The IKAROS Interaction with a Complex Including Chromatin Remodeling and Transcription Elongation Activities Is Required for Hematopoiesis

被引:44
作者
Bottardi, Stefania [1 ]
Mavoungou, Lionel
Pak, Helen
Daou, Salima
Bourgoin, Vincent
Lakehal, Yahia A.
Affar, El Bachir
Milot, Eric
机构
[1] Univ Montreal, Hop Maison Neuve Rosemont, Res Ctr, Montreal, PQ, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
P-TEFB; PROTEIN INTERACTIONS; CELL-DEVELOPMENT; GENE-EXPRESSION; STEM-CELLS; LONG-TERM; GATA-1; BINDING; FAMILY; NURD;
D O I
10.1371/journal.pgen.1004827
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
IKAROS is a critical regulator of hematopoietic cell fate and its dynamic expression pattern is required for proper hematopoiesis. In collaboration with the Nucleosome Remodeling and Deacetylase (NuRD) complex, it promotes gene repression and activation. It remains to be clarified how IKAROS can support transcription activation while being associated with the HDAC-containing complex NuRD. IKAROS also binds to the Positive-Transcription Elongation Factor b (P-TEFb) at gene promoters. Here, we demonstrate that NuRD and P-TEFb are assembled in a complex that can be recruited to specific genes by IKAROS. The expression level of IKAROS influences the recruitment of the NuRD-P-TEFb complex to gene regulatory regions and facilitates transcription elongation by transferring the Protein Phosphatase 1 alpha (PP1 alpha), an IKAROS-binding protein and P-TEFb activator, to CDK9. We show that an IKAROS mutant that is unable to bind PP1 alpha cannot sustain gene expression and impedes normal differentiation of Ik(NULL) hematopoietic progenitors. Finally, the knock-down of the NuRD subunit Mi2 reveals that the occupancy of the NuRD complex at transcribed regions of genes favors the relief of POL II promoter-proximal pausing and thereby, promotes transcription elongation.
引用
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页数:16
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