Experience-dependent brain changes in Angelman syndrome
Nature Neuroscience
May 11, 2009
Sensory-experience dependent modification of visual areas in the brain are disrupted in a mouse model of Angelman syndrome (AS), reports a paper published online this week in Nature Neuroscience.
Angelman syndrome (AS) is a hereditary mental retardation, caused by mutations or deletions in the maternally inherited allele of the UBE3A gene. Normally, visual experience guides the development of brain circuitry in the visual cortex of the brain. Benjamin Philpot and colleagues report that AS mice deficient in UBE3A do not show this sensory-experience dependent maturation process. This experience-dependent plasticity however was restored by sensory deprivation (rearing the mice in a dark environment).
This work points to potential mechanisms that may underlie abnormalities in brain development in human AS, as well as other forms of mental retardation, such as Rett syndrome and Fragile X syndrome.
doi: 10.1038/nn.2327
Research highlights
-
Dec 4
Archaeology: Palaeolithic sea voyage to Japanese islands beyond the horizonScientific Reports
-
Dec 3
Ageing: Cellular rejuvenation restores vision in miceNature
-
Dec 1
Neurodegenerative disease: Two blood molecules may predict Alzheimer’s disease developmentNature Aging
-
Nov 27
Archaeology: Neanderthal thumbs better adapted to holding tools with handlesScientific Reports
-
Nov 26
Evolution: Ancient bird sticks its big beak into the evolutionary recordNature
-
Nov 26
Metabolism: Link between SARS-CoV-2 infection and cholesterol hints at COVID-19 treatment possibilitiesNature Metabolism
