Salient experiences are represented by unique transcriptional signatures in the mouse brain
eLife, ISSN: 2050-084X, Vol: 7
2018
- 29Citations
- 161Captures
- 3Mentions
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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
- Citations29
- Citation Indexes29
- 29
- CrossRef27
- Captures161
- Readers161
- 161
- Mentions3
- News Mentions2
- 2
- Blog Mentions1
- Blog1
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Article Description
It is well established that inducible transcription is essential for the consolidation of salient experiences into long-term memory. However, whether inducible transcription relays information about the identity and affective attributes of the experience being encoded, has not been explored. To this end, we analyzed transcription induced by a variety of rewarding and aversive experiences, across multiple brain regions. Our results describe the existence of robust transcriptional signatures uniquely representing distinct experiences, enabling near-perfect decoding of recent experiences. Furthermore, experiences with shared attributes display commonalities in their transcriptional signatures, exemplified in the representation of valence, habituation and reinforcement. This study introduces the concept of a neural transcriptional code, which represents the encoding of experiences in the mouse brain. This code is comprised of distinct transcriptional signatures that correlate to attributes of the experiences that are being committed to long-term memory.
Bibliographic Details
10.7554/elife.31220; 10.7554/elife.31220.010; 10.7554/elife.31220.003; 10.7554/elife.31220.016; 10.7554/elife.31220.002; 10.7554/elife.31220.001
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85045678255&origin=inward; http://dx.doi.org/10.7554/elife.31220; http://www.ncbi.nlm.nih.gov/pubmed/29412137; https://elifesciences.org/articles/31220#fig2; http://dx.doi.org/10.7554/elife.31220.010; https://elifesciences.org/articles/31220#fig1; http://dx.doi.org/10.7554/elife.31220.003; https://elifesciences.org/articles/31220#fig3; http://dx.doi.org/10.7554/elife.31220.016; https://elifesciences.org/articles/31220#digest; http://dx.doi.org/10.7554/elife.31220.002; https://elifesciences.org/articles/31220#abstract; http://dx.doi.org/10.7554/elife.31220.001; https://elifesciences.org/articles/31220; https://dx.doi.org/10.7554/elife.31220
eLife Sciences Publications, Ltd
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