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Chromosomal assignment of the human erythropoietin gene and its DNA polymorphism.
Author(s) -
M L Law,
Guangyan Cai,
F K Lin,
Qi Wei,
S Z Huang,
J. Hartz,
Herbert C. Morse,
ChihHung Lin,
C. Jones,
FaTen Kao
Publication year - 1986
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.83.18.6920
Subject(s) - biology , genetics , locus (genetics) , microbiology and biotechnology , complementary dna , gene mapping , restriction fragment length polymorphism , gene , southern blot , population , metaphase , chromosome , genotype , demography , sociology
Erythropoietin (EPO), a glycoprotein hormone, is the major physiological regulator of erythrocyte production in mammals. A cDNA clone containing the entire human EPO-coding region was used for Southern blot analysis of a series of human-Chinese hamster somatic cell hybrids containing different combinations of human chromosomes. Synteny analysis revealed 100% concordance between the EPO gene and human chromosome 7. Further localization to the region q11-q22 was accomplished by in situ hybridization of 3H-labeled human EPO cDNA to metaphase chromosomes prepared from both human lymphocytes and the cell hybrid 879-2a that contained human chromosomes 5, 7, 9, 12, and 21. In addition, restriction fragment length polymorphisms were detected at a frequency of approximately 20% in a Chinese population using restriction enzymes either HindIII or HinfI. These polymorphisms were inherited in a Mendelian fashion. Thus, the EPO marker is reasonably polymorphic and should be useful in linkage analysis with other genetic markers on chromosome 7, including the locus for cystic fibrosis.

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