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Volumn 1201, Issue , 2010, Pages 58-64

A role for the CISD2 gene in lifespan control and human disease

Author keywords

aging; CISD2; lifespan; longevity; mitochondria; Wolfram syndrome 2

Indexed keywords

CISD1 PROTEIN; IRON SULFUR PROTEIN; UNCLASSIFIED DRUG; CARRIER PROTEIN; ERIS PROTEIN, HUMAN; MEMBRANE PROTEIN; NERVE PROTEIN; NOXP70 PROTEIN, MOUSE;

EID: 77955284362     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2010.05619.x     Document Type: Conference Paper
Times cited : (64)

References (35)
  • 1
    • 34248359155 scopus 로고    scopus 로고
    • MitoNEETis an iron-containing outer mitochondrial membrane protein that regulates oxidative capacity
    • Wiley, S.E., A.N.Murphy, S.A.Ross, et al. 2007.MitoNEETis an iron-containing outer mitochondrial membrane protein that regulates oxidative capacity. Proc. Natl. Acad. Sci. USA 104: 5318-5323.
    • (2007) Proc. Natl. Acad. Sci. USA , vol.104 , pp. 5318-5323
    • Wiley, S.E.1    Murphy, A.N.2    Ross, S.A.3
  • 2
    • 66149104113 scopus 로고    scopus 로고
    • Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice
    • Chen, Y.F., C.H. Kao, Y.T. Chen, et al. 2009. Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice. Genes Dev. 23: 1183-1194.
    • (2009) Genes Dev , vol.23 , pp. 1183-1194
    • Chen, Y.F.1    Kao, C.H.2    Chen, Y.T.3
  • 3
    • 35548990606 scopus 로고    scopus 로고
    • Crystal structure of human mitoNEET reveals distinct groups of iron sulfur proteins
    • Lin, J., T. Zhou, K. Ye & J. Wang. 2007. Crystal structure of human mitoNEET reveals distinct groups of iron sulfur proteins. Proc. Natl. Acad. Sci. USA 104: 14640-14645.
    • (2007) Proc. Natl. Acad. Sci. USA , vol.104 , pp. 14640-14645
    • Lin, J.1    Zhou, T.2    Ye, K.3    Wang, J.4
  • 4
    • 35448995690 scopus 로고    scopus 로고
    • MitoNEET is a uniquely folded 2Fe 2S outer mitochondrial membrane protein stabilized by pioglitazone
    • Paddock, M.L., S.E. Wiley, H.L. Axelrod, et al. 2007. MitoNEET is a uniquely folded 2Fe 2S outer mitochondrial membrane protein stabilized by pioglitazone. Proc. Natl. Acad. Sci. USA 104: 14342-14347.
    • (2007) Proc. Natl. Acad. Sci. USA , vol.104 , pp. 14342-14347
    • Paddock, M.L.1    Wiley, S.E.2    Axelrod, H.L.3
  • 5
    • 68949175445 scopus 로고    scopus 로고
    • Crystal structure of Miner1: The redox-active 2Fe-2S protein causative in Wolfram Syndrome 2
    • Conlan, A.R., H.L. Axelrod, A.E. Cohen, et al. 2009. Crystal structure of Miner1: the redox-active 2Fe-2S protein causative in Wolfram Syndrome 2. J. Mol. Biol. 392: 143-153.
    • (2009) J. Mol. Biol. , vol.392 , pp. 143-153
    • Conlan, A.R.1    Axelrod, H.L.2    Cohen, A.E.3
  • 6
    • 0942276510 scopus 로고    scopus 로고
    • Identification of a novel mitochondrial protein ("mitoNEET") cross-linked specifically by a thiazolidinedione photoprobe
    • Colca, J.R.,W.G. McDonald, D.J.Waldon, et al. 2004. Identification of a novel mitochondrial protein ("mitoNEET") cross-linked specifically by a thiazolidinedione photoprobe. Am. J. Physiol. Endocrinol. Metab. 286: E252-E260.
    • (2004) Am. J. Physiol. Endocrinol. Metab. , vol.286
    • Colca, J.R.1    McDonald, W.G.2    Waldon, D.J.3
