Role of Transposons in Regulating the Neural Genome and the Mechanisms of Neuropsychiatric Diseases

A Special Issue of Cells (ISSN 2073-4409) belonging to the section "Cellular Neuroscience".

Deadline for manuscript submissions: 20 September 2026 | Viewed by 1742

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Guest Editor
Department of Psychiatry and Human Behavior, University of California, Irvine, CA, USA
Interests: genomics of cognitive traits; brain evolution and paleoneurology; genetics of language; computational neurogenomics

Special Issue Information

Dear Colleagues,

Transposable elements (TEs) constitute over 50% of the human genome, totaling more than 4.5 million elements. Barbara McClintock first discovered TEs in the early 1950s, identifying them as genomic elements capable of moving within the genome and affecting gene expression. Later, in the 1970s, Britten and Davidson recognized their role as major epigenetic factors that regulate gene expression locally (CREs, cis-regulatory elements). Functional sequencing and comparative genomics also uncovered a trans role for TEs, meaning that they are involved in both cis- and trans-regulation independently of their often-lost transposition ability. Since then, there has been extensive research into the diverse regulatory functions of TEs, aided by technological advances. Cis-regulatory TE-derived elements include promoters, enhancers, silencers, and boundary elements. Trans-regulation involves proteins such as transcription factors (TFs) and cofactors, along with non-coding transcripts with regulatory roles, such as enhancer RNAs or long non-coding RNAs. Mechanistically, TEs can influence gene expression both locally, through transcriptional and post-transcriptional mechanisms, and distally, via their encoded products, which encompass non-coding RNAs (ncRNAs) and proteins. Less studied areas include the implication of TEs in trans-generational epigenetic inheritance and the epigenetic dynamics of memory expression. Although the list of potential research topics regarding TEs is long, recent studies have highlighted that cis-regulatory and trans-acting systems evolve at different rates, underscoring the importance of cis-regulatory TEs as targets for evolutionary change.

Given their complex regulatory roles and, in some cases, their exaptation into new protein-coding genes over evolutionary time, TEs act as key drivers of innovation, primarily by shaping and organizing the architecture of the neural genome. Not all innovation processes have stabilized yet, however, which means that TEs not only have adaptive functions but also participate in pathological mechanisms leading to neuropsychiatric disorders. Despite the challenges posed by the species-specific characteristics of TEs, resulting in high human specificity for recent TEs, exciting discoveries continue to emerge. Building on initial findings from just a few years ago, research into the expanded regulatory functions of TEs has progressed toward analyzing their genome-wide roles, using new techniques such as brain organoids and several recently developed molecular and computational tools.

This Special Issue of Cells will highlight current research on TEs in relation to the evolution, development, and mechanistic regulation of the neural genome, as well as their role in the pathogenesis of neuropsychiatric disorders.

Prof. Dr. Fabio M. Macciardi
Guest Editor

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Keywords

  • transposable elements
  • genome evolution
  • central nervous system development
  • neural genome
  • neural gene regulation
  • neuropsychiatric disorders

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Published Papers (1 paper)

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14 pages, 3192 KB  
Article
Sex Differences in B2 SINE RNA Expression and Their Role in Hippocampal Development
by Troy A. Richter, Andrew A. Bartlett, Hannah E. Lapp, Erin T. O’Neil, Ellie K. Pritchard, Guia Guffanti, Susan L. Zup and Richard G. Hunter
Cells 2026, 15(9), 816; https://doi.org/10.3390/cells15090816 - 30 Apr 2026
Viewed by 1247
Abstract
Once dismissed as “junk”, transposable elements (TEs) have recently gained recognition for their regulatory roles, notably in the brain and during development. The brain is hormone-responsive and the hippocampus in particular is sensitive to circulating gonadal hormones. While transcriptionally active, TE function remains [...] Read more.
Once dismissed as “junk”, transposable elements (TEs) have recently gained recognition for their regulatory roles, notably in the brain and during development. The brain is hormone-responsive and the hippocampus in particular is sensitive to circulating gonadal hormones. While transcriptionally active, TE function remains poorly understood, especially in the brain. We and other researchers have shown that one particular TE RNA, B2 SINE ncRNA, is a regulator in the rodent hippocampus, especially after a psychologically stressful event like acute restraint stress. However, it is unknown if B2 SINE ncRNA is necessary for the proper development of hippocampal neurons, and, furthermore, if there are sex differences in this development. This work investigates the differences in the expression of B2 SINE RNA across sexes and its role in the development of primary hippocampal neurons. We utilized pooled locked nucleic acid (LNA) GapmeRs to knock down the expression of B2 SINE RNA, and we treated primary hippocampal neurons with dihydrotestosterone (DHT) to test if there is a difference in dendritic complexity. We used Sholl analysis to quantify branching, number of tips, and Sholl mean. We found a sex difference in both B2 SINE, higher in males compared to females, and ß-actin, lower in males compared to females. Additionally, knocking down B2 SINE RNA results in a reduction in dendritic complexity in male but not in female neurons. Taken together, this work suggests that B2 SINE RNA is expressed differentially and that it plays an important role in the proper development of hippocampal neurons in a sex-dependent manner. Our findings support the identification of a sex-specific biomarker that may enable individualized treatment of conditions influenced by sex. This is the first evidence of the role B2 SINE RNA may play in the regulation of the development of neuronal dendritic structure and the first to show differential regulation by sex. Full article
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