How early mammals evolved night vision to avoid predators
Early mammals evolved in a burst during the Jurassic period, adapting a nocturnal lifestyle when dinosaurs were the dominant daytime predator. How these early mammals evolved night vision to find food and survive has been a mystery, but a new study publishing June 20 in Developmental Cell suggests that rods in the mammalian eye, extremely sensitive to light, developed from color-detecting cone cells during this time to give mammals an edge in low-light conditions.
Cone cells are specialized for certain wavelengths of light to help animals detect color, while rods can detect even a single photon and are specialized for low-light vision. "The majority of mammals have rod-dominant retinas, but if you look at fish, frogs, or birds, the vast majority are cone-dominated–so the evolutionary question has always been, 'What happened?'" says Anand Swaroop, a retina biologist at the National Eye Institute, part of the National Institutes of Health. "We've been working for a long time to understand the fundamental mechanisms behind rod and cone development."
Previous work done by Swaroop and his colleagues showed that a transcription factor called NRL pushes cells in the retina toward maturing into rods by suppressing genes involved in cone development. "We began to wonder if, somehow, the short-wavelength cones were converted into rods during evolution," says Swaroop.
To investigate the origin of rods in mammals, Swaroop and his team examined rod and cone cells taken from mice at different stages of development. Details of an organism's embryonic development often reveal traits carried by its evolutionary ancestors; consider, for instance, how human embryos initially develop gill-like slits and a tail.
The researchers saw that in early stages, two days after the mice were born, developing rod cells expressed genes normally seen in mature short-wavelength cones (which are used in other animals to detect ultraviolet light). When the researchers examined the epigenetics of purified rod cells from mice, they saw that these aspects became repressed by histone and DNA methylations later in development, ten days after the mice were born.
In zebrafish, which are diurnal and cone-dominated, another set of experiments showed that the rod cells didn't resemble cones at all. To investigate when the mammalian elements that turn cones to rods might have originated, the researchers reviewed genomic sequences from a variety of vertebrate animals. The team discovered that the genes responsible for the regulation of NRL became more refined in the placental mammals as the modern retina evolved and were lost in several non-mammalian groups. The origin of this regulatory system appeared to coincide with the evolution of nocturnality in early mammals.
The team concluded that in mammals, the transcription factor NRL became restricted to the photoreceptors in the eye, forcing the cells to change from cones to rods and giving early mammals the edge they needed to take up an active nighttime lifestyle. (Counter-intuitively, humans depend more on cones for our vision, but that's because our ancestors later evolved to take advantage of the daylight hours again.)
"These rod photoreceptors retain the molecular footprint of short-wavelength cones," says Swaroop. "We've provided evidence that by acquiring the regulatory elements for NRL to shift short-wavelength cones into rods, early mammals changed one type of cell from capturing UV light–which isn't necessary at night–to something that is just extremely sensitive to light."
This study was supported by the intramural research program of the National Eye Institute, a Discovery Accelerator Grant from Natural Sciences & Engineering Research Council of Canada, and the National Research Foundation of Korea.
Developmental Cell, Kim, Yang, and Oel et al.: "Recruitment of Rod Photoreceptors from Short Wavelength Sensitive Cones during the Evolution of Nocturnal Vision in Mammals" http://www.cell.com/developmental-cell/fulltext/S1534-5807(16)30336-7
Developmental Cell (@Dev_Cell), published by Cell Press, is a bimonthly, cross-disciplinary journal that brings together the fields of cell biology and developmental biology. Articles provide new biological insight of cell proliferation, intracellular targeting, cell polarity, membrane traffic, cell migration, stem cell biology, chromatin regulation and function, differentiation, morphogenesis and biomechanics, and regeneration and cellular homeostasis. Visit: http://www.cell.com/developmental-cell. To receive Cell Press media alerts, contact [email protected]