MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus
| Autor: | Xueping Fan, Anna Kamp, Ivan P. Moskowitz, Fabiola Quintero-Rivera, Anne W. Higgins, Ronald Berezney, Amy E. Roberts, Kasper Lage, Cynthia C. Morton, Ji Hyun Lee, Ihn Sik Seong, Weining Lu, Ronald V. Lacro, Raymond M. Anchan, Xuchen Hu, Qiongchao J. Xi, Bruce D. Gelb, Joanna Tao, James F. Gusella, Lily Y. Lu, Richard L. Maas, Kim M. Keppler-Noreuil |
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| Rok vydání: | 2015 |
| Předmět: |
Aortic valve
Male Heart disease Heart Valve Diseases Cardiovascular Medical and Health Sciences Translocation Genetic Mice Bicuspid aortic valve Bicuspid Aortic Valve Disease Nuclear Matrix-Associated Proteins Ductus arteriosus 2.1 Biological and endogenous factors Ventricular outflow tract Aetiology Child Ductus Arteriosus Patent Genetics (clinical) Pediatric Genetics & Heredity DUCTUS ARTERIOSUS PATENT RNA-Binding Proteins General Medicine Anatomy Articles Biological Sciences DNA-Binding Proteins Heart Disease medicine.anatomical_structure Aortic Valve Child Preschool cardiovascular system Cardiology Patent Female endocrine system medicine.medical_specialty congenital hereditary and neonatal diseases and abnormalities Adolescent Heart Ventricles Translocation Biology Aortic Coarctation Genetic Insertional Internal medicine Genetics medicine Animals Humans Gene Silencing Preschool Molecular Biology Infant Newborn Infant Ductus Arteriosus Newborn medicine.disease Infant newborn Mutagenesis Insertional Mutagenesis Congenital Structural Anomalies |
| Zdroj: | Human Molecular Genetics Human molecular genetics, vol 24, iss 8 |
| ISSN: | 1460-2083 |
| Popis: | Cardiac left ventricular outflow tract (LVOT) defects represent a common but heterogeneous subset of congenital heart disease for which gene identification has been difficult. We describe a 46,XY,t(1;5)(p36.11;q31.2)dn translocation carrier with pervasive developmental delay who also exhibited LVOT defects, including bicuspid aortic valve (BAV), coarctation of the aorta (CoA) and patent ductus arteriosus (PDA). The 1p breakpoint disrupts the 5' UTR of AHDC1, which encodes AT-hook DNA-binding motif containing-1 protein, and AHDC1-truncating mutations have recently been described in a syndrome that includes developmental delay, but not congenital heart disease [Xia, F., Bainbridge, M.N., Tan, T.Y., Wangler, M.F., Scheuerle, A.E., Zackai, E.H., Harr, M.H., Sutton, V.R., Nalam, R.L., Zhu, W. et al. (2014) De Novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea. Am. J. Hum. Genet., 94, 784-789]. On the other hand, the 5q translocation breakpoint disrupts the 3' UTR of MATR3, which encodes the nuclear matrix protein Matrin 3, and mouse Matr3 is strongly expressed in neural crest, developing heart and great vessels, whereas Ahdc1 is not. To further establish MATR3 3' UTR disruption as the cause of the proband's LVOT defects, we prepared a mouse Matr3(Gt-ex13) gene trap allele that disrupted the 3' portion of the gene. Matr3(Gt-ex13) homozygotes are early embryo lethal, but Matr3(Gt-ex13) heterozygotes exhibit incompletely penetrant BAV, CoA and PDA phenotypes similar to those in the human proband, as well as ventricular septal defect (VSD) and double-outlet right ventricle (DORV). Both the human MATR3 translocation breakpoint and the mouse Matr3(Gt-ex13) gene trap insertion disturb the polyadenylation of MATR3 transcripts and alter Matrin 3 protein expression, quantitatively or qualitatively. Thus, subtle perturbations in Matrin 3 expression appear to cause similar LVOT defects in human and mouse. |
| Databáze: | OpenAIRE |
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