Literature DB >> 8422966

5S rRNA modification in the hyperthermophilic archaea Sulfolobus solfataricus and Pyrodictium occultum.

E Bruenger1, J A Kowalak, Y Kuchino, J A McCloskey, H Mizushima, K O Stetter, P F Crain.   

Abstract

The 5S rRNAs from Sulfolobus solfataricus and Pyrodictium occultum were digested to nucleosides and analyzed using directly-combined HPLC/mass spectrometry. P. occultum 5S rRNA contains two modified nucleoside species, N4-acetylcytidine (ac4C) and N4-acetyl-2'-O-methylcytidine (ac4Cm). Oligonucleotides were generated from P. occultum 5S rRNA by RNase T1 hydrolysis, and their molecular weights were determined using electrospray mass spectrometry and compared with those predicted from the P. occultum 5S RNA gene sequence. Deviation in mass between expected and observed molecular weights permitted ac4Cm to be located at position 35, in the nonanucleotide CAA-CACC[ac4Cm]G, and the ac4C in one or both of two (C,U)G trinucleotides. 2'-O-Methylcytidine is unambiguously characterized in S. solfataricus 5S rRNA, confirming earlier tentative assignments at the analogous sequence position (Stahl, D.A., Luehrsen, K.R., Woese, C.R., and Pace, N.R. (1981) Nucleic Acids Res., Vol. 9, pp. 6129-6137; Dams, E., Londei, P., Cammarano, P., Vandenberghe, A., and De Wachter, R. (1983) Nucleic Acids Res. Vol. 11, pp. 4667-4676). Potential effects of the presence of ac4C and ac4Cm on thermal stabilization of 5S rRNA in thermophiles are discussed.

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Year:  1993        PMID: 8422966     DOI: 10.1096/fasebj.7.1.8422966

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  28 in total

1.  Identification of the mass-silent post-transcriptionally modified nucleoside pseudouridine in RNA by matrix-assisted laser desorption/ionization mass spectrometry.

Authors:  K G Patteson; L P Rodicio; P A Limbach
Journal:  Nucleic Acids Res       Date:  2001-05-15       Impact factor: 16.971

2.  Molecular mass measurement of intact ribonucleic acids via electrospray ionization quadrupole mass spectrometry.

Authors:  P A Limbach; P F Crain; J A McCloskey
Journal:  J Am Soc Mass Spectrom       Date:  1995-01       Impact factor: 3.109

3.  The single pseudouridine residue in Escherichia coli 16S RNA is located at position 516.

Authors:  A Bakin; J A Kowalak; J A McCloskey; J Ofengand
Journal:  Nucleic Acids Res       Date:  1994-09-11       Impact factor: 16.971

Review 4.  Summary: the modified nucleosides of RNA.

Authors:  P A Limbach; P F Crain; J A McCloskey
Journal:  Nucleic Acids Res       Date:  1994-06-25       Impact factor: 16.971

5.  The primary structure of Harpalus rufipes 5S ribosomal RNA: a contribution for understanding insect evolution.

Authors:  M Z Barciszewska; A Gawronski; M Szymanski; V A Erdmann
Journal:  Mol Biol Rep       Date:  1995       Impact factor: 2.316

Review 6.  Mass spectrometry of nucleotides and oligonucleotides.

Authors:  P Miketova; K H Schram
Journal:  Mol Biotechnol       Date:  1997-12       Impact factor: 2.695

7.  Posttranscriptional modifications in 16S and 23S rRNAs of the archaeal hyperthermophile Sulfolobus solfataricus.

Authors:  K R Noon; E Bruenger; J A McCloskey
Journal:  J Bacteriol       Date:  1998-06       Impact factor: 3.490

8.  Mapping posttranscriptional modifications in 5S ribosomal RNA by MALDI mass spectrometry.

Authors:  F Kirpekar; S Douthwaite; P Roepstorff
Journal:  RNA       Date:  2000-02       Impact factor: 4.942

9.  Nucleotide resolution sequencing of N4-acetylcytidine in RNA.

Authors:  Justin M Thomas; Keri M Bryson; Jordan L Meier
Journal:  Methods Enzymol       Date:  2019-03-12       Impact factor: 1.600

10.  A single acetylation of 18 S rRNA is essential for biogenesis of the small ribosomal subunit in Saccharomyces cerevisiae.

Authors:  Satoshi Ito; Yu Akamatsu; Akiko Noma; Satoshi Kimura; Kenjyo Miyauchi; Yoshiho Ikeuchi; Takeo Suzuki; Tsutomu Suzuki
Journal:  J Biol Chem       Date:  2014-08-01       Impact factor: 5.157

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