Conflict-reducing innovations in development enable increased multicellular complexity

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Conflict-reducing innovations in development enable increased multicellular complexity. / Howe, Jack; Cornwallis, Charlie K.; Griffin, Ashleigh S.

In: Proceedings of the Royal Society B: Biological Sciences, Vol. 291, No. 2014, 20232466, 2024.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Howe, J, Cornwallis, CK & Griffin, AS 2024, 'Conflict-reducing innovations in development enable increased multicellular complexity', Proceedings of the Royal Society B: Biological Sciences, vol. 291, no. 2014, 20232466. https://doi.org/10.1098/rspb.2023.2466

APA

Howe, J., Cornwallis, C. K., & Griffin, A. S. (2024). Conflict-reducing innovations in development enable increased multicellular complexity. Proceedings of the Royal Society B: Biological Sciences, 291(2014), [20232466]. https://doi.org/10.1098/rspb.2023.2466

Vancouver

Howe J, Cornwallis CK, Griffin AS. Conflict-reducing innovations in development enable increased multicellular complexity. Proceedings of the Royal Society B: Biological Sciences. 2024;291(2014). 20232466. https://doi.org/10.1098/rspb.2023.2466

Author

Howe, Jack ; Cornwallis, Charlie K. ; Griffin, Ashleigh S. / Conflict-reducing innovations in development enable increased multicellular complexity. In: Proceedings of the Royal Society B: Biological Sciences. 2024 ; Vol. 291, No. 2014.

Bibtex

@article{66aa720575c6492fb26cf82a744cb579,
title = "Conflict-reducing innovations in development enable increased multicellular complexity",
abstract = "Obligately multicellular organisms, where cells can only reproduce as part of the group, have evolved multiple times across the tree of life. Obligate multicellularity has only evolved when clonal groups form by cell division, rather than by cells aggregating, as clonality prevents internal conflict. Yet obligately multicellular organisms still vary greatly in 'multicellular complexity' (the number of cells and cell types): some comprise a few cells and cell types, while others have billions of cells and thousands of types. Here, we test whether variation in multicellular complexity is explained by two conflict-suppressing mechanisms, namely a single-cell bottleneck at the start of development, and a strict separation of germline and somatic cells. Examining the life cycles of 129 lineages of plants, animals, fungi and algae, we show using phylogenetic comparative analyses that an early segregation of the germline stem-cell lineage is key to the evolution of more cell types, driven by a strong correlation in the Metazoa. By contrast, the presence of a strict single-cell bottleneck was not related to either the number of cells or the number of cell types, but was associated with early germline segregation. Our results suggest that segregating the germline earlier in development enabled greater evolutionary innovation, although whether this is a consequence of conflict reduction or other non-conflict effects, such as developmental flexibility, is unclear. ",
keywords = "development, evolution, germline",
author = "Jack Howe and Cornwallis, {Charlie K.} and Griffin, {Ashleigh S.}",
note = "Publisher Copyright: {\textcopyright} 2024 The Authors.",
year = "2024",
doi = "10.1098/rspb.2023.2466",
language = "English",
volume = "291",
journal = "Proceedings of the Royal Society B: Biological Sciences",
issn = "0962-8452",
publisher = "The Royal Society Publishing",
number = "2014",

}

RIS

TY - JOUR

T1 - Conflict-reducing innovations in development enable increased multicellular complexity

AU - Howe, Jack

AU - Cornwallis, Charlie K.

AU - Griffin, Ashleigh S.

N1 - Publisher Copyright: © 2024 The Authors.

PY - 2024

Y1 - 2024

N2 - Obligately multicellular organisms, where cells can only reproduce as part of the group, have evolved multiple times across the tree of life. Obligate multicellularity has only evolved when clonal groups form by cell division, rather than by cells aggregating, as clonality prevents internal conflict. Yet obligately multicellular organisms still vary greatly in 'multicellular complexity' (the number of cells and cell types): some comprise a few cells and cell types, while others have billions of cells and thousands of types. Here, we test whether variation in multicellular complexity is explained by two conflict-suppressing mechanisms, namely a single-cell bottleneck at the start of development, and a strict separation of germline and somatic cells. Examining the life cycles of 129 lineages of plants, animals, fungi and algae, we show using phylogenetic comparative analyses that an early segregation of the germline stem-cell lineage is key to the evolution of more cell types, driven by a strong correlation in the Metazoa. By contrast, the presence of a strict single-cell bottleneck was not related to either the number of cells or the number of cell types, but was associated with early germline segregation. Our results suggest that segregating the germline earlier in development enabled greater evolutionary innovation, although whether this is a consequence of conflict reduction or other non-conflict effects, such as developmental flexibility, is unclear.

AB - Obligately multicellular organisms, where cells can only reproduce as part of the group, have evolved multiple times across the tree of life. Obligate multicellularity has only evolved when clonal groups form by cell division, rather than by cells aggregating, as clonality prevents internal conflict. Yet obligately multicellular organisms still vary greatly in 'multicellular complexity' (the number of cells and cell types): some comprise a few cells and cell types, while others have billions of cells and thousands of types. Here, we test whether variation in multicellular complexity is explained by two conflict-suppressing mechanisms, namely a single-cell bottleneck at the start of development, and a strict separation of germline and somatic cells. Examining the life cycles of 129 lineages of plants, animals, fungi and algae, we show using phylogenetic comparative analyses that an early segregation of the germline stem-cell lineage is key to the evolution of more cell types, driven by a strong correlation in the Metazoa. By contrast, the presence of a strict single-cell bottleneck was not related to either the number of cells or the number of cell types, but was associated with early germline segregation. Our results suggest that segregating the germline earlier in development enabled greater evolutionary innovation, although whether this is a consequence of conflict reduction or other non-conflict effects, such as developmental flexibility, is unclear.

KW - development

KW - evolution

KW - germline

U2 - 10.1098/rspb.2023.2466

DO - 10.1098/rspb.2023.2466

M3 - Journal article

C2 - 38196363

AN - SCOPUS:85182088487

VL - 291

JO - Proceedings of the Royal Society B: Biological Sciences

JF - Proceedings of the Royal Society B: Biological Sciences

SN - 0962-8452

IS - 2014

M1 - 20232466

ER -

ID: 380733915