期刊
ENEURO
卷 9, 期 5, 页码 -出版社
SOC NEUROSCIENCE
DOI: 10.1523/ENEURO.0202-22-2022
关键词
acoustic startle; auditory brainstem response; encephalopsin; light; opsin; panopsin
Opn3 is the first nonvisual opsin gene discovered in mammals and it is expressed in both the central nervous system and peripheral tissues. The behavioral consequences of Opn3 deficiency were investigated and it was found that Opn3-deficient mice perform similarly to wild-type mice in most behavioral tests, but have an attenuated acoustic startle reflex.
Opsin-3 (Opn3, encephalopsin) was the first nonvisual opsin gene discovered in mammals. Since then, several Opn3 functions have been described, and in two cases (adipose tissue, smooth muscle) light sensing activity is implicated. In addition to peripheral tissues, Opn3 is robustly expressed within the central nervous system, for which it derives its name. Despite this expression, no studies have investigated developmental or adult CNS consequences of Opn3 loss-of-function. Here, the behavioral consequences of mice deficient in Opn3 were investigated. Opn3-deficient mice perform comparably to wild-type mice in measures of motor coordination, socialization, anxiety-like behavior, and various aspects of learning and memory. However, Opn3-deficient mice have an attenuated acoustic startle reflex (ASR) relative to lifterrnates. This deficit is not because of changes in hearing sensitivity, although Opn3 was shown to be expressed in auditory and vestibular structures, including cochlear outer hair cells. Interestingly, the ASR was not acutely light-dependent and did not vary between daytime and nighttime trials, despite known functions of Opn3 in photoreception and circadian gene amplitude. Together, these results demonstrate the first role of Opn3 on behavior, although the role of this opsin in the CNS remains largely elusive.
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