  • 7
    • 70349641035 scopus 로고    scopus 로고
    • Cisd2 mediates mitochondrial integrity and life span in mammals
    • Chen, Y.F., C.H. Kao, R. Kirby & T.F. Tsai. 2009. Cisd2 mediates mitochondrial integrity and life span in mammals. Autophagy 5: 1043-1045.
    • (2009) Autophagy , vol.5 , pp. 1043-1045
    • Chen, Y.F.1    Kao, C.H.2    Kirby, R.3    Tsai, T.F.4
  • 8
    • 17944375119 scopus 로고    scopus 로고
    • A genomewide scan for linkage to human exceptional longevity identifies a locus on chromosome 4
    • Puca, A.A., M.J. Daly, S.J. Brewster, et al. 2001. A genomewide scan for linkage to human exceptional longevity identifies a locus on chromosome 4. Proc. Natl. Acad. Sci. USA 98: 10505-10508.
    • (2001) Proc. Natl. Acad. Sci. USA , vol.98 , pp. 10505-10508
    • Puca, A.A.1    Daly, M.J.2    Brewster, S.J.3
  • 10
    • 84934438243 scopus 로고    scopus 로고
    • Fine structure of the autophagosome
    • Eskelinen, E.L. 2008. Fine structure of the autophagosome. Methods Mol. Biol. 445: 11-28.
    • (2008) Methods Mol. Biol. , vol.445 , pp. 11-28
    • Eskelinen, E.L.1
  • 11
    • 0035979750 scopus 로고    scopus 로고
    • Longevity Hints of a 'master gene' for extreme old age
    • Strauss, E. 2001. Longevity. Hints of a 'master gene' for extreme old age. Science 293: 1570-1571.
    • (2001) Science , vol.293 , pp. 1570-1571
    • Strauss, E.1
  • 12
    • 0037470542 scopus 로고    scopus 로고
    • Aging and genome maintenance: Lessons from the mouse?
    • Hasty, P., J. Campisi, J. Hoeijmakers, et al. 2003. Aging and genome maintenance: lessons from the mouse? Science 299: 1355-1359.
    • (2003) Science , vol.299 , pp. 1355-1359
    • Hasty, P.1    Campisi, J.2    Hoeijmakers, J.3
  • 14
    • 62349116477 scopus 로고    scopus 로고
    • Themitochondrial theory of aging: Insight from transgenic and knockout mouse models
    • Jang, Y.C. & H. Van Remmen. 2009. Themitochondrial theory of aging: insight from transgenic and knockout mouse models. Exp. Gerontol. 44: 256-260.
    • (2009) Exp. Gerontol. , vol.44 , pp. 256-260
    • Jang, Y.C.1    Van Remmen, H.2
  • 15
    • 85042595375 scopus 로고    scopus 로고
    • Progress & prospects: Gene therapy in aging
    • Rattan, S.I. & R. Singh. 2009. Progress & prospects: gene therapy in aging. Gene Ther. 16: 3-9.
    • (2009) Gene Ther , vol.16 , pp. 3-9
    • Rattan, S.I.1    Singh, R.2
  • 16
    • 35348939526 scopus 로고    scopus 로고
    • A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible forWolfram syndrome 2
    • Amr, S., C. Heisey, M. Zhang, et al. 2007. A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible forWolfram syndrome 2. Am. J. Hum. Genet. 81: 673-683.
    • (2007) Am. J. Hum. Genet. , vol.81 , pp. 673-683
    • Amr, S.1    Heisey, C.2    Zhang, M.3
  • 17
    • 0030826078 scopus 로고    scopus 로고
    • Wolfram (DIDMOAD) syndrome
    • Barrett, T.G. & S.E. Bundey. 1997. Wolfram (DIDMOAD) syndrome. J. Med. Genet. 34: 838-841.
    • (1997) J. Med. Genet. , vol.34 , pp. 838-841
    • Barrett, T.G.1    Bundey, S.E.2
  • 18
    • 33645395576 scopus 로고    scopus 로고
    • Wolfram/ DIDMOAD syndrome, a heterogenic and molecularly complex neurodegenerative disease
