RELATIONSHIP BETWEEN PLATELET MONOAMINE OXIDASE-B ACTIVITY AND ALLELES AT THE MAOB LOCUS

被引:0
|
作者
GIRMEN, AS
BAENZIGER, J
HOTAMISLIGIL, GS
KONRADI, C
SHALISH, C
SULLIVAN, JL
BREAKEFIELD, XO
机构
[1] MASSACHUSETTS GEN HOSP E,CTR NEUROSCI,BLDG 149,13TH ST,BOSTON,MA 02129
[2] MASSACHUSETTS GEN HOSP,NEUROL SERV,BOSTON,MA
[3] HARVARD UNIV,SCH MED,DEPT MICROBIOL & MOLEC GENET,BOSTON,MA 02115
[4] HARVARD UNIV,SCH MED,NEUROSCI PROGRAM,BOSTON,MA 02115
[5] INDIANA UNIV,MED CTR,ALCOHOL RES CTR,DEPT PSYCHIAT,INDIANAPOLIS,IN 46204
[6] INDIANA UNIV,MED CTR,ALCOHOL RES CTR,DEPT PATHOL,INDIANAPOLIS,IN 46204
关键词
MONOAMINE OXIDASE-B; MONOAMINE OXIDASE-A; PLATELETS; HUMAN; GT-REPEAT ELEMENT;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genetic variations in monoamine oxidase (MAO)-B activity have been proposed to have a contributory role in several neurologic and psychiatric diseases. Variations in activity could affect rates of degradation of exogenous amines, including toxins, precursors of toxins (like 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine), or false transmitters, and of endogenous amines, such as neurotransmitters. In this study a highly polymorphic (GT)n repeat element was used to mark alleles at the MAOB locus. The MAOB allele status and levels of platelet MAO-B activity were determined for 41 control males. No correlation was noted between specific alleles and levels of MAO-B activity in this sample set. This suggests that the structural gene for MAOB is not usually the primary determinant of activity levels in platelets.
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收藏
页码:2063 / 2066
页数:4
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