Dinucleotide repeats in the human surfactant protein-B gene and respiratory-distress syndrome

Author:

Floros J1,Veletza S V1,Kotikalapudi P1,Krizkova L1,Karinch A M1,Friedman C2,Buchter S3,Marks K1

Affiliation:

1. Department of Cellular and Molecular Physiology, Pennsylvania State University College of Medicine, Hershey, PA 17033 U.S.A.

2. Methodist Medical Center, Jackson, MS U.S.A.

3. Emory University School of Medicine, Atlanta, GA, U.S.A.

Abstract

Pulmonary surfactant, a lipoprotein complex, is essential for normal lung function, and deficiency of surfactant can result in respiratory-distress syndrome (RDS) in the prematurely born infant. Some studies have pointed towards a genetic contribution to the aetiology of RDS. Because the surfactant protein B (SP-B) is important for optimal surfactant function and because it is involved in the pathogenesis of pulmonary disease, we investigated the genetic variability of the SP-B gene in individuals with and without RDS. We identified a 2.5 kb BamHI polymorphism and studied its location, nature and frequency. We localized this polymorphism in the first half of intron 4 and found that it is derived by gain or loss in the number of copies of a motif that consists of two elements, a 20 bp conserved sequence and a variable number of CA dinucleotides. Variability in the number of motifs resulting from either deletion (in 55.3% of the cases with the variation) or insertion (44.7%) of motifs was observed in genomic DNAs from unrelated individuals. Analysis of 219 genomic DNAs from infants with (n = 82) and without (n = 137) RDS showed that this insertion/deletion appears with significantly higher frequency in the RDS population (29.3 as against 16.8%, P < 0.05).

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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