Literature DB >> 12175909

Restricted polymorphisms of the mannose-binding lectin gene in a population of Papua New Guinea.

Simone Jüliger1, Peter G Kremsner, Michael P Alpers, John C Reeder, Jürgen F J Kun.   

Abstract

The human mannose-binding lectin (MBL) is an important protein of the innate immune system. MBL is able to eliminate potential pathogens by activating the complement cascade or by opsonisation. We investigated the gene and promoter region of MBL in a population from Papua New Guinea infected with Plasmodium falciparum parasites and measured the appropriate serum concentrations of these individuals. Their serum levels of MBL, detected by ELISA, showed a wide range with concentrations between 632 and 7325 microg/l MBL. A known polymorphism in exon 1 at codon 54 causing an amino acid exchange from Gly to Asp occurred with a low frequency of 3%. Additional to the previously reported polymorphisms in the gene and promoter region of MBL, two novel polymorphic sites were found in the promoter region. One site was in the untranslated region of the MBL gene at position +1 (G-->A, termed R/S), and the second was located upstream of the gene at position -4 (G-->A, termed T/U).

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Year:  2002        PMID: 12175909     DOI: 10.1016/s0027-5107(02)00142-2

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  3 in total

1.  Phylogenetic nomenclature and evolution of mannose-binding lectin (MBL2) haplotypes.

Authors:  Angelica B W Boldt; Iara J Messias-Reason; Diogo Meyer; Carlos G Schrago; Florian Lang; Bertrand Lell; Klaus Dietz; Peter G Kremsner; Maria Luiza Petzl-Erler; Jürgen F J Kun
Journal:  BMC Genet       Date:  2010-05-14       Impact factor: 2.797

2.  Genetic and other factors determining mannose-binding lectin levels in American Indians: the Strong Heart Study.

Authors:  Lyle G Best; Robert E Ferrell; Susan Decroo; Kari E North; Jean W Maccluer; Ying Zhang; Elisa T Lee; Barbara V Howard; Jason Umans; Vittorio Palmieri; Peter Garred
Journal:  BMC Med Genet       Date:  2009-01-22       Impact factor: 2.103

3.  MBL-2 polymorphisms (codon 54 and Y-221X) and low MBL levels are associated with susceptibility to multi organ dysfunction in P. falciparum malaria in Odisha, India.

Authors:  Bidyut K Das; Aditya K Panda
Journal:  Front Microbiol       Date:  2015-07-31       Impact factor: 5.640

  3 in total

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