The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Phylostratigraphic tracking of cancer genes suggests a link to the emergence of multicellularity in metazoa
Open accessAbstract
BACKGROUND: Phylostratigraphy is a method used to correlate the evolutionary origin of founder genes (that is, functional founder protein domains) of gene families with particular macroevolutionary transitions. It is based on a model of genome evolution that suggests that the origin of complex phenotypic innovations will be accompanied by the emergence of such founder genes, the descendants of which can still be traced in extant organisms. The origin of multicellularity can be considered to be a macroevolutionary transition, for which new gene functions would have been required. Cancer should be tightly connected to multicellular life since it can be viewed as a malfunction of interaction between cells in a multicellular organism. A phylostratigraphic tracking of the origin of cancer genes should, therefore, also provide insights into the origin of multicellularity. RESULTS: We find two strong peaks of the emergence of cancer related protein domains, one at the time of the origin of the first cell and the other around the time of the evolution of the multicellular metazoan organisms. These peaks correlate with two major classes of cancer genes, the 'caretakers', which are involved in general functions that support genome stability and the 'gatekeepers', which are involved in cellular signalling and growth processes. Interestingly, this phylogenetic succession mirrors the ontogenetic succession of tumour progression, where mutations in caretakers are thought to precede mutations in gatekeepers. CONCLUSIONS: A link between multicellularity and formation of cancer has often been predicted. However, this has not so far been explicitly tested. Although we find that a significant number of protein domains involved in cancer predate the origin of multicellularity, the second peak of cancer protein domain emergence is, indeed, connected to a phylogenetic level where multicellular animals have emerged. The fact that we can find a strong and consistent signal for this second peak in the phylostratigraphic map implies that a complex multi-level selection process has driven the transition to multicellularity.
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Citations
Cites
A census of human cancer genes
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Evolutionary Dynamics: Exploring the Equations of Life
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Broad phylogenomic sampling improves resolution of the animal tree of life
Dunn, C. W., Hejnol, A., Matus, D. Q., Pang, K., Browne, W. E., Smith, S. A., Seaver, E., Rouse, G. W., Obst, M., Edgecombe, G. D., et al. (2008) · Nature · doi:10.1038/nature06614 · Cited by 1,921 · cited 1×
“However, some recent studies found a limited support for an alternative hypothesis, namely that Porifera together with Cnidaria are the earliest branching clade, while Bilateria is a sister group to these diploblastic animals [29,30].”
ResultThe genome of the choanoflagellate Monosiga brevicollis and the origin of metazoans
King, N., Westbrook, M. J., Young, S. L., Kuo, A., Abedin, M., Chapman, J., Fairclough, S., Hellsten, U., Isogai, Y., Letunic, I., et al. (2008) · Nature · doi:10.1038/nature06617 · Cited by 1,139
The Evolution of Multicellularity: A Minor Major Transition?
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“Based on our previously described phylostratigraphic procedure [1,2], we generated a database of genome sequences divided into 19 phylostrata corresponding to the evolutionary relationships of the major taxa supported by phylogenomic analyses (Figure 1) [15-19].”
BackgroundMethod
Cited by
The evolutionary origin of orphan genes
Tautz, D., & Domazet-Lošo, T. (2011) · Nature Reviews Genetics · doi:10.1038/nrg3053 · Cited by 764
Self-citationCancer across the tree of life: cooperation and cheating in multicellularity
Aktipis, C. A., Boddy, A. M., Jansen, G., Hibner, U., Hochberg, M. E., Maley, C. C., & Wilkinson, G. S. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2014.0219 · Cited by 466
The influence of evolutionary history on human health and disease
Benton, M. L., Abraham, A., LaBella, A. L., Abbot, P., Rokas, A., & Capra, J. A. (2021) · Nature Reviews Genetics · doi:10.1038/s41576-020-00305-9 · Cited by 291
Accelerated Recruitment of New Brain Development Genes into the Human Genome
Zhang, Y. E., Landback, P., Vibranovski, M. D., & Long, M. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1001179 · Cited by 164
Zhao, T., & Schranz, M. E. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1801757116 · Cited by 120
Metadata
- Authors
- Domazet-Lošo, T., & Tautz, D.
- Venue
- BMC Biology
- Published
- 2010-05-21
- Volume
- 8
- Issue
- 1
- Pages
- 66-66
- ISSN
- 1741-7007 (ISSN-L)
- OpenAlex
- W2003567202
- Cited by
- 311
- References
- 7
- FWCI
- 3.34
- Type
- journal article
- Language
- en
- Open access
- gold
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