Mouse Biology Unit, European Molecular Biology Laboratory, Via Ramarini 32, 00015 Monterotondo Scalo, Italy.
Mol Cell. 2013 May 23;50(4):601-8. doi: 10.1016/j.molcel.2013.04.026.
Transposons present an acute challenge to the germline, and mechanisms that repress their activity are essential for transgenerational genomic integrity. LINE1 (L1) is the most successful retrotransposon and is epigenetically repressed by CpG DNA methylation. Here, we identify two additional important mechanisms by which L1 is repressed during spermatogenesis. We demonstrate that the Piwi protein Mili and the piRNA pathway are required to posttranscriptionally silence L1 in meiotic pachytene cells even in the presence of normal L1 DNA methylation. Strikingly, in the absence of both a functional piRNA pathway and DNA methylation, L1 elements are normally repressed in mitotic stages of spermatogenesis. Accordingly, we find that the euchromatic repressive histone H3 dimethylated lysine 9 modification cosuppresses L1 expression therein. We demonstrate the existence of multiple epigenetic mechanisms that in conjunction with the piRNA pathway sequentially enforce L1 silencing and genomic stability during mitotic and meiotic stages of adult spermatogenesis.
转座子对生殖细胞系构成严重威胁,而抑制其活性的机制对于跨代基因组完整性至关重要。LINE1(L1)是最成功的反转录转座子,其活性受到 CpG DNA 甲基化的表观遗传抑制。在这里,我们确定了在精子发生过程中 L1 受到抑制的另外两种重要机制。我们证明,Piwi 蛋白 Mili 和 piRNA 途径在减数分裂前期的精母细胞中即使在正常 L1 DNA 甲基化的情况下也需要进行转录后沉默 L1。引人注目的是,在缺乏功能性 piRNA 途径和 DNA 甲基化的情况下,L1 元件在精母细胞的有丝分裂阶段正常受到抑制。因此,我们发现常染色质抑制性组蛋白 H3 二甲基化赖氨酸 9 修饰也共同抑制了那里的 L1 表达。我们证明了多种表观遗传机制的存在,这些机制与 piRNA 途径一起,在成年精子发生的有丝分裂和减数分裂阶段依次强制沉默 L1 并维持基因组稳定性。