Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader–Willi syndrome

This study defined gene expression changes across different cell types in prefrontal cortex (PFC) of donors with Prader-Willi syndrome (PWS) compared to controls and examined relationships between these changes in blood and PWS symptoms. 8,338 long non-coding RNAs and 17,079 protein-coding genes were examined using single-nucleus RNA-sequencing (snRNA-seq) in the PFC of 8 donors with PWS (4 deletion, 4 non-deletion), and 4 age- and sex-matched neurotypical controls. snRNA-seq analyses showed an increased proportion of interneurons in both PWS groups compared to controls. Fifty-four genes and related pathways were consistently dysregulated across all cell types in the PFC of the PWS group compared to controls, with RPS18 being the only protein-coding gene upregulated in PWS PFC across all comparisons. Increase in RPS18 mRNA levels in peripheral blood mononuclear cells (PBMCs) of another cohort (16 deletion, 20 non-deletion, ages 1-45 years) assessed using droplet digital PCR was found to be associated with intellectual functioning and challenging behaviors, but not autistic traits in children with PWS due to non-deletion (< 13 years old; N = 19). If confirmed in future studies, these findings may lead to development of prognostic biomarkers and therapeutics targeting consistently dysregulated genes and related pathways between brain and periphery.

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Journal
Scientific Reports
Published
2025-12-24
DOI
https://doi.org/10.1038/s41598-025-33041-3
Primary Topic
Genetic Syndromes and Imprinting
Type
article
Field-Weighted Citation Impact
0.00

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article

Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader–Willi syndrome

Mirana Ramialison, Fernando J. Rossello, Helen Heussler, Dinusha Gamage et al.
Scientific Reports
Genetic Syndromes and Imprinting
article

Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader–Willi syndrome

Mirana Ramialison, Fernando J. Rossello, Helen Heussler, Dinusha Gamage, Waheeda A. Hossain, David E. Godler, Merlin G. Butler, David J. Amor, Melissa C. Southey, Michael Duhig, Anthony J Hannan, E. Baker, Olivia Veatch, Minh Bui, Robert D. Nicholls, Shokouh Shahrokhi, Michael See
article en

Abstract

This study defined gene expression changes across different cell types in prefrontal cortex (PFC) of donors with Prader-Willi syndrome (PWS) compared to controls and examined relationships between these changes in blood and PWS symptoms. 8,338 long non-coding RNAs and 17,079 protein-coding genes were examined using single-nucleus RNA-sequencing (snRNA-seq) in the PFC of 8 donors with PWS (4 deletion, 4 non-deletion), and 4 age- and sex-matched neurotypical controls. snRNA-seq analyses showed an increased proportion of interneurons in both PWS groups compared to controls. Fifty-four genes and related pathways were consistently dysregulated across all cell types in the PFC of the PWS group compared to controls, with RPS18 being the only protein-coding gene upregulated in PWS PFC across all comparisons. Increase in RPS18 mRNA levels in peripheral blood mononuclear cells (PBMCs) of another cohort (16 deletion, 20 non-deletion, ages 1-45 years) assessed using droplet digital PCR was found to be associated with intellectual functioning and challenging behaviors, but not autistic traits in children with PWS due to non-deletion (< 13 years old; N = 19). If confirmed in future studies, these findings may lead to development of prognostic biomarkers and therapeutics targeting consistently dysregulated genes and related pathways between brain and periphery.

Scientific ReportsVol. 16(1)
The University of Queensland (AU), The University of Melbourne (AU), Cancer Council Victoria (AU), La Trobe University (AU), Florey Institute of Neuroscience and Mental Health (AU), Australian Regenerative Medicine Institute (AU), Children’s Health Queensland Hospital and Health Service (AU), Monash Health (AU), University of Kansas Medical Center (US), Children's Hospital of Pittsburgh (US), Murdoch Children's Research Institute (AU), Monash University (AU)
Children’s Hospital of Wisconsin Research Institute, Children's Hospital Foundation, Murdoch Children's Research Institute, Novo Nordisk, State Government of Victoria, Medical Research Council, National Health and Medical Research Council, National Institute of Child Health and Human Development
Openalex Percentile: Top 25%
Genetic Syndromes and Imprinting
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