Alagille syndrome mutation update: Comprehensive overview of JAG1 and NOTCH2 mutation frequencies and insight into missense variant classification

被引:103
作者
Gilbert, Melissa A. [1 ,2 ]
Bauer, Robert C. [1 ,2 ]
Rajagopalari, Ramakrishnan [1 ,2 ]
Grochowski, Christopher M. [1 ,2 ]
Chao, Grace [1 ,2 ]
McEldrew, Deborah [1 ,2 ]
Nassur, James A. [1 ,2 ]
Rand, Elizabeth B. [2 ,3 ]
Krock, Bryan L. [1 ,2 ]
Kamath, Binita M. [4 ,5 ]
Krantz, Ian D. [6 ,7 ]
Piccoli, David A. [2 ,3 ]
Loomes, Kathleen M. [2 ,3 ]
Spinner, Nancy B. [1 ,2 ]
机构
[1] Univ Penn, Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Div Genom Diagnost, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Childrens Hosp Philadelphia, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Philadelphia, PA 19104 USA
[4] Hosp Sick Children, Dept Pediat, Div Gastroenterol Hepatol & Nutr, Toronto, ON, Canada
[5] Univ Toronto, Toronto, ON, Canada
[6] Childrens Hosp Philadelphia, Div Human Genet, Roberts Individualized Med Genet Ctr, Philadelphia, PA 19104 USA
[7] Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
Alagille syndrome; JAG1; liver; NOTCH2; COMPOUND HETEROZYGOUS MUTATIONS; ARTERIOHEPATIC DYSPLASIA; FUNCTIONAL-ANALYSIS; CLINICAL-FEATURES; JAGGED1; MUTATIONS; MONOZYGOTIC TWINS; GENETIC DIAGNOSIS; MOUSE MODEL; LIVER; LIGAND;
D O I
10.1002/humu.23879
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Alagille syndrome is an autosomal dominant disease with a known molecular etiology of dysfunctional Notch signaling caused primarily by pathogenic variants in JAGGED1 (JAG1), but also by variants in NOTCH2. The majority of JAG1 variants result in loss of function, however disease has also been attributed to lesser understood missense variants. Conversely, the majority of NOTCH2 variants are missense, though fewer of these variants have been described. In addition, there is a small group of patients with a clear clinical phenotype in the absence of a pathogenic variant. Here, we catalog our single-center study, which includes 401 probands and 111 affected family members amassed over a 27-year period, to provide updated mutation frequencies in JAG1 and NOTCH2 as well as functional validation of nine missense variants. Combining our cohort of 86 novel JAG1 and three novel NOTCH2 variants with previously published data (totaling 713 variants), we present the most comprehensive pathogenic variant overview for Alagille syndrome. Using this data set, we developed new guidance to help with the classification of JAG1 missense variants. Finally, we report clinically consistent cases for which a molecular etiology has not been identified and discuss the potential for next generation sequencing methodologies in novel variant discovery.
引用
收藏
页码:2197 / 2220
页数:24
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