Literature DB >> 20186050

The molecular genetics of congenital heart disease: a review of recent developments.

Michael Wolf1, Craig T Basson.   

Abstract

PURPOSE OF REVIEW: Our understanding of the interactions of genes and pathways during heart development continues to expand with our knowledge of the genetic basis of congenital heart disease. Along with the discovery of specific genes that cause lesions, recent research has focused on the interactions of some previously identified genes. This review focuses on the progress made during the last year. RECENT
FINDINGS: T-box, NK, and GATA transcription factors have known associations with a variety of syndromic and isolated congenital heart defects. Discovery of novel interactions of GATA and T-box transcription factors highlights the direction of recent research. In addition, the critical yet somewhat redundant roles of nkx2.5 and nkx2.7, along with the interaction of nkx2.7 with tbx20, have been elucidated. The contributions of still other transcription factor classes are being elucidated. Further understanding of 22q11.2 deletion and microduplication syndromes and their genetic interactions has also been studied. Recent work also highlights PTPN11 and NOTCH1 in Noonan syndrome.
SUMMARY: The recent developments in the genetics of congenital heart disease are reviewed. In many cases, it is the novel interactions of previously known genes that highlight this year's developments. These interactions will ultimately lead to better understanding of downstream transcriptional or signaling pathways.

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Year:  2010        PMID: 20186050      PMCID: PMC2930935          DOI: 10.1097/HCO.0b013e328337b4ce

Source DB:  PubMed          Journal:  Curr Opin Cardiol        ISSN: 0268-4705            Impact factor:   2.161


  52 in total

1.  Formation of the sinus node head and differentiation of sinus node myocardium are independently regulated by Tbx18 and Tbx3.

Authors:  Cornelia Wiese; Thomas Grieskamp; Rannar Airik; Mathilda T M Mommersteeg; Ajmal Gardiwal; Corrie de Gier-de Vries; Karin Schuster-Gossler; Antoon F M Moorman; Andreas Kispert; Vincent M Christoffels
Journal:  Circ Res       Date:  2008-12-18       Impact factor: 17.367

Review 2.  Bridging the gap between anatomy and molecular genetics for an improved understanding of congenital heart disease.

Authors:  Stella Marie Reamon-Buettner; Katharina Spanel-Borowski; Jürgen Borlak
Journal:  Ann Anat       Date:  2006-05       Impact factor: 2.698

3.  Expression of active Notch1 in avian coronary development.

Authors:  Ke Yang; Yong-Qiu Doughman; Ganga Karunamuni; Shi Gu; Yu-Chung Yang; David M Bader; Michiko Watanabe
Journal:  Dev Dyn       Date:  2009-01       Impact factor: 3.780

4.  Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development.

Authors:  Meenakshi Maitra; Marie K Schluterman; Haley A Nichols; James A Richardson; Cecilia W Lo; Deepak Srivastava; Vidu Garg
Journal:  Dev Biol       Date:  2008-11-20       Impact factor: 3.582

5.  Deletion of JAM-C, a candidate gene for heart defects in Jacobsen syndrome, results in a normal cardiac phenotype in mice.

Authors:  Maoqing Ye; Rabih Hamzeh; Amy Geddis; Nissi Varki; M Benjamin Perryman; Paul Grossfeld
Journal:  Am J Med Genet A       Date:  2009-07       Impact factor: 2.802

6.  The Tbx2+ primary myocardium of the atrioventricular canal forms the atrioventricular node and the base of the left ventricle.

Authors:  Wim T J Aanhaanen; Janynke F Brons; Jorge N Domínguez; M Sameer Rana; Julia Norden; Rannar Airik; Vincent Wakker; Corrie de Gier-de Vries; Nigel A Brown; Andreas Kispert; Antoon F M Moorman; Vincent M Christoffels
Journal:  Circ Res       Date:  2009-05-07       Impact factor: 17.367

7.  Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype-phenotype correlations.

Authors:  Maria Lisa Dentici; Anna Sarkozy; Francesca Pantaleoni; Claudio Carta; Francesca Lepri; Rosangela Ferese; Viviana Cordeddu; Simone Martinelli; Silvana Briuglia; Maria Cristina Digilio; Giuseppe Zampino; Marco Tartaglia; Bruno Dallapiccola
Journal:  Eur J Hum Genet       Date:  2009-01-21       Impact factor: 4.246

8.  Noonan syndrome cardiac defects are caused by PTPN11 acting in endocardium to enhance endocardial-mesenchymal transformation.

