Skip to main content
Top
Published in: BMC Medical Genetics 1/2017

Open Access 01-12-2017 | Research article

Identification of novel candidate variants including COL6A6 polymorphisms in early-onset atopic dermatitis using whole-exome sequencing

Authors: Won Il Heo, Kui Young Park, Taewon Jin, Mi-Kyung Lee, MinJeong Kim, Eung Ho Choi, Hae-Suk Kim, Jung Min Bae, Nam Ju Moon, Seong Jun Seo

Published in: BMC Medical Genetics | Issue 1/2017

Login to get access

Abstract

Background

The prevalence of atopic dermatitis has increased over the last 10 years. Atopic dermatitis tends to run in families and commonly begins to manifest in childhood. The prevalence of atopic dermatitis is as high as 20% in children. Thus, early diagnosis and treatment of atopic dermatitis are important. Understanding its genetic basis is also needed to facilitate early detection.

Methods

To identify family-specific candidate genetic variants associated with early-onset atopic dermatitis in Koreans, we carried out whole-exome sequencing of three separate families with this condition. Additional validation was performed in 112 AD patients and 61 controls using Sanger sequencing.

Results

We focused on both common functional variants with a minor allele frequency higher than 1% and rare variants with a minor allele frequency less than 1%. The relevance of the respective variants was supported by a program that could predict whether the mutations resulted in damaged protein function. Fourteen overlapping genes were identified during exome sequencing. Three variants of the COL6A6 gene appeared in all three families and were in close proximity to atopic dermatitis-related loci on chromosome 3q21. The homozygous frequency for the rs16830494 minor allele (AA) and the rs59021909 (TT) allele and the rs200963433 heterozygous (CT) frequency were all higher in AD cases compared to controls in a population-based case-control study.

Conclusion

Identifying family-specific COL6A6 polymorphisms and genetic variants of other candidate genes associated with AD using WES is a novel approach. Our study suggests that COL6A6 variants may be risk factors for atopic dermatitis. This study provides a genetic basis for early-onset AD diagnosis in Korean patients and the development of new therapies.

