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Reconstructing the last common ancestor of all eukaryotes.

Authors :
Richards TA
Eme L
Archibald JM
Leonard G
Coelho SM
de Mendoza A
Dessimoz C
Dolezal P
Fritz-Laylin LK
Gabaldón T
Hampl V
Kops GJPL
Leger MM
Lopez-Garcia P
McInerney JO
Moreira D
Muñoz-Gómez SA
Richter DJ
Ruiz-Trillo I
Santoro AE
Sebé-Pedrós A
Snel B
Stairs CW
Tromer EC
van Hooff JJE
Wickstead B
Williams TA
Roger AJ
Dacks JB
Wideman JG
Source :
PLoS biology [PLoS Biol] 2024 Nov 25; Vol. 22 (11), pp. e3002917. Date of Electronic Publication: 2024 Nov 25.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Understanding the origin of eukaryotic cells is one of the most difficult problems in all of biology. A key challenge relevant to the question of eukaryogenesis is reconstructing the gene repertoire of the last eukaryotic common ancestor (LECA). As data sets grow, sketching an accurate genomics-informed picture of early eukaryotic cellular complexity requires provision of analytical resources and a commitment to data sharing. Here, we summarise progress towards understanding the biology of LECA and outline a community approach to inferring its wider gene repertoire. Once assembled, a robust LECA gene set will be a useful tool for evaluating alternative hypotheses about the origin of eukaryotes and understanding the evolution of traits in all descendant lineages, with relevance in diverse fields such as cell biology, microbial ecology, biotechnology, agriculture, and medicine. In this Consensus View, we put forth the status quo and an agreed path forward to reconstruct LECA's gene content.<br />Competing Interests: The authors have declared that no competing interests exist.<br /> (Copyright: © 2024 Richards et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)

Details

Language :
English
ISSN :
1545-7885
Volume :
22
Issue :
11
Database :
MEDLINE
Journal :
PLoS biology
Publication Type :
Academic Journal
Accession number :
39585925
Full Text :
https://doi.org/10.1371/journal.pbio.3002917