Department of Developmental Immunology, Max Planck Institute of Immunobiology and Epigenetics, Stuebeweg 51, 79108, Freiburg, Germany.
Center for Bioscience Research and Education, Utsunomiya University, 350 Mine-machi, Utsunomiya, Tochigi, 321-8505, Japan.
Nat Commun. 2020 Sep 9;11(1):4505. doi: 10.1038/s41467-020-18289-9.
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.
脊椎动物跨代遗传表观遗传信息的证据很少。配子中异常的 DNA 甲基化模式可能为向后代传递奠定了基础。在这里,我们描述了斑马鱼中 dnmt1 的一种可行的低功能等位基因,它导致精子和体细胞组织中 CpG 二核苷酸的广泛去甲基化。我们发现纯合突变体基本上是正常的,除了淋巴生成严重受损,影响 T 细胞发育的幼虫和成年阶段。由基因型野生型鱼类传递的幼虫(而非成年)T 细胞发育受损表型。我们进一步发现,在传递和不传递的雄性精子 DNA 中有大约 200 个差异甲基化区域,包括与 runt3 和 rptor 基因相关的高甲基化位点,其活性降低与幼虫 T 细胞发育受损有关。我们的结果表明,幼虫 T 细胞发育对跨代遗传的表观突变特别敏感。