Development and Differentiation Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Department of Functional Genomics, University of Science and Technology (UST), Yuseong-gu, Daejeon, 34141, South Korea.
Bioessays. 2018 Sep;40(9):e1800058. doi: 10.1002/bies.201800058. Epub 2018 Jun 13.
In human cancers, histone methyltransferase SETDB1 (SET domain, bifurcated 1) is frequently overexpressed but its significance in carcinogenesis remains elusive. A recent study shows that SETDB1 downregulation induces de-repression of retroelements and innate immunity in cancer cells. The possibility of SETDB1 functioning as a surveillant of retroelement expression is discussed in this study: the cytoplasmic presence of retroelement-derived nucleic acids (RdNAs) drives SETDB1 into the nucleus by the RNA-interference route, rendering the corresponding retroelement transcriptionally inert. These RdNAs could, therefore, be signals of genome instability sent out for SETDB1 present in the cytoplasm to maintain genome integrity.
在人类癌症中,组蛋白甲基转移酶 SETDB1(SET 域,分叉 1)经常过表达,但它在肿瘤发生中的意义仍不清楚。最近的一项研究表明,SETDB1 的下调会诱导癌细胞中逆转录元件和先天免疫的去抑制。在这项研究中讨论了 SETDB1 作为逆转录元件表达的监测者的可能性:逆转录元件衍生的核酸(RdNAs)的细胞质存在通过 RNA 干扰途径将 SETDB1 带入细胞核,使相应的逆转录元件转录失活。因此,这些 RdNAs 可能是基因组不稳定性发出的信号,以便细胞质中存在的 SETDB1 来维持基因组完整性。