Home LiteratureArticle Details
PMID: 9363890 Published · ppublish English Journal Article

Mutation of the mouse klotho gene leads to a syndrome resembling ageing.

Nature ·Vol. 390 ·No. 6655 ·1997-11-06 ·Pages 45-51

Kuro-o M, Matsumura Y, Aizawa H, Kawaguchi H, Suga T, Utsugi T, Ohyama Y, Kurabayashi M, Kaname T, Kume E, Iwasaki H, Iida A, Shiraki-Iida T, Nishikawa S, Nagai R, Nabeshima YI

Abstract

A new gene, termed klotho, has been identified that is involved in the suppression of several ageing phenotypes. A defect in klotho gene expression in the mouse results in a syndrome that resembles human ageing, including a short lifespan, infertility, arteriosclerosis, skin atrophy, osteoporosis and emphysema. The gene encodes a membrane protein that shares sequence similarity with the beta-glucosidase enzymes. The klotho gene product may function as part of a signalling pathway that regulates ageing in vivo and morbidity in age-related diseases.

MeSH Terms
Aging/genetics,pathology Amino Acid Sequence Animals Arteriosclerosis/genetics,pathology Atrophy Calcinosis/genetics,pathology Cloning, Molecular Emphysema/genetics Female Genitalia/pathology Humans Male Membrane Proteins/genetics,physiology Mice Mice, Inbred BALB C Mice, Inbred C3H Mice, Inbred C57BL Mice, Transgenic Molecular Sequence Data Mutagenesis, Insertional Osteoporosis/genetics,pathology Phenotype Pituitary Gland/pathology Sequence Homology, Amino Acid Skin/pathology Syndrome Thymus Gland/pathology
Chemicals
Membrane Proteins
Authors & Affiliations
16 authors, click to expand affiliations / ORCID
Kuro-o M
Division of Molecular Genetics, National Institute of Neuroscience, Kodaira, Tokyo, Japan. kuroo@ncnaxp.ncnp.go.jp
Matsumura Y
Aizawa H
Kawaguchi H
Suga T
Utsugi T
Ohyama Y
Kurabayashi M
Kaname T
Kume E
Iwasaki H
Iida A
Shiraki-Iida T
Nishikawa S
Nagai R
Nabeshima Y I
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1997-11-06
Pages
45-51
Language
English
Region
England
NLM ID
0410462
Subset
IM
Databases
GENBANK
AB005141, AB005142, AB010088, AB010089, AB010090, AB010091
Corrections
CommentIn
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