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PMID: 11110912 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Evolution of two-component signal transduction.

Molecular biology and evolution ·Vol. 17 ·No. 12 ·2000-12-00 ·Pages 1956-70

Koretke KK, Lupas AN, Warren PV, Rosenberg M, Brown JR

Abstract

Two-component signal transduction (TCST) systems are the principal means for coordinating responses to environmental changes in bacteria as well as some plants, fungi, protozoa, and archaea. These systems typically consist of a receptor histidine kinase, which reacts to an extracellular signal by phosphorylating a cytoplasmic response regulator, causing a change in cellular behavior. Although several model systems, including sporulation and chemotaxis, have been extensively studied, the evolutionary relationships between specific TCST systems are not well understood, and the ancestry of the signal transduction components is unclear. Phylogenetic trees of TCST components from 14 complete and 6 partial genomes, containing 183 histidine kinases and 220 response regulators, were constructed using distance methods. The trees showed extensive congruence in the positions of 11 recognizable phylogenetic clusters. Eukaryotic sequences were found almost exclusively in one cluster, which also showed the greatest extent of domain variability in its component proteins, and archaeal sequences mainly formed species-specific clusters. Three clusters in different parts of the kinase tree contained proteins with serine-phosphorylating activity. All kinases were found to be monophyletic with respect to other members of their superfamily, such as type II topoisomerases and Hsp90. Structural analysis further revealed significant similarity to the ATP-binding domain of eukaryotic protein kinases. TCST systems are of bacterial origin and radiated into archaea and eukaryotes by lateral gene transfer. Their components show extensive coevolution, suggesting that recombination has not been a major factor in their differentiation. Although histidine kinase activity is prevalent, serine kinases have evolved multiple times independently within this family, accompanied by a loss of the cognate response regulator(s). The structural and functional similarity between TCST kinases and eukaryotic protein kinases raises the possibility of a distant evolutionary relationship.

MeSH Terms
Amino Acid Sequence Animals Archaeal Proteins/genetics Evolution, Molecular Gene Transfer, Horizontal Genetic Linkage Histidine Kinase Molecular Sequence Data Phosphorylation Phylogeny Protein Kinases/genetics Protein Structure, Tertiary Sequence Homology Signal Transduction
Chemicals
Archaeal Proteins Protein Kinases Histidine Kinase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Koretke K K
SmithKline Beecham Pharmaceuticals, Collegeville, Pennsylvania 19426-0989, USA.
Lupas A N
Warren P V
Rosenberg M
Brown J R
Article Info
Journal
Molecular biology and evolution
Abbr.
Mol Biol Evol
ISSN
0737-4038
Published
2000-12-00
Pages
1956-70
Language
English
Region
United States
NLM ID
8501455
Subset
IM
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