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  Transgenerational inheritance of impaired larval T cell development in zebrafish

Iwanami, N., Lawir, D.-F., Sikora, K., Meara, C. O., Takeshita, K., Schorpp, M., et al. (2020). Transgenerational inheritance of impaired larval T cell development in zebrafish. Nature Communications, 11, 4505. doi:10.1038/s41467-020-18289-9.

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Norimasa et al. 2020.pdf (Verlagsversion), 2MB
 
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 Urheber:
Iwanami, Norimasa1, Autor           
Lawir, Divine-Fondzenyuy1, Autor
Sikora, Katarzyna1, Autor
Meara, Connor O1, Autor
Takeshita, Kohei2, Autor
Schorpp, Michael1, Autor           
Boehm, Thomas1, Autor           
Affiliations:
1Department of Developmental Immunology, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243647              
2External Organizations, ou_persistent22              

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 Zusammenfassung: Evidence for transgenerational inheritance of epigenetic information in vertebrates is scarce. Aberrant patterns of DNA methylation in gametes may set the stage for transmission into future generations. Here, we describe a viable hypomorphic allele of dnmt1 in zebrafish that causes widespread demethylation of CpG dinucleotides in sperm and somatic tissues. We find that homozygous mutants are essentially normal, with the exception of drastically impaired lymphopoiesis, affecting both larval and adult phases of T cell development. The phenotype of impaired larval (but not adult) T cell development is transmitted to subsequent generations by genotypically wildtype fish. We further find that about 200 differentially methylated regions in sperm DNA of transmitting and non-transmitting males, including hypermethylated sites associated with runx3 and rptor genes, whose reduced activities are associated with impaired larval T cell development. Our results indicate a particular sensitivity of larval T cell development to transgenerationally inherited epimutations.

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Sprache(n): eng - English
 Datum: 2020-09-09
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1038/s41467-020-18289-9
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Titel: Nature Communications
  Kurztitel : Nat. Commun.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: London : Nature Publishing Group
Seiten: - Band / Heft: 11 Artikelnummer: - Start- / Endseite: 4505 Identifikator: ISSN: 2041-1723
CoNE: https://pure.mpg.de/cone/journals/resource/2041-1723