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Chloé Savignac

Doctorat - McGill
Superviseur⋅e principal⋅e
Sujets de recherche
Apprentissage automatique médical
Biologie computationnelle
Neurosciences computationnelles

Publications

Mitochondria‐nucleus crosstalk characterizes Alzheimer's disease across 1,5 million brain cells
Emerging insight from stem cell research reinforces Alzheimer's disease (AD) to affect mitochondrial protein expression. Compelling new evid… (voir plus)ence points to mitochondrial reactive oxygen species (ROS) as potential driving player in Aβ toxicity, mediated through glial cells and ultimately impacting neuronal health. A comprehensive understanding of how oxidative phosphorylation variations relate to cell function remains largely unexplored, especially through a cell type lens. Leveraging today's largest single‐nucleus RNA sequencing dataset of AD, we unveil how cell‐type‐specific mitochondrial alterations reverberate in the nuclear transcriptome, in 424 AD patients and healthy controls from ROSMAP. By adopting a supervised latent factor modelling approach, we identified distinct gene modules capturing unique aspects of the mitochondrial crosstalk in 6 major brain cell types across 5,427 nuclear and 13 mitochondrial genes. We found that nuclear‐mitochondrial crosstalk varies distinctly with cell identity, reflecting metabolic demands and functional specialization. In neurons and oligodendrocytes, ATP synthase (complex V) takes a central role, whereas type 1 NADH dehydrogenase (complex I) is more prominent in astrocytes, microglia, and OPCs. Screening across >1 million gene expression profiles from ∼20,000 drug perturbations identified mitochondrial‐nuclear signatures that resemble those activated by parthenolide and niclosamide—two chemical compounds previously associated with oxidative stress and cytotoxicity via ubiquitination—as most predictive of AD. Microglia and OPCs achieved the highest overall classification accuracy, with stronger predictive performance observed in males than in females. Mapping gene module expressions to the Allen Human Brain Atlas revealed shared whole‐brain patterns highlighting the precuneus, which we implicated in ubiquitin‐cascade‐enriched modules. Clinical phenotyping revealed that males with higher AD risk, as indicated by their mitochondrial‐nuclear scores on glial gene modules, exhibited a greater pathological burden, including higher amyloid load, Parkinson's‐like symptoms, and neuroticism‐related traits. Finally, by comparing our findings with 2.5 million CRISPRi‐based perturbations, we identified neural signatures associated with female‐biased transcription factors and fatty acid biosynthesis, while glial signatures were linked to DNA damage and oxidative stress. By integrating multiple layers of biological data from established reference atlases, our analysis of mitochondria‐nuclear crosstalk revealed distinct transcriptional signatures associated with AD risk in glial and neural cells, with these associations exhibiting sex‐biased patterns.
Recovering undersampled single-cell transcriptomes with HyperCell
Abstract

Single-cell transcriptomic technology has now matured, allowing quantification of mRNA transcripts corres… (voir plus)ponding to tens of thousands of genes within a cell. However, still only a small fraction of these mRNA is captured and measured by today’s single-cell assays. There are likely hundreds of thousands of mRNA copies present within a typical human cell, yet these assays omit a majority of the transcripts that are actually present. This introduces technical noise, especially non-biological variability and excessive sparsity, which frustrates downstream analysis and potentially skews biological conclusions. To overcome these challenges, we here develop HyperCell, a probabilistic deep learning approach that explicitly models this undersampling to produce estimates of each cell’s original gene transcript abundances across the whole transcriptome. We demonstrate that our framework offers benefits in various mRNA modeling settings, by i) correctly differentiating between spurious sampling-induced and real biological zeros, outperforming existing approaches, ii) estimating the total mRNA content of cells across states to reduce contamination due to background transcripts, iii) reducing contamination due to background transcripts, and iv) helping to counteract biases that may appear during typical differential gene expression analyses using widespread normalization approaches. Our approach to correcting for the technical noise introduced by the single-cell experimental process brings us closer to studying biology, starting from the true transcriptome of cells.

Cell type transcriptomics reveal shared genetic mechanisms in Alzheimer’s and Parkinson’s disease
Edward A. Fon
Alain Dagher
Yasser Iturria-Medina
Jo Anne Stratton
David A Bennett
Historically, Alzheimer’s disease (AD) and Parkinson’s disease (PD) have been investigated as two distinct disorders of the brain. Howev… (voir plus)er, a few similarities in neuropathology and clinical symptoms have been documented over the years. Traditional single gene-centric genetic studies, including GWAS and differential gene expression analyses, have struggled to unravel the molecular links between AD and PD. To address this, we tailor a pattern-learning framework to analyze synchronous gene co-expression at sub-cell-type resolution. Utilizing recently published single-nucleus AD (70,634 nuclei) and PD (340,902 nuclei) datasets from postmortem human brains, we systematically extract and juxtapose disease-critical gene modules. Our findings reveal extensive molecular similarities between AD and PD gene cliques. In neurons, disrupted cytoskeletal dynamics and mitochondrial stress highlight convergence in key processes; glial modules share roles in T-cell activation, myelin synthesis, and synapse pruning. This multi-module sub-cell-type approach offers insights into the molecular basis of shared neuropathology in AD and PD.
Cell type transcriptomics reveal shared genetic mechanisms in Alzheimer’s and Parkinson’s disease
Edward A. Fon
Alain Dagher
Yasser Iturria-Medina
Jo Anne Stratton
David A Bennett
Historically, Alzheimer’s disease (AD) and Parkinson’s disease (PD) have been investigated as two distinct disorders of the brain. Howev… (voir plus)er, a few similarities in neuropathology and clinical symptoms have been documented over the years. Traditional single gene-centric genetic studies, including GWAS and differential gene expression analyses, have struggled to unravel the molecular links between AD and PD. To address this, we tailor a pattern-learning framework to analyze synchronous gene co-expression at sub-cell-type resolution. Utilizing recently published single-nucleus AD (70,634 nuclei) and PD (340,902 nuclei) datasets from postmortem human brains, we systematically extract and juxtapose disease-critical gene modules. Our findings reveal extensive molecular similarities between AD and PD gene cliques. In neurons, disrupted cytoskeletal dynamics and mitochondrial stress highlight convergence in key processes; glial modules share roles in T-cell activation, myelin synthesis, and synapse pruning. This multi-module sub-cell-type approach offers insights into the molecular basis of shared neuropathology in AD and PD.
Large language models auto-profile conscious awareness changes under psychedelic drug effects
Robin Carhart-Harris
Steven Laureys
Abstract

