Broad Institute, Cambridge, MA 02142, USA.
Cell. 2011 Jan 21;144(2):296-309. doi: 10.1016/j.cell.2011.01.004.
Though many individual transcription factors are known to regulate hematopoietic differentiation, major aspects of the global architecture of hematopoiesis remain unknown. Here, we profiled gene expression in 38 distinct purified populations of human hematopoietic cells and used probabilistic models of gene expression and analysis of cis-elements in gene promoters to decipher the general organization of their regulatory circuitry. We identified modules of highly coexpressed genes, some of which are restricted to a single lineage but most of which are expressed at variable levels across multiple lineages. We found densely interconnected cis-regulatory circuits and a large number of transcription factors that are differentially expressed across hematopoietic states. These findings suggest a more complex regulatory system for hematopoiesis than previously assumed.
尽管已知许多单个转录因子可调节造血分化,但造血发生的全局结构的主要方面仍不清楚。在这里,我们对 38 种不同的人类造血细胞进行了基因表达谱分析,并使用基因表达概率模型和基因启动子顺式元件分析来破译其调控回路的一般结构。我们鉴定了高度共表达基因的模块,其中一些基因模块局限于单个谱系,但大多数基因模块在多个谱系中以可变水平表达。我们发现了密集连接的顺式调控回路和大量在造血状态下差异表达的转录因子。这些发现表明造血的调控系统比以前假设的更为复杂。