Literature DB >> 17337617

Cleft lip with or without cleft palate: implication of the heavy chain of non-muscle myosin IIA.

Marcella Martinelli, Mariateresa Di Stazio, Luca Scapoli, Jlenia Marchesini, Filomena Di Bari, Furio Pezzetti, Francesco Carinci, Annalisa Palmieri, Paolo Carinci, Anna Savoia.   

Abstract

Non-syndromic cleft lip with or without palate (CL/P) is one of the most common malformations among live births, but most of the genetic components and environmental factors involved remain to be identified. Among the different causes, MYH9, the gene encoding for the heavy chain of non-muscle myosin IIA, was considered a potential candidate, because it was found to be abundantly and specifically expressed in epithelial cells of palatal shelves before fusion. After fusion, its expression level was shown to decrease and to become limited to epithelial triangles before disappearing, as fusion is completed. To determine whether MYH9 plays a role in CL/P aetiology, a family-based association analysis was performed in 218 case/parent triads using single-nucleotide polymorphism (SNP) markers. Pairwise and multilocus haplotype analyses identified linkage disequilibrium between polymorphism alleles at the MYH9 locus and the disease. The strongest deviation from a null hypothesis of random sharing was obtained with two adjacent SNPs, rs3752462 and rs2009930 (global p value = 0.001), indicating that MYH9 might be a predisposing factor for CL/P, although its pathogenetic role needs to be investigated more accurately.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17337617      PMCID: PMC2740885          DOI: 10.1136/jmg.2006.047837

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  34 in total

Review 1.  Myosins: a diverse superfamily.

Authors:  J R Sellers
Journal:  Biochim Biophys Acta       Date:  2000-03-17

2.  GOLD--graphical overview of linkage disequilibrium.

Authors:  G R Abecasis; W O Cookson
Journal:  Bioinformatics       Date:  2000-02       Impact factor: 6.937

3.  Pedigree disequilibrium tests for multilocus haplotypes.

Authors:  Frank Dudbridge
Journal:  Genet Epidemiol       Date:  2003-09       Impact factor: 2.135

Review 4.  Recent developments in orofacial cleft genetics.

Authors:  Francesco Carinci; Furio Pezzetti; Luca Scapoli; Marcella Martinelli; Anna Avantaggiato; Paolo Carinci; Ernesto Padula; Ugo Baciliero; Fernando Gombos; Gregorio Laino; Rosario Rullo; Roberto Cenzi; Fredrick Carls; Mauro Tognon
Journal:  J Craniofac Surg       Date:  2003-03       Impact factor: 1.046

5.  Medial edge epithelial cell fate during palatal fusion.

Authors:  C Martínez-Alvarez; C Tudela; J Pérez-Miguelsanz; S O'Kane; J Puerta; M W Ferguson
Journal:  Dev Biol       Date:  2000-04-15       Impact factor: 3.582

6.  Programmed cell death is required for palate shelf fusion and is regulated by retinoic acid.

Authors:  Rodrigo Cuervo; Concepción Valencia; Roshantha A S Chandraratna; Luis Covarrubias
Journal:  Dev Biol       Date:  2002-05-01       Impact factor: 3.582

7.  Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome.

Authors:  Samuel Deutsch; Alexandra Rideau; Marie-Luce Bochaton-Piallat; Giuseppe Merla; Antoine Geinoz; Giulio Gabbiani; Torsten Schwede; Thomas Matthes; Stylianos E Antonarakis; Photis Beris
Journal:  Blood       Date:  2003-03-20       Impact factor: 22.113

8.  Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations.

Authors:  Shinji Kunishima; Tadashi Matsushita; Tetsuhito Kojima; Masahiro Sako; Fumihiro Kimura; Eun-Kyeong Jo; Chikako Inoue; Tadashi Kamiya; Hidehiko Saito
Journal:  Lab Invest       Date:  2003-01       Impact factor: 5.662

9.  Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.

Authors:  Shinji Kondo; Brian C Schutte; Rebecca J Richardson; Bryan C Bjork; Alexandra S Knight; Yoriko Watanabe; Emma Howard; Renata L L Ferreira de Lima; Sandra Daack-Hirsch; Achim Sander; Donna M McDonald-McGinn; Elaine H Zackai; Edward J Lammer; Arthur S Aylsworth; Holly H Ardinger; Andrew C Lidral; Barbara R Pober; Lina Moreno; Mauricio Arcos-Burgos; Consuelo Valencia; Claude Houdayer; Michel Bahuau; Danilo Moretti-Ferreira; Antonio Richieri-Costa; Michael J Dixon; Jeffrey C Murray
Journal:  Nat Genet       Date:  2002-09-03       Impact factor: 38.330

10.  MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness.

Authors:  Marco Seri; Alessandro Pecci; Filomena Di Bari; Roberto Cusano; Maria Savino; Emanuele Panza; Alessandra Nigro; Patrizia Noris; Simone Gangarossa; Bianca Rocca; Paolo Gresele; Nicola Bizzaro; Paola Malatesta; Pasi A Koivisto; Ilaria Longo; Roberto Musso; Carmine Pecoraro; Achille Iolascon; Umberto Magrini; Juan Rodriguez Soriano; Alessandra Renieri; Gian Marco Ghiggeri; Roberto Ravazzolo; Carlo L Balduini; Anna Savoia
Journal:  Medicine (Baltimore)       Date:  2003-05       Impact factor: 1.889

View more
  7 in total

1.  New insights in orofacial cleft: epidemiological and genetic studies on italian samples.

Authors:  L Tettamanti; A Avantaggiato; M Nardone; A Palmieri; A Tagliabue
Journal:  Oral Implantol (Rome)       Date:  2017-04-10

2.  Cleft palate only: current concepts.

Authors:  L Tettamanti; A Avantaggiato; M Nardone; J Silvestre-Rangil; A Tagliabue
Journal:  Oral Implantol (Rome)       Date:  2017-04-10

3.  Nonsyndromic cleft lip and palate: CRISPLD genes and the folate gene pathway connection.

Authors:  Brett T Chiquet; Robin Henry; Amber Burt; John B Mulliken; Samuel Stal; Susan H Blanton; Jacqueline T Hecht
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2010-11-15

4.  Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.

Authors:  Brett T Chiquet; Syed S Hashmi; Robin Henry; Amber Burt; John B Mulliken; Samuel Stal; Molly Bray; Susan H Blanton; Jacqueline T Hecht
Journal:  Eur J Hum Genet       Date:  2008-08-20       Impact factor: 4.246

5.  A point mutation in Myh10 causes major defects in heart development and body wall closure.

Authors:  Xuefei Ma; Robert S Adelstein
Journal:  Circ Cardiovasc Genet       Date:  2014-05-13

6.  Convergence and extrusion are required for normal fusion of the mammalian secondary palate.

Authors:  Seungil Kim; Ace E Lewis; Vivek Singh; Xuefei Ma; Robert Adelstein; Jeffrey O Bush
Journal:  PLoS Biol       Date:  2015-04-07       Impact factor: 8.029

7.  Nonsynonymous variants in MYH9 and ABCA4 are the most frequent risk loci associated with nonsyndromic orofacial cleft in Taiwanese population.

Authors:  Hsiu-Huei Peng; Nai-Chung Chang; Kuo-Ting Chen; Jang-Jih Lu; Pi-Yueh Chang; Shih-Cheng Chang; Yah-Huei Wu-Chou; Yi-Ting Chou; Wanni Phang; Po-Jen Cheng
Journal:  BMC Med Genet       Date:  2016-08-15       Impact factor: 2.103

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.