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KRAB 锌指蛋白 ZFP708 介导 RMER19B 逆转录转座子的表观遗传抑制。

The KRAB-zinc-finger protein ZFP708 mediates epigenetic repression at RMER19B retrotransposons.

机构信息

Developmental Epigenetics and Disease Group, IMCB, A*STAR, 138673, Singapore.

Methyltransferases in Development and Disease Group, IMCB, A*STAR, 138673, Singapore.

出版信息

Development. 2019 Jul 10;146(19):dev170266. doi: 10.1242/dev.170266.

Abstract

Global epigenetic reprogramming is vital to purge germ cell-specific epigenetic features to establish the totipotent state of the embryo. This process transpires to be carefully regulated and is not an undirected, radical erasure of parental epigenomes. The TRIM28 complex has been shown to be crucial in embryonic epigenetic reprogramming by regionally opposing DNA demethylation to preserve vital parental information to be inherited from germline to soma. Yet the DNA-binding factors guiding this complex to specific targets are largely unknown. Here, we uncover and characterize a novel, maternally expressed, TRIM28-interacting KRAB zinc-finger protein: ZFP708. It recruits the repressive TRIM28 complex to RMER19B retrotransposons to evoke regional heterochromatin formation. ZFP708 binding to these hitherto unknown TRIM28 targets is DNA methylation and H3K9me3 independent. ZFP708 mutant mice are viable and fertile, yet embryos fail to inherit and maintain DNA methylation at ZFP708 target sites. This can result in activation of RMER19B-adjacent genes, while ectopic expression of ZFP708 results in transcriptional repression. Finally, we describe the evolutionary conservation of ZFP708 in mice and rats, which is linked to the conserved presence of the targeted RMER19B retrotransposons in these species.

摘要

全球表观遗传重编程对于清除生殖细胞特异性的表观遗传特征以建立胚胎的全能状态至关重要。这个过程被精心调控,不是对亲本表观基因组的无定向、彻底清除。TRIM28 复合物已被证明在胚胎表观遗传重编程中至关重要,它通过区域拮抗 DNA 去甲基化来保留重要的亲本信息,以便从生殖细胞遗传到体细胞。然而,指导该复合物到特定靶标的 DNA 结合因子在很大程度上是未知的。在这里,我们发现并表征了一种新的、母系表达的、与 TRIM28 相互作用的 KRAB 锌指蛋白:ZFP708。它招募抑制性的 TRIM28 复合物到 RMER19B 反转录转座子上,引发区域异染色质形成。ZFP708 与这些迄今为止未知的 TRIM28 靶标的结合是独立于 DNA 甲基化和 H3K9me3 的。ZFP708 突变小鼠具有活力和生育能力,但胚胎无法继承和维持 ZFP708 靶位点的 DNA 甲基化。这可能导致 RMER19B 邻近基因的激活,而 ZFP708 的异位表达则导致转录抑制。最后,我们描述了 ZFP708 在小鼠和大鼠中的进化保守性,这与这些物种中靶向 RMER19B 反转录转座子的保守存在有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/6803371/cf701649b849/develop-146-170266-g1.jpg

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