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Discordant MZ Twins With Cleft Lip and Palate: A Model for Identifying Genes in Complex Traits


Author(s): Maria Adela Mansilla | Jane Kimani | Laura E Mitchell | Kaare Christensen | Dorret I Boomsma | Sandy Daack-Hirsch | Buena Nepomucena | Diego F Wyszynski | Temis M Felix | Nicholas G Martin | Jeffrey C Murray
doi: 10.1375/twin.8.1.39
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  Twin Research and Human Genetics
 
Print ISSN: 1832-4274
Volume: 8 | Issue: 1
Cover date: February 2005
Page(s): 39-46
 
 
  Abstract

Monozygotic (MZ) twins may be discordant for complex traits due to differential environmental exposure in utero, epigenetic variability in imprinting, X chromosome inactivation, or stochastic effects. Occasionally MZ twins may be discordant for chromosomal and single gene disorders due to somatic mosaicism. For complex traits, which are due to the interactive effects of multiple genes and environmental factors, the affected twin of a discordant MZ pair offers the possibility for identifying somatic mutations in candidate genes. DNA sequencing of candidate genes in discordant MZ twins can identify those rare etiologic mutational events responsible for the different phenotypes since the confounding effects of common single nucleotide polymorphisms are eliminated, as DNA sequences should be identical in MZ pairs. In this report we describe the extensive DNA sequencing of 18 candidate genes in a sample of MZ and dizygotic (DZ) twins with nonsyndromic cleft lip with or without cleft palate. We were unable to identify any somatic differences in approximately 34 Kb of DNA sequenced in 13 MZ pairs, for a total of approximately 900 Kb of sequence comparisons, supporting the hypothesis that nonetiologic posttwinning mutations are rare. While no etiologic variants were identified in this study, sequence comparisons of discordant MZ twins can serve as a tool for identifying etiologic mutations in clefting and other complex traits.

 
  Author(s) affiliations
 
1University of Iowa, Department of Pediatrics, Iowa City, Iowa, United States of America.
2University of Iowa, Department of Pediatrics, Iowa City, Iowa, United States of America.
3The Texas A & M University System, Health Science Center, Institute of Biosciences and Technology, Houston, Texas, United States of America.
4Institute of Public Health, University of Southern Denmark: Main Campus, Odense University, Odense, Denmark.
5Department of Biological Psychology, Vrije Universiteit, Amsterdam, the Netherlands.
6University of Iowa, Department of Pediatrics, Iowa City, Iowa, United States of America.
7Hope Foundation, Bacolod City, Philippines.
8Boston University School of Medicine, Genetics Program, Boston, Massachusetts, United States of America.
9Medical Genetics Service, Hospital de Clinicas de Porto Alegre, Porto Alegre, Brazil.
10Genetic Epidemiology Unit, Queensland Institute of Medical Research, Brisbane, Australia.
11University of Iowa, Department of Pediatrics, Iowa City, Iowa, United States of America; Institute of Public Health, University of Southern Denmark: Main Campus, Odense University, Odense, Denmark.
*Address for correspondence: Jeffrey C. Murray, University of Iowa, Department of Pediatrics, 2182 ML, S Grand Avenue, Iowa City, Iowa 52242, USA.
 
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X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate.
Jane W. Kimani, Min Shi, Sandra Daack-Hirsch, Kaare Christensen, Danilo Moretti-Ferreira, Mary L. Marazita, L. Leigh Field, John W. Canady, Jeffrey C. Murray.
American Journal of Medical Genetics Part A |  143a |  24 |  3267
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