Skip Navigation

This Article
Right arrow Print PDF (726K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (204)
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Woese, C.R.
Right arrow Articles by Noller, H.F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Woese, C.R.
Right arrow Articles by Noller, H.F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1980, Vol. 8, No. 10 2275-2294
© 1980


Articles

Secondary structure model for bacterial 16S ribosomal RNA: phylogenetic, enzymatic and chemical evidence

C.R. Woese, L.J. Magrum, R. Gupta, R.B. Siegel, D.A. Stahl, J. Kop, N. Crawford, R. Brosius, R. Gutell, J.J. Hogan and H.F. Noller

Department of Genetics and Development, University of Illinois Urbana, IL 61801, USA Thimann Laboratories, University of California at Santa Cruz Santa Cruz, CA 95064, USA

Received May 2, 1980. We have derived a secondary structure model for 16S ribosomal RNA on the basis of comparative sequence analysis, chemical modification studies and nuclease susceptibility data. Nucleotide sequences of the E. coli and B. brevis 16S rRNA chains, and of RNAse T1 oligomer catalogs from 16S rRNAs of over 100 species of eubacteria were used for phylogenetic comparison. Chemical modification of G by glyoxal, A by m-chloroperbenzoic acid and C by bisulfite In naked 16S rRNA, and G by kethoxal in active and inactive 30S ribosomal subunits was taken as an indication of single stranded structure. Further support for the structure was obtained from susceptibility to RNases A and T1. These three approaches are in excellent agreement. The structure contains fifty helical elements organized into four major domains, in which 46 percent of the nucleotides of 16S rRNA are involved in base pairing. Phylogenetic comparison shows that highly conserved sequences are found principally in unpaired regions of the molecule. No knots are created by the structure.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
Z. Liu, C. Lozupone, M. Hamady, F. D. Bushman, and R. Knight
Short pyrosequencing reads suffice for accurate microbial community analysis
Nucleic Acids Res., September 25, 2007; 35(18): e120 - e120.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
S. Smit, J. Widmann, and R. Knight
Evolutionary rates vary among rRNA structural elements
Nucleic Acids Res., May 11, 2007; 35(10): 3339 - 3354.
[Abstract] [Full Text] [PDF]


Home page
RNAHome page
N. Kirthi, B. Roy-Chaudhuri, T. Kelley, and G. M. Culver
A novel single amino acid change in small subunit ribosomal protein S5 has profound effects on translational fidelity
RNA, December 1, 2006; 12(12): 2080 - 2091.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
A. Zemann, A. op de Bekke, M. Kiefmann, J. Brosius, and J. Schmitz
Evolution of small nucleolar RNAs in nematodes.
Nucleic Acids Res., January 1, 2006; 34(9): 2676 - 2685.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
A. Yassin, K. Fredrick, and A. S. Mankin
Deleterious mutations in small subunit ribosomal RNA identify functional sites and potential targets for antibiotics
PNAS, November 15, 2005; 102(46): 16620 - 16625.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
C. Pichon and B. Felden
From The Cover: Small RNA genes expressed from Staphylococcus aureusgenomic and pathogenicity islands with specific expression among pathogenic strains
PNAS, October 4, 2005; 102(40): 14249 - 14254.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
H. F. Noller
RNA Structure: Reading the Ribosome
Science, September 2, 2005; 309(5740): 1508 - 1514.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. Miranda-Rios, M. Navarro, and M. Soberon
A conserved RNA structure (thi box) is involved in regulation of thiamin biosynthetic gene expression in bacteria
PNAS, July 19, 2001; (2001) 161168098.
[Abstract] [Full Text] [PDF]


Home page
Microbiol. Mol. Biol. Rev.Home page
R. S. Gupta
Protein Phylogenies and Signature Sequences: A Reappraisal of Evolutionary Relationships among Archaebacteria, Eubacteria, and Eukaryotes
Microbiol. Mol. Biol. Rev., December 1, 1998; 62(4): 1435 - 1491.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
S Stern, T Powers, L. Changchien, and H. Noller
RNA-protein interactions in 30S ribosomal subunits: folding and function of 16S rRNA
Science, May 19, 1989; 244(4906): 783 - 790.
[Abstract] [PDF]


Home page
ScienceHome page
R. GUPTA, J. M. LANTER, and C. R. WOESE
Sequence of the 16S Ribosomal RNA from Halobacterium volcanii, an Archaebacterium
Science, August 12, 1983; 221(4611): 656 - 659.
[Abstract] [PDF]


Home page
ScienceHome page
H. Noller and C. Woese
Secondary structure of 16S ribosomal RNA
Science, April 24, 1981; 212(4493): 403 - 411.
[Abstract] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. Miranda-Rios, M. Navarro, and M. Soberon
From the Cover: A conserved RNA structure (thi box) is involved in regulation of thiamin biosynthetic gene expression in bacteria
PNAS, August 14, 2001; 98(17): 9736 - 9741.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.