HEIndividual fellowship2022–2024

FOX-mTN · Dissecting FOXO-mediated Transcription Noise to Stall Cellular Dysfunction in Ageing

Horizon Europe — Marie Skłodowska-Curie Actions

Duration
2022-06-01 → 2024-05-31
EU contribution
€156,779
Participants
1
Scheme
HORIZON-TMA-MSCA-PF-EF

Lines connect the coordinator with its partners.

Results in brief

Dissecting FOXO-mediated Transcription Noise to Stall Cellular Dysfunction in Ageing

Ageing is the result of accumulated cellular dysfunction and loss of tissue homeostasis, which culminates in age-related pathologies. Tissue homeostasis relies on the balance between cell removal, proliferation, and regeneration, which is disturbed during ageing, and is particularly important for the vascular endothelium. Previous research, conducted by our group and collaborators, has shed light on the indispensable role of FOXO1 in endothelial homeostasis. Dysregulation of FOXO1, either through its loss or overexpression, has been linked to vascular abnormalities such as overgrowth and rarefaction, leading to the emergence of vascular malformations in diverse tissues including the retina, skeletal muscle, and liver. Conversely, the decline in cellular function observed during ageing can also stem from defects in quality control mechanisms, such as those governing gene expression. For instance, ageing is associated with an increase in transcriptional noise and the accumulation of aberrant RNA molecules. However, the extent and significance of this phenomenon in both healthy and aged tissues remain poorly understood, despite its potential impact on cellular fitness during ageing. Our project adopted a multidisciplinary approach that integrates computational multi-omics analyses and genetic manipulation techniques in both human cells and mouse models. The primary objective was to gain fresh insights into the emergence of transcriptional noise, elucidate its dependence on FOXO dysregulation, and unravel its implications for cellular homeostasis. By unravelling these intricate relationships, our aim was to contribute to a deeper understanding of the molecular mechanisms underlying ageing-related cellular dysfunction, with special emphasis on vascular health, and pave the way for potential therapeutic interventions. In parallel, we sought to enhance the computational biology field by providing training opportunities for students and young researchers in computational approaches. The field is rapidly evolving in terms of applications, breadth of scope and the extent of what can be accomplished. However, there is a big demand for bioinformatics skills in research, particularly in Portugal, even though many life scientists had no contact with programming languages. This effort will contribute to strengthening national and European cooperation, not only in the topics covered in this project but also in a variety of other fields where computational biology is required.

Data: CORDIS, © European Union

Project objective

Ageing is the result of accumulated cellular dysfunction and loss of tissue homeostasis, which often leads to the emergence of age-related pathologies such as cancer and cardiovascular disorders. The disruption of tissue homeostasis during ageing is particularly critical in the case of the vascular endothelium. The signaling interface and barrier to external factors is provided by a single layer of endothelial cells in a quiescent state. The maintenance of this quiescent state plays an important role in vascular aging and development of cardiovascular diseases. Previous studies have shown that the FOXO1 is a critical driver of endothelial quiescence, where its loss and overexpression leads to vascular overgrowth and rarefaction, respectively. My preliminary analyses show that gene expression levels of FOXO family varies in aged-tissues and that FOXO1/3/4 mutant mice display significant vascular malformation in the retina. On the other hand, ageing is associated with an increase of transcriptional noise and accumulation of aberrant RNA, which if not eliminated, may lead to cellular dysfunction. My preliminary data shows that even healthy tissues have significant levels of transcriptional noise, while old individuals present higher levels of such aberrant transcription. However, transcription noise is an unexplored phenomenon impacting cell homeostasis. In addition, my analyses also show that FOXO1 overexpression in cultured human endothelial cells leads to higher levels of transcription noise. Given the accumulating evidence and my preliminary findings, I propose to explore how the dysregulation of FOXO transcription factors increases transcription noise, promoting functional decline of the vascular endothelium through ageing. Understanding the cascade events that drive this transcription aberrancy can have a significant impact on the prevention of cellular function decline and delay a wide range of ageing illnesses.

Original text from CORDIS.

Participants

  • NOVA ID FCT - ASSOCIACAO PARA A INOVACAO E DESENVOLVIMENTO DA FCT · CaparicaCoordinatorPortugal

Links

Data: CORDIS, © European Union