메뉴 건너뛰기




Volumn 18, Issue 1, 1998, Pages 388-399

Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: Studies with PEX5-defective CHO cell mutants

Author keywords

[No Author keywords available]

Indexed keywords

ACETYL COENZYME A ACYLTRANSFERASE; AMINO ACID; COMPLEMENTARY DNA; DNA; PROTEIN; RECEPTOR;

EID: 0031962116     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/mcb.18.1.388     Document Type: Article
Times cited : (182)

References (48)
  • 1
    • 0030946632 scopus 로고    scopus 로고
    • Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata
    • Braverman, N., G. Steel, C. Obie, A. Moser, H. Moser, S. J. Gould, and D. Valle. 1997. Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata. Nat. Genet. 15:369-376.
    • (1997) Nat. Genet. , vol.15 , pp. 369-376
    • Braverman, N.1    Steel, G.2    Obie, C.3    Moser, A.4    Moser, H.5    Gould, S.J.6    Valle, D.7
  • 2
    • 0030951104 scopus 로고    scopus 로고
    • Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders
    • Chang, C.-C., W.-H. Lee, H. Moser, D. Valle, and S. J. Gould. 1997. Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders. Nat. Genet. 15:385-388.
    • (1997) Nat. Genet. , vol.15 , pp. 385-388
    • Chang, C.-C.1    Lee, W.-H.2    Moser, H.3    Valle, D.4    Gould, S.J.5
  • 3
    • 0028817372 scopus 로고
    • Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
    • Dodt, G., N. Braverman, C. S. Wong, A. Moser, H. W. Moser, P. Watkins, D. Valle, and S. J. Gould. 1995. Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders. Nat. Genet. 9:115-125.
    • (1995) Nat. Genet. , vol.9 , pp. 115-125
    • Dodt, G.1    Braverman, N.2    Wong, C.S.3    Moser, A.4    Moser, H.W.5    Watkins, P.6    Valle, D.7    Gould, S.J.8
  • 4
    • 0029840399 scopus 로고    scopus 로고
    • The SH3 domain of the Saccharomyces cerevisiae peroxisomal membrane protein Pex13p functions as a docking site for Pex5p, a mobile receptor for the import of PTS1-containing proteins
    • Elgersma, Y., L. Kwast, A. Klein, T. Voorn-Brouwer, M. van den Berg, B. Metzig, T. America, H. K. Tabak, and B. Distel. 1996. The SH3 domain of the Saccharomyces cerevisiae peroxisomal membrane protein Pex13p functions as a docking site for Pex5p, a mobile receptor for the import of PTS1-containing proteins. J. Cell Biol. 135:97-109.
    • (1996) J. Cell Biol. , vol.135 , pp. 97-109
    • Elgersma, Y.1    Kwast, L.2    Klein, A.3    Voorn-Brouwer, T.4    Van Den Berg, M.5    Metzig, B.6    America, T.7    Tabak, H.K.8    Distel, B.9
  • 5
    • 0029795490 scopus 로고    scopus 로고
    • Identification of Pex13p, a peroxisomal membrane receptor for the PTS1 recognition factor
    • Erdmann, R., and G. Blobel. 1996. Identification of Pex13p, a peroxisomal membrane receptor for the PTS1 recognition factor. J. Cell Biol. 135:111-121.
    • (1996) J. Cell Biol. , vol.135 , pp. 111-121
    • Erdmann, R.1    Blobel, G.2
  • 6
    • 0028916868 scopus 로고
    • Identification and characterization of the putative human peroxisomal C-terminal targeting signal import receptor
    • Fransen, M., C. Brees, E. Baumgart, J. C. Vanhooren, M. Baes, G. P. Mannaerts, and P. P. V. Veldhoven. 1995. Identification and characterization of the putative human peroxisomal C-terminal targeting signal import receptor. J. Biol. Chem. 270:7731-7736.
