4.8 Article

Characterization of transcriptional networks in blood stem and progenitor cells using high-throughput single-cell gene expression analysis

期刊

NATURE CELL BIOLOGY
卷 15, 期 4, 页码 363-+

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/ncb2709

关键词

-

资金

  1. Medical Research Council
  2. Leukaemia and Lymphoma Research
  3. Leukaemia and Lymphoma Society
  4. Cancer Research UK
  5. Wellcome Trust
  6. Biotechnology and Biological Sciences Research Council [BB/I00050X/1] Funding Source: researchfish
  7. Cancer Research UK [12765] Funding Source: researchfish
  8. Medical Research Council [MC_PC_12009, MC_UU_12009/5, G0501838, G1000801h, G0801073, G0900951, MC_UU_12009/2] Funding Source: researchfish
  9. National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs) [G0900729/1] Funding Source: researchfish
  10. BBSRC [BB/I00050X/1] Funding Source: UKRI
  11. MRC [G0501838, G0900951, MC_UU_12009/2, G0801073, MC_UU_12009/5] Funding Source: UKRI

向作者/读者索取更多资源

Cellular decision-making is mediated by a complex interplay of external stimuli with the intracellular environment, in particular transcription factor regulatory networks. Here we have determined the expression of a network of 18 key haematopoietic transcription factors in 597 single primary blood stem and progenitor cells isolated from mouse bone marrow. We demonstrate that different stem/progenitor populations are characterized by distinctive transcription factor expression states, and through comprehensive bioinformatic analysis reveal positively and negatively correlated transcription factor pairings, including previously unrecognized relationships between Gata2, Gfi1 and Gfi1b. Validation using transcriptional and transgenic assays confirmed direct regulatory interactions consistent with a regulatory triad in immature blood stem cells, where Gata2 may function to modulate cross-inhibition between Gfi1 and Gfi1b. Single-cell expression profiling therefore identifies network states and allows reconstruction of network hierarchies involved in controlling stem cell fate choices, and provides a blueprint for studying both normal development and human disease.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据