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Assignment of the Complement Serine Protease Genes C1r and C1s to Chromosome 12 Region 12p13

Overview
Journal Hum Genet
Specialty Genetics
Date 1988 Apr 1
PMID 2834284
Citations 7
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Abstract

C1r and C1s are distinct, but structurally and functionally similar, serine protease zymogens responsible for the enzymatic activity of the first component of complement (C1). Recent comparisons indicate a significant degree of sequence similarity between C1r and C1s and support the hypothesis that they are related by gene duplication. Complementary DNA probes for human C1r and C1s do not cross-hybridize even at mild stringency conditions and are therefore gene-specific. Using a panel of 25 human-rodent cell hybrids, we have independently assigned the C1r and the C1s genes to chromosome 12. In situ hybridization analyses were consistent with these assignments, showing in addition that both C1r and C1s are located on the short arm of the chromosome in the region p13. These data suggest that the homologous C1r and C1s genes have remained closely linked after duplication of a common ancestor. The C1r and C1s loci also provide useful polymorphic DNA markers for the short arm of chromosome 12.

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References
1.
Gee P, Douglas G, McAlpine P, Hamerton J . Proceedings: Synteny of the IDH-1 and MDH-1 gene loci in man and probable assignment to chromosome 2. Cytogenet Cell Genet. 1974; 13(1):89-90. DOI: 10.1159/000130242. View

2.
Franckle U . Regional localization of the human genes for malate dehydrogenase-1 and isocitrate dehydrogenase-1 on chromosome 2 by interspecific hybridization using human cells with the balanced reciprocal translocation t(1;2) (q32;q13). Birth Defects Orig Artic Ser. 1975; 11(3):138-42. View

3.
Jongsma A, Los W, Hagemeijer A . Proceedings: Evidence for synteny between the human loci for triose phosphate isomerase, lactate dehydrogenase-B, and peptidase-B and the regional mapping of these loci on chromosome 12. Cytogenet Cell Genet. 1974; 13(1):106-7. DOI: 10.1159/000130248. View

4.
Van Cong N, Weil D, FINAZ C, Cohen-Haguenauer O, Gross M, De Tand M . Panel of twenty-five independent man-rodent hybrids for human genetic marker mapping. Ann Genet. 1986; 29(1):20-6. View

5.
Lewis W, Harris H . Human red cell peptidases. Nature. 1967; 215(5099):351-5. DOI: 10.1038/215351a0. View