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Early embryonic mutations reveal dynamics of somatic and germ cell lineages in mice

De novo mutations accumulate with zygotic cell divisions. However, the occurrence of these mutations and the way they are inherited by somatic cells and germ cells remain unclear. Here, we present a novel method to reconstruct cell lineages. We identified mosaic mutations in mice using deep whole-ge...

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Autores principales: Uchimura, Arikuni, Matsumoto, Hirotaka, Satoh, Yasunari, Minakuchi, Yohei, Wakayama, Sayaka, Wakayama, Teruhiko, Higuchi, Mayumi, Hashimoto, Masakazu, Fukumura, Ryutaro, Toyoda, Atsushi, Gondo, Yoichi, Yagi, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104692/
https://www.ncbi.nlm.nih.gov/pubmed/35534232
http://dx.doi.org/10.1101/gr.276363.121
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author Uchimura, Arikuni
Matsumoto, Hirotaka
Satoh, Yasunari
Minakuchi, Yohei
Wakayama, Sayaka
Wakayama, Teruhiko
Higuchi, Mayumi
Hashimoto, Masakazu
Fukumura, Ryutaro
Toyoda, Atsushi
Gondo, Yoichi
Yagi, Takeshi
author_facet Uchimura, Arikuni
Matsumoto, Hirotaka
Satoh, Yasunari
Minakuchi, Yohei
Wakayama, Sayaka
Wakayama, Teruhiko
Higuchi, Mayumi
Hashimoto, Masakazu
Fukumura, Ryutaro
Toyoda, Atsushi
Gondo, Yoichi
Yagi, Takeshi
author_sort Uchimura, Arikuni
collection PubMed
description De novo mutations accumulate with zygotic cell divisions. However, the occurrence of these mutations and the way they are inherited by somatic cells and germ cells remain unclear. Here, we present a novel method to reconstruct cell lineages. We identified mosaic mutations in mice using deep whole-genome sequencing and reconstructed embryonic cell lineages based on the variant allele frequencies of the mutations. The reconstructed trees were confirmed using nuclear transfer experiments and the genotyping of approximately 50 offspring of each tree. The most detailed tree had 32 terminal nodes and showed cell divisions from the fertilized egg to germ cell– and somatic cell–specific lineages, indicating at least five independent cell lineages that would be selected as founders of the primordial germ cells. The contributions of each lineage to germ cells and offspring varied widely. At the emergence of the germ cell–specific lineages, 10–15 embryonic mutations had accumulated, suggesting that the pregastrulation mutation rate is 1.0 mutation per mitosis. Subsequent mutation rates were 0.7 for germ cells and 13.2 for tail fibroblasts. Our results show a new framework to assess embryonic lineages; further, we suggest an evolutionary strategy for preserving heterogeneity owing to postzygotic mutations in offspring.
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spelling pubmed-91046922022-05-27 Early embryonic mutations reveal dynamics of somatic and germ cell lineages in mice Uchimura, Arikuni Matsumoto, Hirotaka Satoh, Yasunari Minakuchi, Yohei Wakayama, Sayaka Wakayama, Teruhiko Higuchi, Mayumi Hashimoto, Masakazu Fukumura, Ryutaro Toyoda, Atsushi Gondo, Yoichi Yagi, Takeshi Genome Res Method De novo mutations accumulate with zygotic cell divisions. However, the occurrence of these mutations and the way they are inherited by somatic cells and germ cells remain unclear. Here, we present a novel method to reconstruct cell lineages. We identified mosaic mutations in mice using deep whole-genome sequencing and reconstructed embryonic cell lineages based on the variant allele frequencies of the mutations. The reconstructed trees were confirmed using nuclear transfer experiments and the genotyping of approximately 50 offspring of each tree. The most detailed tree had 32 terminal nodes and showed cell divisions from the fertilized egg to germ cell– and somatic cell–specific lineages, indicating at least five independent cell lineages that would be selected as founders of the primordial germ cells. The contributions of each lineage to germ cells and offspring varied widely. At the emergence of the germ cell–specific lineages, 10–15 embryonic mutations had accumulated, suggesting that the pregastrulation mutation rate is 1.0 mutation per mitosis. Subsequent mutation rates were 0.7 for germ cells and 13.2 for tail fibroblasts. Our results show a new framework to assess embryonic lineages; further, we suggest an evolutionary strategy for preserving heterogeneity owing to postzygotic mutations in offspring. Cold Spring Harbor Laboratory Press 2022-05 /pmc/articles/PMC9104692/ /pubmed/35534232 http://dx.doi.org/10.1101/gr.276363.121 Text en © 2022 Uchimura et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Method
Uchimura, Arikuni
Matsumoto, Hirotaka
Satoh, Yasunari
Minakuchi, Yohei
Wakayama, Sayaka
Wakayama, Teruhiko
Higuchi, Mayumi
Hashimoto, Masakazu
Fukumura, Ryutaro
Toyoda, Atsushi
Gondo, Yoichi
Yagi, Takeshi
Early embryonic mutations reveal dynamics of somatic and germ cell lineages in mice
title Early embryonic mutations reveal dynamics of somatic and germ cell lineages in mice
title_full Early embryonic mutations reveal dynamics of somatic and germ cell lineages in mice
title_fullStr Early embryonic mutations reveal dynamics of somatic and germ cell lineages in mice
title_full_unstemmed Early embryonic mutations reveal dynamics of somatic and germ cell lineages in mice
title_short Early embryonic mutations reveal dynamics of somatic and germ cell lineages in mice
title_sort early embryonic mutations reveal dynamics of somatic and germ cell lineages in mice
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104692/
https://www.ncbi.nlm.nih.gov/pubmed/35534232
http://dx.doi.org/10.1101/gr.276363.121
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