Familial Diarrhea Syndrome Caused by an Activating GUCY2C Mutation

被引:151
作者
Fiskerstrand, Torunn [1 ,4 ]
Arshad, Najla [6 ]
Haukanes, Bjorn Ivar [1 ]
Tronstad, Rune Rose [3 ]
Pham, Khanh Do-Cong [2 ]
Johansson, Stefan [1 ,5 ]
Havik, Bjarte [1 ,4 ]
Tonder, Siv L. [1 ]
Levy, Shawn E. [7 ]
Brackman, Damien [3 ]
Boman, Helge [1 ]
Biswas, Kabir Hassan [6 ]
Apold, Jaran [1 ]
Hovdenak, Nils [2 ]
Visweswariah, Sandhya S. [6 ]
Knappskog, Per M. [1 ,4 ]
机构
[1] Haukeland Hosp, Ctr Med Genet & Mol Med, N-5021 Bergen, Norway
[2] Haukeland Hosp, Dept Internal Med, N-5021 Bergen, Norway
[3] Haukeland Hosp, Dept Pediat, N-5021 Bergen, Norway
[4] Univ Bergen, Dept Clin Med, Bergen, Norway
[5] Univ Bergen, Dept Biomed, Bergen, Norway
[6] Indian Inst Sci, Dept Mol Reprod Dev & Genet, Bangalore 560012, Karnataka, India
[7] HudsonAlpha Inst Biotechnol, Huntsville, AL USA
关键词
VASOACTIVE INTESTINAL POLYPEPTIDE; FUNCTIONAL ABDOMINAL-PAIN; IRRITABLE-BOWEL-SYNDROME; CROHNS-DISEASE; CLINICAL MANAGEMENT; NITRIC-OXIDE; CYCLASE-C; INFLAMMATION; DYSFUNCTION; MICE;
D O I
10.1056/NEJMoa1110132
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Familial diarrhea disorders are, in most cases, severe and caused by recessive mutations. We describe the cause of a novel dominant disease in 32 members of a Norwegian family. The affected members have chronic diarrhea that is of early onset, is relatively mild, and is associated with increased susceptibility to inflammatory bowel disease, small-bowel obstruction, and esophagitis. METHODS We used linkage analysis, based on arrays with single-nucleotide polymorphisms, to identify a candidate region on chromosome 12 and then sequenced GUCY2C, encoding guanylate cyclase C (GC-C), an intestinal receptor for bacterial heat-stable enterotoxins. We performed exome sequencing of the entire candidate region from three affected family members, to exclude the possibility that mutations in genes other than GUCY2C could cause or contribute to susceptibility to the disease. We carried out functional studies of mutant GC-C using HEK293T cells. RESULTS We identified a heterozygous missense mutation (c.2519G -> T) in GUCY2C in all affected family members and observed no other rare variants in the exons of genes in the candidate region. Exposure of the mutant receptor to its ligands resulted in markedly increased production of cyclic guanosine monophosphate (cGMP). This may cause hyperactivation of the cystic fibrosis transmembrane regulator (CFTR), leading to increased chloride and water secretion from the enterocytes, and may thus explain the chronic diarrhea in the affected family members. CONCLUSIONS Increased GC-C signaling disturbs normal bowel function and appears to have a proinflammatory effect, either through increased chloride secretion or additional effects of elevated cellular cGMP. Further investigation of the relevance of genetic variants affecting the GC-C-CFTR pathway to conditions such as Crohn's disease is warranted. (Funded by Helse Vest [Western Norway Regional Health Authority] and the Department of Science and Technology, Government of India.)
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收藏
页码:1586 / 1595
页数:10
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