Division of Hematology/Oncology, Children's Hospital Boston and Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Stem Cell Institute, Harvard Medical School, Boston, MA 02115, USA.
Dev Cell. 2012 Oct 16;23(4):796-811. doi: 10.1016/j.devcel.2012.09.003. Epub 2012 Oct 4.
Gene-distal enhancers are critical for tissue-specific gene expression, but their genomic determinants within a specific lineage at different stages of development are unknown. Here we profile chromatin state maps, transcription factor occupancy, and gene expression profiles during human erythroid development at fetal and adult stages. Comparative analyses of human erythropoiesis identify developmental stage-specific enhancers as primary determinants of stage-specific gene expression programs. We find that erythroid master regulators GATA1 and TAL1 act cooperatively within active enhancers but confer little predictive value for stage specificity. Instead, a set of stage-specific coregulators collaborates with master regulators and contributes to differential gene expression. We further identify and validate IRF2, IRF6, and MYB as effectors of an adult-stage expression program. Thus, the combinatorial assembly of lineage-specific master regulators and transcriptional coregulators within developmental stage-specific enhancers determines gene expression programs and temporal regulation of transcriptional networks in a mammalian genome.
基因远端增强子对于组织特异性基因表达至关重要,但在不同发育阶段的特定谱系中,其基因组决定因素尚不清楚。在这里,我们在胎儿和成人阶段对人类红细胞生成过程中的染色质状态图谱、转录因子占据和基因表达谱进行了分析。对人类红细胞生成的比较分析确定了发育阶段特异性增强子是阶段特异性基因表达程序的主要决定因素。我们发现,红细胞主要调控因子 GATA1 和 TAL1 在活性增强子中协同作用,但对阶段特异性的预测价值不大。相反,一组阶段特异性共调控因子与主要调控因子合作,有助于差异基因表达。我们进一步鉴定并验证了 IRF2、IRF6 和 MYB 作为成人阶段表达程序的效应因子。因此,在哺乳动物基因组中,谱系特异性主要调控因子和转录共调控因子在发育阶段特异性增强子中的组合组装决定了基因表达程序和转录网络的时间调节。