Skip Navigation

This Article
Right arrow Print PDF (738K)
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 (42)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Doelling, J. H.
Right arrow Articles by Frankin, N. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Doelling, J. H.
Right arrow Articles by Frankin, N. C.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1989, Vol. 17, No. 14 5565
© 1989


MOLECULAR BIOLOGY

Effects of all single base substitutions in the loop of boxB on antitermination of transcription by bacteriophage {lambda}'s N protein

Jed H. Doelling and Naomi C. Frankin

Department of Biology, University of Utah Salt Lake City, UT 84112, USA

Received March 21, 1989. Revised June 9, 1989. Accepted June 9, 1989.

The ’N‘ antitermination proteins of lambdoid bacteriophages are essential for overcoming multiple transcription terminators located within the major early operons of these phages (1). In order for N proteins to function, a genome sequence specifying N utilization, nut, must belocated within an operon, between the promoter and the terminators (2). Two components have been identified within nut: 8-base baxA, conserved among different phages and implicated in the recognition of host NusA protein, required for N function (3); 15-base boxB, an interrupted palindrome (4), diverged in sequence among different lambdoid phages and hypothesized to be the site of recognition for different N proteins, also diverged in sequence (5). Here we apply a plasmid for testing termination and antitermination of transcription (6) to identify mutations at all positions in the 5–7 base loop of {lambda}'s boxB. Almost every base change at any position within the 5–7 base boxB loop was found to constrain antitermination of transcription by the N protein of bacteriophage {lambda}. Theseobservations extend previous mutational knowledge of nut(7) and are consistant with the hypothesisthat the boxB loop is the direct site of recognition for N protein. Variations among the effects of different base changes suggest differential contacts between N protein and bases of the boxB loop, whether in DNA or RNA.


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
J. Bacteriol.Home page
A. I. Cocozaki, I. R. Ghattas, and C. A. Smith
Bacteriophage P22 Antitermination boxB Sequence Requirements Are Complex and Overlap with Those of {lambda}
J. Bacteriol., June 15, 2008; 190(12): 4263 - 4271.
[Abstract] [Full Text] [PDF]


Home page
RNAHome page
C. D. CILLEY and J. R. WILLIAMSON
Structural mimicry in the phage {phi}21 N peptide-boxB RNA complex
RNA, June 1, 2003; 9(6): 663 - 676.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
Y. Ikawa, K. Tsuda, S. Matsumura, S. Atsumi, and T. Inoue
Putative intermediary stages for the molecular evolution from a ribozyme to a catalytic RNP
Nucleic Acids Res., March 1, 2003; 31(5): 1488 - 1496.
[Abstract] [Full Text] [PDF]


Home page
RNAHome page
H. PELED-ZEHAVI, S. HORIYA, C. DAS, K. HARADA, and A. D. FRANKEL
Selection of RRE RNA binding peptides using a kanamycin antitermination assay
RNA, February 1, 2003; 9(2): 252 - 261.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. Mogridge, T.-F. Mah, and J. Greenblatt
Involvement of boxA Nucleotides in the Formation of a Stable Ribonucleoprotein Complex Containing the Bacteriophage lambda  N Protein
J. Biol. Chem., February 13, 1998; 273(7): 4143 - 4148.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
H. R. Wilson, L. Kameyama, J.-g. Zhou, G. Guarneros, and D. L. Court
Translational repression by a transcriptional elongation factor
Genes & Dev., September 1, 1997; 11(17): 2204 - 2213.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
L. Su, J. T. Radek, L. A. Labeots, K. Hallenga, P. Hermanto, H. Chen, S. Nakagawa, M. Zhao, S. Kates, and M. A. Weiss
An RNA enhancer in a phage transcriptional antitermination complex functions as a structural switch
Genes & Dev., September 1, 1997; 11(17): 2214 - 2226.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
J Mogridge, T F Mah, and J Greenblatt
A protein-RNA interaction network facilitates the template-independent cooperative assembly on RNA polymerase of a stable antitermination complex containing the lambda N protein.
Genes & Dev., November 15, 1995; 9(22): 2831 - 2845.
[Abstract] [PDF]


Home page
Genes Dev.Home page
J R Nodwell and J Greenblatt
The nut site of bacteriophage lambda is made of RNA and is bound by transcription antitermination factors on the surface of RNA polymerase.
Genes & Dev., November 1, 1991; 5(11): 2141 - 2151.
[Abstract] [PDF]


Home page
Genes Dev.Home page
D I Friedman, E R Olson, L L Johnson, D Alessi, and M G Craven
Transcription-dependent competition for a host factor: the function and optimal sequence of the phage lambda boxA transcription antitermination signal.
Genes & Dev., December 1, 1990; 4(12a): 2210 - 2222.
[Abstract] [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.