期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 291, 期 19, 页码 9883-9893出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M116.716498
关键词
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资金
- Japanese Ministry of Education, Culture, Sports, Science, and Technology [26708001, 26115706, 26620005, 25104009, 15H02391]
- Grants-in-Aid for Scientific Research [26708001, 26115706, 26620005, 25104009, 15H02391] Funding Source: KAKEN
In addition to the well-known light-driven outward proton pumps, novel ion-pumping rhodopsins functioning as outward Na+ and inward Cl- pumps have been recently found in eubacteria. They convert light energy into transmembrane electrochemical potential difference, similar to the prototypical archaeal H+ pump bacteriorhodopsin (BR) and Cl- pump halorhodopsin (HR). The H+, Na+, and Cl- pumps possess the conserved respective DTE, NDQ, and NTQ motifs in the helix C, which likely serve as their functional determinants. To verify this hypothesis, we attempted functional interconversion between selected pumps from each category by mutagenesis. Introduction of the proton-pumping motif resulted in successful Na+ -> H+ functional conversion. Introduction of the respective characteristic motifs with several additional mutations leads to successful Na+ -> Cl- and Cl- -> 3 H+ functional conversions, whereas remaining conversions (H+ -> Na+, H+ -> Cl-, Cl- -> Na+) were unsuccessful when mutagenesis of 4-6 residues was used. Phylogenetic analysis suggests that a H+ pump is the common ancestor of all of these rhodopsins, from which Cl- pumps emerged followed by Na+ pumps. We propose that successful functional conversions of these ion pumps are achieved exclusively when mutagenesis reverses the evolutionary amino acid sequence changes. Dependence of the observed functional conversions on the direction of evolution strongly suggests that the essential structural mechanism of an ancestral function is retained even after the gain of a new function during natural evolution, which can be evoked by a few mutations. By contrast, the gain of a new function needs accumulation of multiple mutations, which may not be easily reproduced by limited mutagenesis in vitro.
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