Literature DB >> 26191260

Genotyping analysis of 3 RET polymorphisms demonstrates low somatic mutation rate in Chinese Hirschsprung disease patients.

Zhen Zhang1, Qian Jiang2, Qi Li1, Wei Cheng3, Guoliang Qiao1, Ping Xiao4, Liang Gan1, Lin Su5, Chunyue Miao6, Long Li1.   

Abstract

BACKGROUND: Genetic mosaicism has been reported for both coding and non-coding sequences in the RET gene in Hirschsprung disease (HSCR) patients. This study aimed to investigate somatic mutation rate in Chinese population by comparing both homozygous genotype percentage and risk allele frequency of 3 RET single nucleotide polymorphisms (SNPs) among blood and colon samples.
METHODS: DNA was extracted from 59 HSCR blood samples, 59 control blood samples and 76 fresh frozen colon tissue samples (grouped into ganglionic, transitional and aganglionic level). Genotype status of rs2435357 and rs2506030 was examined by competitive allele specific hydrolysis probes (Taqman) PCR technology, and rs2506004 was examined by Sanger sequencing. Homozygous genotype percentage and risk allele frequency were calculated for each type of sample and compared by chi-square test. P<0.05 was regarded as being statistically significant.
RESULTS: Colon tissue DNA samples showed similar frequency of SNPs as that of the blood DNA samples in HSCR patients, both of which are significantly higher than the control blood group (rs2435357 TT genotype: 71.2%, 74.7% versus 22.0% in HSCR blood, HSCR colon and control blood DNA respectively, P=0.000; rs2506004 AA genotype: 72.4%, 83.1% versus 25.5%, P=0.000; rs2506030 GG genotype: 79.7%, 77.2% versus 54.2%, P=0.000 and 0.004). With respect to DNA extracted from ganglionic, transitional and aganglionic levels, no statistically significant difference was demonstrated in those 3 regions (rs2435357: P=0.897; rs2506004: P=0.740; rs2506030: P=0.901).
CONCLUSION: Our data does not support the notion that high frequency of somatic changes as an underlying etiology of Chinese HSCR population.

Entities:  

Keywords:  Hirschsprung disease; RET proto-oncogene; fresh frozen colon; genetic mosaicism

Mesh:

Substances:

Year:  2015        PMID: 26191260      PMCID: PMC4503131     

Source DB:  PubMed          Journal:  Int J Clin Exp Pathol        ISSN: 1936-2625


  23 in total

1.  Comparison of genomic DNA extraction techniques from whole blood samples: a time, cost and quality evaluation study.

Authors:  Diego Chacon-Cortes; Larisa M Haupt; Rod A Lea; Lyn R Griffiths
Journal:  Mol Biol Rep       Date:  2012-01-07       Impact factor: 2.316

2.  Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia.

Authors:  Paolo Prontera; Gabriela Stangoni; Carmela Ardisia; Daniela Rogaia; Amedea Mencarelli; Emilio Donti
Journal:  Am J Med Genet A       Date:  2011-03-17       Impact factor: 2.802

3.  Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability.

Authors:  Eileen Sproat Emison; Merce Garcia-Barcelo; Elizabeth A Grice; Francesca Lantieri; Jeanne Amiel; Grzegorz Burzynski; Raquel M Fernandez; Li Hao; Carl Kashuk; Kristen West; Xiaoping Miao; Paul K H Tam; Paola Griseri; Isabella Ceccherini; Anna Pelet; Anne-Sophie Jannot; Loic de Pontual; Alexandra Henrion-Caude; Stanislas Lyonnet; Joke B G M Verheij; Robert M W Hofstra; Guillermo Antiñolo; Salud Borrego; Andrew S McCallion; Aravinda Chakravarti
Journal:  Am J Hum Genet       Date:  2010-07-09       Impact factor: 11.025

4.  RET and NRG1 interplay in Hirschsprung disease.

Authors:  Hongsheng Gui; Wai-Kiu Tang; Man-Ting So; Petroola Proitsi; Pak C Sham; Paul K Tam; Elly Sau-Wai Ngan; Elly Sau-Wai Ngan; Stacey S Cherny; Maria-Mercè Garcia-Barceló
Journal:  Hum Genet       Date:  2013-02-12       Impact factor: 4.132

5.  Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association.

Authors:  Stacey Arnold; Anna Pelet; Jeanne Amiel; Salud Borrego; Robert Hofstra; Paul Tam; Isabella Ceccherini; Stanislas Lyonnet; Stephanie Sherman; Aravinda Chakravarti
Journal:  Hum Mutat       Date:  2009-05       Impact factor: 4.878

6.  Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.