Trial registration

Trial registration number: IRB NO. C2008030 (133); Name of registry: The collection research of clinical data and patient blood to identify genetic and protein biomarker of atopic dermatitis; Date of registration: 09-July-2008.
Trial registration number: IRB NO. C2015258 (1716); Name of registry: The collection study of patient blood and clinical data for the development of the prognosis prediction and early diagnosis of atopic dermatitis; Date of registration: 15-jan-2016.
Appendix
Available only for authorised users
Literature
1.
go back to reference Hoffjan S, Stemmler S. Unravelling the complex genetic background of atopic dermatitis: from genetic association results towards novel therapeutic strategies. Arch Dermatol Res. 2015;307(8):659–70. Hoffjan S, Stemmler S. Unravelling the complex genetic background of atopic dermatitis: from genetic association results towards novel therapeutic strategies. Arch Dermatol Res. 2015;307(8):659–70.
2.
go back to reference Uehara M, Kimura C. Descendant family history of atopic dermatitis. Acta Derm Venereol. 1993;73(1):62–3.PubMed Uehara M, Kimura C. Descendant family history of atopic dermatitis. Acta Derm Venereol. 1993;73(1):62–3.PubMed
3.
go back to reference Kryukov GV, Pennacchio LA, Sunyaev SR. Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. Am J Hum Genet. 2007;80(4):727–39.CrossRefPubMedPubMedCentral Kryukov GV, Pennacchio LA, Sunyaev SR. Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. Am J Hum Genet. 2007;80(4):727–39.CrossRefPubMedPubMedCentral
4.
go back to reference Nutten S. Atopic dermatitis: global epidemiology and risk factors. Ann Nutr Metab. 2015;66 Suppl 1:8–16.CrossRefPubMed Nutten S. Atopic dermatitis: global epidemiology and risk factors. Ann Nutr Metab. 2015;66 Suppl 1:8–16.CrossRefPubMed
5.
go back to reference Rabbani B, Tekin M, Mahdieh N. The promise of whole-exome sequencing in medical genetics. J Hum Genet. 2014;59(1):5–15.CrossRefPubMed Rabbani B, Tekin M, Mahdieh N. The promise of whole-exome sequencing in medical genetics. J Hum Genet. 2014;59(1):5–15.CrossRefPubMed
6.
go back to reference Pabinger S, Dander A, Fischer M, Snajder R, Sperk M, Efremova M, Krabichler B, Speicher MR, Zschocke J, Trajanoski Z. A survey of tools for variant analysis of next-generation genome sequencing data. Brief Bioinform. 2014;15(2):256–78.CrossRefPubMed Pabinger S, Dander A, Fischer M, Snajder R, Sperk M, Efremova M, Krabichler B, Speicher MR, Zschocke J, Trajanoski Z. A survey of tools for variant analysis of next-generation genome sequencing data. Brief Bioinform. 2014;15(2):256–78.CrossRefPubMed
7.
go back to reference Asimit J, Zeggini E. Testing for rare variant associations in complex diseases. Genome Med. 2009;1(11):24.PubMed Asimit J, Zeggini E. Testing for rare variant associations in complex diseases. Genome Med. 2009;1(11):24.PubMed
9.
go back to reference Gibson G. Rare and common variants: twenty arguments. Nat Rev Genet. 2011;13(2):135–45.CrossRef Gibson G. Rare and common variants: twenty arguments. Nat Rev Genet. 2011;13(2):135–45.CrossRef
10.
go back to reference Sharma M, Mehla K, Batra J, Ghosh B. Association of a chromosome 1q21 locus in close proximity to a late cornified envelope-like proline-rich 1 (LELP1) gene with total serum IgE levels. J Hum Genet. 2007;52(4):378–83.CrossRefPubMed Sharma M, Mehla K, Batra J, Ghosh B. Association of a chromosome 1q21 locus in close proximity to a late cornified envelope-like proline-rich 1 (LELP1) gene with total serum IgE levels. J Hum Genet. 2007;52(4):378–83.CrossRefPubMed
11.
