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Saez, M. A.

Publications and source records attributed to Saez, M. A..

2 recordsLinked to original sources

Exploring Single-Cell Gene Regulatory Dynamics in Rett Syndrome

Rett syndrome is a monogenic disorder with an incidence of 95% in women, characterized by the complexity of studying the associated phenotype due to the heterogeneity in patient tissues from the stochastic silencing of the affected X chromosome. Furthermore, we are largely unaware of the cascade of alterations that occur in neurons due to transcriptional changes induced by the affected MECP2 gene. To address these challenges, an in-depth network analysis was implemented using organoid single-cell transcriptomic data derived from human patients. We performed a Weighted correlation network analysis and trajectory analysis to understand the differences in the developmental processes between samples, we followed by the generation of gene regulatory networks for each relevant cell developmental pathways to assess the master regulator that are involved in this process, with the differential expressed genes with potential therapeutic implications being identified by integration with SFARI and Genes4Epi. The results were adapted into dynamic Boolean models fitted with the transcriptomic data for validation in which we evaluated the attractor field from each reachable state. These approaches allowed us to explore differences in regulatory behavior in the developmental pathways. Our study provides an insight that pinpoints the cellular stages on which the regulation and compensatory mechanism activate and regulate Rett syndrome. We identified 19 Master regulators for the Dopaminergic developmental trajectory, as well as 34 Master regulator genes for the Gabaergic developmental trajectory. Dynamic Boolean modeling of these systems showcased a comprehensive understanding of the disrupted developmental pathways of Rett syndrome, highlighting the transitional states of potential within maturation trajectories as the key point of divergence in regulation for Rett syndrome. After complementing with enrichment and clinical relevant variant analysis, we identify the key actors in this system as NR2F1 and TCF4, with TCF4 suggesting a symmetrical compensatory relationship with MeCP2, and NR2F1 as possible link with wider developmental conditions, this concluded with highlighting the possibility of regulation in this condition being affected by the MAPK-ERK pathway of transcriptional regulation, offering a novel angle for targeted research.

neuroscience↗

Transcriptional and Histone acetylation changes associated with CRE elements expose key factors governing the regulatory circuit in early stage of Huntington's disease models.

Huntingtons disease (HD) is a disorder caused by an abnormal expansion of trinucleotide CAG repeats within the huntingtin (Htt) gene. Under normal conditions, the CREB Binding Protein interacts with CREB elements and acetylates Lysine 27 of Histone 3 to direct the expression of several genes. However, mutant Htt causes depletion of CBP which in turn induces altered histone acetylation patterns and transcriptional deregulation. Here, we have studied differential expression analysis and H3K27ac variation in 4- and 6-week-old R6/2 mice as a model of juvenile HD. Analysis of differential gene expression and acetylation levels were integrated into Gene Regulatory Networks revealing key regulators involved in the altered transcription cascade. Our results show changes in acetylation and gene expression levels that are related to impaired neuronal development and key regulators clearly defined in 6-week-old mice are proposed to drive the downstream regulatory cascade in HD. Here we describe the first approach to determine the relationship among epigenetic changes in the early stages of HD. We determined the existence of changes in pre-symptomatic stages of HD, a starting point for early onset indicators of the progression of this disease.

genomics↗