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Detection of Lesch‐Nyhan Syndrome Carriers: Analysis of hair roots for HPRT by agarose gel electrophoresis and autoradiography
Author(s) -
Bakay Bohdan,
TuckerPian Charmaine,
Seegmiller J. E.
Publication year - 1980
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1980.tb00166.x
Subject(s) - hypoxanthine guanine phosphoribosyltransferase , agarose , lesch–nyhan syndrome , agarose gel electrophoresis , microbiology and biotechnology , hair dyes , chemistry , biology , biochemistry , dna , gene , organic chemistry , dyeing , mutant
Flat agarose gel electrophoresis and autoradiography were used to analyze HPRT and APRT activity in individual hair roots collected from the scalps of females to determine the presence of HPRT‐deficient cells. Autoradiographs of hair‐root lysates of normal homozygous females contained two well‐separated dark zones representing HPRT and APRT activities. In contrast, some hair roots from carriers of HPRT deficiency contained two zones of activity with the same relative proportion of APRT and HPRT as hair roots of normal homozygotes, while others contained decreased amounts of HPRT activity. These hair roots consisted of HPRT+ and HPRT ‐ cells. In addition, some hair roots from heterozygous carriers contained APRT but no HPRT activity. Such hair roots consisted of HPRT‐ cells only.