylation and expression analyses. We then focused on the differentially methylated CpG85 island located in intron 2 of RB1 and showing parent-of-origin-specific DNA methylation. This differential methylation promotes expression of the maternal c.1981C>T allele. We propose that the maternally inherited c.1981C>T/p.Arg661Trp allele retains sufficient tumor suppressor activity to prevent retinoblastoma development. In contrast, when the mutation is paternally transmitted, the low residual activity would mimic a null mutation and subsequently lead to retinoblastoma. This implies that the c.1981C>T mutation is not deleterious per se but needs to be destabilized in order to reach pRb haploinsufficiency and initiate tumorigenesis. We suggest that this phenomenon might be a general mechanism to explain phenotypic differences in low penetrance Rb families.
视网膜母细胞瘤(Rb)是最常见的儿童眼内肿瘤,由RB1肿瘤抑制基因的两个等位基因失活所致。如杂合性缺失研究所示,第二个等位基因最常丢失。RB1种系携带者通常会发生双侧肿瘤,但一些Rb家族表现出低外显率和可变表达性。为了解析其潜在机制,对23个不相关的低外显率家系进行了研究,这些家系分离出常见的c.1981C>T/p.Arg661Trp突变和其他低外显率突变。在分离c.1981C>T突变的家系中,我们首次通过Fisher精确检验证明了传递携带者的性别与外显率之间的相关性:当突变分别从母亲和父亲遗传时,未受影响的概率分别为90.3%和32.5%(p值 = 7.10(-7))。有趣的是,在分离其他低外显率等位基因的家系中也观察到了类似的相关性。因此,我们研究了印记修饰基因在低外显率Rb中的假定作用。我们首先通过MED4甲基化和表达分析排除了MED4驱动的机制。然后,我们聚焦于位于RB1内含子2中的差异甲基化CpG85岛,该岛显示出亲本来源特异性的DNA甲基化。这种差异甲基化促进了母本c.1981C>T等位基因的表达。我们提出,母系遗传的c.1981C>T/p.Arg661Trp等位基因保留了足够的肿瘤抑制活性以预防视网膜母细胞瘤的发生。相反,当突变由父系传递时,低残留活性会模拟无效突变,随后导致视网膜母细胞瘤。这意味着c.1981C>T突变本身并非有害,但需要不稳定才能达到pRb单倍体不足并启动肿瘤发生。我们认为这种现象可能是解释低外显率Rb家系表型差异的一种普遍机制。