Posttranscriptional modification of tRNA in psychrophilic bacteria

被引:91
作者
Dalluge, JJ
Hamamoto, T
Horikoshi, K
Morita, RY
Stetter, KO
McCloskey, JA
机构
[1] UNIV UTAH, DEPT MED CHEM, SALT LAKE CITY, UT 84112 USA
[2] UNIV UTAH, DEPT BIOCHEM, SALT LAKE CITY, UT 84132 USA
[3] RIKEN, JAPAN MARINE SCI & TECHNOL CTR, DEEPSTAR PROGRAM, WAKO, SAITAMA 35101, JAPAN
[4] OREGON STATE UNIV, DEPT MICROBIOL, CORVALLIS, OR 97331 USA
[5] OREGON STATE UNIV, COLL OCEANOG, CORVALLIS, OR 97331 USA
[6] UNIV REGENSBURG, LEHRSTUHL MIKROBIOL, D-93049 REGENSBURG, GERMANY
关键词
D O I
10.1128/jb.179.6.1918-1923.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Posttranscriptional modification in tRNA is known to play a multiplicity of functional roles, including maintenance of tertiary structure and cellular adaptation to environmental factors such as temperature. Nucleoside modification has been studied in unfractionated tRNA from three psychrophilic bacteria (ANT-300 and Vibrio sp. strains 5710 and 29-6) and one psychrotrophic bacterium (Lactobacillus bavaricus). Based on analysis of total enzymatic hydrolysates by liquid chromatography-mass spectrometry, unprecedented low amounts of modification were found in the psychrophiles, particularly from the standpoint of structural diversity of modifications observed. Thirteen to 15 different forms of posttranscriptional modification were found in the psychrophiles, and 10 were found in L. bavaricus, compared nith approximately 29 known to occur in bacterial mesophiles and 24 to 31 known to occur in the archaeal hyperthermophiles. The four most abundant modified nucleosides in tRNA from each organism were dihydrouridine, pseudouridine, 7-methylguanosine, and 5-methyluridine. The molar abundances of the latter three nucleosides were comparable to those found in tRNA from Escherichia coli. By contrast, the high levels of dihydrouridine observed in all three psychrophiles are unprecedented for any organism in any of the three phylogenetic domains. tRNA from these organisms contains 40 to 70% more dihydrouridine, on average, than that of the mesophile E. coli or the psychrotroph L. bavaricus. This finding supports the concept that a functional role for dihydrouridine is in maintenance of conformational flexibility of RNA, especially important to organisms growing under conditions where the dynamics of thermal motion are severely compromised. This is in contrast to the role of modifications contained in RNA from thermophiles, which is to reduce regional RNA flexibility and provide structural stability to RNA for adaptation to high temperature.
引用
收藏
页码:1918 / 1923
页数:6
相关论文
共 59 条
  • [1] EFFECT OF GROWTH TEMPERATURES ON IN-VIVO RIBOSE METHYLATION OF BACILLUS-STEAROTHERMOPHILUS TRANSFER-RNA
    AGRIS, PF
    KOH, H
    SOLL, D
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1973, 154 (01) : 277 - 282
  • [2] Baross J. A., 1978, MICROBIAL LIFE EXTRE, P9
  • [3] TRANSFER-RNA MODIFICATION
    BJORK, GR
    ERICSON, JU
    GUSTAFSSON, CED
    HAGERVALL, TG
    JONSSON, YH
    WIKSTROM, PM
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 : 263 - 287
  • [4] Bjork GR, 1992, TRANSFER RNA PROTEIN, P23
  • [5] BUCK M, 1983, ANAL BIOCHEM, V129, P1, DOI 10.1016/0003-2697(83)90044-1
  • [6] A PHYLOGENETIC ANALYSIS OF AQUIFEX-PYROPHILUS
    BURGGRAF, S
    OLSEN, GJ
    STETTER, KO
    WOESE, CR
    [J]. SYSTEMATIC AND APPLIED MICROBIOLOGY, 1992, 15 (03) : 352 - 356
  • [7] The RNA modification database
    Crain, PF
    McCloskey, JA
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (01) : 126 - 127
  • [8] PREPARATION AND ENZYMATIC-HYDROLYSIS OF DNA AND RNA FOR MASS-SPECTROMETRY
    CRAIN, PF
    [J]. METHODS IN ENZYMOLOGY, 1990, 193 : 782 - 790
  • [9] Quantitative measurement of dihydrouridine in RNA using isotope dilution liquid chromatography mass spectrometry (LC/MS)
    Dalluge, JJ
    Hashizume, T
    McCloskey, JA
    [J]. NUCLEIC ACIDS RESEARCH, 1996, 24 (16) : 3242 - 3245
  • [10] Conformational flexibility in RNA: The role of dihydrouridine
    Dalluge, JJ
    Hashizume, T
    Sopchik, AE
    McCloskey, JA
    Davis, DR
    [J]. NUCLEIC ACIDS RESEARCH, 1996, 24 (06) : 1073 - 1079