HEIndividual fellowship2023–2025

PhaeoCREEvol · Regulatory sequence evolution during major transitions in complex multicellularity in the brown algal radiation

Horizon Europe — Marie Skłodowska-Curie Actions

Duration
2023-10-01 → 2025-09-30
EU contribution
€173,847
Participants
1
Scheme
HORIZON-TMA-MSCA-PF-EF

Lines connect the coordinator with its partners.

Results in brief

Regulatory sequence evolution during major transitions in complex multicellularity in the brown algal radiation

How complex multicellularity evolves is a fundamental question in biology. The two most complex multicellular groups, animals and plants, each share many core development genes with their unicellular relatives. Thus, it has been hypothesised that increases in gene regulatory sequences, rather than the acquisition of novel genes, may play a central role in the evolution of complexity. However, the ancient origins of developmental complexity in animals and plants has made it difficult to reconstruct the evolutionary steps involved. Brown algae represent the third most complex lineage on Earth and are vastly understudied relative to animals and plants. They evolved only ~250 million years ago, making them one of the youngest groups with complex multicellularity. Furthermore, extant brown algae exhibit extensive diversity in their complexity, ranging from relatively simple branched filaments (e.g., Ectocarpus) to complex three-dimensional thalli (e.g., kelps). Similar diversity exists in life cycles, sexual systems and genome sizes. Critically, there have been several independent transitions in complexity in the group. Taken together, the recent emergence and diversity of brown algae presents an elegant natural experiment in which to ask what genetic changes coincide with, and have potentially driven, transitions in complexity. PhaeoCREEvol set out to answer this fundamental question. The project aimed to do this using two key methods. First, it would utilise comparative genomics analyses across the diversity of brown algae (~50 available genomes) to identify conserved noncoding sequences that likely have regulatory function (also known as cis-regulatory elements, or CREs). Second, it would employ multiomics approaches such as ATAC-seq to functionally identify CREs in five species of varying complexity. Combining these data, we would ask whether transitions to greater developmental complexity are associated with lineage-specific increases in CREs. We also aimed to ask how these CREs are acquired, specifically looking at the role of transposable elements, mobile genetic elements that are known to drive CRE evolution in animals and plants. Finally, we set out to ask whether distal gene regulation had emerged in the most complex brown algae using HiC data, mirroring the evolution of long-range gene enhancers in vertebrates and some angiosperms. The projects main ambitions were to provide fundamental insights in evolutionary biology. Additionally, brown algae are of substantial ecological and economic significance, with brown algal forests forming keystone habitats across 25% of coastlines globally. PhaeoCREEVol also aimed to increase our understanding of brown algal genomics and genetics, bringing benefits to global biodiversity and food security.

Data: CORDIS, © European Union

Project objective

Brown algae are a multicellular clade that display remarkable diversity in developmental and physiological complexity, and in life history traits. They evolved independently and more recently than animals and plants, making them a uniquely powerful system to characterise the genomic changes that underlie the emergence of complex multicellularity. I will specifically test the hypothesis that cis-regulatory element (CRE) evolution plays a leading role the evolution of complexity. Harnessing large-scale multiomics datasets, I will quantify lineage-specific rates of CRE gains and losses, and attempt to link these events to transitions in complexity. I will combine signatures of constraint from a 59-species whole-genome alignment with functional epigenomic data (ATAC-seq, ChIP-seq) from five representative species to produce fine-scale maps of deeply conserved and recently acquired CREs. To understand the mechanisms of CRE evolution, I will annotate transposable elements (TEs) and quantify variation in TE diversity, abundance and activity. I will characterise what roles TEs have had in CRE dissemination. I will also explore between-species variation in the proportion of proximal and distal CREs. I will analyse high-resolution Hi-C data for four species to ask what effect distal regulation has on 3D genome organisation (i.e. are distal CREs and the genes they regulate topologically associated?). PhaeoCREEvol will inform upon the rates and mechanisms of CRE evolution during the emergence of complexity, providing a highly pertinent comparison to animals and plants. This will increase our knowledge of regulatory evolution in general, while shedding light onto the fundamental biology of a largely unstudied eukaryotic group. Brown algae play critical ecological roles and have significant potential to mitigate climate change, enhance global food security, and deliver novel industrial solutions, providing key motivations to better understand their genetics and evolution.

Original text from CORDIS.

Participants

  • MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV · MUNCHENCoordinatorGermany

Links

Data: CORDIS, © European Union