Literature DB >> 23121717

A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients.

Josine C C Widdershoven1, Mark Bowser, Molly B Sheridan, Donna M McDonald-McGinn, Elaine H Zackai, Cynthia B Solot, Richard E Kirschner, Frits A Beemer, Bernice E Morrow, Marcella Devoto, Beverly S Emanuel.   

Abstract

OBJECTIVE: Palatal anomalies are one of the identifying features of 22q11.2 deletion syndrome (22q11.2DS) affecting about one third of patients. To identify genetic variants that increase the risk of cleft or palatal anomalies in 22q11.2DS patients, we performed a candidate gene association study in 101 patients with 22q11.2DS genotyped with the Affymetrix genome-wide human SNP array 6.0.
METHODS: Patients from Children's Hospital of Philadelphia, USA and Wilhelmina Children's Hospital Utrecht, The Netherlands were stratified based on palatal phenotype (overt cleft, submucosal cleft, bifid uvula). SNPs in 21 candidate genes for cleft palate were analyzed for genotype-phenotype association. In addition, TBX1 sequencing was carried out. Quality control and association analyses were conducted using the software package PLINK.
RESULTS: Genotype and phenotype data of 101 unrelated patients (63 non-cleft subjects (62.4%), 38 cleft subjects (37.6%)) were analyzed. A Total of 39 SNPs on 10 genes demonstrated a p-value ≤0.05 prior to correction. The most significant SNPs were found on FGF10. However none of the SNPs remained significant after correcting for multiple testing.
CONCLUSIONS: Although these results are promising, analysis of additional samples will be required to confirm that variants in these regions influence risk for cleft palate or palatal anomalies in 22q11.2DS patients.
Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.

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Year:  2012        PMID: 23121717      PMCID: PMC4098838          DOI: 10.1016/j.ijporl.2012.10.009

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  27 in total

1.  MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.

Authors:  M J van den Boogaard; M Dorland; F A Beemer; H K van Amstel
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Review 2.  About face: signals and genes controlling jaw patterning and identity in vertebrates.

Authors:  Joy M Richman; Sang-Hwy Lee
Journal:  Bioessays       Date:  2003-06       Impact factor: 4.345

3.  DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1.

Authors:  L A Jerome; V E Papaioannou
Journal:  Nat Genet       Date:  2001-03       Impact factor: 38.330

4.  TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.

Authors:  S Merscher; B Funke; J A Epstein; J Heyer; A Puech; M M Lu; R J Xavier; M B Demay; R G Russell; S Factor; K Tokooya; B S Jore; M Lopez; R K Pandita; M Lia; D Carrion; H Xu; H Schorle; J B Kobler; P Scambler; A Wynshaw-Boris; A I Skoultchi; B E Morrow; R Kucherlapati
Journal:  Cell       Date:  2001-02-23       Impact factor: 41.582

5.  TGF-beta mediated FGF10 signaling in cranial neural crest cells controls development of myogenic progenitor cells through tissue-tissue interactions during tongue morphogenesis.

Authors:  Ryoichi Hosokawa; Kyoko Oka; Takayoshi Yamaza; Junichi Iwata; Mark Urata; Xun Xu; Pablo Bringas; Kazuaki Nonaka; Yang Chai
Journal:  Dev Biol       Date:  2010-02-26       Impact factor: 3.582

6.  Family-based analysis of MSX1 haplotypes for association with oral clefts.

Authors:  M Daniele Fallin; Jacqueline B Hetmanski; Jiwan Park; Alan F Scott; Roxann Ingersoll; Hans A Fuernkranz; Iain McIntosh; Terri H Beaty
Journal:  Genet Epidemiol       Date:  2003-09       Impact factor: 2.135

7.  Identification of SATB2 as the cleft palate gene on 2q32-q33.

Authors:  David R FitzPatrick; Ian M Carr; Lorna McLaren; Jack P Leek; Patrick Wightman; Kathy Williamson; Philippe Gautier; Niolette McGill; Caroline Hayward; Helen Firth; Alex F Markham; Judy A Fantes; David T Bonthron
Journal:  Hum Mol Genet       Date:  2003-07-29       Impact factor: 6.150

8.  Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!

