Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice

Yi Fan Chen, Cheng Heng Kao, Ya Ting Chen, Chih Hao Wang, Chia Yu Wu, Ching Yen Tsai, Fu Chin Liu, Chu Wen Yang, Yau Huei Wei, Ming Ta Hsu, Shih Feng Tsai, Ting Fen Tsai

Research output: Contribution to journalArticle

127 Citations (Scopus)

Abstract

CISD2, the causative gene for Wolfram syndrome 2 (WFS2), is a previously uncharacterized novel gene. Significantly, the CISD2 gene is located on human chromosome 4q, where a genetic component for longevity maps. Here we show for the first time that CISD2 is involved in mammalian life-span control. Cisd2 deficiency in mice causes mitochondrial breakdown and dysfunction accompanied by autophagic cell death, 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. Our study also reveals that Cisd2 is primarily localized in the mitochondria and that mitochondrial degeneration appears to have a direct phenotypic consequence that triggers the accelerated aging process in Cisd2 knockout mice; furthermore, mitochondrial degeneration exacerbates with age, and the autophagy increases in parallel to the development of the premature aging phenotype. Additionally, our Cisd2 knockout mouse work provides strong evidence supporting an earlier clinical hypothesis that WFS is in part a mitochondria-mediated disorder; specifically, we propose that mutation of CISD2 causes the mitochondria-mediated disorder WFS2 in humans. Thus, this mutant mouse provides an animal model for mechanistic investigation of Cisd2 protein function and help with a pathophysiological understanding of WFS2.

Original languageEnglish
Pages (from-to)1183-1194
Number of pages12
JournalGenes and Development
Volume23
Issue number10
DOIs
Publication statusPublished - May 15 2009
Externally publishedYes

Fingerprint

Premature Aging
Mitochondria
Autophagy
Knockout Mice
Genes
Nerve Degeneration
Human Chromosomes
Animal Models
Phenotype
Muscles
Mutation
Wolfram Syndrome 2
Proteins

Keywords

  • Autophagy
  • Cisd2
  • Knockout mice
  • Mitochondria
  • Premature aging
  • Wolfram syndrome 2

ASJC Scopus subject areas

  • Genetics
  • Developmental Biology
  • Medicine(all)

Cite this

Chen, Y. F., Kao, C. H., Chen, Y. T., Wang, C. H., Wu, C. Y., Tsai, C. Y., ... Tsai, T. F. (2009). Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice. Genes and Development, 23(10), 1183-1194. https://doi.org/10.1101/gad.1779509

Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice. / Chen, Yi Fan; Kao, Cheng Heng; Chen, Ya Ting; Wang, Chih Hao; Wu, Chia Yu; Tsai, Ching Yen; Liu, Fu Chin; Yang, Chu Wen; Wei, Yau Huei; Hsu, Ming Ta; Tsai, Shih Feng; Tsai, Ting Fen.

In: Genes and Development, Vol. 23, No. 10, 15.05.2009, p. 1183-1194.

Research output: Contribution to journalArticle

Chen, YF, Kao, CH, Chen, YT, Wang, CH, Wu, CY, Tsai, CY, Liu, FC, Yang, CW, Wei, YH, Hsu, MT, Tsai, SF & Tsai, TF 2009, 'Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice', Genes and Development, vol. 23, no. 10, pp. 1183-1194. https://doi.org/10.1101/gad.1779509
Chen, Yi Fan ; Kao, Cheng Heng ; Chen, Ya Ting ; Wang, Chih Hao ; Wu, Chia Yu ; Tsai, Ching Yen ; Liu, Fu Chin ; Yang, Chu Wen ; Wei, Yau Huei ; Hsu, Ming Ta ; Tsai, Shih Feng ; Tsai, Ting Fen. / Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice. In: Genes and Development. 2009 ; Vol. 23, No. 10. pp. 1183-1194.
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