go back to reference Christensen U, Moller-Larsen S, Nyegaard M, Haagerup A, Hedemand A, Brasch-Andersen C, Kruse TA, Corydon TJ, Deleuran M, Borglum AD. Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21. Hum Genet. 2009;126(4):549–57.CrossRefPubMed Christensen U, Moller-Larsen S, Nyegaard M, Haagerup A, Hedemand A, Brasch-Andersen C, Kruse TA, Corydon TJ, Deleuran M, Borglum AD. Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21. Hum Genet. 2009;126(4):549–57.CrossRefPubMed
13.
go back to reference DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet. 2011;43(5):491–8.CrossRefPubMedPubMedCentral DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet. 2011;43(5):491–8.CrossRefPubMedPubMedCentral
14.
go back to reference Cingolani P, Platts A, le Wang L, Coon M, Nguyen T, Wang L, Land SJ, Lu X, Ruden DM. A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3. Fly. 2012;6(2):80–92.CrossRefPubMedPubMedCentral Cingolani P, Platts A, le Wang L, Coon M, Nguyen T, Wang L, Land SJ, Lu X, Ruden DM. A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3. Fly. 2012;6(2):80–92.CrossRefPubMedPubMedCentral
15.
go back to reference Cibulskis K, Lawrence MS, Carter SL, Sivachenko A, Jaffe D, Sougnez C, Gabriel S, Meyerson M, Lander ES, Getz G. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat Biotechnol. 2013;31(3):213–9.CrossRefPubMedPubMedCentral Cibulskis K, Lawrence MS, Carter SL, Sivachenko A, Jaffe D, Sougnez C, Gabriel S, Meyerson M, Lander ES, Getz G. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat Biotechnol. 2013;31(3):213–9.CrossRefPubMedPubMedCentral
16.
go back to reference Carlsten C, Dimich-Ward H, Ferguson A, Watson W, Rousseau R, Dybuncio A, Becker A, Chan-Yeung M. Atopic dermatitis in a high-risk cohort: natural history, associated allergic outcomes, and risk factors. Ann Allergy Asthma Immunol. 2013;110(1):24–8.CrossRefPubMed Carlsten C, Dimich-Ward H, Ferguson A, Watson W, Rousseau R, Dybuncio A, Becker A, Chan-Yeung M. Atopic dermatitis in a high-risk cohort: natural history, associated allergic outcomes, and risk factors. Ann Allergy Asthma Immunol. 2013;110(1):24–8.CrossRefPubMed
17.
18.
go back to reference Sabatelli P, Gara SK, Grumati P, Urciuolo A, Gualandi F, Curci R, Squarzoni S, Zamparelli A, Martoni E, Merlini L, et al. Expression of the collagen VI alpha5 and alpha6 chains in normal human skin and in skin of patients with collagen VI-related myopathies. J Invest Dermatol. 2011;131(1):99–107.CrossRefPubMed Sabatelli P, Gara SK, Grumati P, Urciuolo A, Gualandi F, Curci R, Squarzoni S, Zamparelli A, Martoni E, Merlini L, et al. Expression of the collagen VI alpha5 and alpha6 chains in normal human skin and in skin of patients with collagen VI-related myopathies. J Invest Dermatol. 2011;131(1):99–107.CrossRefPubMed
19.
go back to reference Lee YA, Wahn U, Kehrt R, Tarani L, Businco L, Gustafsson D, Andersson F, Oranje AP, Wolkertstorfer A, v Berg A, et al. A major susceptibility locus for atopic dermatitis maps to chromosome 3q21. Nat Genet. 2000;26(4):470–3.CrossRefPubMed Lee YA, Wahn U, Kehrt R, Tarani L, Businco L, Gustafsson D, Andersson F, Oranje AP, Wolkertstorfer A, v Berg A, et al. A major susceptibility locus for atopic dermatitis maps to chromosome 3q21. Nat Genet. 2000;26(4):470–3.CrossRefPubMed
20.
go back to reference Becker KG, Barnes KC. Underlying disease specificity of genetic loci in atopic dermatitis. J Invest Dermatol. 2001;117(5):1325–7.CrossRefPubMed Becker KG, Barnes KC. Underlying disease specificity of genetic loci in atopic dermatitis. J Invest Dermatol. 2001;117(5):1325–7.CrossRefPubMed
21.
go back to reference Soderhall C, Marenholz I, Kerscher T, Ruschendorf F, Esparza-Gordillo J, Worm M, Gruber C, Mayr G, Albrecht M, Rohde K, et al. Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis. PLoS Biol. 2007;5(9):e242.CrossRefPubMedPubMedCentral Soderhall C, Marenholz I, Kerscher T, Ruschendorf F, Esparza-Gordillo J, Worm M, Gruber C, Mayr G, Albrecht M, Rohde K, et al. Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis. PLoS Biol. 2007;5(9):e242.CrossRefPubMedPubMedCentral