    • (1995) J. Biol. Chem. , vol.270 , pp. 7731-7736
    • Fransen, M.1    Brees, C.2    Baumgart, E.3    Vanhooren, J.C.4    Baes, M.5    Mannaerts, G.P.6    Veldhoven, P.P.V.7
  • 7
    • 0030477744 scopus 로고    scopus 로고
    • Approaches to studies on peroxisome biogenesis and human peroxisome-deficient disorders
    • Fujiki, Y. 1996. Approaches to studies on peroxisome biogenesis and human peroxisome-deficient disorders. Ann. N. Y. Acad. Sci. 804:491-501.
    • (1996) Ann. N. Y. Acad. Sci. , vol.804 , pp. 491-501
    • Fujiki, Y.1
  • 8
    • 0030725335 scopus 로고    scopus 로고
    • Molecular defects in genetic diseases of peroxisomes
    • Fujiki, Y. 1997. Molecular defects in genetic diseases of peroxisomes. Biochim. Biophys. Acta 1361:235-250.
    • (1997) Biochim. Biophys. Acta , vol.1361 , pp. 235-250
    • Fujiki, Y.1
  • 10
    • 0029795686 scopus 로고    scopus 로고
    • Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTS1 receptor
    • Gould, S. J., J. E. Kalish, J. C. Morrell, J. Bjorkman, A. J. Urquhart, and D. I. Crane. 1996. Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTS1 receptor. J. Cell Biol. 135:85-95.
    • (1996) J. Cell Biol. , vol.135 , pp. 85-95
    • Gould, S.J.1    Kalish, J.E.2    Morrell, J.C.3    Bjorkman, J.4    Urquhart, A.J.5    Crane, D.I.6
  • 13
    • 0027168271 scopus 로고
    • The pas8 mutant of Pichia pastoris exhibits the peroxisomal protein import deficiencies of Zellweger syndrome cells - The PAS8 protein binds to the COOH-terminal tripeptide peroxisomal targeting signal, and is a member of the TPR protein family
    • McCollum, D., E. Monosov, and S. Subramani. 1993. The pas8 mutant of Pichia pastoris exhibits the peroxisomal protein import deficiencies of Zellweger syndrome cells - the PAS8 protein binds to the COOH-terminal tripeptide peroxisomal targeting signal, and is a member of the TPR protein family. J. Cell Biol. 121:761-774.
    • (1993) J. Cell Biol. , vol.121 , pp. 761-774
    • McCollum, D.1    Monosov, E.2    Subramani, S.3
  • 14
    • 0026643496 scopus 로고
    • Carboxyl-terminal consensus Ser-Lys-Leu-related tripeptide of peroxisomal proteins functions in vitro as a minimal peroxisome-targeting signal
    • Miura, S., I. Kasuya-Arai, H. Mori, S. Miyazawa, T. Osumi, T. Hashimoto, and Y. Fujiki. 1992. Carboxyl-terminal consensus Ser-Lys-Leu-related tripeptide of peroxisomal proteins functions in vitro as a minimal peroxisome-targeting signal. J. Biol. Chem. 267:14405-14411.
    • (1992) J. Biol. Chem. , vol.267 , pp. 14405-14411
    • Miura, S.1    Kasuya-Arai, I.2    Mori, H.3    Miyazawa, S.4    Osumi, T.5    Hashimoto, T.6    Fujiki, Y.7
  • 16
    • 0024528893 scopus 로고
    • Peroxisome targeting signal of rat liver acyl-coenzyme a oxidase resides at the carboxy terminus
    • Miyazawa, S., T. Osumi, T. Hashimoto, K. Ohno, S. Miura, and Y. Fujiki. 1989. Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus. Mol. Cell. Biol. 9:83-91.
    • (1989) Mol. Cell. Biol. , vol.9 , pp. 83-91
    • Miyazawa, S.1    Osumi, T.2    Hashimoto, T.3    Ohno, K.4    Miura, S.5    Fujiki, Y.6
  • 18
    • 0028332245 scopus 로고
    • Differential protein import deficiencies in human peroxisome assembly disorders
    • Motley, A., E. Hettema, B. Distel, and H. Tabak. 1994. Differential protein import deficiencies in human peroxisome assembly disorders. J. Cell Biol. 125:755-767.
