Centre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, QC H3T1C5, Canada.
Am J Hum Genet. 2013 Oct 3;93(4):765-72. doi: 10.1016/j.ajhg.2013.08.014. Epub 2013 Sep 26.
Anophthalmia and/or microphthalmia, pulmonary hypoplasia, diaphragmatic hernia, and cardiac defects are the main features of PDAC syndrome. Recessive mutations in STRA6, encoding a membrane receptor for the retinol-binding protein, have been identified in some cases with PDAC syndrome, although many cases have remained unexplained. Using whole-exome sequencing, we found that two PDAC-syndrome-affected siblings, but not their unaffected sibling, were compound heterozygous for nonsense (c.355C>T [p.Arg119(∗)]) and frameshift (c.1201_1202insCT [p.Ile403Serfs(∗)15]) mutations in retinoic acid receptor beta (RARB). Transfection studies showed that p.Arg119(∗) and p.Ile403Serfs(∗)15 altered RARB had no transcriptional activity in response to ligands, confirming that the mutations induced a loss of function. We then sequenced RARB in 15 subjects with anophthalmia and/or microphthalmia and at least one other feature of PDAC syndrome. Surprisingly, three unrelated subjects with microphthalmia and diaphragmatic hernia showed de novo missense mutations affecting the same codon; two of the subjects had the c.1159C>T (Arg387Cys) mutation, whereas the other one carried the c.1159C>A (p.Arg387Ser) mutation. We found that compared to the wild-type receptor, p.Arg387Ser and p.Arg387Cys altered RARB induced a 2- to 3-fold increase in transcriptional activity in response to retinoic acid ligands, suggesting a gain-of-function mechanism. Our study thus suggests that both recessive and dominant mutations in RARB cause anophthalmia and/or microphthalmia and diaphragmatic hernia, providing further evidence of the crucial role of the retinoic acid pathway during eye development and organogenesis.
先天性无眼症和/或小眼球症、肺发育不全、膈疝和心脏缺陷是 PDAC 综合征的主要特征。虽然许多病例仍未得到解释,但已在一些 PDAC 综合征病例中发现编码视黄醇结合蛋白膜受体的 STRA6 隐性突变。使用全外显子组测序,我们发现 2 名受 PDAC 综合征影响的兄弟姐妹,但不受影响的兄弟姐妹均为视黄酸受体 β (RARB) 的无意义 (c.355C>T [p.Arg119(∗)]) 和移码 (c.1201_1202insCT [p.Ile403Serfs(∗)15]) 复合杂合突变。转染研究表明,p.Arg119(∗) 和 p.Ile403Serfs(∗)15 改变的 RARB 对配体无转录活性,证实突变导致功能丧失。然后,我们对 15 名患有先天性无眼症和/或小眼球症以及至少一个 PDAC 综合征其他特征的受试者进行了 RARB 测序。令人惊讶的是,3 名患有小眼球症和膈疝的无亲缘关系的受试者出现了影响同一密码子的新生错义突变;其中 2 名受试者携带 c.1159C>T (Arg387Cys) 突变,而另一名携带 c.1159C>A (p.Arg387Ser) 突变。我们发现,与野生型受体相比,p.Arg387Ser 和 p.Arg387Cys 改变的 RARB 对视黄酸配体的转录活性增加了 2 至 3 倍,提示存在获得性功能机制。因此,我们的研究表明,RARB 的隐性和显性突变均可导致先天性无眼症和/或小眼球症和膈疝,进一步证明了视黄酸通路在眼睛发育和器官发生中的关键作用。