2005 Fiscal Year Final Research Report Summary
Regulation of hematopoiesis through a novel nuclear receptor coactivator TRAP/Mediator complex
| Project/Area Number |
16590941
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Hematology
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| Research Institution | Kobe University |
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Principal Investigator |
ITO Mitsuhiro Kobe University, Hospital, Assistant Professor, 医学部附属病院, 助手 (50362794)
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| Project Period (FY) |
2004 – 2005
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| Keywords | Transcriptional Mediator / TRAP220 / MED1 / myelomonocytic differentiation / retinoic acid receptor / vitamin D receptor |
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| Research Abstract |
The TRAP/Mediator complex, the metazoan counterpart of the yeast Mediator complex, is master transcriptional regulatory complex composed of approximately 30 subunits. It was originally isolated as a thyroid hormone receptor (TR)-associated protein (TRAP) complex that mediates TR-activated transcription from DNA templates in vitro and probably acts in vivo after the action of other receptor-interacting coactivators involved in chromatin remodeling. The TRAP220/MED1 subunit of the TRAP/Mediator complex is proposed to act on a variety of major and specific biological events, including growth, differentiation and homeostasis, through physical interaction with nuclear receptors. The vitamin D receptor (VDR) and retinoic acid receptor (RAR), coupled with retinoid X receptor (RXR), are nuclear receptors which have important roles for monopoiesis and granulopoiesis, respectively. The functional role of TRAP220/MED1 in nuclear receptor-mediated monopoiesis and granulopoiesis is presented. Since
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TRAP220 knockout mice were mortal before definitive hematopoiesis becomes dominant, the function of TRAP220/MED1 in adult hematopoiesis was mostly unknown. However, these embryos appeared to have normal composition of nucleated erythroid cells. Therefore, the E9.0 yolk sac-derived hematopoietic precursor cells were used to differentiate into definitive hematopoietic colony forming units. The number of monocytic colonies (CFU-M) was significantly lower in knockouts, while the numbers of other colonies (CFU-GEMM, CFU-GM, CFU-G and CFU-E) were comparable. Then, the HL-60 acute promyelocytic leukemia cells were used to elucidate directly and mechanistically the roles of TRAP220/MED1 in RAR- and VDR-dependent differentiation of the hematopoietic precursor cells. Flow cytometric analyses showed that HL-60 cells, wherein TRAP220/MED1 was down-regulated, did not differentiate efficiently into monocytes and granulocytes by ligand stimulation. The expression of direct target genes of VDR or RAR, as well as the differentiation marker genes, was low in the knockdown cells. These results indicated a crucial role of TRAP220/MED1 in the optimal VDR- and RAR-mediated myelomonocytic differentiation processes in mammalian hematopoiesis. Less
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Research Products
(14 results)