    • (1994) J. Cell Biol. , vol.125 , pp. 755-767
    • Motley, A.1    Hettema, E.2    Distel, B.3    Tabak, H.4
  • 20
    • 0040624512 scopus 로고
    • Generation of protein-reactive antibodies by short peptides is an event of high frequency: Implications for the structural basis of immune recognition
    • Niman, H. L., R. A. Houghten, L. E. Walker, R. A. Reisfeld, I. A. Wilson, J. M. Hogle, and R. A. Lerner. 1983. Generation of protein-reactive antibodies by short peptides is an event of high frequency: implications for the structural basis of immune recognition. Proc. Natl. Acad. Sci. USA 80:4949-4953.
    • (1983) Proc. Natl. Acad. Sci. USA , vol.80 , pp. 4949-4953
    • Niman, H.L.1    Houghten, R.A.2    Walker, L.E.3    Reisfeld, R.A.4    Wilson, I.A.5    Hogle, J.M.6    Lerner, R.A.7
  • 21
    • 0031586033 scopus 로고    scopus 로고
    • Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III
    • Okumoto, K., A. Bogaki, K. Tateishi, T. Tsukamoto, T. Osumi, N. Shimozawa, Y. Suzuki, T. Orii, and Y. Fujiki. 1997. Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III. Exp. Cell Res. 233:11-20.
    • (1997) Exp. Cell Res. , vol.233 , pp. 11-20
    • Okumoto, K.1    Bogaki, A.2    Tateishi, K.3    Tsukamoto, T.4    Osumi, T.5    Shimozawa, N.6    Suzuki, Y.7    Orii, T.8    Fujiki, Y.9
  • 22
    • 0031279088 scopus 로고    scopus 로고
    • PEX12 encodes an integral membrane protein of peroxisomes
    • Okumoto, K., and Y. Fujiki. 1997. PEX12 encodes an integral membrane protein of peroxisomes. Nat. Genet. 17:265-266.
    • (1997) Nat. Genet. , vol.17 , pp. 265-266
    • Okumoto, K.1    Fujiki, Y.2
  • 23
    • 2642611565 scopus 로고    scopus 로고
    • Submitted for publication
    • Okumoto, K., et al. Submitted for publication.
    • Okumoto, K.1
  • 25
    • 1842335689 scopus 로고    scopus 로고
    • Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor
    • Purdue, P. E., J. W. Zhang, M. Skoneczny, and P. B. Lazarow. 1997. Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor. Nat. Genet. 15:381-384.
    • (1997) Nat. Genet. , vol.15 , pp. 381-384
    • Purdue, P.E.1    Zhang, J.W.2    Skoneczny, M.3    Lazarow, P.B.4
  • 26
    • 0026574020 scopus 로고
    • Peroxisome assembly mutations in humans: Structural heterogeneity in Zellweger syndrome
    • Santos, M. J., S. Hoefler, A. B. Moser, H. W. Moser, and P. B. Lazarow. 1992. Peroxisome assembly mutations in humans: structural heterogeneity in Zellweger syndrome. J. Cell. Physiol. 151:103-112.
    • (1992) J. Cell. Physiol. , vol.151 , pp. 103-112
    • Santos, M.J.1    Hoefler, S.2    Moser, A.B.3    Moser, H.W.4    Lazarow, P.B.5
  • 27
    • 0029979607 scopus 로고    scopus 로고
    • Common principles of protein translocation across membranes
    • Washington, D.C.
    • Schatz, G., and B. Dobberstein. 1996. Common principles of protein translocation across membranes. Science (Washington, D.C.) 271:1519-1526.
    • (1996) Science , vol.271 , pp. 1519-1526
    • Schatz, G.1    Dobberstein, B.2
  • 28
    • 0026492894 scopus 로고
    • Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome
    • Shimozawa, N., T. Tsukamoto, Y. Suzuki, T. Orii, and Y. Fujiki. 1992. Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome. J. Clin. Invest. 90:1864-1870.