    • Domenech, E., M. Gomez-Zaera & V. Nunes. 2006. Wolfram/ DIDMOAD syndrome, a heterogenic and molecularly complex neurodegenerative disease. Pediatr. Endocrinol. Rev. 3: 249-257.
    • (2006) Pediatr. Endocrinol. Rev. , vol.3 , pp. 249-257
    • Domenech, E.1    Gomez-Zaera, M.2    Nunes, V.3
  • 19
    • 0027275218 scopus 로고
    • Wolfram syndrome: A mitochondrial-mediated disorder?
    • Bu, X. & J.I. Rotter. 1993. Wolfram syndrome: a mitochondrial- mediated disorder? Lancet 342: 598-600.
    • (1993) Lancet , vol.342 , pp. 598-600
    • Bu, X.1    Rotter, J.I.2
  • 20
    • 0027515138 scopus 로고
    • Wolfram syndrome: Mitochondrial disorder
    • Vora, A.J. & J.S. Lilleyman. 1993.Wolfram syndrome: mitochondrial disorder. Lancet 342: 1059.
    • (1993) Lancet , vol.342 , pp. 1059
    • Vora, A.J.1    Lilleyman, J.S.2
  • 21
    • 0027337386 scopus 로고
    • Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD,Wolfram syndrome)
    • Rötig, A., V. Cormier, P. Chatelain, et al. 1993. Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD,Wolfram syndrome). J. Inherit. Metab. Dis. 16: 527-530.
    • (1993) J. Inherit. Metab. Dis. , vol.16 , pp. 527-530
    • Rötig, A.1    Cormier, V.2    Chatelain, P.3
  • 22
    • 19144366747 scopus 로고    scopus 로고
    • Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion
    • Barrientos, A., J. Casademont, A. Saiz, et al. 1996. Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion. Am. J. Hum. Genet. 58: 963-970.
    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 963-970
    • Barrientos, A.1    Casademont, J.2    Saiz, A.3
  • 23
    • 0026753325 scopus 로고
    • Mitochondrial abnormalities in the DIDMOAD syndrome
    • Bundey, S., K. Poulton, H.Whitwell, et al. 1992. Mitochondrial abnormalities in the DIDMOAD syndrome. J. Inherit. Metab. Dis. 15: 315-319.
    • (1992) J. Inherit. Metab. Dis. , vol.15 , pp. 315-319
    • Bundey, S.1    Poulton, K.2    Whitwell, H.3
  • 24
    • 0031024138 scopus 로고    scopus 로고
    • Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinctmitochondrial DNA haplotypes
    • Hofmann, S., R. Bezold, M. Jaksch, et al. 1997. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinctmitochondrial DNA haplotypes. Genomics 39: 8-18.
    • (1997) Genomics , vol.39 , pp. 8-18
    • Hofmann, S.1    Bezold, R.2    Jaksch, M.3
  • 25
    • 0034081869 scopus 로고    scopus 로고
    • The mitochondrial genome inWolframsyndrome
    • Barrett, T.G., M. Scott-Brown, A. Seller, et al. 2000. The mitochondrial genome inWolframsyndrome. J.Med.Genet. 37: 463-466.
    • (2000) J. Med. Genet. , vol.37 , pp. 463-466
    • Barrett, T.G.1    Scott-Brown, M.2    Seller, A.3
  • 26
    • 17344362695 scopus 로고    scopus 로고
    • A gene encoding a transmembrane protein ismutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)
    • Inoue, H., Y. Tanizawa, J. Wasson, et al. 1998. A gene encoding a transmembrane protein ismutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome). Nat. Genet. 20: 143-148.
    • (1998) Nat. Genet. , vol.20 , pp. 143-148
    • Inoue, H.1    Tanizawa, Y.2    Wasson, J.3
  • 27
    • 0031761895 scopus 로고    scopus 로고
    • Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein
    • Strom, T.M., K. Hörtnagel, S. Hofmann, et al. 1998. Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein. Hum. Mol. Genet. 7: 2021-2028.
    • (1998) Hum. Mol. Genet. , vol.7 , pp. 2021-2028
    • Strom, T.M.1    Hörtnagel, K.2    Hofmann, S.3
  • 28
    • 0035283066 scopus 로고    scopus 로고
    • WFS1 (Wolfram syndrome 1) gene product: Predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain
    • Takeda, K., H. Inoue, Y. Tanizawa, et al. 2001. WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain. Hum.Mol. Genet. 10: 477-484.
    • (2001) Hum. Mol. Genet. , vol.10 , pp. 477-484
    • Takeda, K.1    Inoue, H.2    Tanizawa, Y.3
  • 29
    • 2942731683 scopus 로고    scopus 로고
    • Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion
    • Ishihara,H., S. Takeda, A. Tamura, et al. 2004. Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion. Hum. Mol. Genet. 13: 1159-1170.
    • (2004) Hum. Mol. Genet. , vol.13 , pp. 1159-1170
    • Ishihara, H.1    Takeda, S.2    Tamura, A.3
  • 30
    • 27744523525 scopus 로고    scopus 로고
    • Mice conditionally lacking the Wolfram gene in pancreatic islet beta cells exhibit diabetes as a result of enhanced endoplasmic reticulum stress and apoptosis
    • Riggs, A.C., E. Bernal-Mizrachi, M. Ohsugi, et al. 2005.Mice conditionally lacking the Wolfram gene in pancreatic islet beta cells exhibit diabetes as a result of enhanced endoplasmic reticulum stress and apoptosis. Diabetologia 48: 2313-2321.
    • (2005) Diabetologia , vol.48 , pp. 2313-2321
    • Riggs, A.C.1    Bernal-Mizrachi, E.2    Ohsugi, M.3
  • 31
    • 33745202552 scopus 로고    scopus 로고
    • WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic beta-cells
    • Yamada, T., H. Ishihara, A. Tamura, et al. 2006. WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic beta-cells. Hum. Mol. Genet. 15: 1600-1609.
    • (2006) Hum. Mol. Genet. , vol.15 , pp. 1600-1609
    • Yamada, T.1    Ishihara, H.2    Tamura, A.3
  • 33
    • 0031466720 scopus 로고    scopus 로고
    • Optic atrophy inWolfram (DIDMOAD) syndrome
    • Barrett, T.G., S.E. Bundey, A.R. Fielder & P.A. Good. 1997. Optic atrophy inWolfram (DIDMOAD) syndrome. Eye 11: 882-888.
    • (1997) Eye , vol.11 , pp. 882-888
    • Barrett, T.G.1    Bundey, S.E.2    Fielder, A.R.3    Good, P.A.4
  • 34
    • 33644759358 scopus 로고    scopus 로고
    • Genetic analysis of the diabetes-prone C57BLKS/J mouse strain reveals genetic contribution from multiple strains
    • Mao, H.Z., E.T. Roussos&M. Ṕeterfy. 2006. Genetic analysis of the diabetes-prone C57BLKS/J mouse strain reveals genetic contribution from multiple strains. Biochim. Biophys. Acta 1762: 440-446.
    • (2006) Biochim. Biophys. Acta , vol.1762 , pp. 440-446
    • Mao, H.Z.1    Roussos, E.T.2    Ṕeterfy, M.3
  • 35
    • 0038529802 scopus 로고    scopus 로고
    • Impact of genetic background and ablation of insulin receptor substrate (IRS)-3 on IRS-2 knock-out mice
    • Terauchi, Y., J. Matsui, R. Suzuki, et al. 2003. Impact of genetic background and ablation of insulin receptor substrate (IRS)-3 on IRS-2 knock-out mice. J. Biol. Chem. 278: 14284-14290.
    • (2003) J. Biol. Chem. , vol.278 , pp. 14284-14290
    • Terauchi, Y.1    Matsui, J.2    Suzuki, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.