MULTIFACTORIAL INHERITANCE OF NEURAL-TUBE DEFECTS - LOCALIZATION OF THE MAJOR GENE AND RECOGNITION OF MODIFIERS IN CT MUTANT MICE

被引:103
作者
NEUMANN, PE
FRANKEL, WN
LETTS, VA
COFFIN, JM
COPP, AJ
BERNFIELD, M
机构
[1] HARVARD UNIV,CHILDRENS HOSP,SCH MED,DEPT NEUROL,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,JOINT PROGRAM NEONATOL,BOSTON,MA 02115
[3] TUFTS UNIV,SCH MED,DEPT MOLEC BIOL,BOSTON,MA 02111
[4] JACKSON LAB,BAR HARBOR,ME 04609
[5] UNIV LONDON,INST CHILD HLTH,LONDON WC1N 1EH,ENGLAND
关键词
D O I
10.1038/ng0494-357
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Neural tube defects (NTD) in humans have been considered to have a multifactorial aetiology, however the participating genes have not been identified. The curly-tail (ct) mutant mouse develops NTD that resemble the human malformations in location, pathology and associated abnormalities. Moreover, there appears to be multifactorial influence on the incidence of NTD in offspring of curly-tail mice. We now describe a linkage analysis that localizes the ct gene to distal chromosome 4 in mice. Further analysis using recombinant inbred strains demonstrates the presence of at least three modifier loci that influence the incidence of NTD. This study provides definitive evidence for multifactorial inheritance in a mouse model of human NTD.
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页码:357 / 362
页数:6
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