Functional divergence of the circadian clock proteins in prokaryotes

被引:15
作者
Dvornyk, V
Knudsen, B
机构
[1] Creighton Univ, Osteoporosis Res Ctr, Omaha, NE 68131 USA
[2] Creighton Univ, Dept Biomed Sci, Omaha, NE 68131 USA
[3] Univ Florida, Dept Zool, Gainesville, FL 32611 USA
关键词
circadian genes; cyanobacteria; functional divergence; rate shift;
D O I
10.1007/s10709-005-3146-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cyanobacteria are only prokaryotes known so far to have a circadian system. It may be based either on two (kaiB and kaiC) or three (kaiA, kaiB and kaiC) circadian genes. The homologs of two circadian proteins, KaiB and KaiC, form four major subfamilies (K1-K4) and also occur in some other prokaryotes. Using the likelihood-ratio tests, we studied a rate shift at the functional divergence of the proteins from the different subfamilies. It appears that only two of the subfamilies (K1 and K2) perform circadian functions. We identified in total 92 sites that have significantly different rates of evolution between the clades K1/K2 and K3/K4; 67 sites (15 in KaiB and 52 in KaiC) been evolving significantly slower in K1/K2 than the overall average for the entire sequence. Many critical sites are located in the identified functionally important motifs and regions, e.g. one of the Walker's motif As, DXXG motif, and two KaiA-binding domains of KaiC. There are also 36 sites (similar to 5%) with rate shift between K1 and K2. The rate shift at these sites may be related to the interaction with KaiA. Rate shift analyses have identified residues whose manipulation in the Kai proteins may lead to better understanding of their functions in the two different types of the cyanobacterial circadian system.
引用
收藏
页码:247 / 254
页数:8
相关论文
共 34 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]  
ASHIER M, 1998, SCIENCE, V281, P1519
[3]  
BOURNE HR, 1991, NATURE, V349, P117, DOI 10.1038/349117a0
[4]   A cyanobacterial circadian timing mechanism [J].
Ditty, JL ;
Williams, SB ;
Golden, SS .
ANNUAL REVIEW OF GENETICS, 2003, 37 :513-543
[5]   Molecular evolution of ldpA, a gene mediating the circadian input signal in cyanobacteria [J].
Dvornyk, V .
JOURNAL OF MOLECULAR EVOLUTION, 2005, 60 (01) :105-112
[6]   Structure and molecular phylogeny of sasA genes in cyanobacteria:: Insights into evolution of the prokaryotic circadian system [J].
Dvornyk, V ;
Deng, HW ;
Nevo, E .
MOLECULAR BIOLOGY AND EVOLUTION, 2004, 21 (08) :1468-1476
[7]   Origin and evolution of circadian clock genes in prokaryotes [J].
Dvornyk, V ;
Vinogradova, O ;
Nevo, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (05) :2495-2500
[8]   Statistical methods for testing functional divergence after gene duplication [J].
Gu, X .
MOLECULAR BIOLOGY AND EVOLUTION, 1999, 16 (12) :1664-1674
[9]   Maximum-likelihood approach for gene family evolution under functional divergence [J].
Gu, X .
MOLECULAR BIOLOGY AND EVOLUTION, 2001, 18 (04) :453-464
[10]   A KaiC-interacting sensory histidine kinase, SasA, necessary to sustain robust circadian oscillation in cyanobacteria [J].
Iwasaki, H ;
Williams, SB ;
Kitayama, Y ;
Ishiura, M ;
Golden, SS ;
Kondo, T .
CELL, 2000, 101 (02) :223-233