Skip Navigation

Nucleic Acids Research 2004 32(22):e182; doi:10.1093/nar/gnh179
This Article
Right arrow Full Text Freely available
Right arrow Print PDF (281K) 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 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 arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Wen, J.-D.
Right arrow Articles by Gray, D. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wen, J.-D.
Right arrow Articles by Gray, D. M.
Related Collections
Right arrow Nucleic acid amplification
Right arrow Protein-nucleic acid interaction
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Published online 15 December 2004

Nucleic Acids Research, Vol. 32 No. 22 © Oxford University Press 2004; all rights reserved

Selection of genomic sequences that bind tightly to Ff gene 5 protein: primer-free genomic SELEX

Jin-Der Wen and Donald M. Gray*

Department of Molecular and Cell Biology, Mail Stop FO 3.1, The University of Texas at Dallas, PO Box 830688, Richardson, TX 75083-0688, USA

* To whom correspondence should be addressed. Tel: +1 972 883 2513; Fax: +1 972 883 2409; Email: dongray{at}utdallas.edu
Present address: Jin-Der Wen, Department of Chemistry, 104 Lewis Hall, The University of California, Berkeley, Berkeley, CA 94720-1460, USA

Received August 28, 2004; Revised and Accepted November 24, 2004

Single-stranded DNA or RNA libraries used in SELEX experiments usually include primer-annealing sequences for PCR amplification. In genomic SELEX, these fixed sequences may form base pairs with the central genomic fragments and interfere with the binding of target molecules to the genomic sequences. In this study, a method has been developed to circumvent these artificial effects. Primer-annealing sequences are removed from the genomic library before selection with the target protein and are then regenerated to allow amplification of the selected genomic fragments. A key step in the regeneration of primer-annealing sequences is to employ thermal cycles of hybridization-extension, using the sequences from unselected pools as templates. The genomic library was derived from the bacteriophage fd, and the gene 5 protein (g5p) from the phage was used as a target protein. After four rounds of primer-free genomic SELEX, most cloned sequences overlapped at a segment within gene 6 of the viral genome. This sequence segment was pyrimidine-rich and contained no stable secondary structures. Compared with a neighboring genomic fragment, a representative sequence from the family of selected sequences had about 23-fold higher g5p-binding affinity. Results from primer-free genomic SELEX were compared with the results from two other genomic SELEX protocols.


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
J. Zhang, E. Li, and G. J. Olsen
Protein-coding gene promoters in Methanocaldococcus (Methanococcus) jannaschii
Nucleic Acids Res., June 1, 2009; 37(11): 3588 - 3601.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
G. Bai, L. A. McCue, and K. A. McDonough
Characterization of Mycobacterium tuberculosis Rv3676 (CRPMt), a Cyclic AMP Receptor Protein-Like DNA Binding Protein
J. Bacteriol., November 15, 2005; 187(22): 7795 - 7804.
[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.