Ravens Sarina, Yu Changwei, Ye Tao, Stierle Matthieu, Tora Laszlo
Cellular Signalling and Nuclear Dynamics Programme, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), CNRS UMR 7104, INSERM U964, Université de Strasbourg (UdS), BP 10142, 1 Rue Laurent Fries, CU de Strasbourg, 67404 Illkirch Cedex, France.
Microarrays and Deep Sequencing Platform, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), CNRS UMR 7104, INSERM U964, UdS, BP 10142, CU de Strasbourg, 67404 Illkirch Cedex, France.
Epigenetics Chromatin. 2015 Nov 6;8:45. doi: 10.1186/s13072-015-0039-z. eCollection 2015.
Tip60 (KAT5) is the histone acetyltransferase (HAT) of the mammalian Tip60/NuA4 complex. While Tip60 is important for early mouse development and mouse embryonic stem cell (mESC) pluripotency, the function of Tip60 as reflected in a genome-wide context is not yet well understood.
Gel filtration of nuclear mESCs extracts indicate incorporation of Tip60 into large molecular complexes and exclude the existence of large quantities of "free" Tip60 within the nuclei of ESCs. Thus, monitoring of Tip60 binding to the genome should reflect the behaviour of Tip60-containing complexes. The genome-wide mapping of Tip60 binding in mESCs by chromatin immunoprecipitation (ChIP) coupled with high-throughput sequencing (ChIP-seq) shows that the Tip60 complex is present at promoter regions of predominantly active genes that are bound by RNA polymerase II (Pol II) and contain the H3K4me3 histone mark. The coactivator HAT complexes, Tip60- and Mof (KAT8)-containing (NSL and MSL), show a global overlap at promoters, whereas distinct binding profiles at enhancers suggest different regulatory functions of each essential HAT complex. Interestingly, Tip60 enrichment peaks at about 200 bp downstream of the transcription start sites suggesting a function for the Tip60 complexes in addition to histone acetylation. The comparison of genome-wide binding profiles of Tip60 and c-Myc, a somatic cell reprogramming factor that binds predominantly to active genes in mESCs, demonstrate that Tip60 and c-Myc co-bind at 50-60 % of their binding sites. We also show that the Tip60 complex binds to a subset of bivalent developmental genes and defines a set of mESC-specific enhancer as well as super-enhancer regions.
Our study suggests that the Tip60 complex functions as a global transcriptional co-activator at most active Pol II promoters, co-regulates the ESC-specific c-Myc network, important for ESC self-renewal and cell metabolism and acts at a subset of active distal regulatory elements, or super enhancers, in mESCs.
Tip60(KAT5)是哺乳动物Tip60/NuA4复合物的组蛋白乙酰转移酶(HAT)。虽然Tip60对小鼠早期发育和小鼠胚胎干细胞(mESC)多能性很重要,但在全基因组范围内Tip60的功能尚未得到充分理解。
对核mESC提取物进行凝胶过滤表明Tip60掺入大分子复合物中,并排除了ESCs细胞核内存在大量“游离”Tip60的可能性。因此,监测Tip60与基因组的结合应能反映含Tip60复合物的行为。通过染色质免疫沉淀(ChIP)结合高通量测序(ChIP-seq)对mESCs中Tip60结合进行全基因组定位,结果表明Tip60复合物存在于主要由RNA聚合酶II(Pol II)结合且含有H3K4me3组蛋白标记的活跃基因的启动子区域。共激活因子HAT复合物,即含Tip60和Mof(KAT8)的复合物(NSL和MSL),在启动子处呈现全局重叠,而在增强子处不同的结合图谱表明每个必需HAT复合物具有不同的调控功能。有趣的是,Tip60富集峰出现在转录起始位点下游约200 bp处,这表明Tip60复合物除了具有组蛋白乙酰化功能外还具有其他功能。对Tip60和c-Myc(一种主要结合mESCs中活跃基因的体细胞重编程因子)全基因组结合图谱的比较表明,Tip60和c-Myc在其50 - 60%的结合位点共结合。我们还表明,Tip60复合物与一组二价发育基因结合,并定义了一组mESC特异性增强子以及超级增强子区域。
我们的研究表明,Tip60复合物在大多数活跃的Pol II启动子处作为全局转录共激活因子发挥作用,共同调节对ESC自我更新和细胞代谢很重要的ESC特异性c-Myc网络,并作用于mESCs中一部分活跃的远端调控元件或超级增强子。