Shedding Light on Animal Cryptochromes

Anyone who’s neglected a houseplant for any length of time knows that plants can’t survive without light. But it’s more complicated than that; in addition to serving as an energy source, light is used by plants as a signal to sense and respond to the environment. For example, both red and blue light send the signal for maturation and flower and seed development. Depriving a plant of such light signals disrupts a variety of growth processes such as early seedling development, leaf and stem expansion, and initiation of flowering, as well as circadian clock entrainment. Cryptochromes are photoreceptor proteins used by plants to mediate the effects of blue light; they are also found in animals like flies and mice, where they help to regulate the circadian clock. In plants, exposure to blue light results in the reduction (gain of electrons) of flavin pigments that are bound by the cryptochrome. Blue light activates plant cryptochromes by reducing the flavins, but researchers weren’t sure exactly how blue light activates fly cryptochromes, or if mammalian cryptochromes even respond to light at all. In a new study, Nathalie Hoang et al. set out to determine how animal cryptochromes respond to blue light, and if mammalian cryptochromes are capable of blue light activation. The researchers performed a series of experiments to measure the effects of blue light irradiation on cryptochromes in living flies and in insect cell lines (Sf21) expressing high levels of fly or human cryptochrome (Dmcry and Hscry1, respectively). They found that not only is the bound flavin molecule in an intermediately reduced, unpaired electron (radical) state in activated animal cryptochromes, similar to what is seen in plants, but that mammalian cryptochrome is fully capable of responding to light in living animals. Although you might think that animal cryptochromes are activated the same way that plant cryptochromes are, in fact, plant and animal cryptochromes evolved independently from different DNA photolyase proteins, which rely on energy from blue light to repair DNA damaged by ultraviolet radiation. Like plant cryptochromes, DNA photolyases have a bound flavin molecule. However, in plant cryptochromes, flavin goes from a fully oxidized resting state (able to receive electrons) to a radical intermediate state when activated by blue light, whereas flavins bound by DNA photolyases are generally completely reduced. After first confirming that flavin was indeed the photoreactive pigment in living flies and in the cell lines, and that it is fully oxidized in the resting state (as in plant cryptochromes), the researchers sought to more fully characterize what was happening to animal cryptochromes in living cells irradiated with blue light. To do this, they exposed Sf21 cells to blue light and then measured changes in levels of oxidized flavins based on a decrease in absorption at 450 nm, the wavelength at which protein-bound oxidized flavins absorb the most energy. They found that in both Dmcryand Hscry1-expressing cells, excitation progressively decreased over time, indicating that the crytochrome-bound flavin molecules were being reduced. To determine whether animal cryptochrome was being reduced to a radical intermediate state, as in plant cryptochromes, or to a fully reduced state, as in DNA photolyases, the researchers performed whole-cell electron paramagnetic resonance (EPR) spectroscopy (a technique used to detect radicals) on the Sf21 cells. They found that a radical accumulated in the cryptochrome-expressing cells after irradiation with blue light that was not found in control, non–cryptochrome expressing Sf21 cells, indicating that the activation of both Dmcry and Hscry involves light-dependent flavin reduction and accumulation of active, radical cryptochrome. In plant cryptochromes, the biologically active signaling state induced by blue light is reversed by doi:10.1371/journal.pbio.0060168.g001