Authors:  Maria-Mercè Garcia-Barcelo; Clara Sze-Man Tang; Elly Sau-Wai Ngan; Vincent Chi-Hang Lui; Yan Chen; Man-Ting So; Thomas Yuk-Yu Leon; Xiao-Ping Miao; Cathy Ka-Yee Shum; Feng-Qin Liu; Ming-Yiu Yeung; Zhen-Wei Yuan; Wei-Hong Guo; Lei Liu; Xiao-Bing Sun; Liu-Ming Huang; Jin-Fa Tou; You-Qiang Song; Danny Chan; Kenneth M C Cheung; Kenneth Kak-Yuen Wong; Stacey S Cherny; Pak-Chung Sham; Paul Kwong-Hang Tam
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-05       Impact factor: 11.205

7.  Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.

Authors:  Jinfa Tou; Li Wang; Li Liu; Ying Wang; Rong Zhong; Shengyu Duan; Weiguang Liu; Qixing Xiong; Qinglong Gu; Hong Yang; Hui Li
Journal:  BMC Med Genet       Date:  2011-02-25       Impact factor: 2.103

8.  Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease.

Authors:  Qian Jiang; Yen-Yi Ho; Li Hao; Courtney Nichols Berrios; Aravinda Chakravarti
Journal:  PLoS One       Date:  2011-06-21       Impact factor: 3.240

Review 9.  Enteric nervous system development: migration, differentiation, and disease.

Authors:  Jonathan I Lake; Robert O Heuckeroth
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2013-05-02       Impact factor: 4.052

10.  Genome-wide copy number analysis uncovers a new HSCR gene: NRG3.

Authors:  Clara Sze-Man Tang; Guo Cheng; Man-Ting So; Benjamin Hon-Kei Yip; Xiao-Ping Miao; Emily Hoi-Man Wong; Elly Sau-Wai Ngan; Vincent Chi-Hang Lui; You-Qiang Song; Danny Chan; Kenneth Cheung; Zhen-Wei Yuan; Liu Lei; Patrick Ho-Yu Chung; Xue-Lai Liu; Kenneth Kak-Yuen Wong; Christian R Marshall; Stephen W Scherer; Steve Scherer; Stacey S Cherny; Pak-Chung Sham; Paul Kwong-Hang Tam; Maria-Mercè Garcia-Barceló
Journal:  PLoS Genet       Date:  2012-05-10       Impact factor: 5.917

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  5 in total

Review 1.  Hirschsprung's disease: clinical dysmorphology, genes, micro-RNAs, and future perspectives.

Authors:  Consolato Maria Sergi; Oana Caluseriu; Hunter McColl; David D Eisenstat
Journal:  Pediatr Res       Date:  2016-09-28       Impact factor: 3.756

2.  Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.

Authors:  Dehua Yang; Jun Yang; Shuai Li; Meng Jiang; Guoqing Cao; Li Yang; Xi Zhang; Ying Zhou; Kang Li; Shao-Tao Tang
Journal:  Sci Rep       Date:  2017-03-03       Impact factor: 4.379

3.  ASSOCIATION OF RS2435357 AND RS1800858 POLYMORPHISMS IN RET PROTO-ONCOGENE WITH HIRSCHSPRUNG DISEASE: SYSTEMATIC REVIEW AND META-ANALYSIS.

Authors:  Abdolhamid Amooee; Mohamad Hosein Lookzadeh; Seyed Reza Mirjalili; Seyed Mohsen Miresmaeili; Kazem Aghili; Masoud Zare-Shehneh; Hossein Neamatzadeh
Journal:  Arq Bras Cir Dig       Date:  2019-10-21

4.  Is There Any Mosaicism in REarranged During Transfection Variant in Hirschsprung Disease's Patients?

Authors:  Kristy Iskandar; Susan Simanjaya; Taufik Indrawan; Alvin Santoso Kalim; Didik Setyo Heriyanto
Journal:  Front Pediatr       Date:  2022-03-10       Impact factor: 3.418

5.  The Somatic Mutation Paradigm in Congenital Malformations: Hirschsprung Disease as a Model.

Authors:  Katherine C MacKenzie; Rhiana Garritsen; Rajendra K Chauhan; Yunia Sribudiani; Bianca M de Graaf; Tim Rugenbrink; Rutger Brouwer; Wilfred F J van Ijcken; Ivo de Blaauw; Alice S Brooks; Cornelius E J Sloots; Conny J H M Meeuwsen; René M Wijnen; Donald F Newgreen; Alan J Burns; Robert M W Hofstra; Maria M Alves; Erwin Brosens
Journal:  Int J Mol Sci       Date:  2021-11-16       Impact factor: 5.923

  5 in total

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