Format

Send to

Choose Destination
Tissue Antigens. 2013 Dec;82(6):410-5. doi: 10.1111/tan.12232. Epub 2013 Oct 17.

Characterization of mannose-binding lectin (MBL) variants by allele-specific sequencing of MBL2 and determination of serum MBL protein levels.

Author information

1
Department of Transplantation Immunology, Institute of Immunology, University of Heidelberg, Heidelberg, Germany.

Abstract

Mannose-binding lectin (MBL) is a major component of the lectin pathway of complement activation. High and low MBL levels have been associated with susceptibility and severity of a variety of infectious and autoimmune diseases. Several single-nucleotide polymorphisms (SNPs) in the promoter region and exon 1 of the MBL2 gene are responsible for variations in serum MBL levels. We developed a sequence-based typing method for allele-specific MBL2 genotyping and measured serum MBL protein levels in 24 German blood donors. We identified the common MBL2 haplotypes including five promoter polymorphisms in linkage with the Q allele and correlated serum MBL levels with the respective genotypes. The genotyping method presented here could provide a basis for confirmatory studies in larger cohorts.

KEYWORDS:

MBL2; haplotypes; mannoseā€binding lectin; sequencing

PMID:
24134411
DOI:
10.1111/tan.12232
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center