4.8 Article

MiR-150 controls B cell differentiation by targeting the transcription factor c-myb

期刊

CELL
卷 131, 期 1, 页码 146-159

出版社

CELL PRESS
DOI: 10.1016/j.cell.2007.07.021

关键词

-

资金

  1. NCI NIH HHS [R01 CA085842, CA85842] Funding Source: Medline
  2. NIAID NIH HHS [AI054636, AI059294, R01 AI059294, AI064345] Funding Source: Medline

向作者/读者索取更多资源

MiR-150 is a microRNA ( miRNA) specifically expressed in mature lymphocytes, but not their progenitors. A top predicted target of miR-150 is c-Myb, a transcription factor controlling multiple steps of lymphocyte development. Combining loss- and gain-of-function gene targeting approaches for miR-150 with conditional and partial ablation of c-Myb, we show that miR150 indeed controls c-Myb expression in vivo in a dose-dependent manner over a narrow range of miRNA and c-Myb concentrations and that this dramatically affects lymphocyte development and response. Our results identify a key transcription factor as a critical target of a stage-specifically expressed miRNA in lymphocytes and suggest that this and perhaps other miRNAs have evolved to control the expression of just a few critical target proteins in particular cellular contexts.

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