A system-level, molecular evolutionary analysis of mammalian phototransduction
Abstract Background Visual perception is initiated in the photoreceptor cells of the retina via the phototransduction system. This system has shown marked evolution during mammalian divergence in such complex attributes as activation time and recovery time. We have performed a molecular evolutionary analysis of proteins involved in mammalian phototransduction in order to unravel how the action of natural selection has been distributed throughout the system to evolve such traits. Results We found selective pressures to be non-randomly distributed according to both a simple protein classification scheme and a protein-interaction network representation of the signaling pathway. Proteins which are topologically central in the signaling pathway, such as the G proteins, as well as retinoid cycle chaperones and proteins involved in photoreceptor cell-type determination, were found to be more constrained in their evolution. Proteins peripheral to the pathway, such as ion channels and exchangers, as well as the retinoid cycle enzymes, have experienced a relaxation of selective pressures. Furthermore, signals of positive selection were detected in two genes: the short-wave (blue) opsin (OPN1SW) in hominids and the rod-specific N a +/ C a 2+, K + ion exchanger (SLC24A1) in rodents. Conclusions The functions of the proteins involved in phototransduction and the topology of the interactions between them have imposed non-random constraints on their evolution. Thus, in shaping or conserving system-level phototransduction traits, natural selection has targeted the underlying proteins in a concerted manner.
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Format: | artículo biblioteca |
Language: | English |
Published: |
BioMed Central
2013-02-23
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Online Access: | http://dx.doi.org/10.1186/1471-2148-13-52 http://hdl.handle.net/10261/73645 http://dx.doi.org/10.13039/501100006280 http://dx.doi.org/10.13039/501100002809 http://dx.doi.org/10.13039/501100004837 |
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