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Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis.RRAS中的激活突变是RAS病谱系中一种表型的基础,并促进白血病发生。
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The RASopathies.RAS 相关疾病。
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MiR-124 inhibits the growth of glioblastoma through the downregulation of SOS1.miR-124 通过下调 SOS1 抑制神经胶质瘤的生长。
Mol Med Rep. 2013 Aug;8(2):345-9. doi: 10.3892/mmr.2013.1561. Epub 2013 Jun 28.
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Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome.RIT1 中的功能获得性突变导致努南综合征,一种 RAS/MAPK 通路综合征。
Am J Hum Genet. 2013 Jul 11;93(1):173-80. doi: 10.1016/j.ajhg.2013.05.021. Epub 2013 Jun 20.
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NMR-based functional profiling of RASopathies and oncogenic RAS mutations.基于 NMR 的 RAS 通路病和致癌性 RAS 突变的功能谱分析。
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Differential allelic expression of IL13 and CSF2 genes associated with asthma.IL13 和 CSF2 基因的等位基因表达差异与哮喘有关。
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Skewed allele-specific expression of the NF1 gene in normal subjects: a possible mechanism for phenotypic variability in neurofibromatosis type 1.正常受试者中NF1基因的等位基因特异性表达偏倚:1型神经纤维瘤病表型变异性的一种可能机制。
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SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations.Noonan 综合征中的 SOS1 突变:分子谱、致病性影响的结构见解以及基因型-表型相关性。
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努南综合征家族中SOS1的差异等位基因表达及激活型SOS1 c.755C变异体的过表达

Differential allelic expression of SOS1 and hyperexpression of the activating SOS1 c.755C variant in a Noonan syndrome family.

作者信息

Moncini Silvia, Bonati Maria Teresa, Morella Ilaria, Ferrari Luca, Brambilla Riccardo, Riva Paola

机构信息

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale, Università degli Studi di Milano, Milan, Italy.

IRCCS Istituto Auxologico Italiano, Milan, Italy.

出版信息

Eur J Hum Genet. 2015 Nov;23(11):1531-7. doi: 10.1038/ejhg.2015.20. Epub 2015 Feb 25.

DOI:10.1038/ejhg.2015.20
PMID:25712082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4613488/
Abstract

Noonan syndrome (NS) is a genetic condition characterized by congenital heart defects, short stature and characteristic facial features. We here present the case of a girl with moderate learning disabilities, delayed language development, craniofacial features and skin anomalies reminiscent of NS. After a mutation screening of the known NS genes PTPN11, SOS1, RAF1, KRAS, GRB2, BRAF and SHOC2 we found the heterozygous c.755T>C variant in SOS1 causing the p.I252T amino-acid substitution, which was considered possibly pathogenetic by bioinformatic predictions. The same variant was present in the proband's mother, displaying some NS features, and maternal grandfather showing no NS traits, but also by a healthy subject in 1000 genomes project database without phenotype informations. The functional analysis revealed that SOS1 c.755C activated the RAS-ERK intracellular pathway, whereas no effects on RAC-JNK cascade have been detected. After a comparison between the sequence of SOS1 cDNA from peripheral blood and SOS1 genomic DNA, we showed for the first time a differential allelic expression of the SOS1 gene in healthy individuals, thus occurring as a physiologic condition. Interestingly, we found that the mutated allele C was 50% more expressed than the wild-type allele T in all familial carriers. The comparable amount of SOS1 mRNA between mutated individuals and the controls indicates that the variant does not affect SOS1 expression. The present study provides a first evidence of allelic imbalance of SOS1 and pinpoints this condition as a possible mechanism underlying a different penetrance of some SOS1-mutated alleles in unrelated carriers.

摘要

努南综合征(NS)是一种遗传性疾病,其特征为先天性心脏缺陷、身材矮小和典型的面部特征。我们在此报告一例患有中度学习障碍、语言发育迟缓、颅面特征和皮肤异常的女孩病例,这些表现让人联想到努南综合征。在对已知的努南综合征基因PTPN11、SOS1、RAF1、KRAS、GRB2、BRAF和SHOC2进行突变筛查后,我们在SOS1基因中发现了杂合的c.755T>C变异,该变异导致p.I252T氨基酸替换,通过生物信息学预测认为其可能具有致病性。先证者的母亲也存在相同变异,有一些努南综合征特征,而外祖父无努南综合征特征,但在1000基因组计划数据库中的一名无表型信息的健康个体中也发现了该变异。功能分析显示,SOS1 c.755C激活了RAS-ERK细胞内信号通路,而未检测到对RAC-JNK级联反应的影响。在比较外周血SOS1 cDNA序列和SOS1基因组DNA后,我们首次在健康个体中发现了SOS1基因的差异等位基因表达,这是一种生理状态。有趣的是,我们发现所有家族携带者中,突变等位基因C的表达比野生型等位基因T高50%。突变个体与对照组之间SOS1 mRNA的量相当,表明该变异不影响SOS1的表达。本研究首次提供了SOS1等位基因失衡的证据,并指出这种情况可能是一些SOS1突变等位基因在无关携带者中具有不同外显率的潜在机制。