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Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36.
Zaveri, Hitisha P; Beck, Tyler F; Hernández-García, Andrés; Shelly, Katharine E; Montgomery, Tara; van Haeringen, Arie; Anderlid, Britt-Marie; Patel, Chirag; Goel, Himanshu; Houge, Gunnar; Morrow, Bernice E; Cheung, Sau Wai; Lalani, Seema R; Scott, Daryl A.
Afiliación
  • Zaveri HP; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
  • Beck TF; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
  • Hernández-García A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
  • Shelly KE; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
  • Montgomery T; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • van Haeringen A; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Anderlid BM; Clinical Genetic Department, Karolinska University Hospital and Institution of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Patel C; Department of Clinical Genetics, Birmingham Women's Hospital, Birmingham, United Kingdom.
  • Goel H; Faculty of Health and Medicine, University of Newcastle, Callaghan, New South Wales, Australia.
  • Houge G; Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway.
  • Morrow BE; Department of Genetics, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Cheung SW; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
  • Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
  • Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America ; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas, United States of America.
PLoS One ; 9(1): e85600, 2014.
Article en En | MEDLINE | ID: mdl-24454898
Cardiovascular malformations and cardiomyopathy are among the most common phenotypes caused by deletions of chromosome 1p36 which affect approximately 1 in 5000 newborns. Although these cardiac-related abnormalities are a significant source of morbidity and mortality associated with 1p36 deletions, most of the individual genes that contribute to these conditions have yet to be identified. In this paper, we use a combination of clinical and molecular cytogenetic data to define five critical regions for cardiovascular malformations and two critical regions for cardiomyopathy on chromosome 1p36. Positional candidate genes which may contribute to the development of cardiovascular malformations associated with 1p36 deletions include DVL1, SKI, RERE, PDPN, SPEN, CLCNKA, ECE1, HSPG2, LUZP1, and WASF2. Similarly, haploinsufficiency of PRDM16-a gene which was recently shown to be sufficient to cause the left ventricular noncompaction-SKI, PRKCZ, RERE, UBE4B and MASP2 may contribute to the development of cardiomyopathy. When treating individuals with 1p36 deletions, or providing prognostic information to their families, physicians should take into account that 1p36 deletions which overlie these cardiac critical regions may portend to cardiovascular complications. Since several of these cardiac critical regions contain more than one positional candidate gene-and large terminal and interstitial 1p36 deletions often overlap more than one cardiac critical region-it is likely that haploinsufficiency of two or more genes contributes to the cardiac phenotypes associated with many 1p36 deletions.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 1 / Enfermedades Cardiovasculares / Eliminación de Gen / Anomalías Cardiovasculares Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 1 / Enfermedades Cardiovasculares / Eliminación de Gen / Anomalías Cardiovasculares Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos