Research Article: Parallel and Convergent Evolution of the Dim-Light Vision Gene RH1 in Bats (Order: Chiroptera)

Date Published: January 21, 2010

Publisher: Public Library of Science

Author(s): Yong-Yi Shen, Jie Liu, David M. Irwin, Ya-Ping Zhang, Konrad Scheffler. http://doi.org/10.1371/journal.pone.0008838

Abstract: Rhodopsin, encoded by the gene Rhodopsin (RH1), is extremely sensitive to light, and is responsible for dim-light vision. Bats are nocturnal mammals that inhabit poor light environments. Megabats (Old-World fruit bats) generally have well-developed eyes, while microbats (insectivorous bats) have developed echolocation and in general their eyes were degraded, however, dramatic differences in the eyes, and their reliance on vision, exist in this group. In this study, we examined the rod opsin gene (RH1), and compared its evolution to that of two cone opsin genes (SWS1 and M/LWS). While phylogenetic reconstruction with the cone opsin genes SWS1 and M/LWS generated a species tree in accord with expectations, the RH1 gene tree united Pteropodidae (Old-World fruit bats) and Yangochiroptera, with very high bootstrap values, suggesting the possibility of convergent evolution. The hypothesis of convergent evolution was further supported when nonsynonymous sites or amino acid sequences were used to construct phylogenies. Reconstructed RH1 sequences at internal nodes of the bat species phylogeny showed that: (1) Old-World fruit bats share an amino acid change (S270G) with the tomb bat; (2) Miniopterus share two amino acid changes (V104I, M183L) with Rhinolophoidea; (3) the amino acid replacement I123V occurred independently on four branches, and the replacements L99M, L266V and I286V occurred each on two branches. The multiple parallel amino acid replacements that occurred in the evolution of bat RH1 suggest the possibility of multiple convergences of their ecological specialization (i.e., various photic environments) during adaptation for the nocturnal lifestyle, and suggest that further attention is needed on the study of the ecology and behavior of bats.

Partial Text: Vision plays an extraordinary role in animals and is often basic for their survival. Due to the high degree of variation in light conditions and presence of various wavelengths of light in different environments, the evolution of vision to various photic environments and lifestyles is among the most significant mammalian adaptations [1]. Most mammals have two vision systems, one based on cone photoreceptors and one on rod photoreceptors. The rods are 100 times more sensitive to light than the cones, and are responsible for night vision (dim-light vision) [2], however, they are not sensitive to color. In contrast, cones provide color sensitivity which is due to the presence of two types of cone photoreceptors in most mammals: cones with long/middle wavelength (L/M or red/green) opsin and cones with short wavelength (S or blue) opsin. The size and shape of eyes, photoreceptor organization, and color sensitivity differ dramatically depending upon an animals’ specific needs and photic environments [3]. Some primates have undergone one or more duplications of M/L opsin genes, thus have become trichromatic [4], [5], [6]. In contrast, many nocturnal primates, carnivores, and rodents have lost the functional short wavelength opsin, and depend upon rods to maximize their visual sensitivities to the available dim-light rather than to color discrimination [7], [8], [9], [10].

We successfully amplified cDNAs for the rod pigment gene (RH1) from retina total RNA for all bats used in this study. The aligned bat RH1 nucleotide sequence was 834bp in length, of which 147 were variable, but only 24 of these sites cause amino acid sequence variation (Figure 1). No insertion/deletion mutations or changes that result in stop codons were found in the sequences suggesting that all bats have a RH1 that function in dim-light vision. For the two color vision genes, the M/LWS gene was successfully amplified for all bat species (Figure S1), while the SWS1 gene failed to amplify in all Rhinolophoidea and Rousettus species, implying the loss of function of short wavelength opsin in this species, in agreement with a recent study [20].

Source:

http://doi.org/10.1371/journal.pone.0008838

 

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