Mutations in GDI1 are responsible for X-linked non-specific mental retardation

被引:272
作者
D'Adamo, P
Menegon, A
Lo Nigro, C
Grasso, M
Gulisano, M
Tamanini, F
Bienvenu, T
Gedeon, AK
Oostra, B
Wu, SK
Tandon, A
Valtorta, F
Balch, WE
Chelly, J
Toniolo, D [1 ]
机构
[1] CNR, Inst Genet Biochem & Evolut, I-27100 Pavia, Italy
[2] Galliera Hosp, Lab Human Genet, Genoa, Italy
[3] HSR, DIBIT, Milan, Italy
[4] Inst Cochin Genet Mol, F-75014 Paris, France
[5] Womens & Childrens Hosp, Dept Cytogenet & Mol Genet, Adelaide, SA, Australia
[6] Erasmus Univ, Dept Clin Genet, NL-3000 DR Rotterdam, Netherlands
[7] Scripps Res Inst, Dept Mol & Cell Biol, La Jolla, CA USA
[8] Univ Milan, Dept Med Pharmacol, Milan, Italy
关键词
D O I
10.1038/487
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Rab GDP-dissociation inhibitors (GDI) are evolutionarily conserved proteins that play an essential role in the recycling of Rab GTPases required for vesicular transport through the secretory pathway We have found mutations in the GDI1 gene (which encodes alpha GDI) in two families affected with X-linked non-specific mental retardation. One of the mutations caused a non-conservative substitution (L92P) which reduced binding and recycling of RAB3A, the second was a null mutation. Our results show that both functional and developmental alterations in the neuron may account for the severe impairment of learning abilities as a consequence of mutations in GDI1, emphasizing its critical role in development of human intellectual and learning abilities.
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页码:134 / 139
页数:6
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