Affiliation:
1. Circadian and Visual Neuroscience, Wellcome Trust Centre for Human Genetics, University of OxfordRoosevelt Drive, Oxford OX3 7BN, UK
2. School of Animal Biology, University of Western AustraliaCrawley, Western Australia 6009, Australia
3. Faculty of Medical and Human Sciences, University of ManchesterManchester M13 9PT, UK
Abstract
Melanopsin confers photosensitivity to a subset of retinal ganglion cells and is responsible for many non-image-forming tasks, like the detection of light for circadian entrainment. Recently, two melanopsin genes,
Opn4m
and
Opn4x,
were described in non-mammalian vertebrates. However, only one form,
Opn4m,
has been described in the mammals, although studies to date have been limited to the placentals and have not included the marsupials.
We report here the isolation and characterization of an
Opn4
gene from an Australian marsupial, the fat-tailed dunnart (
Sminthopsis crassicaudata
), and present evidence which suggests that the
Opn4x
gene was lost before the placental/marsupial split.
In situ
hybridization shows that the expression of
Opn4
in the dunnart eye is restricted to a subset of ganglion cells, a pattern previously reported for rodents and primates. These Opn4-positive cells are randomly distributed across the dunnart retina. We also undertook a comparative analysis with the South American marsupial, the grey short-tailed opossum (
Monodelphis domestica)
, and two placental mammals, mouse and human. This approach reveals that the two marsupials show a higher sequence identity than that seen between rodents and primates, despite separating at approximately the same point in time, some 65–85 Myr ago.
Subject
General Agricultural and Biological Sciences,General Environmental Science,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine
Cited by
30 articles.
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