Localised Cdr1as activity is required for fear extinction memory
Neurobiology of Learning and Memory, ISSN: 1074-7427, Vol: 203, Page: 107777
2023
- 6Citations
- 4Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations6
- Citation Indexes6
- CrossRef5
- Captures4
- Readers4
Article Description
Circular RNAs (circRNAs) comprise a novel class of regulatory RNAs that are abundant in the brain, particularly within synapses. They are highly stable, dynamically regulated, and display a range of functions, including serving as decoys for microRNAs and proteins and, in some cases, circRNAs also undergo translation. Early work in animal models revealed an association between circRNAs and neurodegenerative and neuropsychiatric disorders; however, little is known about the link between circRNA function and memory. To address this, we examined circRNA in synaptosomes derived from the medial prefrontal cortex of fear extinction-trained male C57BL/6J mice and found 12,837 circRNAs that were enriched at the synapse, including cerebellar degeneration-related protein 1 antisense RNA ( Cdr1as). Targeted knockdown of Cdr1as in the neural processes of the infralimbic cortex led to impaired fear extinction memory. These findings highlight the involvement of localised circRNA activity at the synapse in memory formation.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1074742723000588; http://dx.doi.org/10.1016/j.nlm.2023.107777; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85162007613&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37257557; https://linkinghub.elsevier.com/retrieve/pii/S1074742723000588; https://dx.doi.org/10.1016/j.nlm.2023.107777
Elsevier BV
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