    • (1992) J. Clin. Invest. , vol.90 , pp. 1864-1870
    • Shimozawa, N.1    Tsukamoto, T.2    Suzuki, Y.3    Orii, T.4    Fujiki, Y.5
  • 29
    • 0026523576 scopus 로고
    • A human gene responsible for Zellweger syndrome that affects peroxisome assembly
    • Washington, D.C.
    • Shimozawa, N., T. Tsukamoto, Y. Suzuki, T. Orii, Y. Shirayoshi, T. Mori, and Y. Fujiki. 1992. A human gene responsible for Zellweger syndrome that affects peroxisome assembly. Science (Washington, D.C.) 255:1132-1134.
    • (1992) Science , vol.255 , pp. 1132-1134
    • Shimozawa, N.1    Tsukamoto, T.2    Suzuki, Y.3    Orii, T.4    Shirayoshi, Y.5    Mori, T.6    Fujiki, Y.7
  • 30
    • 0029047855 scopus 로고
    • Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders
    • Slawecki, M. L., G. Dodt, S. Steinberg, A. B. Moser, H. W. Moser, and S. J. Gould. 1995. Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders. J. Cell Sci. 108: 1817-1829.
    • (1995) J. Cell Sci. , vol.108 , pp. 1817-1829
    • Slawecki, M.L.1    Dodt, G.2    Steinberg, S.3    Moser, A.B.4    Moser, H.W.5    Gould, S.J.6
  • 31
    • 0027333416 scopus 로고
    • Protein import into peroxisomes and biogenesis of the organelle
    • Subramani, S. 1993. Protein import into peroxisomes and biogenesis of the organelle. Annu. Rev. Cell Biol. 9:445-478.
    • (1993) Annu. Rev. Cell Biol. , vol.9 , pp. 445-478
    • Subramani, S.1
  • 32
    • 0025941962 scopus 로고
    • A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase
    • Swinkels, B. W., S. J. Gould, A. G. Bodnar, R. A. Rachubinski, and S. Subramani. 1991. A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase. EMBO J. 10:3255-3262.
    • (1991) EMBO J. , vol.10 , pp. 3255-3262
    • Swinkels, B.W.1    Gould, S.J.2    Bodnar, A.G.3    Rachubinski, R.A.4    Subramani, S.5
  • 33
    • 0030799396 scopus 로고    scopus 로고
    • Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals
    • Tateishi, K., K. Okumoto, N. Shimozawa, T. Tsukamoto, T. Osumi, Y. Suzuki, N. Kondo, I. Okano, and Y. Fujiki. 1997. Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals. Eur. J. Cell Biol. 73:352-359.
    • (1997) Eur. J. Cell Biol. , vol.73 , pp. 352-359
    • Tateishi, K.1    Okumoto, K.2    Shimozawa, N.3    Tsukamoto, T.4    Osumi, T.5    Suzuki, Y.6    Kondo, N.7    Okano, I.8    Fujiki, Y.9
  • 34
    • 0029087571 scopus 로고
    • The Pichia pastoris peroxisomal protein PAS8p is the receptor for the C-terminal tripeptide peroxisome targeting signal
    • Terlecky, S. R., W. M. Nuttley, D. McCollum, E. Sock, and S. Subramani. 1995. The Pichia pastoris peroxisomal protein PAS8p is the receptor for the C-terminal tripeptide peroxisome targeting signal. EMBO J. 14:3627-3634.
    • (1995) EMBO J. , vol.14 , pp. 3627-3634
    • Terlecky, S.R.1    Nuttley, W.M.2    McCollum, D.3    Sock, E.4    Subramani, S.5
  • 36
  • 37
    • 0026064431 scopus 로고
    • Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant
    • Tsukamoto, T., S. Miura, and Y. Fujiki. 1991. Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant. Nature (London) 350:77-81.
