New Insights into BS69 Functions*

New Insights into BS69 Functions*
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DOI:
10.1074/jbc.m600573200
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发表时间:
2006-06
影响因子:
4.8
通讯作者:
Guillaume Velasco;S. Grkovic;S. Ansieau
Guillaume Velasco;S. Grkovic;S. Ansieau
中科院分区:
生物学2区
文献类型:
--
作者:
Guillaume Velasco;S. Grkovic;S. Ansieau

文献摘要

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BS69蛋白通常被描述为与各种转录因子相关的共阻遏物。然而,由于缺乏可靠的BS69抗体,该假设主要依赖于标记蛋白的过表达。我们首次提出了一个完整的序列的BS 69和有价值的工具来表征内源性蛋白质。我们发现,全长BS69蛋白,以及次要的选择性剪接亚型,是无处不在的表达,核,并与染色质和有丝分裂染色体。因此,BS69与一组染色质重塑因子相互作用,包括ATP依赖性解旋酶、组蛋白脱乙酰酶和组蛋白甲基转移酶,以及E2F6转录因子。这些数据加强了BS69在基因抑制中的作用,并将BS69与染色质重塑联系起来。
The BS69 protein has been commonly described as a co-repressor associated with various transcription factors. However, this hypothesis relied predominately on overexpression of tagged proteins due to the lack of a reliable BS69 antibody. We present for the first time a complete sequence of BS69 and valuable tools to characterize the endogenous protein. We show that the full-length BS69 protein, as well as minor alternatively spliced isoforms, is ubiquitously expressed, nuclear, and associates with chromatin and mitotic chromosomes. Accordingly, BS69 interacts with a set of chromatin remodeling factors, including ATP-dependent helicases, histone deacetylases, and histone methyltransferases, as well as the E2F6 transcription factor. These data strengthen a role for BS69 in gene repression and link BS69 to chromatin remodeling.