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YOSHIDA Keita
Department School of Medicine, School of Medicine Position Assistant Professor |
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| Article types | Original article |
| Language | English |
| Peer review | Peer reviewed |
| Title | Germ cell regeneration-mediated, enhanced mutagenesis in the ascidian Ciona intestinalis reveals flexible germ cell formation from different somatic cells. |
| Journal | Formal name：Developmental biology Abbreviation：Dev Biol ISSN code：1095-564X(Electronic)0012-1606(Linking) |
| Domestic / Foregin | Foregin |
| Volume, Issue, Page | 423(2),pp.111-125 |
| Author and coauthor | Yoshida Keita†, Hozumi Akiko, Treen Nicholas, Sakuma Tetsushi, Yamamoto Takashi, Shirae-Kurabayashi Maki, Sasakura Yasunori* |
| Authorship | Lead author |
| Publication date | 2017/03 |
| Summary | The ascidian Ciona intestinalis has a high regeneration capacity that enables the regeneration of artificially removed primordial germ cells (PGCs) from somatic cells. We utilized PGC regeneration to establish efficient methods of germ line mutagenesis with transcription activator-like effector nucleases (TALENs). When PGCs were artificially removed from animals in which a TALEN pair was expressed, somatic cells harboring mutations in the target gene were converted into germ cells, this germ cell population exhibited higher mutation rates than animals not subjected to PGC removal. PGC regeneration enables us to use TALEN expression vectors of specific somatic tissues for germ cell mutagenesis. Unexpectedly, cis elements for epidermis, neural tissue and muscle could be used for germ cell mutagenesis, indicating there are multiple sources of regenerated PGCs, suggesting a flexibility of differentiated Ciona somatic cells to regain totipotency. Sperm and eggs of a single hermaphroditic, PGC regenerated animal typically have different mutations, suggesting they arise from different cells. PGCs can be generated from somatic cells even though the maternal PGCs are not removed, suggesting that the PGC regeneration is not solely an artificial event but could have an endogenous function in Ciona. This study provides a technical innovation in the genome-editing methods, including easy establishment of mutant lines. Moreover, this study suggests cellular mechanisms and the potential evolutionary significance of PGC regeneration in Ciona. |
| DOI | 10.1016/j.ydbio.2017.01.022 |
| Document No. | 28161521 |