Haobin Ren
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Haobin Ren has a total of 33 co-authors. Here are the top co-authors by number of shared publications:
- Esmi Lau Zajaczkowski
Cognitive Neuroepigenetics Laboratory, The Queensland Brain Institute, University of Queensland
2 shared publications - Mason Musgrove
Centre for RNA in Neuroscience, University of Queensland, Brisbane, QLD, Australia
2 shared publications - Qiongyi Zhao
The University of Queensland
2 shared publications - Timothy William Bredy
The University of Queensland
2 shared publications Wei Wei
2 shared publications- Wei-Siang Liau
Cognitive Neuroepigenetics Laboratory, The Queensland Brain Institute, University of Queensland
2 shared publications
Latest Publications
- Open Access
A mobile circular DNA element drives memory-related processes in mice
Extrachromosomal circular DNAs (ecDNAs) are double stranded, closed loop DNA molecules that act independently of the genome. Here we report the discovery of a brain-enriched ecDNA, ecCldn34d , that regulates the transcriptional state of plasticity-related genes and is temporally associated with the stability of fear memories. ecDNA therefore represents a novel class of mobile DNA elements that are involved in experience-dependent neuroadaptation.
Open AccessA mobile circular DNA element drives memory-related processes in mice
Extrachromosomal circular DNAs (ecDNAs) are double stranded, closed loop DNA molecules that act independently of the genome. Here we report the discovery of a brain-enriched ecDNA, ecCldn34d , that regulates the transcriptional state of plasticity-related genes and is temporally associated with the stability of fear memories. ecDNA therefore represents a novel class of mobile DNA elements that are involved in experience-dependent neuroadaptation.
- 15 July 2025
- Published by University of Queensland Library
Explore extrachromosomal circular DNA in the brain and in fear-related learning and memory
The University of Queensland's institutional repository, UQ eSpace, aims to create global visibility and accessibility of UQ’s scholarly research.
- 15 July 2025
- Published by University of Queensland Library
Explore extrachromosomal circular DNA in the brain and in fear-related learning and memory
The University of Queensland's institutional repository, UQ eSpace, aims to create global visibility and accessibility of UQ’s scholarly research.
- Open Access
- 22 November 2023
- Published by Springer Nature in Nature Communications
- Vol. 14 (1) , 1-16
Fear extinction is regulated by the activity of long noncoding RNAs at the synapse
Long noncoding RNAs (lncRNAs) represent a multidimensional class of regulatory molecules that are involved in many aspects of brain function. Emerging evidence indicates that lncRNAs are localized to the synapse; however, a direct role for their activity in this subcellular compartment in memory formation has yet to be demonstrated. Using lncRNA capture-seq, we identified a specific set of lncRNAs that accumulate in the synaptic compartment within the infralimbic prefrontal cortex of adult male C57/Bl6 mice. Among these was a splice variant related to the stress-associated lncRNA, Gas5. RNA immunoprecipitation followed by mass spectrometry and single-molecule imaging revealed that this Gas5 isoform, in association with the RNA binding proteins G3BP2 and CAPRIN1, regulates the activity-dependent trafficking and clustering of RNA granules. In addition, we found that cell-type-specific, activity-dependent, and synapse-specific knockdown of the Gas5 variant led to impaired fear extinction memory. These findings identify a new mechanism of fear extinction that involves the dynamic interaction between local lncRNA activity and RNA condensates in the synaptic compartment.
- 22 November 2023
- Published by Springer Nature in Nature Communications
- Vol. 14 (1) , 1-16
Open AccessFear extinction is regulated by the activity of long noncoding RNAs at the synapse
Long noncoding RNAs (lncRNAs) represent a multidimensional class of regulatory molecules that are involved in many aspects of brain function. Emerging evidence indicates that lncRNAs are localized to the synapse; however, a direct role for their activity in this subcellular compartment in memory formation has yet to be demonstrated. Using lncRNA capture-seq, we identified a specific set of lncRNAs that accumulate in the synaptic compartment within the infralimbic prefrontal cortex of adult male C57/Bl6 mice. Among these was a splice variant related to the stress-associated lncRNA, Gas5. RNA immunoprecipitation followed by mass spectrometry and single-molecule imaging revealed that this Gas5 isoform, in association with the RNA binding proteins G3BP2 and CAPRIN1, regulates the activity-dependent trafficking and clustering of RNA granules. In addition, we found that cell-type-specific, activity-dependent, and synapse-specific knockdown of the Gas5 variant led to impaired fear extinction memory. These findings identify a new mechanism of fear extinction that involves the dynamic interaction between local lncRNA activity and RNA condensates in the synaptic compartment.