Abstract
CISD2, the causative gene for Wolfram syndrome 2 (WFS2), is a previously uncharacterized novel gene. Using a mouse genetic approach, this work demonstrated for the first time that Cisd2 is involved in mammalian life span control. Cisd2 deficiency in mice leads to mitochondrial breakdown and dysfunction; this is accompanied by cell death with autophagic features and these events precede the two earliest manifestations of nerve and muscle degeneration. Together, they lead to a panel of phenotypic features suggestive of premature aging. This work effectively links Cisd2 gene function, mitochondrial integrity and aging in mammals.
| Original language | English |
|---|---|
| Pages (from-to) | 1043-1045 |
| Number of pages | 3 |
| Journal | Autophagy |
| Volume | 5 |
| Issue number | 7 |
| DOIs | |
| State | Published - 01 10 2009 |
Keywords
- Autophagy
- Cisd2
- Knockout mice
- Mitochondria
- Premature aging
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