Deciphering the origins of cell differentiation and developmental gene regulation in animals

This project investigates chromatin-based transcriptional regulation in choanoflagellates to understand the evolution of animal cell differentiation and gene regulation mechanisms.

Subsidie
€ 1.872.506
2024

Projectdetails

Introduction

During animal development, the process of cell differentiation gives rise to terminally differentiated cell types with cell-type-specific gene expression programs. In the most closely related group to animals, the choanoflagellates, cell differentiation occurs but cells do not commit irreversibly to specific fates. Instead, they transition through cell identities as they progress through their life cycle, known as temporal cell differentiation.

Background

Animal cell differentiation is thought to have evolved from temporal differentiation, but the mechanisms are largely unknown due to a lack of information on the molecular processes underpinning temporal differentiation.

Research Proposal

This proposal will test the hypothesis that chromatin-based transcriptional regulation underlies temporal cell differentiation in choanoflagellates. Utilizing S. rosetta as a model, I will:

  1. Compare transcription and chromatin across cell types using genome-wide omics techniques.
  2. Assess the role of different histone modifications in cell-fate transitions.
  3. Discover whether various aspects of animal developmental gene regulation, e.g., the use of repressive histone modifications in cell-type-specific gene regulation, are also utilized in choanoflagellates.

I will also examine the cis-regulatory landscape in S. rosetta and use both molecular and functional assays to:

  • Examine the types of cis-regulatory elements present.
  • Investigate if enhancer elements are used to regulate gene expression.

Finally, I will test the role of selected chromatin regulators in temporal cell differentiation and cell-type-specific gene expression.

Significance

This ground-breaking work will be the first to study these processes in choanoflagellates, thus pioneering the comparison between definitive cell differentiation, seen in animals, and choanoflagellate temporal differentiation. In a broader context, this will deliver fundamental new insights into the evolution of animal gene regulation during development.

Financiële details & Tijdlijn

Financiële details

Subsidiebedrag€ 1.872.506
Totale projectbegroting€ 1.872.506

Tijdlijn

Startdatum1-4-2024
Einddatum31-3-2029
Subsidiejaar2024

Partners & Locaties

Projectpartners

  • UNIVERSITY OF GALWAYpenvoerder

Land(en)

Ireland

Vergelijkbare projecten binnen European Research Council

ERC Starting...

From cell shape to organism shape: the cellular basis for the evolutionary origin of animal morphogenesis

This project investigates the evolution of cellular mechanisms in animal morphogenesis by studying choanoflagellates, aiming to uncover insights into pre-metazoan developmental gene functions.

€ 1.492.753
ERC Starting...

Timing cell cycles in multicellular development

DevCycle aims to uncover the mechanisms of cell-cycle regulation during intestinal development in nematodes, providing insights for tissue engineering and disease control.

€ 1.500.000
ERC Consolid...

Animal cell types across evolutionary timescales: from regulatory characters to cell phylogenies

This project aims to elucidate the evolutionary processes of cell type diversity in Cnidaria through comparative genomics and phylogenetic analysis, enhancing our understanding of animal adaptation and evolution.

€ 1.999.960
ERC Consolid...

The impact of 3D regulatory landscapes on the evolution of developmental programs

The 3D-REVOLUTION project aims to explore how changes in 3D regulatory landscapes influence gonadal sex determination and evolutionary gene regulation using advanced genomic techniques.

€ 1.998.217
ERC Starting...

Uncovering the role and regulation of 3D DNA-RNA nuclear dynamics in controlling cell fate decisions

This project aims to elucidate the interplay between 3D genome organization and transcriptome dynamics in early mouse embryos to identify factors influencing cell fate decisions.

€ 1.500.000