BDNF-DT and BDNF-AS-DT: novel genes in the BDNF locus

Divergent transcription from bidirectional promoters is frequently observed in eukaryotic genomes, but the biological relevance of divergent RNA transcripts (DT) is unknown. We identified and characterized BDNF-DT, a novel DT gene, and BDNF-AS-DT, a novel readthrough gene, in the locus containing BDNF, a gene with key roles in neuronal development, differentiation, and synaptic plasticity. BDNF-DT is independent from the known BDNF antisense (BDNF-AS), and its expression is developmentally regulated and positively correlated with BDNF in human postmortem dorsolateral prefrontal cortex (DLPFC). BDNF-DT and BDNF-AS-DT expression increase after induced depolarization, but the temporal dynamics follow expression of BDNF, suggesting a regulatory role. Moreover, CRISPR-mediated upregulation of BDNF in human neural progenitor cells drives BDNF-DT expression. Finally, BDNF-DT shows higher expression in DLPFC from patients diagnosed with schizophrenia compared to neurotypical controls, and genetically predicted lower expression of the BDNF-AS-DT readthrough transcript is associated with schizophrenia and with the schizophrenia-associated C allele of the rs6265 single-nucleotide polymorphism. These findings identify BDNF-DT and BDNF-AS-DT as novel, low-abundance genes that show coordinated expression with BDNF and association with schizophrenia risk, though their biological significance requires further validation given detection limitations and the need to establish causal roles.

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Publication Details

Journal
Molecular Psychiatry
Published
2026-06-30
DOI
https://doi.org/10.1038/s41380-026-03695-0
Primary Topic
Nerve injury and regeneration
Type
article
Field-Weighted Citation Impact
0.00

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article

BDNF-DT and BDNF-AS-DT: novel genes in the BDNF locus

Gianluca Ursini, Keri Martinowich, Joel E. Kleinman, Q Chen et al.
Molecular Psychiatry
Nerve injury and regeneration
article

BDNF-DT and BDNF-AS-DT: novel genes in the BDNF locus

Gianluca Ursini, Keri Martinowich, Joel E. Kleinman, Q Chen, Giovanna Punzi, Nuri Smith, Joo Heon Shin, Kristen R. Maynard, Daniel R. Weinberger, Svitlana V. Bach, Thomas M. Hyde, Leonardo Collado‐Torres, Stephanie C. Page, Sreya Mukherjee, Geo Pertea
article en

Abstract

Divergent transcription from bidirectional promoters is frequently observed in eukaryotic genomes, but the biological relevance of divergent RNA transcripts (DT) is unknown. We identified and characterized BDNF-DT, a novel DT gene, and BDNF-AS-DT, a novel readthrough gene, in the locus containing BDNF, a gene with key roles in neuronal development, differentiation, and synaptic plasticity. BDNF-DT is independent from the known BDNF antisense (BDNF-AS), and its expression is developmentally regulated and positively correlated with BDNF in human postmortem dorsolateral prefrontal cortex (DLPFC). BDNF-DT and BDNF-AS-DT expression increase after induced depolarization, but the temporal dynamics follow expression of BDNF, suggesting a regulatory role. Moreover, CRISPR-mediated upregulation of BDNF in human neural progenitor cells drives BDNF-DT expression. Finally, BDNF-DT shows higher expression in DLPFC from patients diagnosed with schizophrenia compared to neurotypical controls, and genetically predicted lower expression of the BDNF-AS-DT readthrough transcript is associated with schizophrenia and with the schizophrenia-associated C allele of the rs6265 single-nucleotide polymorphism. These findings identify BDNF-DT and BDNF-AS-DT as novel, low-abundance genes that show coordinated expression with BDNF and association with schizophrenia risk, though their biological significance requires further validation given detection limitations and the need to establish causal roles.

Molecular Psychiatry
National Institutes of Health (US), Johns Hopkins University (US), Johns Hopkins Medicine (US), Behavioral Pharma (United States) (US), National Center for Advancing Translational Sciences (US), Lieber Institute for Brain Development (US)
National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Mental Health, National Institute on Drug Abuse, National Human Genome Research Institute, NIH Office of the Director, National Cancer Institute, National Institute of Neurological Disorders and Stroke, Common Fund
Zero hunger
Openalex Percentile: Top 11%
Nerve injury and regeneration
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