Spatial constraints govern competition of mutant clones in human epidermis
Spatial constraints govern competition of mutant clones in human epidermis
Deep sequencing can detect somatic DNA mutations in tissues permitting inference of clonal relationships. This has been applied to human epidermis, where sun exposure leads to the accumulation of mutations and an increased risk of skin cancer. However, previous studies have yielded conflicting conclusions about the relative importance of positive selection and neutral drift in clonal evolution. Here, we sequenced larger areas of skin than previously, focusing on cancer-prone skin spanning five decades of life. The mutant clones identified were too large to be accounted for solely by neutral drift. Rather, using mathematical modelling and computational lattice-based simulations, we show that observed clone size distributions can be explained by a combination of neutral drift and stochastic nucleation of mutations at the boundary of expanding mutant clones that have a competitive advantage. These findings demonstrate that spatial context and cell competition cooperate to determine the fate of a mutant stem cell.
Lynch, M. D.
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Lynch, C. N. S.
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Craythorne, E.
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Liakath-Ali, K.
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Mallipeddi, R.
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Barker, J. N.
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Watt, F. M.
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October 2017
Lynch, M. D.
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Lynch, C. N. S.
f5307f22-cbef-4767-8dbb-6a48c8d48ec0
Craythorne, E.
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Liakath-Ali, K.
8d5a020c-e976-4901-9195-68f4bc0de74e
Mallipeddi, R.
fb8126c0-26e2-4ebe-90c0-80cfccc3b19c
Barker, J. N.
51e95e30-f54c-4a61-8196-70dd7f67cc72
Watt, F. M.
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Lynch, M. D., Lynch, C. N. S., Craythorne, E., Liakath-Ali, K., Mallipeddi, R., Barker, J. N. and Watt, F. M.
(2017)
Spatial constraints govern competition of mutant clones in human epidermis.
Nature Communications, 8, [1119].
(doi:10.1038/s41467-017-00993-8).
Abstract
Deep sequencing can detect somatic DNA mutations in tissues permitting inference of clonal relationships. This has been applied to human epidermis, where sun exposure leads to the accumulation of mutations and an increased risk of skin cancer. However, previous studies have yielded conflicting conclusions about the relative importance of positive selection and neutral drift in clonal evolution. Here, we sequenced larger areas of skin than previously, focusing on cancer-prone skin spanning five decades of life. The mutant clones identified were too large to be accounted for solely by neutral drift. Rather, using mathematical modelling and computational lattice-based simulations, we show that observed clone size distributions can be explained by a combination of neutral drift and stochastic nucleation of mutations at the boundary of expanding mutant clones that have a competitive advantage. These findings demonstrate that spatial context and cell competition cooperate to determine the fate of a mutant stem cell.
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Published date: October 2017
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Local EPrints ID: 494677
URI: http://eprints.soton.ac.uk/id/eprint/494677
ISSN: 2041-1723
PURE UUID: a5395453-f2a1-435c-8fd8-6f6ce6c8ddee
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Date deposited: 11 Oct 2024 17:12
Last modified: 12 Oct 2024 03:01
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Author:
M. D. Lynch
Author:
C. N. S. Lynch
Author:
E. Craythorne
Author:
K. Liakath-Ali
Author:
R. Mallipeddi
Author:
J. N. Barker
Author:
F. M. Watt
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