Literature DB >> 33047712

[Exploring parent-of-origin effects for non-syndromic cleft lip with or without cleft palate on PTCH1, PTCH2, SHH, SMO genes in Chinese case-parent trios].

W Y Li1, M Y Wang1, R Zhou1, S Y Wang1, H C Zheng1, H P Zhu2, Z B Zhou2, T Wu1,3, H Wang1, B Shi4.   

Abstract

OBJECTIVE: Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect, affecting 1.4 per 1 000 live births, and multiple genetic and environmental risk factors influencing its risk. All the known genetic risk factors accounted for a small proportion of the heritability. Several authors have suggested parent-of-origin effects (PoO) may play an important role in the etiology of this complex and heterogeneous malformation. To clarify the genetic association between PTCH1, PTCH2, SHH and SMO in hedgehog (HH) pathway and NSCL/P, as well as testing for potential PoO effects in Chinese case-parent trios.
METHODS: We tested for transmission disequilibrium tests (TDT) and PoO effects using 83 common single nucleotide polymorphic (SNP) markers of HH pathway genes from 806 NSCL/P case-parent trios. These trios were drawn from an international consortium established for a genome-wide association studies (GWAS) of non-syndromic oral clefts of multiple ethnicities. DNA samples were collected from each trio. Single marker and haplotype based analysis were performed both in TDT tests and PoO effects. SNPs were excluded if they (ⅰ) had a call rate of &#60; 95%, (ⅱ) had a minor allele frequency (MAF) of &#60; 0.05, (ⅲ) had Mendelian errors over all trios of >5%, (ⅳ) had a genotype distribution in the parents that deviated from the Hardy-Weinberg equilibrium (HWE) (<i>P</i> &#60; 0.000 1). The process was done using Plink (version 1.07, <a href="http://pngu.mgh.harvard.edu/~purcell/plink/data.shtml" target="_blank">http://pngu.mgh.harvard.edu/~purcell/plink/data.shtml</a>). TDT test was performed in Plink v1.07. A log-linear model was used to explore PoO effects using Haplin v6.2.1 as implemented in R package v3.4.2. Significance level was assessed using the Bonferroni correction.
RESULTS: A total of 18 SNPs were dropped due to low MAF, thus leaving 65 SNPs available for the analysis. Thus the Bonferroni threshold was 7.7×10-4 (0.05/65). Nominal significant association with NSCL/P was found at a SNP (rs4448343 in PTCH1, P=0.023) and six haplotypes (rs10512249-rs4448343, rs1461208-rs7786445, rs10512249-rs4448343, rs16909865-rs10512249-rs4448343, rs1461208-rs7786445-rs12698335, and rs288756-rs288758-rs1151790, P < 0.05). A total of six haplotypes (rs288765-rs1233563, rs12537550-rs11765352, rs872723-rs288765-rs1233563, rs288765-rs1233563-rs288756, rs6459952-rs12537550-rs11765352, and rs12537550-rs11765352-rs6971211) showed PoO effect (P < 0.05). None of the results remained significant after the Bonferroni correction (P>7.7×10-4).
CONCLUSION: Neither significant association between SNPs within HH pathway and the risk of NSCL/P nor PoO effects was seen in this study.

Entities:  

Keywords:  Hedgehog pathway; Non-syndromic cleft lip with or without cleft palate; Parent-of-origin effects

Mesh:

Substances:

Year:  2020        PMID: 33047712      PMCID: PMC7653437     

Source DB:  PubMed          Journal:  Beijing Da Xue Xue Bao Yi Xue Ban        ISSN: 1671-167X


  33 in total

1.  A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population.

Authors:  Tânia Kawasaki de Araujo; Rodrigo Secolin; Têmis Maria Félix; Liliane Todeschini de Souza; Marshall Ítalo Barros Fontes; Isabella Lopes Monlleó; Josiane de Souza; Agnes Cristina Fett-Conte; Erlane Marques Ribeiro; Ana Carolina Xavier; Adriana Augusto de Rezende; Milena Simioni; Ândrea Kely Campos Ribeiro-dos-Santos; Sidney Emanuel Batista dos Santos; Vera Lúcia Gil-da-Silva-Lopes
Journal:  J Craniomaxillofac Surg       Date:  2015-08-13       Impact factor: 2.078

Review 2.  Prevalence of Orofacial Clefts among Live Births in China: A Systematic Review and Meta-Analysis.

