HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Jagged1 (JAG1) mutations in patients with tetralogy of Fallot or pulmonic stenosis.

Abstract
Mutations in the Notch pathway ligand Jagged1 (JAG1) cause Alagille syndrome (AGS), as well as cardiac defects in seemingly nonsyndromic individuals. To estimate the frequency of JAG1 mutations in cases with right-sided cardiac defects not otherwise diagnosed with AGS, we screened 94 cases with tetralogy of Fallot (TOF) and 50 with pulmonic stenosis/peripheral pulmonary stenosis (PS/PPS) or pulmonary valve atresia with intact ventricular septum (PA) for mutations. Sequence changes were identified in three TOF and three PS/PPS/PA patients, that were not present in 100 controls. We identified one frameshift and two missense mutations in the TOF cases, and one frameshift and two missense mutations in cases with PS/PPS/PA. The four missense mutations were assayed for their effect on protein localization, posttranslational modification, and ability to activate Notch signaling. The missense mutants displayed heterogeneous behavior in these assays, some with complete haploinsufficiency, suggesting that there are additional modifiers leading to organ specific features. We identified functionally significant mutations in 2% (2/94) of TOF patients and 4% (2/50) of PS/PPS/PA patients. Patients with right-sided cardiac defects should be carefully screened for features of AGS or a family history of cardiac defects that might suggest the presence of a JAG1 mutation.
AuthorsRobert C Bauer, Ayanna O Laney, Rosemarie Smith, Jennifer Gerfen, Jennifer J D Morrissette, Stacy Woyciechowski, Jennifer Garbarini, Kathleen M Loomes, Ian D Krantz, Zsolt Urban, Bruce D Gelb, Elizabeth Goldmuntz, Nancy B Spinner
JournalHuman mutation (Hum Mutat) Vol. 31 Issue 5 Pg. 594-601 (May 2010) ISSN: 1098-1004 [Electronic] United States
PMID20437614 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Copyright(c) 2010 Wiley-Liss, Inc.
Chemical References
  • Calcium-Binding Proteins
  • Intercellular Signaling Peptides and Proteins
  • JAG1 protein, human
  • Jag1 protein, mouse
  • Jagged-1 Protein
  • Membrane Proteins
  • Serrate-Jagged Proteins
Topics
  • Alagille Syndrome (genetics)
  • Animals
  • Calcium-Binding Proteins (genetics, metabolism)
  • DNA Mutational Analysis
  • Female
  • Glycosylation
  • Humans
  • Intercellular Signaling Peptides and Proteins (genetics, metabolism)
  • Jagged-1 Protein
  • Male
  • Membrane Proteins (genetics, metabolism)
  • Mice
  • Mutation
  • Mutation, Missense
  • NIH 3T3 Cells
  • Pedigree
  • Protein Processing, Post-Translational
  • Pulmonary Valve Stenosis (genetics)
  • Serrate-Jagged Proteins
  • Signal Transduction (genetics)
  • Tetralogy of Fallot (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: