van Woerden Geeske M, Senden Richelle, de Konink Charlotte, Trezza Rossella A, Baban Anwar, Bassetti Jennifer A, van Bever Yolande, Bird Lynne M, van Bon Bregje W, Brooks Alice S, Guan Qiaoning, Klee Eric W, Marcelis Carlo, Rosado Joel M, Schimmenti Lisa A, Shikany Amy R, Terhal Paulien A, Nicole Weaver Kathryn, Wessels Marja W, van Wieringen Hester, Hurst Anna C, Gooch Catherine F, Steindl Katharina, Joset Pascal, Rauch Anita, Tartaglia Marco, Niceta Marcello, Elgersma Ype, Demirdas Serwet
Department of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
Hum Mutat. 2022 Oct;43(10):1377-1395. doi: 10.1002/humu.24425. Epub 2022 Jul 29.
Mitogen-activated protein 3 kinase 7 (MAP3K7) encodes the ubiquitously expressed transforming growth factor β-activated kinase 1, which plays a crucial role in many cellular processes. Mutationsin the MAP3K7 gene have been linked to two distinct disorders: frontometaphyseal dysplasia type 2 (FMD2) and cardiospondylocarpofacial syndrome (CSCF). The fact that different mutations can induce two distinct phenotypes suggests a phenotype/genotype correlation, but no side-by-side comparison has been done thus far to confirm this. Here, we significantly expand the cohort and the description of clinical phenotypes for patients with CSCF and FMD2 who carry mutations in MAP3K7. Our findings support that in contrast to FMD2-causing mutations, CSCF-causing mutations in MAP3K7 have a loss-of-function effect. Additionally, patients with pathogenic mutations in MAP3K7 are at risk for (severe) cardiac disease, have symptoms associated with connective tissue disease, and we show overlap in clinical phenotypes of CSCF with Noonan syndrome (NS). Together, we confirm a molecular fingerprint of FMD2- versus CSCF-causing MAP3K7 mutations and conclude that mutations in MAP3K7 should be considered in the differential diagnosis of patients with syndromic congenital cardiac defects and/or cardiomyopathy, syndromic connective tissue disorders, and in the differential diagnosis of NS.
丝裂原活化蛋白3激酶7(MAP3K7)编码普遍表达的转化生长因子β激活激酶1,其在许多细胞过程中起关键作用。MAP3K7基因的突变与两种不同的疾病有关:2型额骨干骺端发育异常(FMD2)和心脊柱腕面部综合征(CSCF)。不同的突变可诱发两种不同的表型,这一事实表明存在表型/基因型相关性,但迄今为止尚未进行过并行比较以证实这一点。在此,我们显著扩大了携带MAP3K7突变的CSCF和FMD2患者的队列规模并对其临床表型进行了描述。我们的研究结果支持,与导致FMD2的突变不同,MAP3K7中导致CSCF的突变具有功能丧失效应。此外,MAP3K7存在致病突变的患者有患(严重)心脏病的风险,有与结缔组织病相关的症状,并且我们发现CSCF的临床表型与努南综合征(NS)存在重叠。我们共同确认了导致FMD2与CSCF的MAP3K7突变的分子特征,并得出结论,在对患有综合征性先天性心脏缺陷和/或心肌病、综合征性结缔组织疾病的患者进行鉴别诊断以及在对NS进行鉴别诊断时,应考虑MAP3K7的突变。