INHIBITION OF MYELOID DIFFERENTIATION BY THE HELIX-LOOP-HELIX PROTEIN ID

INHIBITION OF MYELOID DIFFERENTIATION BY THE HELIX-LOOP-HELIX PROTEIN ID
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DOI:
10.1126/science.1372755
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发表时间:
1992-03-27
期刊:
影响因子:
56.9
通讯作者:
KADESCH, T
KADESCH, T
中科院分区:
综合性期刊1区
文献类型:
--
作者:
KREIDER, BL;BENEZRA, R;KADESCH, T

文献摘要

被引文献

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Id是一种螺旋-环-螺旋(helix-loop-helix,HLH)蛋白,其抑制参与细胞类型特异性转录和细胞谱系定型的几种碱性螺旋-环-螺旋(basic helix-loop-helix,bHLH)蛋白的活性。髓样前体细胞系32 DC 13(G)表达Id信使RNA,当用粒细胞集落刺激因子诱导细胞终末分化时,Id信使RNA瞬时减少。伴随着Id信使RNA的减少,在核提取物中出现了DNA结合蛋白,其识别了典型的E盒基序,一些bHLH蛋白的DNA结合位点。Id互补DNA在32 DC 13(G)细胞中的组成型表达阻断了它们的分化能力和诱导E-box结合活性。这些结果表明,Id,因此,bHLH蛋白的功能在骨髓分化的过程中。
Id is a helix-loop-helix (HLH) protein that represses activity of several basic helix-loop-helix (bHLH) proteins involved in cell type-specific transcription and cell lineage commitment. The myeloid precursor cell line 32DC13(G) expressed Id messenger RNA, which was transiently decreased when cells were induced to terminally differentiate with granulocyte-colony-stimulating factor. Concomitant with the decrease of Id messenger RNA was the appearance in nuclear extracts of DNA binding proteins that recognized a canonical E-box motif, a DNA binding site for some bHLH proteins. Constitutive expression of an Id complementary DNA in 32DC13(G) cells blocked their ability to differentiate and to induce E-box-binding activity. These results suggest that Id and, hence, bHLH proteins function in the process of myeloid differentiation.