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Genetic variants and monoallelic expression of surfactant protein-D in inflammatory bowel disease.

Authors :
Lin Z
John G
Hegarty JP
Berg A
Yu W
Wang Y
Kelly AA
Peterson BZ
Poritz LS
Floros J
Koltun WA
Source :
Annals of human genetics [Ann Hum Genet] 2011 Sep; Vol. 75 (5), pp. 559-68. Date of Electronic Publication: 2011 Jul 25.
Publication Year :
2011

Abstract

Surfactant protein-D (SP-D) is expressed on mucosal surfaces and functions in the innate immune response to microorganisms. We studied the genetic association of the two nonsynonymous SP-D single nucleotide polymorphisms (SNPs) rs721917 and rs2243639 in 256 inflammatory bowel disease (IBD) cases (123 CD and 133 UC) and 376 unrelated healthy individuals from an IBD population from Central Pennsylvania. Case-control analysis revealed a significant association of rs2243639 with susceptibility to Crohn's disease (CD) (p= 0.0036), but not ulcerative colitis (UC) (p= 0.883), and no association of rs721917 with CD (p= 0.328) or UC (p= 0.218). Using intestinal tissues from 19 individuals heterozygous for each SNP, we compared allelic expression of these two SNPs between diseased and matched normal tissues. rs2243639 exhibited balanced biallelic (BB) expression; while rs721917 exhibited differential allelic expression (BB 37%, imbalanced biallelic [IB] 45%, and dominant monoallelic [DM] 18%). Comparison of allelic expression pattern between diseased and matched normal tissues, 13 of 19 individuals (14 UC, 5 CD) showed a similar pattern. The six patients exhibiting a different pattern were all UC patients. The results suggest that differential allelic expression may affect penetrance of the SNP rs721917 disease-susceptibility allele in IBD. The potential impact of SP-D monoallelic expression on incomplete penetrance is discussed.<br /> (© 2011 The Authors Annals of Human Genetics © 2011 Blackwell Publishing Ltd/University College London.)

Details

Language :
English
ISSN :
1469-1809
Volume :
75
Issue :
5
Database :
MEDLINE
Journal :
Annals of human genetics
Publication Type :
Academic Journal
Accession number :
21790524
Full Text :
https://doi.org/10.1111/j.1469-1809.2011.00662.x