Institute of Biochemistry, Medical Faculty, Justus-Liebig-University, Member of the German Center for Lung Research, D-35392, Giessen, Germany.
Department of Pathology, Universities of Giessen and Marburg Lung Center, Excellence Cluster Cardio-Pulmonary System, D-35392, Giessen, Germany.
Sci Rep. 2017 Jun 14;7(1):3547. doi: 10.1038/s41598-017-03708-7.
The multi-subunit CCR4 (carbon catabolite repressor 4)-NOT (Negative on TATA) complex serves as a central coordinator of all different steps of eukaryotic gene expression. Here we performed a systematic and comparative analysis of cells where the CCR4-NOT subunits CNOT1, CNOT2 or CNOT3 were individually downregulated using doxycycline-inducible shRNAs. Microarray experiments showed that downregulation of either CNOT subunit resulted in elevated expression of major histocompatibility complex class II (MHC II) genes which are found in a gene cluster on chromosome 6. Increased expression of MHC II genes after knock-down or knock-out of either CNOT subunit was seen in a variety of cell systems and also in naïve macrophages from CNOT3 conditional knock-out mice. CNOT2-mediated repression of MHC II genes occurred also in the absence of the master regulator class II transactivator (CIITA) and did not cause detectable changes of the chromatin structure at the chromosomal MHC II locus. CNOT2 downregulation resulted in an increased de novo transcription of mRNAs whereas tethering of CNOT2 to a regulatory region governing MHC II expression resulted in diminished transcription. These results expand the known repertoire of CCR4-NOT members for immune regulation and identify CNOT proteins as a novel group of corepressors restricting class II expression.
多亚基 CCR4(碳源代谢物阻遏物 4)-NOT(TATA 阴性)复合物作为真核基因表达所有不同步骤的中央协调因子。在这里,我们使用强力霉素诱导型 shRNA 对单个下调 CCR4-NOT 亚基 CNOT1、CNOT2 或 CNOT3 的细胞进行了系统和比较分析。微阵列实验表明,下调任一 CNOT 亚基都会导致主要组织相容性复合体 II(MHC II)基因的表达升高,这些基因位于染色体 6 上的一个基因簇中。在各种细胞系统中,以及在 CNOT3 条件性敲除小鼠的幼稚巨噬细胞中,敲低或敲除任一 CNOT 亚基后 MHC II 基因的表达增加。即使在缺乏主调控因子 II 类转录激活物(CIITA)的情况下,CNOT2 也介导 MHC II 基因的抑制,并且不会导致染色体 MHC II 基因座上染色质结构的可检测变化。CNOT2 下调导致新转录的 mRNA 增加,而 CNOT2 与调控 MHC II 表达的调节区的连接导致转录减少。这些结果扩展了 CCR4-NOT 成员在免疫调节中的已知功能,并将 CNOT 蛋白确定为限制 II 类表达的新的核心抑制因子组。