Authors:  Toshiyuki Araki; Gordon Chan; Susan Newbigging; Lily Morikawa; Roderick T Bronson; Benjamin G Neel
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-27       Impact factor: 11.205

9.  Investigation of somatic NKX2-5 mutations in congenital heart disease.

Authors:  J M Draus; M A Hauck; M Goetsch; E H Austin; A Tomita-Mitchell; M E Mitchell
Journal:  J Med Genet       Date:  2009-02       Impact factor: 6.318

10.  Nkx2.7 and Nkx2.5 function redundantly and are required for cardiac morphogenesis of zebrafish embryos.

Authors:  Chi-Tang Tu; Tzu-Ching Yang; Huai-Jen Tsai
Journal:  PLoS One       Date:  2009-01-22       Impact factor: 3.240

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  25 in total

1.  Initial deployment of the cardiogenic gene regulatory network in the basal chordate, Ciona intestinalis.

Authors:  Arielle Woznica; Maximilian Haeussler; Ella Starobinska; Jessica Jemmett; Younan Li; David Mount; Brad Davidson
Journal:  Dev Biol       Date:  2012-05-14       Impact factor: 3.582

2.  A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects.

Authors:  Fei Long; Xike Wang; Shaohai Fang; Yuejuan Xu; Kun Sun; Sun Chen; Rang Xu
Journal:  PLoS One       Date:  2013-08-29       Impact factor: 3.240

Review 3.  Syndromic Hirschsprung's disease and associated congenital heart disease: a systematic review.

Authors:  Johannes W Duess; Prem Puri
Journal:  Pediatr Surg Int       Date:  2015-07-09       Impact factor: 1.827

Review 4.  The programming of cardiovascular disease.

Authors:  K L Thornburg
Journal:  J Dev Orig Health Dis       Date:  2015-07-15       Impact factor: 2.401

5.  Associations between maternal genotypes and metabolites implicated in congenital heart defects.

Authors:  Shimul Chowdhury; Charlotte A Hobbs; Stewart L MacLeod; Mario A Cleves; Stepan Melnyk; S Jill James; Ping Hu; Stephen W Erickson
Journal:  Mol Genet Metab       Date:  2012-09-27       Impact factor: 4.797

6.  NEXN inhibits GATA4 and leads to atrial septal defects in mice and humans.

Authors:  Fan Yang; Lei Zhou; Qiguang Wang; Xin You; Ying Li; Yong Zhao; Xiaonan Han; Zai Chang; Xin He; Chunyan Cheng; Chong Wu; Wen-Jing Wang; Fang-Yuan Hu; Ting Zhao; Yang Li; Ming Zhao; Gu-Yan Zheng; Jie Dong; Chun Fan; Juxian Yang; Xianmin Meng; Youyi Zhang; Xianyang Zhu; Jingwei Xiong; Xiao-Li Tian; Huiqing Cao
Journal:  Cardiovasc Res       Date:  2014-05-27       Impact factor: 10.787

7.  A single GATA factor plays discrete, lineage specific roles in ascidian heart development.

Authors:  Katerina Ragkousi; Jeni Beh; Sarah Sweeney; Ella Starobinska; Brad Davidson
Journal:  Dev Biol       Date:  2011-01-14       Impact factor: 3.582

8.  Myocardin regulates BMP10 expression and is required for heart development.

Authors:  Jianhe Huang; John Elicker; Nina Bowens; Xi Liu; Lan Cheng; Thomas P Cappola; Xiaohong Zhu; Michael S Parmacek
Journal:  J Clin Invest       Date:  2012-09-17       Impact factor: 14.808

Review 9.  An Assessment of the Therapeutic Landscape for the Treatment of Heart Disease in the RASopathies.

Authors:  Jae-Sung Yi; Sravan Perla; Anton M Bennett
Journal:  Cardiovasc Drugs Ther       Date:  2022-02-14       Impact factor: 3.727

10.  The genotype and expression of the TGFβ2 gene in children with congenital conotruncal defects.

Authors:  Yingying Meng; Xiaojing Ma; Jing Zhang; Huijun Wang; Duan Ma; Guoying Huang
Journal:  Pediatr Cardiol       Date:  2013-05-28       Impact factor: 1.655

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