Laboratory of Chromatin Biology and Epigenetics, Department of Biology, Indian Institute of Science Education and Research, Pune, India.
Centre of Excellence in Epigenetics, Department of Life Sciences, Shiv Nadar University, Delhi-NCR, India.
Life Sci Alliance. 2023 Mar 21;6(5). doi: 10.26508/lsa.202201619. Print 2023 May.
The evolution of the first body axis in the animal kingdom and its extensive ability to regenerate makes , a Cnidarian, an excellent model system for understanding the underlying epigenetic mechanisms. We identify that monomethyltransferase SETD8 is critical for regeneration in because of its conserved interaction with β-catenin to fine-tune the associated gene regulatory network. Inhibition of SETD8 activity abolishes head and foot regeneration in Furthermore, we show that H4K20me1, the histone mark imparted by SETD8, colocalizes with the transcriptional activation machinery locally at the β-catenin-bound TCF/LEF-binding sites on the promoters of head-associated genes, marking an epigenetic activation mode. In contrast, genome-wide analysis of the H4K20me1 occupancy revealed a negative correlation with transcriptional activation. We propose that H4K20me1 acts as a general repressive histone mark in Cnidaria and describe its dichotomous role in transcriptional regulation in .
动物王国中第一体轴的进化及其广泛的再生能力,使刺胞动物成为理解潜在表观遗传机制的极佳模型系统。我们发现,由于 SETD8 与 β-catenin 的保守相互作用,可精细调节相关基因调控网络,因此单甲基转移酶 SETD8 对再生至关重要。SETD8 活性的抑制会破坏海葵的头部和足部再生。此外,我们还表明,由 SETD8 赋予的 H4K20me1 组蛋白标记与转录激活机制在 β-catenin 结合的 TCF/LEF 结合位点上局部共定位在头部相关基因的启动子上,标志着一种表观遗传激活模式。相比之下,H4K20me1 占据的全基因组分析显示与转录激活呈负相关。我们提出 H4K20me1 作为刺胞动物中的一种普遍的抑制组蛋白标记,并描述其在海葵转录调控中的二分角色。