Identification and characterization of polymorphisms at the HSA α1-acid glycoprotein (ORM*) gene locus in Caucasians

Catherine M. Owczarek, Aleksander L. Owczarek, Philip G. Board
Published: March 28, 2002
Genet. Mol. Res. 1 (1) : 96-105

Cite this Article:
C.M. Owczarek, A.L. Owczarek, P.G. Board (2002). Identification and characterization of polymorphisms at the HSA α1-acid glycoprotein (ORM*) gene locus in Caucasians. Genet. Mol. Res. 1(1): 96-105.

About the Authors
Catherine M. Owczarek, Aleksander L. Owczarek, Philip G. Board.
Corresponding author: C.M. Owczarek
E-mail: catherine.owczarek@med.monash.edu.au

ABSTRACT

Human α1-acid glycoprotein (AGP) or orosomucoid (ORM) is a major acute phase protein that is thought to play a crucial role in maintaining homeostasis. Human AGP is the product of a cluster of at least two adjacent genes located on HSA chromosome 9. Using a range of restriction endonucleases we have investigated DNA variation at the locus encoding the AGP genes in a group of healthy Caucasians. Polymorphisms were identified using BamHI, EcoRI, BglII, PvuII, HindIII, TaqI and MspI. Nonrandom associations were found between the BamHI, EcoRI and BglII RFLPs. The RFLPs detected with PvuII, TaqI and MspI were all located in exon 6 of both AGP genes. The duplication of an AGP gene was observed in 11% of the individuals studied and was in linkage disequilibrium with the TaqI RFLP. The identification and characterization of these polymorphisms should prove useful for other population and forensic studies.

Human α1-acid glycoprotein (AGP) or orosomucoid (ORM) is a major acute phase protein that is thought to play a crucial role in maintaining homeostasis. Human AGP is the product of a cluster of at least two adjacent genes located on HSA chromosome 9. Using a range of restriction endonucleases we have investigated DNA variation at the locus encoding the AGP genes in a group of healthy Caucasians. Polymorphisms were identified using BamHI, EcoRI, BglII, PvuII, HindIII, TaqI and MspI. Nonrandom associations were found between the BamHI, EcoRI and BglII RFLPs. The RFLPs detected with PvuII, TaqI and MspI were all located in exon 6 of both AGP genes. The duplication of an AGP gene was observed in 11% of the individuals studied and was in linkage disequilibrium with the TaqI RFLP. The identification and characterization of these polymorphisms should prove useful for other population and forensic studies.

Keywords: Human a1-acid glycoprotein, RFLP, Linkage disequilibrium.

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