Authors:  Mengying Wang; Yuan Yuan; Zifan Wang; Dongjing Liu; Zhuqing Wang; Feng Sun; Ping Wang; Hongping Zhu; Jing Li; Tao Wu; Terri H Beaty
Journal:  Birth Defects Res       Date:  2017-06-21       Impact factor: 2.344

3.  A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.

Authors:  Struan F A Grant; Kai Wang; Haitao Zhang; Wendy Glaberson; Kiran Annaiah; Cecilia E Kim; Jonathan P Bradfield; Joseph T Glessner; Kelly A Thomas; Maria Garris; Edward C Frackelton; F George Otieno; Rosetta M Chiavacci; Hyun-Duck Nah; Richard E Kirschner; Hakon Hakonarson
Journal:  J Pediatr       Date:  2009-08-04       Impact factor: 4.406

Review 4.  Development of the upper lip: morphogenetic and molecular mechanisms.

Authors:  Rulang Jiang; Jeffrey O Bush; Andrew C Lidral
Journal:  Dev Dyn       Date:  2006-05       Impact factor: 3.780

5.  Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.

Authors:  Elisabeth Mangold; Kerstin U Ludwig; Stefanie Birnbaum; Carlotta Baluardo; Melissa Ferrian; Stefan Herms; Heiko Reutter; Nilma Almeida de Assis; Taofik Al Chawa; Manuel Mattheisen; Michael Steffens; Sandra Barth; Nadine Kluck; Anna Paul; Jessica Becker; Carola Lauster; Gül Schmidt; Bert Braumann; Martin Scheer; Rudolf H Reich; Alexander Hemprich; Simone Pötzsch; Bettina Blaumeiser; Susanne Moebus; Michael Krawczak; Stefan Schreiber; Thomas Meitinger; Hans-Erich Wichmann; Regine P Steegers-Theunissen; Franz-Josef Kramer; Sven Cichon; Peter Propping; Thomas F Wienker; Michael Knapp; Michele Rubini; Peter A Mossey; Per Hoffmann; Markus M Nöthen
Journal:  Nat Genet       Date:  2009-12-20       Impact factor: 38.330

6.  Patched1 is required in neural crest cells for the prevention of orofacial clefts.

Authors:  Vicki Metzis; Andrew D Courtney; Markus C Kerr; Charles Ferguson; Maria C Rondón Galeano; Robert G Parton; Brandon J Wainwright; Carol Wicking
Journal:  Hum Mol Genet       Date:  2013-07-29       Impact factor: 6.150

Review 7.  Nevoid basal cell carcinoma syndrome (Gorlin syndrome).

Authors:  Lorenzo Lo Muzio
Journal:  Orphanet J Rare Dis       Date:  2008-11-25       Impact factor: 4.123

8.  Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.

Authors:  Jae Woong Sull; Kung-Yee Liang; Jacqueline B Hetmanski; Margaret Daniele Fallin; Roxann G Ingersoll; Jiwan Park; Yah-Huei Wu-Chou; Philip K Chen; Samuel S Chong; Felicia Cheah; Vincent Yeow; Beyoung Yun Park; Sun Ha Jee; Ethylin Wang Jabs; Richard Redett; Euiju Jung; Ingo Ruczinski; Alan F Scott; Terri H Beaty
Journal:  Genet Epidemiol       Date:  2008-09       Impact factor: 2.135

9.  Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts.

Authors:  Paras Garg; Kerstin U Ludwig; Anne C Böhmer; Michele Rubini; Regine Steegers-Theunissen; Peter A Mossey; Elisabeth Mangold; Andrew J Sharp
Journal:  Eur J Hum Genet       Date:  2013-10-30       Impact factor: 4.246

10.  Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.

Authors:  Yanqin Yu; Xianbo Zuo; Miao He; Jinping Gao; Yuchuan Fu; Chuanqi Qin; Liuyan Meng; Wenjun Wang; Yaling Song; Yong Cheng; Fusheng Zhou; Gang Chen; Xiaodong Zheng; Xinhuan Wang; Bo Liang; Zhengwei Zhu; Xiazhou Fu; Yujun Sheng; Jiebing Hao; Zhongyin Liu; Hansong Yan; Elisabeth Mangold; Ingo Ruczinski; Jianjun Liu; Mary L Marazita; Kerstin U Ludwig; Terri H Beaty; Xuejun Zhang; Liangdan Sun; Zhuan Bian
Journal:  Nat Commun       Date:  2017-02-24       Impact factor: 14.919

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.