Published September 3, 2024 | Version v1
Journal article Open

Two KaiABC systems control circadian oscillations in one cyanobacterium

Description

The circadian clock of cyanobacteria, which predicts daily environmental changes, typically includes a standard oscillator consisting of proteins KaiA, KaiB, and KaiC. However, several cyanobacteria have diverse Kai protein homologs of unclear function. In particular, Synechocystis sp. PCC 6803 harbours, in addition to a canonical kaiABC gene cluster (named kaiAB1C1), two further kaiB and kaiC homologs (kaiB2, kaiB3, kaiC2, kaiC3). Here, we identify a chimeric KaiA homolog, named KaiA3, encoded by a gene located upstream of kaiB3. At the N-terminus, KaiA3 is similar to response-regulator receiver domains, whereas its C-terminal domain resembles that of KaiA. Homology analysis shows that a KaiA3-KaiB3-KaiC3 system exists in several cyanobacteria and other bacteria. Using the Synechocystis sp. PCC 6803 homologs, we observe circadian oscillations in KaiC3 phosphorylation in vitro in the presence of KaiA3 and KaiB3. Mutations of kaiA3 affect KaiC3 phosphorylation, leading to growth defects under both mixotrophic and chemoheterotrophic conditions. KaiC1 and KaiC3 exhibit phase-locked free-running phosphorylation rhythms. Deletion of either system (∆kaiAB1C1 or ∆kaiA3B3C3) alters the period of the cellular backscattering rhythm. Furthermore, both oscillators are required to maintain high-amplitude, self-sustained backscatter oscillations with a period of approximately 24 h, indicating their interconnected nature.

Data availability

Raw and processed data generated in this study are available on figshare: Raw data: https://doi.org/10.6084/m9.figshare.25218143. Processed Data: https://doi.org/10.6084/m9.figshare.25218137, Alignments: https://doi.org/10.6084/m9.figshare.25218122, Phylogeny: https://doi.org/10.6084/m9.figshare.25218134), processed KaiA3 hits are also available as Supplementary Data S1. The mass spectrometry proteomics data generated in this study have been deposited in the ProteomeXchange Consortium database (http://proteomecentral.proteomexchange.org) via the PRIDE partner repository, with the dataset identifier PXD042846 (analysis of KaiC3 phosphorylation) https://ftp.pride.ebi.ac.uk/pride/data/archive/2024/07/PXD042846, PXD042845 (screening of KaiC3 and KaiC1 binding partners) https://ftp.pride.ebi.ac.uk/pride/data/archive/2024/07/PXD042845, and summarized data are available as Supplementary Data S2 and S3. Datasets S1 to S4 are available as Supplementary Data. Source data are provided with this paper.

The script for reciprocal BLAST analysis is available at https://github.com/schmelling/reciprocal_BLAST/blob/master/notebooks/. The script for backscatter data analysis is available at https://github.com/flo-sti/cyano-backscatter. Raw data, Biolection and LUA protocols are available as Supplementary Data S4.

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Additional details

Identifiers

DOI
10.1038/s41467-024-51914-5
Other
oai:uchicago.tind.io:13353

Funding

German Research Foundation
397695561
German Research Foundation
WI2014/5-3
German Research Foundation
WI2014/10-1
German Research Foundation
WI2014/10-2
German Research Foundation
AX 84/1-3
German Research Foundation
MA 4918/4-1
German Research Foundation
SFB1535 - Project ID 458090666
German Research Foundation
Germany’s Excellence Strategy
National Institutes of Health
R01 GM135382

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Molecular Genetics and Cell Biology