메뉴 건너뛰기




Volumn 5, Issue 11, 2010, Pages

The ubiquitin ligase Ubr2, a recognition E3 component of the N-end rule pathway, stabilizes Tex19.1 during spermatogenesis

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; PROTEIN TEX19.1; UBIQUITIN LIGASE UBR2; UBIQUITIN PROTEIN LIGASE E3; UNCLASSIFIED DRUG; CYSTEINE; METHIONINE; NUCLEAR PROTEIN; TEX19 PROTEIN, MOUSE; UBIQUITIN PROTEIN LIGASE; UBR2 PROTEIN, MOUSE;

EID: 78649496203     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0014017     Document Type: Article
Times cited : (35)

References (27)
  • 1
    • 0023003380 scopus 로고
    • In vivo half-life of a protein is a function of its amino-terminal residue
    • Bachmair A, Finley D, Varshavsky A (1986) In vivo half-life of a protein is a function of its amino-terminal residue. Science 234(4773): 179-186.
    • (1986) Science , vol.234 , Issue.4773 , pp. 179-186
    • Bachmair, A.1    Finley, D.2    Varshavsky, A.3
  • 2
    • 35548974677 scopus 로고    scopus 로고
    • The mammalian N-end rule pathway: New insights into its components and physiological roles
    • Tasaki T, Kwon YT (2007) The mammalian N-end rule pathway: New insights into its components and physiological roles. Trends Biochem Sci 32(11): 520-528.
    • (2007) Trends Biochem Sci , vol.32 , Issue.11 , pp. 520-528
    • Tasaki, T.1    Kwon, Y.T.2
  • 3
    • 27144557281 scopus 로고    scopus 로고
    • The N-end rule pathway as a nitric oxide sensor controlling the levels of multiple regulators
    • Hu RG, Sheng J, Qi X, Xu Z, Takahashi TT, et al. (2005) The N-end rule pathway as a nitric oxide sensor controlling the levels of multiple regulators. Nature 437(7061): 981-986.
    • (2005) Nature , vol.437 , Issue.7061 , pp. 981-986
    • Hu, R.G.1    Sheng, J.2    Qi, X.3    Xu, Z.4    Takahashi, T.T.5
  • 4
    • 0037025163 scopus 로고    scopus 로고
    • An essential role of N-terminal arginylation in cardiovascular development
    • Kwon YT, Kashina AS, Davydov IV, Hu RG, An JY, et al. (2002) An essential role of N-terminal arginylation in cardiovascular development. Science 297(5578): 96-99.
    • (2002) Science , vol.297 , Issue.5578 , pp. 96-99
    • Kwon, Y.T.1    Kashina, A.S.2    Davydov, I.V.3    Hu, R.G.4    An, J.Y.5
  • 5
    • 27244444724 scopus 로고    scopus 로고
    • RGS4 and RGS5 are in vivo substrates of the N-end rule pathway
    • Lee MJ, Tasaki T, Moroi K, An JY, Kimura S, et al. (2005) RGS4 and RGS5 are in vivo substrates of the N-end rule pathway. Proc Natl Acad Sci U S A 102(42): 15030-15035.
    • (2005) Proc Natl Acad Sci U S A , vol.102 , Issue.42 , pp. 15030-15035
    • Lee, M.J.1    Tasaki, T.2    Moroi, K.3    An, J.Y.4    Kimura, S.5
  • 6
    • 59449093066 scopus 로고    scopus 로고
    • The substrate recognition domains of the N-end rule pathway
    • Tasaki T, Zakrzewska A, Dudgeon DD, Jiang Y, Lazo JS, et al. (2009) The substrate recognition domains of the N-end rule pathway. J Biol Chem 284(3): 1884-1895.
    • (2009) J Biol Chem , vol.284 , Issue.3 , pp. 1884-1895
    • Tasaki, T.1    Zakrzewska, A.2    Dudgeon, D.D.3    Jiang, Y.4    Lazo, J.S.5
  • 7
    • 0037936841 scopus 로고    scopus 로고
    • Degradation of DIAP1 by the N-end rule pathway is essential for regulating apoptosis
    • Ditzel M, Wilson R, Tenev T, Zachariou A, Paul A, et al. (2003) Degradation of DIAP1 by the N-end rule pathway is essential for regulating apoptosis. Nat Cell Biol 5(5): 467-473.
    • (2003) Nat Cell Biol , vol.5 , Issue.5 , pp. 467-473
    • Ditzel, M.1    Wilson, R.2    Tenev, T.3    Zachariou, A.4    Paul, A.5
  • 8
    • 0035912183 scopus 로고    scopus 로고
    • Degradation of a cohesin subunit by the N-end rule pathway is essential for chromosome stability
    • Rao H, Uhlmann F, Nasmyth K, Varshavsky A (2001) Degradation of a cohesin subunit by the N-end rule pathway is essential for chromosome stability. Nature 410(6831): 955-959.
    • (2001) Nature , vol.410 , Issue.6831 , pp. 955-959
    • Rao, H.1    Uhlmann, F.2    Nasmyth, K.3    Varshavsky, A.4
  • 9
    • 76649112438 scopus 로고    scopus 로고
