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

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.

journal_name

Nature

journal_title

Nature

authors

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

doi

10.1038/36285

subject

Has Abstract

pub_date

1997-11-06 00:00:00

pages

45-51

issue

6655

eissn

0028-0836

issn

1476-4687

journal_volume

390

pub_type

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