labA: a novel gene required for negative feedback regulation of the cyanobacterial circadian clock protein KaiC

  1. Yasuhito Taniguchi1,
  2. Mitsunori Katayama1,3,
  3. Rie Ito1,
  4. Naoki Takai1,
  5. Takao Kondo1,2,4, and
  6. Tokitaka Oyama1,2,5
  1. 1 Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan;
  2. 2 Solution Oriented Research for Science and Technology (SORST), Japan Science and Technology Corporation, Furo-cho, Chikusa, Nagoya 464-8602, Japan

Abstract

In the cyanobacterium Synechococcus elongatus PCC 7942, circadian timing is transmitted from the KaiABC-based central oscillator to the transcription factor RpaA via the KaiC-interacting histidine kinase SasA to activate transcription, thereby generating rhythmic circadian gene expression. However, KaiC can also repress circadian gene expression, including its own. The mechanism and significance of this negative feedback regulation have been unclear. Here, we report a novel gene, labA (low-amplitude and bright), that is required for negative feedback regulation of KaiC. Disruption of labA abolished transcriptional repression caused by overexpression of KaiC and elevated the trough levels of circadian gene expression, resulting in a low-amplitude phenotype. In contrast, overexpression of labA significantly lowered circadian gene expression. Furthermore, genetic analysis indicated that labA and sasA function in parallel pathways to regulate kaiBC expression, whereas rpaA functions downstream from labA for kaiBC expression. These results suggest that temporal information from the KaiABC-based oscillator diverges into a LabA-dependent negative pathway and a SasA-dependent positive pathway, and then converges onto RpaA to generate robust circadian gene expression. It is likely that quantitative information of KaiC is transmitted to RpaA through LabA, whereas SasA mediates the state of the KaiABC-based oscillator.

Keywords

Footnotes

  • 3 Present address: Department of Life Sciences (Biology), University of Tokyo, Komaba 3-8-1, Meguro-ku, Tokyo 153-8902, Japan.

  • 4 Corresponding authors.

    4 E-MAIL kondo{at}bio.nagoya-u.ac.jp; FAX 81-52-789-2963.

  • 5 E-MAIL oyama{at}biol1.bio.nagoya-u.ac.jp; FAX 81-52-789-2963.

  • Supplemental material is available at http://www.genesdev.org.

  • Article is online at http://www.genesdev.org/cgi/doi/10.1101/gad.1488107

    • Received August 30, 2006.
    • Accepted November 17, 2006.
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