Simultaneous detection of ACP1 and GC genotypes using PCR/SSCP

被引:3
作者
Dissing, J
Thymann, M
Hopkinson, D
机构
[1] Univ Copenhagen, Inst Forens Med, Res Lab, DK-2100 Copenhagen, Denmark
[2] UCL, Galton Lab, Human Biochem Genet Unit, London, England
关键词
ACP1; GC; acid phosphatase; phosphotyrosine phosphatase; group specific component; SSCP; alleles; classical genetic markers;
D O I
10.1046/j.1469-1809.2003.00011.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The classical enzyme and protein markers ACP1 and GC have gained new importance because of the biological functions of their gene products. ACPI encodes a low molecular weight enzyme which is now recognized as a phosphotyrosine phosphatase with a role in the regulation of signal transduction pathways, and GC-globulin acts both as a transporter of vitamin D and as a plasma actin scavenger and plays a role in macrophage activation. These two polymorphisms were phenotyped for decades on the basis of electrophoretic isozyme or protein patterns; the gene structures are now known. Nucleotide substitutions determining the common alleles are close enough at each locus to be contained in one short PCR product. We have developed a simple, rapid and reliable multiplex method based on PCR and SSCP which allows the simultaneous determination of the common ACPI and GC genotypes.
引用
收藏
页码:81 / 85
页数:5
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