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Somatic Mutation Analysis in Salix suchowensis Reveals Early-Segregated Cell Lineages

Long-lived plants face the challenge of ever-increasing mutational burden across their long lifespan. Early sequestration of meristematic stem cells is supposed to efficiently slow down this process, but direct measurement of somatic mutations that accompanies segregated cell lineages in plants is s...

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Autores principales: Ren, Yifan, He, Zhen, Liu, Pingyu, Traw, Brian, Sun, Shucun, Tian, Dacheng, Yang, Sihai, Jia, Yanxiao, Wang, Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662653/
https://www.ncbi.nlm.nih.gov/pubmed/34562099
http://dx.doi.org/10.1093/molbev/msab286
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author Ren, Yifan
He, Zhen
Liu, Pingyu
Traw, Brian
Sun, Shucun
Tian, Dacheng
Yang, Sihai
Jia, Yanxiao
Wang, Long
author_facet Ren, Yifan
He, Zhen
Liu, Pingyu
Traw, Brian
Sun, Shucun
Tian, Dacheng
Yang, Sihai
Jia, Yanxiao
Wang, Long
author_sort Ren, Yifan
collection PubMed
description Long-lived plants face the challenge of ever-increasing mutational burden across their long lifespan. Early sequestration of meristematic stem cells is supposed to efficiently slow down this process, but direct measurement of somatic mutations that accompanies segregated cell lineages in plants is still rare. Here, we tracked somatic mutations in 33 leaves and 22 adventitious roots from 22 stem-cuttings across eight major branches of a shrub willow (Salix suchowensis). We found that most mutations propagated separately in leaves and roots, providing clear evidence for early segregation of underlying cell lineages. By combining lineage tracking with allele frequency analysis, our results revealed a set of mutations shared by distinct branches, but were exclusively present in leaves and not in roots. These mutations were likely propagated by rapidly dividing somatic cell lineages which survive several iterations of branching, distinct from the slowly dividing axillary stem cell lineages. Leaf is thus contributed by both slowly and rapidly dividing cell lineages, leading to varied fixation chances of propagated mutations. By contrast, each root likely arises from a single founder cell within the adventitious stem cell lineages. Our findings give straightforward evidence that early segregation of meristems slows down mutation accumulation in axillary meristems, implying a plant “germline” paralog to the germline of animals through convergent evolution.
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spelling pubmed-86626532021-12-10 Somatic Mutation Analysis in Salix suchowensis Reveals Early-Segregated Cell Lineages Ren, Yifan He, Zhen Liu, Pingyu Traw, Brian Sun, Shucun Tian, Dacheng Yang, Sihai Jia, Yanxiao Wang, Long Mol Biol Evol Discoveries Long-lived plants face the challenge of ever-increasing mutational burden across their long lifespan. Early sequestration of meristematic stem cells is supposed to efficiently slow down this process, but direct measurement of somatic mutations that accompanies segregated cell lineages in plants is still rare. Here, we tracked somatic mutations in 33 leaves and 22 adventitious roots from 22 stem-cuttings across eight major branches of a shrub willow (Salix suchowensis). We found that most mutations propagated separately in leaves and roots, providing clear evidence for early segregation of underlying cell lineages. By combining lineage tracking with allele frequency analysis, our results revealed a set of mutations shared by distinct branches, but were exclusively present in leaves and not in roots. These mutations were likely propagated by rapidly dividing somatic cell lineages which survive several iterations of branching, distinct from the slowly dividing axillary stem cell lineages. Leaf is thus contributed by both slowly and rapidly dividing cell lineages, leading to varied fixation chances of propagated mutations. By contrast, each root likely arises from a single founder cell within the adventitious stem cell lineages. Our findings give straightforward evidence that early segregation of meristems slows down mutation accumulation in axillary meristems, implying a plant “germline” paralog to the germline of animals through convergent evolution. Oxford University Press 2021-09-25 /pmc/articles/PMC8662653/ /pubmed/34562099 http://dx.doi.org/10.1093/molbev/msab286 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Ren, Yifan
He, Zhen
Liu, Pingyu
Traw, Brian
Sun, Shucun
Tian, Dacheng
Yang, Sihai
Jia, Yanxiao
Wang, Long
Somatic Mutation Analysis in Salix suchowensis Reveals Early-Segregated Cell Lineages
title Somatic Mutation Analysis in Salix suchowensis Reveals Early-Segregated Cell Lineages
title_full Somatic Mutation Analysis in Salix suchowensis Reveals Early-Segregated Cell Lineages
title_fullStr Somatic Mutation Analysis in Salix suchowensis Reveals Early-Segregated Cell Lineages
title_full_unstemmed Somatic Mutation Analysis in Salix suchowensis Reveals Early-Segregated Cell Lineages
title_short Somatic Mutation Analysis in Salix suchowensis Reveals Early-Segregated Cell Lineages
title_sort somatic mutation analysis in salix suchowensis reveals early-segregated cell lineages
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662653/
https://www.ncbi.nlm.nih.gov/pubmed/34562099
http://dx.doi.org/10.1093/molbev/msab286
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