Publications by authors named "F N L Vitorino"

The gut microbiota has emerged as a pivotal regulator of host inflammatory processes after traumatic brain injury (TBI). However, the mechanisms by which the gut microbiota communicates to the brain in TBI are still under investigation. We previously reported that gut microbiota depletion (GMD) using antibiotics after TBI resulted in increased microglial activation, reduced neurogenesis, and reduced T cell infiltration.

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The "Histone Code" is comprised of specific types and positions of post-translational modifications (PTMs) which produce biological signals for gene regulation and have potential as biomarkers for medical diagnostics. Previous work has shown that electron-based fragmentation improves the sequence coverage and confidence of labile PTM position assignment. Here, we evaluated two derivatization methods (e.

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Article Synopsis
  • Methylation of histone 3 lysine 36 (H3K36me) is crucial for gene expression regulation, but understanding the specific enzymes involved remains unclear.* -
  • In mouse stem cells, research reveals that H3K36me2 is mainly added by NSD1 and NSD2 in intergenic regions, while H3K36me1/3 are found in exons, correlating with gene activity; SETD2 is key for H3K36me3 deposition.* -
  • The study identifies a hierarchy among methyltransferases (K36MTs) for adding H3K36me1/2, with NSD1 being the most dominant, while NSD3
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Trypanosoma cruzi, the causative agent of Chagas disease, has a complex life cycle that involves triatomine insects as vectors and mammals as hosts. The differentiation of epimastigote forms into metacyclic trypomastigotes within the insect vector is crucial for the parasite's life cycle progression. Factors influencing this process, including temperature, pH, and nutritional stress, along with specific metabolite availability, play a pivotal role.

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Metabolic control of chromatin and gene expression is emerging as a key, but largely unexplored aspect of gene regulation. In the brain, metabolic-epigenetic interactions can influence critical neuronal functions. Here, we use a combination of behavioral, proteomic and genomic approaches to demonstrate that the intermediary metabolite acetate enhances memory in a brain region- and sex-specific manner.

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