HMRF1L is a human mitochondrial translation release factor involved in the decoding of the termination codons UAA and UAG

被引:36
作者
Nozaki, Yusuke [1 ]
Matsunaga, Noriko [1 ]
Ishizawa, Toshihiro [1 ]
Ueda, Takuya [1 ]
Takeuchi, Nono [1 ]
机构
[1] Univ Tokyo, Grad Sch Frontier Sci, Dept Med Genome Sci, Kashiwa, Chiba 2778562, Japan
关键词
D O I
10.1111/j.1365-2443.2008.01181.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
While all essential mammalian mitochondrial factors involved in the initiation and elongation phases of translation have been cloned and well characterized, little is known about the factors involved in the termination process. In the present work, we report the functional analysis of human mitochondrial translation release factors (RF). Here, we show that HMRF1, which had been previously denoted as a human mitochondrial RF, was inactive in in vitro translation system, although it is a mitochondrial protein. Instead, we identified another human mitochondrial RF candidate, HMRF1L, and demonstrated that HMRF1L is indeed a mitochondrial protein that functions specifically as an RF for the decoding of mitochondrial UAA and UAG termination codons in vitro. The identification of the functional mitochondrial RF brings us much closer to a detailed understanding of the translational termination process in mammalian mitochondria as well as to the unraveling of the molecular mechanism of diseases caused by the dys-regulation of translational termination in human mitochondria.
引用
收藏
页码:429 / 438
页数:10
相关论文
共 60 条
  • [1] Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease
    Abahuni, Nadine
    Gispert, Suzana
    Bauer, Peter
    Riess, Olaf
    Krueger, Rejko
    Becker, Tim
    Auburger, Georg
    [J]. NEUROSCIENCE LETTERS, 2007, 414 (02) : 126 - 129
  • [2] SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME
    ANDERSON, S
    BANKIER, AT
    BARRELL, BG
    DEBRUIJN, MHL
    COULSON, AR
    DROUIN, J
    EPERON, IC
    NIERLICH, DP
    ROE, BA
    SANGER, F
    SCHREIER, PH
    SMITH, AJH
    STADEN, R
    YOUNG, IG
    [J]. NATURE, 1981, 290 (5806) : 457 - 465
  • [3] [Anonymous], TRANSLATIONAL CONTRO
  • [4] The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1
    Antonicka, Hana
    Sasarman, Florin
    Kennaway, Nancy G.
    Shoubridge, Eric A.
    [J]. HUMAN MOLECULAR GENETICS, 2006, 15 (11) : 1835 - 1846
  • [5] BARRELL BG, 1979, NATURE, V282, P189, DOI 10.1038/282189a0
  • [6] SEQUENCE AND GENE ORGANIZATION OF MOUSE MITOCHONDRIAL-DNA
    BIBB, MJ
    VANETTEN, RA
    WRIGHT, CT
    WALBERG, MW
    CLAYTON, DA
    [J]. CELL, 1981, 26 (02) : 167 - 180
  • [7] Toward the full set of human mitochondrial aminoacyl-tRNA synthetases:: Characterization of AspRS and TyrRS
    Bonnefond, L
    Fender, A
    Rudinger-Thirion, J
    Giegé, R
    Florentz, C
    Sissler, M
    [J]. BIOCHEMISTRY, 2005, 44 (12) : 4805 - 4816
  • [8] Expression and characterization of the human mitochondrial leucyl-tRNA synthetase
    Bullard, JM
    Cai, YC
    Spremulli, LL
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2000, 1490 (03): : 245 - 258
  • [9] Expression and characterization of a human mitochondrial phenylalanyl-tRNA synthetase
    Bullard, JN
    Cai, YC
    Demeler, B
    Spremulli, LL
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1999, 288 (04) : 567 - 577
  • [10] Cytoplasmic and mitochondrial protein translation in axonal and dendritic terminal arborization
    Chihara, Takahiro
    Luginbuhl, David
    Luo, Liqun
    [J]. NATURE NEUROSCIENCE, 2007, 10 (07) : 828 - 837