Psychedelic experiences open a colorful view into drug-induced changes in conscious awareness. Small-samp… (voir plus)le studies on psychedelic drug action have gained traction in recent years. Yet, today’s means for measuring changes in subjective experience are mostly limited to legacy questionnaires of pre-assumed relevance, which could be complemented by bottom-up explorations of semantic facets that underlie experience reports. Here, we show how to harness large language models (LLMs) to i) design from scratch, ii) annotate at scale, and iii) evaluate with rigor a vast portfolio of experience dimensions during psychoactive drug influence, yielding > 2 million automatic dimension ratings that would otherwise have been done by hand. Investigator-independent LLM scoring of these drug effects on the human mind alone allowed to robustly discriminate the unique mental effects of 30 psychoactive substances. Successful knowledge integration of how psychedelics mediate shifts in subjective awareness will be an unavoidable milestone towards charting the full drug design space.

APOE alleles are associated with sex-specific structural differences in brain regions affected in Alzheimer's disease and related dementia
Sylvia Villeneuve
AmanPreet Badhwar
Kimia Shafighi
Chris Zajner
Vaibhav Sharma
Sarah A. Gagliano Taliun
Sali Farhan
Judes Poirier
Alzheimer’s disease is marked by intracellular tau aggregates in the medial temporal lobe (MTL) and extracellular amyloid aggregates in th… (voir plus)e default network (DN). Here, we examined codependent structural variations between the MTL’s most vulnerable structure, the hippocampus (HC), and the DN at subregion resolution in individuals with Alzheimer’s disease and related dementia (ADRD). By leveraging the power of the approximately 40,000 participants of the UK Biobank cohort, we assessed impacts from the protective APOE ɛ2 and the deleterious APOE ɛ4 Alzheimer’s disease alleles on these structural relationships. We demonstrate ɛ2 and ɛ4 genotype effects on the inter-individual expression of HC-DN co-variation structural patterns at the population level. Across these HC-DN signatures, recurrent deviations in the CA1, CA2/3, molecular layer, fornix’s fimbria, and their cortical partners related to ADRD risk. Analyses of the rich phenotypic profiles in the UK Biobank cohort further revealed male-specific HC-DN associations with air pollution and female-specific associations with cardiovascular traits. We also showed that APOE ɛ2/2 interacts preferentially with HC-DN co-variation patterns in estimating social lifestyle in males and physical activity in females. Our structural, genetic, and phenotypic analyses in this large epidemiological cohort reinvigorate the often-neglected interplay between APOE ɛ2 dosage and sex and link APOE alleles to inter-individual brain structural differences indicative of ADRD familial risk.
<i>APOE</i> ɛ2 vs <i>APOE</i> ɛ4 dosage shows sex-specific links to hippocampus-default network subregion co-variation
Sylvia Villeneuve
AmanPreet Badhwar
Kimia Shafighi
Chris Zajner
Vaibhav Sharma
Sarah A Gagliano Taliun
Sali Farhan
Judes Poirier
Alzheimer’s disease and related dementias (ADRD) are marked by intracellular tau aggregates in the medial-temporal lobe (MTL) and extracel… (voir plus)lular amyloid aggregates in the default network (DN). Here, we sought to clarify ADRD-related co-dependencies between the MTL’s most vulnerable structure, the hippocampus (HC), and the highly associative DN at a subregion resolution. We confronted the effects of APOE ɛ2 and ɛ4, rarely investigated together, with their impact on HC-DN co-variation regimes at the population level. In a two-pronged decomposition of structural brain scans from ∼40,000 UK Biobank participants, we located co-deviating structural patterns in HC and DN subregions as a function of ADRD family risk. Across the disclosed HC-DN signatures, recurrent deviations in the CA1, CA2/3, molecular layer, fornix’s fimbria, and their cortical partners related to ADRD risk. Phenome-wide profiling of HC-DN co- variation expressions from these population signatures revealed male-specific associations with air-pollution, and female-specific associations with cardiovascular traits. We highlighted three main factors associated with brain-APOE associations across the different gene variants: happiness, and satisfaction with friendships, and with family. We further showed that APOE ɛ2/2 interacts preferentially with HC-DN co-variation patterns in estimating social lifestyle in males and physical activity in females. Our findings reinvigorate the often-neglected interplay between APOE ɛ2 dosage and sex, which we have linked to fine-grained structural divergences indicative of ADRD susceptibility.