22.
go back to reference Merner ND, Chandler MR, Bourassa C, Liang B, Khanna AR, Dion P, Rouleau GA, Kahle KT. Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia. Front Cell Neurosci. 2015;9:386.CrossRefPubMedPubMedCentral Merner ND, Chandler MR, Bourassa C, Liang B, Khanna AR, Dion P, Rouleau GA, Kahle KT. Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia. Front Cell Neurosci. 2015;9:386.CrossRefPubMedPubMedCentral
23.
go back to reference Palmer LJ, Barnes KC, Burton PR, Chen H, Cookson WO, Deichmann KA, Elston RC, Holloway JW, Jacobs KB, Laitinen T, et al. Meta-analysis for linkage to asthma and atopy in the chromosome 5q31-33 candidate region. Hum Mol Genet. 2001;10(8):891–9.CrossRefPubMed Palmer LJ, Barnes KC, Burton PR, Chen H, Cookson WO, Deichmann KA, Elston RC, Holloway JW, Jacobs KB, Laitinen T, et al. Meta-analysis for linkage to asthma and atopy in the chromosome 5q31-33 candidate region. Hum Mol Genet. 2001;10(8):891–9.CrossRefPubMed
24.
go back to reference Guo RJ, Huang E, Ezaki T, Patel N, Sinclair K, Wu J, Klein P, Suh ER, Lynch JP. Cdx1 inhibits human colon cancer cell proliferation by reducing beta-catenin/T-cell factor transcriptional activity. J Biol Chem. 2004;279(35):36865–75.CrossRefPubMed Guo RJ, Huang E, Ezaki T, Patel N, Sinclair K, Wu J, Klein P, Suh ER, Lynch JP. Cdx1 inhibits human colon cancer cell proliferation by reducing beta-catenin/T-cell factor transcriptional activity. J Biol Chem. 2004;279(35):36865–75.CrossRefPubMed
25.
go back to reference Lim X, Nusse R. Wnt signaling in skin development, homeostasis, and disease. Cold Spring Harb Perspect Biol. 2013;5(2). Lim X, Nusse R. Wnt signaling in skin development, homeostasis, and disease. Cold Spring Harb Perspect Biol. 2013;5(2).
26.
go back to reference Kim SY, Yang SW, Kim HL, Kim SH, Kim SJ, Park SM, Son M, Ryu S, Pyo YS, Lee JS, et al. Association between P478S polymorphism of the filaggrin gene & atopic dermatitis. Indian J Med Res. 2013;138(6):922–7.PubMedPubMedCentral Kim SY, Yang SW, Kim HL, Kim SH, Kim SJ, Park SM, Son M, Ryu S, Pyo YS, Lee JS, et al. Association between P478S polymorphism of the filaggrin gene & atopic dermatitis. Indian J Med Res. 2013;138(6):922–7.PubMedPubMedCentral
27.
go back to reference Rupnik H, Rijavec M, Korošec P. Filaggrin loss‐of‐function mutations are not associated with atopic dermatitis that develops in late childhood or adulthood. Br J Dermatol. 2015;172(2):455–61.CrossRefPubMed Rupnik H, Rijavec M, Korošec P. Filaggrin loss‐of‐function mutations are not associated with atopic dermatitis that develops in late childhood or adulthood. Br J Dermatol. 2015;172(2):455–61.CrossRefPubMed
28.
29.
go back to reference Holloway JW, Lonjou C, Beghe B, Peng Q, Gaunt TR, Gomes I, Hall IP, Dewar JC, Wilkinson J, Thomas NS, et al. Linkage analysis of the 5q31-33 candidate region for asthma in 240 UK families. Genes Immun. 2001;2(1):20–4.CrossRefPubMed Holloway JW, Lonjou C, Beghe B, Peng Q, Gaunt TR, Gomes I, Hall IP, Dewar JC, Wilkinson J, Thomas NS, et al. Linkage analysis of the 5q31-33 candidate region for asthma in 240 UK families. Genes Immun. 2001;2(1):20–4.CrossRefPubMed
Metadata
Title
Identification of novel candidate variants including COL6A6 polymorphisms in early-onset atopic dermatitis using whole-exome sequencing
Authors
Won Il Heo
Kui Young Park
Taewon Jin
Mi-Kyung Lee
MinJeong Kim
Eung Ho Choi
Hae-Suk Kim
Jung Min Bae
Nam Ju Moon
Seong Jun Seo
Publication date
01-12-2017
Publisher
BioMed Central
Published in
BMC Medical Genetics / Issue 1/2017
Electronic ISSN: 1471-2350
DOI
https://doi.org/10.1186/s12881-017-0368-9

Other articles of this Issue 1/2017

BMC Medical Genetics 1/2017 Go to the issue