RRC ID |
44922
|
著者 |
Ohnishi T, Murata T, Watanabe A, Hida A, Ohba H, Iwayama Y, Mishima K, Gondo Y, Yoshikawa T.
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タイトル |
Defective craniofacial development and brain function in a mouse model for depletion of intracellular inositol synthesis.
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ジャーナル |
J Biol Chem
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Abstract |
myo-Inositol is an essential biomolecule that is synthesized by myo-inositol monophosphatase (IMPase) from inositol monophosphate species. The enzymatic activity of IMPase is inhibited by lithium, a drug used for the treatment of mood swings seen in bipolar disorder. Therefore, myo-inositol is thought to have an important role in the mechanism of bipolar disorder, although the details remain elusive. We screened an ethyl nitrosourea mutant mouse library for IMPase gene (Impa) mutations and identified an Impa1 T95K missense mutation. The mutant protein possessed undetectable enzymatic activity. Homozygotes died perinatally, and E18.5 embryos exhibited striking developmental defects, including hypoplasia of the mandible and asymmetric fusion of ribs to the sternum. Perinatal lethality and morphological defects in homozygotes were rescued by dietary myo-inositol. Rescued homozygotes raised on normal drinking water after weaning exhibited a hyper-locomotive trait and prolonged circadian periods, as reported in rodents treated with lithium. Our mice should be advantageous, compared with those generated by the conventional gene knock-out strategy, because they carry minimal genomic damage, e.g. a point mutation. In conclusion, our results reveal critical roles for intracellular myo-inositol synthesis in craniofacial development and the maintenance of proper brain function. Furthermore, this mouse model for cellular inositol depletion could be beneficial for understanding the molecular mechanisms underlying the clinical effect of lithium and myo-inositol-mediated skeletal development.
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巻・号 |
289(15)
|
ページ |
10785-10796
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公開日 |
2014-4-11
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DOI |
10.1074/jbc.M113.536706
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PII |
S0021-9258(20)40341-2
|
PMID |
24554717
|
PMC |
PMC4036449
|
MeSH |
Amino Acid Sequence
Animals
Behavior, Animal
Bipolar Disorder / drug therapy
Brain / metabolism*
Brain Diseases / drug therapy
Circadian Rhythm
Disease Models, Animal
Ethylnitrosourea / chemistry
Female
Gene Library
Genotype
Homozygote
Humans
Inositol / biosynthesis*
Lithium / pharmacology*
Male
Mice
Mice, Inbred C57BL
Molecular Sequence Data
Mutagenesis
Mutation
Mutation, Missense
Phosphoric Monoester Hydrolases / genetics
Phosphoric Monoester Hydrolases / metabolism*
Recombinant Proteins / metabolism
Sequence Homology, Amino Acid
Time Factors
|
IF |
4.238
|
引用数 |
13
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WOS 分野
|
BIOCHEMISTRY & MOLECULAR BIOLOGY
|
リソース情報 |
ヒト・動物細胞 |
|