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首页> 外文期刊>Journal of Cellular Physiology >Core binding factor β (CBFβ) is retained in the midbody during cytokinesis
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Core binding factor β (CBFβ) is retained in the midbody during cytokinesis

机译:核心绑定因子β(CBFβ)是保留的中间体在胞质分裂

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摘要

Core Binding Factor β (CBFβ) is complexed with the RUNX family of transcription factors in the nucleus to support activation or repression of genes related to bone (RUNX2), hematopoiesis (RUNX1) and gastrointestinal (RUNX3) development. Furthermore, RUNX proteins contribute to the onset and progression of different types of cancer. Although CBFβ localizes to cytoskeletal architecture, its biological role in the cytoplasmic compartment remains to be established. Additionally, the function and localization of CBFβ during the cell cycle are important questions relevant to its biological role. Here we show that CBFβ dynamically distributes in different stages of cell division and importantly is present during telophase at the midbody, a temporal structure important for successful cytokinesis. A functional role for CBFβ localization at the midbody is supported by striking defects in cytokinesis that include polyploidy and abscission failure following siRNA-mediated downregulation of endogenous CBFβ or overexpression of the inv(16) fusion protein CBFβ-SMMHC. Our results suggest that CBFβ retention in the midbody during cytokinesis reflects a novel function that contributes to epigenetic control.
机译:核心绑定因子β(CBFβ)包裹着RUNX家族的转录因子核支持激活或镇压与骨相关基因(RUNX2)造血作用(RUNX1)和胃肠道(RUNX3)发展。此外,RUNX蛋白质做出贡献不同类型的发展癌症。架构,其生物作用胞质间还有待建立。本地化的CBFβ细胞周期期间重要的问题相关的生物的角色。分布在不同的细胞分裂阶段在末期,重要的是礼物中间体,重要的时间结构成功的胞质分裂。CBFβ本地化支持中间体胞质分裂,包括缺陷多倍体和离层失败后的差别siRNA-mediated对这些内生CBFβ或超表达的发票(16)融合蛋白CBFβ-SMMHC。胞质分裂期间保留的中间体反映了一种新颖的功能,导致表观遗传控制。

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