Authors:  D M McDonald-McGinn; M K Tonnesen; A Laufer-Cahana; B Finucane; D A Driscoll; B S Emanuel; E H Zackai
Journal:  Genet Med       Date:  2001 Jan-Feb       Impact factor: 8.822

9.  FGF10 maintains stem cell compartment in developing mouse incisors.

Authors:  Hidemitsu Harada; Takashi Toyono; Kuniaki Toyoshima; Masahiro Yamasaki; Nobuyuki Itoh; Shigeaki Kato; Keisuke Sekine; Hideyo Ohuchi
Journal:  Development       Date:  2002-03       Impact factor: 6.868

10.  Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate.

Authors:  Ritva Rice; Bradley Spencer-Dene; Elaine C Connor; Amel Gritli-Linde; Andrew P McMahon; Clive Dickson; Irma Thesleff; David P C Rice
Journal:  J Clin Invest       Date:  2004-06       Impact factor: 14.808

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  7 in total

Review 1.  22q11.2 deletion syndrome.

Authors:  Donna M McDonald-McGinn; Kathleen E Sullivan; Bruno Marino; Nicole Philip; Ann Swillen; Jacob A S Vorstman; Elaine H Zackai; Beverly S Emanuel; Joris R Vermeesch; Bernice E Morrow; Peter J Scambler; Anne S Bassett
Journal:  Nat Rev Dis Primers       Date:  2015-11-19       Impact factor: 52.329

Review 2.  The 22q11.2 Microdeletion in Pediatric Patients with Cleft Lip, Palate, or Both and Congenital Heart Disease: A Systematic Review.

Authors:  Diana Cárdenas-Nieto; Maribel Forero-Castro; Clara Esteban-Pérez; Julio Martínez-Lozano; Ignacio Briceño-Balcázar
Journal:  J Pediatr Genet       Date:  2019-10-23

3.  A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome.

Authors:  Matthew Jensen; R Frank Kooy; Tony J Simon; Edwin Reyniers; Santhosh Girirajan; Flora Tassone
Journal:  Eur J Med Genet       Date:  2017-11-28       Impact factor: 2.708

4.  22q and two: 22q11.2 deletion syndrome and coexisting conditions.

Authors:  Jennifer L Cohen; Terrence B Crowley; Daniel E McGinn; Carey McDougall; Marta Unolt; Michele P Lambert; Beverly S Emanuel; Elaine H Zackai; Donna M McDonald-McGinn
Journal:  Am J Med Genet A       Date:  2018-09-23       Impact factor: 2.802

Review 5.  Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome.

Authors:  Blaine Crowley; Melanie Ruffner; Donna M McDonald McGinn; Kathleen E Sullivan
Journal:  Am J Med Genet A       Date:  2018-01-17       Impact factor: 2.802

6.  Association of Nucleotide Variants of GRHL3, IRF6, NAT2, SDC2, BCL3, and PVRL1 Genes with Nonsyndromic Cleft Lip With/Without Cleft Palate in Multigenerational Families: A Retrospective Study.

Authors:  Praveen Kumar Neela; Srinivas Reddy Gosla; Akhter Husain; Vasavi Mohan; Sravya Thumoju; B V Rajeshwari
Journal:  Contemp Clin Dent       Date:  2021-06-14

7.  MicroRNA-17-92, a direct Ap-2α transcriptional target, modulates T-box factor activity in orofacial clefting.

Authors:  Jun Wang; Yan Bai; Hong Li; Stephanie B Greene; Elzbieta Klysik; Wei Yu; Robert J Schwartz; Trevor J Williams; James F Martin
Journal:  PLoS Genet       Date:  2013-09-19       Impact factor: 5.917

  7 in total

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