Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 155 (2009), 635-641; DOI  10.1099/mic.0.022343-0
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Clerico, E. M.
Right arrow Articles by Golden, S. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Clerico, E. M.
Right arrow Articles by Golden, S. S.
Agricola
Right arrow Articles by Clerico, E. M.
Right arrow Articles by Golden, S. S.
Microbiology 155 (2009), 635-641; DOI  10.1099/mic.0.022343-0
© 2009 Society for General Microbiology

Stability and lability of circadian period of gene expression in the cyanobacterium Synechococcus elongatus

Eugenia M. Clerico{dagger}, Vincent M. Cassone and Susan S. Golden

Department of Biology, Texas A&M University, 3258 TAMU, College Station, TX 77843-3258, USA

Correspondence
Susan S. Golden
sgolden{at}tamu.edu

Molecular aspects of the circadian clock in the cyanobacterium Synechococcus elongatus have been described in great detail. Three-dimensional structures have been determined for the three proteins, KaiA, KaiB and KaiC, that constitute a central oscillator of the clock. Moreover, a temperature-compensated circadian rhythm of KaiC phosphorylation can be reconstituted in vitro with the addition of KaiA, KaiB and ATP. These data suggest a relatively simple circadian system in which a single oscillator provides temporal information for all downstream processes. However, in vivo the situation is more complex, and additional components contribute to the maintenance of a normal period, the resetting of relative phases of circadian oscillations, and the control of rhythms of gene expression. We show here that two well-studied promoters in the S. elongatus genome report different circadian periods of expression under a given set of conditions in wild-type as well as mutant genetic backgrounds. Moreover, the period differs between these promoters with respect to modulation by light intensity, growth phase, and the presence or absence of a promoter-recognition subunit of RNA polymerase. These data contrast sharply with the current clock model in which a single Kai-based oscillator governs circadian period. Overall, these findings suggest that complex interactions among the circadian oscillator, perhaps other oscillators, and other cellular machinery result in a clock that is plastic and sensitive to the environment and to the physiological state of the cell.


Abbreviations: CT, circadian time; LL, constant light; WT, wild-type

{dagger}Present address: Department of Biochemistry and Molecular Biology, University of Massachusetts, Lederle Research Graduate Tower, 710 North Pleasant St, Amherst, MA 01003, USA.




This article has been cited by other articles:


Home page
J. Bacteriol.Home page
Y. Chen, Y.-I. Kim, S. R. Mackey, C. K. Holtman, A. LiWang, and S. S. Golden
A Novel Allele of kaiA Shortens the Circadian Period and Strengthens Interaction of Oscillator Components in the Cyanobacterium Synechococcus elongatus PCC 7942
J. Bacteriol., July 1, 2009; 191(13): 4392 - 4400.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2009 Society for General Microbiology.