    • (1991) Nature (London) , vol.350 , pp. 77-81
    • Tsukamoto, T.1    Miura, S.2    Fujiki, Y.3
  • 39
    • 0027965618 scopus 로고
    • Peroxisome assembly factor-1: Nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis
    • Tsukamoto, T., N. Shimozawa, and Y. Fujiki. 1994. Peroxisome assembly factor-1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis. Mol. Cell. Biol. 14:5458-5465.
    • (1994) Mol. Cell. Biol. , vol.14 , pp. 5458-5465
    • Tsukamoto, T.1    Shimozawa, N.2    Fujiki, Y.3
  • 40
    • 0025342563 scopus 로고
    • Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes
    • Tsukamoto, T., S. Yokota, and Y. Fujiki. 1990. Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes. J. Cell Biol. 110:651-660.
    • (1990) J. Cell Biol. , vol.110 , pp. 651-660
    • Tsukamoto, T.1    Yokota, S.2    Fujiki, Y.3
  • 42
    • 0027138676 scopus 로고
    • PAS10 is a tetratricopeptide-repeat protein that is essential for the import of most matrix proteins into peroxisomes of Saccharomyces cerevisiae
    • Van der Leij, I., M. M. Franse, Y. Elgersma, B. Distel, and H. F. Tabak. 1993. PAS10 is a tetratricopeptide-repeat protein that is essential for the import of most matrix proteins into peroxisomes of Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. USA 90:11782-11786.
    • (1993) Proc. Natl. Acad. Sci. USA , vol.90 , pp. 11782-11786
    • Van Der Leij, I.1    Franse, M.M.2    Elgersma, Y.3    Distel, B.4    Tabak, H.F.5
  • 43
    • 0027482051 scopus 로고
    • Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders
    • Wendland, M., and S. Subramani. 1993. Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders. J. Clin. Invest. 92:2462-2468.
    • (1993) J. Clin. Invest. , vol.92 , pp. 2462-2468
    • Wendland, M.1    Subramani, S.2
  • 44
    • 0029024783 scopus 로고
    • Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders
    • Wiemer, E. A., W. M. Nuttley, B. L. Bertolaet, X. Li, U. Francke, M. J. Wheelock, U. K. Anne, K. R. Johnson, and S. Subramani. 1995. Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders. J. Cell Biol. 130:51-65.
    • (1995) J. Cell Biol. , vol.130 , pp. 51-65
    • Wiemer, E.A.1    Nuttley, W.M.2    Bertolaet, B.L.3    Li, X.4    Francke, U.5    Wheelock, M.J.6    Anne, U.K.7    Johnson, K.R.8    Subramani, S.9
  • 46
    • 0029888487 scopus 로고    scopus 로고
    • The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor
    • Yahraus, T., N. Braverman, G. Dodt, J. E. Kalish, J. C. Morrell, H. W. Moser, D. Valle, and S. J. Gould. 1996. The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor. EMBO J. 15:2914-2923.
    • (1996) EMBO J. , vol.15 , pp. 2914-2923
    • Yahraus, T.1    Braverman, N.2    Dodt, G.3    Kalish, J.E.4    Morrell, J.C.5    Moser, H.W.6    Valle, D.7    Gould, S.J.8
  • 47
    • 0023782245 scopus 로고
    • A possible role for plasmalogens in protecting animal cells against photosensitized killing
    • Zoeller, R. A., O. H. Morand, and C. R. H. Raetz. 1988. A possible role for plasmalogens in protecting animal cells against photosensitized killing. J. Biol. Chem. 263:11590-11596.
    • (1988) J. Biol. Chem. , vol.263 , pp. 11590-11596
    • Zoeller, R.A.1    Morand, O.H.2    Raetz, C.R.H.3
  • 48
    • 0022537701 scopus 로고
    • Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly
    • Zoeller, R. A., and C. R. H. Raetz. 1986. Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly. Proc. Natl. Acad. Sci. USA 83:5170-5174.
    • (1986) Proc. Natl. Acad. Sci. USA , vol.83 , pp. 5170-5174
    • Zoeller, R.A.1    Raetz, C.R.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.