Common origin of sterol biosynthesis points to a feeding strategy shift in Neoproterozoic animals
T. Brunoir,
C. Mulligan,
A. Sistiaga,
K. M. Vuu,
P. M. Shih,
S. S. O’Reilly,
R. E. Summons and
D. A. Gold ()
Additional contact information
T. Brunoir: University of California, Davis
C. Mulligan: University of California, Davis
A. Sistiaga: University of Copenhagen
K. M. Vuu: Joint BioEnergy Institute, Lawrence Berkeley National Laboratory
P. M. Shih: Joint BioEnergy Institute, Lawrence Berkeley National Laboratory
S. S. O’Reilly: Atlantic Technological University, ATU Sligo, Ash Lane
R. E. Summons: Atmospheric, and Planetary Sciences. Massachusetts Institute of Technology
D. A. Gold: University of California, Davis
Nature Communications, 2023, vol. 14, issue 1, 1-8
Abstract:
Abstract Steranes preserved in sedimentary rocks serve as molecular fossils, which are thought to record the expansion of eukaryote life through the Neoproterozoic Era ( ~ 1000-541 Ma). Scientists hypothesize that ancient C27 steranes originated from cholesterol, the major sterol produced by living red algae and animals. Similarly, C28 and C29 steranes are thought to be derived from the sterols of prehistoric fungi, green algae, and other microbial eukaryotes. However, recent work on annelid worms–an advanced group of eumetazoan animals–shows that they are also capable of producing C28 and C29 sterols. In this paper, we explore the evolutionary history of the 24-C sterol methyltransferase (smt) gene in animals, which is required to make C28+ sterols. We find evidence that the smt gene was vertically inherited through animals, suggesting early eumetazoans were capable of C28+ sterol synthesis. Our molecular clock of the animal smt gene demonstrates that its diversification coincides with the rise of C28 and C29 steranes in the Neoproterozoic. This study supports the hypothesis that early eumetazoans were capable of making C28+ sterols and that many animal lineages independently abandoned its biosynthesis around the end-Neoproterozoic, coinciding with the rise of abundant eukaryotic prey.
Date: 2023
References: View references in EconPapers View complete reference list from CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/s41467-023-43545-z Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43545-z
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-023-43545-z
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().