    • UBR2 mediates transcriptional silencing during spermatogenesis via histone ubiquitination
    • An JY, Kim EA, Jiang Y, Zakrzewska A, Kim DE, et al. (2010) UBR2 mediates transcriptional silencing during spermatogenesis via histone ubiquitination. Proc Natl Acad Sci U S A 107(5): 1912-1917.
    • (2010) Proc Natl Acad Sci U S A , vol.107 , Issue.5 , pp. 1912-1917
    • An, J.Y.1    Kim, E.A.2    Jiang, Y.3    Zakrzewska, A.4    Kim, D.E.5
  • 10
    • 0032472322 scopus 로고    scopus 로고
    • The N-end rule pathway controls the import of peptides through degradation of a transcriptional repressor
    • Byrd C, Turner GC, Varshavsky A (1998) The N-end rule pathway controls the import of peptides through degradation of a transcriptional repressor. EMBO J 17(1): 269-277.
    • (1998) EMBO J , vol.17 , Issue.1 , pp. 269-277
    • Byrd, C.1    Turner, G.C.2    Varshavsky, A.3
  • 11
    • 33749057086 scopus 로고    scopus 로고
    • Spatiotemporal regulation of c-fos by ERK5 and the E3 ubiquitin ligase UBR1, and its biological role
    • Sasaki T, Kojima H, Kishimoto R, Ikeda A, Kunimoto H, et al. (2006) Spatiotemporal regulation of c-fos by ERK5 and the E3 ubiquitin ligase UBR1, and its biological role. Mol Cell 24(1): 63-75.
    • (2006) Mol Cell , vol.24 , Issue.1 , pp. 63-75
    • Sasaki, T.1    Kojima, H.2    Kishimoto, R.3    Ikeda, A.4    Kunimoto, H.5
  • 12
    • 28444458475 scopus 로고    scopus 로고
    • Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (johansonblizzard syndrome)
    • Zenker M, Mayerle J, Lerch MM, Tagariello A, Zerres K, et al. (2005) Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (johansonblizzard syndrome). Nat Genet 37(12): 1345-1350.
    • (2005) Nat Genet , vol.37 , Issue.12 , pp. 1345-1350
    • Zenker, M.1    Mayerle, J.2    Lerch, M.M.3    Tagariello, A.4    Zerres, K.5
  • 13
    • 0242664014 scopus 로고    scopus 로고
    • Female lethality and apoptosis of spermatocytes in mice lacking the UBR2 ubiquitin ligase of the N-end rule pathway
    • Kwon YT, Xia Z, An JY, Tasaki T, Davydov IV, et al. (2003) Female lethality and apoptosis of spermatocytes in mice lacking the UBR2 ubiquitin ligase of the N-end rule pathway. Mol Cell Biol 23(22): 8255-8271.
    • (2003) Mol Cell Biol , vol.23 , Issue.22 , pp. 8255-8271
    • Kwon, Y.T.1    Xia, Z.2    An, J.Y.3    Tasaki, T.4    Davydov, I.V.5
  • 14
    • 0035071815 scopus 로고    scopus 로고
    • An abundance of X-linked genes expressed in spermatogonia
    • Wang PJ, McCarrey JR, Yang F, Page DC (2001) An abundance of X-linked genes expressed in spermatogonia. Nat Genet 27(4): 422-426.
    • (2001) Nat Genet , vol.27 , Issue.4 , pp. 422-426
    • Wang, P.J.1    McCarrey, J.R.2    Yang, F.3    Page, D.C.4
  • 15
    • 52949118505 scopus 로고    scopus 로고
    • Deletion of the pluripotency-associated tex19.1 gene causes activation of endogenous retroviruses and defective spermatogenesis in mice
    • Ollinger R, Childs AJ, Burgess HM, Speed RM, Lundegaard PR, et al. (2008) Deletion of the pluripotency-associated tex19.1 gene causes activation of endogenous retroviruses and defective spermatogenesis in mice. PLoS Genet 4(9): e1000199.
    • (2008) PLoS Genet , vol.4 , Issue.9
    • Ollinger, R.1    Childs, A.J.2    Burgess, H.M.3    Speed, R.M.4    Lundegaard, P.R.5
  • 16
    • 43049143946 scopus 로고    scopus 로고
    • Tex19, a mammalian-specific protein with a restricted expression in pluripotent stem cells and germ line
    • Kuntz S, Kieffer E, Bianchetti L, Lamoureux N, Fuhrmann G, et al. (2008) Tex19, a mammalian-specific protein with a restricted expression in pluripotent stem cells and germ line. Stem Cells 26(3): 734-744.
    • (2008) Stem Cells , vol.26 , Issue.3 , pp. 734-744
    • Kuntz, S.1    Kieffer, E.2    Bianchetti, L.3    Lamoureux, N.4    Fuhrmann, G.5
  • 17
    • 26444490659 scopus 로고    scopus 로고
    • Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse
    • Wang PJ, Page DC, McCarrey JR (2005) Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse. Hum Mol Genet 14(19): 2911-2918.
