THE EFFECT OF T-LYMPHOCYTE CLONALITY ON THE CALCULATED HPRT MUTATION FREQUENCY OCCURRING IN-VIVO IN HUMANS

被引:37
作者
ONEILL, JP [1 ]
NICKLAS, JA [1 ]
HUNTER, TC [1 ]
BATSON, OB [1 ]
ALLEGRETTA, M [1 ]
FALTA, MT [1 ]
BRANDA, RF [1 ]
ALBERTINI, RJ [1 ]
机构
[1] UNIV VERMONT,DEPT MED,GENET LAB,BURLINGTON,VT 05401
来源
MUTATION RESEARCH-ENVIRONMENTAL MUTAGENESIS AND RELATED SUBJECTS | 1994年 / 313卷 / 2-3期
关键词
HUMAN T-LYMPHOCYTE; HPRT MUTATION; T-LYMPHOCYTE CLONALITY; T-CELL RECEPTOR GENE REARRANGEMENT; IN VIVO MUTATION;
D O I
10.1016/0165-1161(94)90052-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The frequency of 6-thioguanine resistant (TG(r)) mutant T-lymphocytes arising in vivo in humans can be quantified with a cell cloning assay. However, the in vivo proliferation of T-lymphocytes that may include TG(r) mutant cells can distort the relationship between mutation events and the resulting frequency of mutant cells. The T-cell receptor (TCR) gene rearrangement pattern of T-cell colonies can be used as an independent measure of clonality. Analysis of T-cell 'clonality' in 413 wild type and 1736 TG(r) mutant isolates from 58 individuals shows that mutant clonality is a frequent occurrence (35/58 individuals = 60.3%). However, a major effect on the mutant frequency corrected for clonality (the calculated 'mutation frequency') was found only in nine samples all of which had mutant frequencies greater than 40 x 10(-6).
引用
收藏
页码:215 / 225
页数:11
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