Affiliation:
1. Division of Biological Science, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya 464-01, and National Institute for Basic Biology, Okazaki, Aichi 444, Japan
Abstract
ABSTRACT
We cloned the pS1K1 plasmid in the process of apparently “complementing” a circadian clock mutant of cyanobacterium
Synechococcus
sp. strain PCC 7942, SP22, which has a 22-h period (T. Kondo, N. F. Tsinoremas, S. S. Golden, C. H. Johnson, S. Kutsuna, and M. Ishiura, Science 266:1233–1236, 1994). Sequence analysis revealed that SP22 did not have a mutation in the genomic DNA segment carried on pS1K1, and the
sp22
mutation was later found in a recently cloned new clock gene,
kaiC
. Therefore, the period-extender gene
pex
that was carried on pS1K1 was a suppressor gene for the
sp22
mutation. The
pex
gene encoded a protein of 148 amino acid residues. No meaningful homologs were found in DNA or protein databases including the
Synechocystis
genome database. The
pex
gene was transcribed from 129 and 164 bp upstream of the translation initiation codon as 0.6-kb transcripts. The Pex protein was detected as a fusion protein with a molecular mass of 15 kDa by the epitope tag fusion method using a c-Myc epitope tag. Disruption of the
pex
gene in wild-type cells shortened the period of the rhythms by 1 h, although it did not affect other properties of the rhythms, whereas its overexpression extended the period by 3 h with a concomitant reduction in the amplitude of the rhythms. In various clock mutants examined, overexpression caused arrhythmicity. Thus, Pex is likely to function as a modifier of the circadian clock in
Synechococcus.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
80 articles.
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