    • (2005) Hum Mol Genet , vol.14 , Issue.19 , pp. 2911-2918
    • Wang, P.J.1    Page, D.C.2    McCarrey, J.R.3
  • 18
    • 0030578416 scopus 로고    scopus 로고
    • Organization of SCP1 protein molecules within synaptonemal complexes of the rat
    • Schmekel K, Meuwissen RL, Dietrich AJ, Vink AC, van Marle J, et al. (1996) Organization of SCP1 protein molecules within synaptonemal complexes of the rat. Exp Cell Res 226(1): 20-30.
    • (1996) Exp Cell Res , vol.226 , Issue.1 , pp. 20-30
    • Schmekel, K.1    Meuwissen, R.L.2    Dietrich, A.J.3    Vink, A.C.4    van Marle, J.5
  • 19
    • 22344442015 scopus 로고    scopus 로고
    • Mouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formation
    • de Vries FA, de Boer E, van den Bosch M, Baarends WM, Ooms M, et al. (2005) Mouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formation. Genes Dev 19(11): 1376-1389.
    • (2005) Genes Dev , vol.19 , Issue.11 , pp. 1376-1389
    • de Vries, F.A.1    de Boer, E.2    van den Bosch, M.3    Baarends, W.M.4    Ooms, M.5
  • 20
    • 33646770606 scopus 로고    scopus 로고
    • Mouse SYCP2 is required for synaptonemal complex assembly and chromosomal synapsis during male meiosis
    • Yang F, De La Fuente R, Leu NA, Baumann C, McLaughlin KJ, et al. (2006) Mouse SYCP2 is required for synaptonemal complex assembly and chromosomal synapsis during male meiosis. J Cell Biol 173(4): 497-507.
    • (2006) J Cell Biol , vol.173 , Issue.4 , pp. 497-507
    • Yang, F.1    de la Fuente, R.2    Leu, N.A.3    Baumann, C.4    McLaughlin, K.J.5
  • 21
    • 0029098294 scopus 로고
    • Complementary deoxyribonucleic acid cloning and characterization of mSP-10: The mouse homologue of human acrosomal protein SP-10
    • Reddi PP, Naaby-Hansen S, Aguolnik I, Tsai JY, Silver LM, et al. (1995) Complementary deoxyribonucleic acid cloning and characterization of mSP-10: The mouse homologue of human acrosomal protein SP-10. Biol Reprod 53(4): 873-881.
    • (1995) Biol Reprod , vol.53 , Issue.4 , pp. 873-881
    • Reddi, P.P.1    Naaby-Hansen, S.2    Aguolnik, I.3    Tsai, J.Y.4    Silver, L.M.5
  • 22
    • 19544366597 scopus 로고    scopus 로고
    • RECQL4, mutated in the rothmund-thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway
    • Yin J, Kwon YT, Varshavsky A, Wang W (2004) RECQL4, mutated in the rothmund-thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway. Hum Mol Genet 13(20): 2421-2430.
    • (2004) Hum Mol Genet , vol.13 , Issue.20 , pp. 2421-2430
    • Yin, J.1    Kwon, Y.T.2    Varshavsky, A.3    Wang, W.4
  • 23
    • 0032939991 scopus 로고    scopus 로고
    • Mutations in RECQL4 cause a subset of cases of rothmund-thomson syndrome
    • Kitao S, Shimamoto A, Goto M, Miller RW, Smithson WA, et al. (1999) Mutations in RECQL4 cause a subset of cases of rothmund-thomson syndrome. Nat Genet 22(1): 82-84.
    • (1999) Nat Genet , vol.22 , Issue.1 , pp. 82-84
    • Kitao, S.1    Shimamoto, A.2    Goto, M.3    Miller, R.W.4    Smithson, W.A.5
  • 24
    • 0242609126 scopus 로고    scopus 로고
    • Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases
    • Siitonen HA, Kopra O, Kaariainen H, Haravuori H, Winter RM, et al. (2003) Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases. Hum Mol Genet 12(21): 2837-2844.
    • (2003) Hum Mol Genet , vol.12 , Issue.21 , pp. 2837-2844
    • Siitonen, H.A.1    Kopra, O.2    Kaariainen, H.3    Haravuori, H.4    Winter, R.M.5
  • 25
    • 0034608802 scopus 로고    scopus 로고
    • Exploring the sequence space for tetracycline-dependent transcriptional activators: Novel mutations yield expanded range and sensitivity
    • Urlinger S, Baron U, Thellmann M, Hasan MT, Bujard H, et al. (2000) Exploring the sequence space for tetracycline-dependent transcriptional activators: Novel mutations yield expanded range and sensitivity. Proc Natl Acad Sci U S A 97(14): 7963-7968.
    • (2000) Proc Natl Acad Sci U S A , vol.97 , Issue.14 , pp. 7963-7968
    • Urlinger, S.1    Baron, U.2    Thellmann, M.3    Hasan, M.T.4    Bujard, H.5
  • 26


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.