DETERMINATION OF THE MUTATIONS RESPONSIBLE FOR THE LESCH-NYHAN SYNDROME IN 17 SUBJECTS

被引:36
作者
TARLE, SA
DAVIDSON, BL
WU, VC
ZIDAR, FJ
SEEGMILLER, JE
KELLEY, WN
PALELLA, TD
机构
[1] UNIV MICHIGAN,DEPT INTERNAL MED,CTR MULTIPURPOSE ARTHRITIS,1150 W MED CTR DR,BOX 0680,ANN ARBOR,MI 48109
[2] RACKHAM ARTHRITIS RES UNIT,DEPT INTERNAL MED,ANN ARBOR,MI 48109
[3] UNIV CALIF SAN DIEGO,INST RES AGING,LA JOLLA,CA 92093
[4] UNIV PENN,SCH MED,PHILADELPHIA,PA 19104
关键词
D O I
10.1016/0888-7543(91)90341-B
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Hypoxanthine - guanine phosphoribosyltransferase (HPRT) is a purine salvage enzyme that catalyzes the conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate. Previous studies of mutant HPRT proteins analyzed at the molecular level have shown a significant heterogeneity. This investigation further verifies this heterogeneity and identifies insertions, deletions, and point mutations. The direct sequencing of the polymerase chain reaction-amplified product of reverse-transcribed HPRT mRNA enabled the rapid identification of the mutations found in 17 previously uncharacterized cell lines derived from patients with the Lesch-Nyhan syndrome. © 1991.
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页码:499 / 501
页数:3
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