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PU.1启动子的淋巴细胞特异性和髓细胞特异性活性由八聚体和ets转录因子的组合作用决定。

Lymphoid- and myeloid-specific activity of the PU.1 promoter is determined by the combinatorial action of octamer and ets transcription factors.

作者信息

Kistler B, Pfisterer P, Wirth T

机构信息

ZMBH, Zentrum für Molekulare Biologie Heidelberg, Germany.

出版信息

Oncogene. 1995 Sep 21;11(6):1095-106.

PMID:7566969
Abstract

The putative oncogene PU.1/Spi-1 is a member of the ets-family of transcription factors normally expressed in a subset of hematopoietic cell types. Here we have characterized the role of the PU.1 promoter region for the cell-type specific expression. The proximal 120 bp are sufficient to mediate a high level of activity specifically in B cells and macrophages. Three important motifs could be identified within this region. Two of them, an ets binding site (EBS) and a variant octamer motif were most important for cell-type-specific promoter activity in B cells and macrophages. An additional Sp1 motif stimulates basal activity of this promoter element. The relative contribution to overall activity of octamer motif and EBS differs in B cells and macrophages. In B cells, both octamer motif and EBS combine to mediate high level activity, whereas in macrophages the EBS predominantly confers promoter activity. Both the Oct1 and Oct2 transcription factors, presumably in combination with a B-cell-restricted coactivator, are responsible for the activity of the variant octamer motif in B cells. Interestingly, the PU.1 transcription factor can functionally interact with the EBS in its own promoter, suggesting a positive feedback regulation.

摘要

假定的癌基因PU.1/Spi-1是ets转录因子家族的成员,通常在一部分造血细胞类型中表达。在此,我们阐述了PU.1启动子区域在细胞类型特异性表达中的作用。近端120个碱基对足以介导在B细胞和巨噬细胞中特异性的高水平活性。在该区域内可鉴定出三个重要基序。其中两个,一个ets结合位点(EBS)和一个变体八聚体基序,对B细胞和巨噬细胞中的细胞类型特异性启动子活性最为重要。另一个Sp1基序刺激该启动子元件的基础活性。八聚体基序和EBS对总体活性的相对贡献在B细胞和巨噬细胞中有所不同。在B细胞中,八聚体基序和EBS共同作用以介导高水平活性,而在巨噬细胞中,EBS主要赋予启动子活性。Oct1和Oct2转录因子,可能与一种B细胞限制性共激活因子结合,负责B细胞中变体八聚体基序的活性。有趣的是,PU.1转录因子可在其自身启动子中与EBS发生功能相互作用,提示存在正反馈调节。

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