Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (425K) Freely available
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 ISI Web of Science
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 (13)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Sandman, K. E.
Right arrow Articles by Noren, C. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sandman, K. E.
Right arrow Articles by Noren, C. J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 2000, Vol. 28, No. 3 755-761
© 2000 Oxford University Press

The efficiency of Escherichia coli selenocysteine insertion is influenced by the immediate downstream nucleotide

Karen E. Sandman and Christopher J. Noren*

New England Biolabs, 32 Tozer Road, Beverly, MA 01915, USA

Selenocysteine (Sec) incorporation requires the TGA opal codon and a downstream Sec insertion sequence (SECIS), which can be partially randomized and cloned into M13 pIII fusion constructs for phage display. This combinatorial approach provides a convenient non-radioactive assay that couples phage production to opal suppression. Two SECIS libraries were prepared, with the immediate downstream nucleotide either randomized (TGAN) or fixed as thymidine (TGAT). The TGAN library resulted in a majority of clones with a downstream purine and selenium-independent phage production, implicating the endo­genous tryptophan-inserting opal suppression pathway. Although the addition of sodium selenite to the growth medium did not affect phage production, it did increase the level of Sec insertion, as shown by the chemical reactivity of the resulting phage. The TGAT phage library yielded clones with strictly selenium-dependent phage production and reactivity consistent with the presence of Sec. These clones were prone to spontaneous mutation upon further propagation, however, resulting in loss of the selenium-dependent phenotype. We conclude that the immediate downstream nucleotide determines whether the endogenous opal suppression pathway competes with co-translational Sec insertion.

* To whom correspondence should be addressed. Tel: +1 978 927 5054; Fax: +1 978 921 1350; Email: noren@neb.com


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
D. Su, Y. Li, and V. N. Gladyshev
Selenocysteine insertion directed by the 3'-UTR SECIS element in Escherichia coli
Nucleic Acids Res., April 29, 2005; 33(8): 2486 - 2492.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
H.-Y. Kim and V. N. Gladyshev
Methionine Sulfoxide Reduction in Mammals: Characterization of Methionine-R-Sulfoxide Reductases
Mol. Biol. Cell, March 1, 2004; 15(3): 1055 - 1064.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Camps, J. Naukkarinen, B. P. Johnson, and L. A. Loeb
Targeted gene evolution in Escherichia coli using a highly error-prone DNA polymerase I
PNAS, August 19, 2003; 100(17): 9727 - 9732.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
K. E. Sandman, D. F. Tardiff, L. A. Neely, and C. J. Noren
Revised Escherichia coli selenocysteine insertion requirements determined by in vivo screening of combinatorial libraries of SECIS variants
Nucleic Acids Res., April 15, 2003; 31(8): 2234 - 2241.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Hazebrouck, L. Camoin, Z. Faltin, A. D. Strosberg, and Y. Eshdat
Substituting Selenocysteine for Catalytic Cysteine 41 Enhances Enzymatic Activity of Plant Phospholipid Hydroperoxide Glutathione Peroxidase Expressed in Escherichia coli
J. Biol. Chem., September 8, 2000; 275(37): 28715 - 28721.
[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.