Aird Katherine M, Iwasaki Osamu, Kossenkov Andrew V, Tanizawa Hideki, Fatkhutdinov Nail, Bitler Benjamin G, Le Linh, Alicea Gretchen, Yang Ting-Lin, Johnson F Brad, Noma Ken-Ichi, Zhang Rugang
Gene Expression and Regulation Program, The Wistar Institute, Philadelphia, PA 19104.
Center for Systems and Computational Biology, The Wistar Institute, Philadelphia, PA 19104.
J Cell Biol. 2016 Nov 7;215(3):325-334. doi: 10.1083/jcb.201608026. Epub 2016 Oct 31.
Cellular senescence is a stable cell growth arrest that is characterized by the silencing of proliferation-promoting genes through compaction of chromosomes into senescence-associated heterochromatin foci (SAHF). Paradoxically, senescence is also accompanied by increased transcription of certain genes encoding for secreted factors such as cytokines and chemokines, known as the senescence-associated secretory phenotype (SASP). How SASP genes are excluded from SAHF-mediated global gene silencing remains unclear. In this study, we report that high mobility group box 2 (HMGB2) orchestrates the chromatin landscape of SASP gene loci. HMGB2 preferentially localizes to SASP gene loci during senescence. Loss of HMGB2 during senescence blunts SASP gene expression by allowing for spreading of repressive heterochromatin into SASP gene loci. This correlates with incorporation of SASP gene loci into SAHF. Our results establish HMGB2 as a novel master regulator that orchestrates SASP through prevention of heterochromatin spreading to allow for exclusion of SASP gene loci from a global heterochromatin environment during senescence.
细胞衰老表现为一种稳定的细胞生长停滞,其特征是通过将染色体压缩成衰老相关异染色质灶(SAHF)来使促进增殖的基因沉默。矛盾的是,衰老还伴随着某些编码分泌因子(如细胞因子和趋化因子)的基因转录增加,即衰老相关分泌表型(SASP)。SASP基因如何从SAHF介导的全局基因沉默中被排除仍不清楚。在本研究中,我们报告高迁移率族蛋白盒2(HMGB2)协调SASP基因位点的染色质格局。衰老过程中,HMGB2优先定位于SASP基因位点。衰老过程中HMGB2的缺失通过允许抑制性异染色质扩散到SASP基因位点而削弱SASP基因表达。这与SASP基因位点并入SAHF相关。我们的结果表明,HMGB2是一种新型的主要调节因子,通过防止异染色质扩散来协调SASP,从而在衰老过程中将SASP基因位点从全局异染色质环境中排除。