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Molecular and clonal analysis of in vivo hprt (hypoxanthine-guanine phosphoribosyl-transferase) mutations in human cells

Conference ·
OSTI ID:6708412
; ; ;  [1]; ;  [2]
  1. Vermont Univ., Burlington, VT (USA). Genetics Lab.
  2. Chemical Industry Inst. of Toxicology, Research Triangle Park, NC (USA)

There is no longer doubt that gene mutations occur in vivo in human somatic cells, and that methods can be developed to detect, quantify and study them. Four assays are now available for such purpose; two detecting mutations that arise in bone marrow erythroid stem cells and two defining mutations that occur in T-lymphocytes. The red cell assays measure changes in mature red blood cells that involve either the blood group glycophorin-A locus or the hemoglobin loci; the lymphocyte assays score for genetic events at either the X-chromosomal hypoxanthine-guanine phosphoribosyl-transferase (hprt) locus. We describe here our attempts in studying in vivo gene mutations in human T-lymphocytes. 35 refs., 3 figs., 3 tabs.

Research Organization:
Vermont Univ., Burlington, VT (USA)
Sponsoring Organization:
DOE/ER
DOE Contract Number:
FG02-87ER60502
OSTI ID:
6708412
Report Number(s):
CONF-8907145-2; ON: DE90015561
Country of Publication:
United States
Language:
English