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Conflict-reducing innovations in development enable increased multicellular complexity

Howe, Jack ; Cornwallis, Charlie K. LU and Griffin, Ashleigh S. (2024) In Proceedings of the Royal Society B: Biological Sciences 291(2014).
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... (More)

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.

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author
; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
development, evolution, germline
in
Proceedings of the Royal Society B: Biological Sciences
volume
291
issue
2014
article number
20232466
publisher
Royal Society Publishing
external identifiers
  • pmid:38196363
  • scopus:85182088487
ISSN
0962-8452
DOI
10.1098/rspb.2023.2466
language
English
LU publication?
yes
id
7644eaa6-2919-4ba3-b7c6-8a4d5b744272
date added to LUP
2024-02-21 14:16:57
date last changed
2024-04-21 10:00:39
@article{7644eaa6-2919-4ba3-b7c6-8a4d5b744272,
  abstract     = {{<p>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.</p>}},
  author       = {{Howe, Jack and Cornwallis, Charlie K. and Griffin, Ashleigh S.}},
  issn         = {{0962-8452}},
  keywords     = {{development; evolution; germline}},
  language     = {{eng}},
  number       = {{2014}},
  publisher    = {{Royal Society Publishing}},
  series       = {{Proceedings of the Royal Society B: Biological Sciences}},
  title        = {{Conflict-reducing innovations in development enable increased multicellular complexity}},
  url          = {{http://dx.doi.org/10.1098/rspb.2023.2466}},
  doi          = {{10.1098/rspb.2023.2466}},
  volume       = {{291}},
  year         = {{2024}},
}