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Tightly bound to DNA proteins: Possible universal substrates for intranuclear processes

  作者 Sjakste, N; Bielskiene, K; Bagdoniene, L; Labeikyte, D; Gutcaits, A; Vassetzky, Y; Sjakste, T  
  选自 期刊  Gene;  卷期  2012年492-1;  页码  54-64  
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[摘要]Tightly bound to DNA proteins (TBPs) are a protein group that remains attached to DNA after its deproteinization by phenol, chloroform or salting-out. TBP are bound to DNA with covalent phosphotriester or non-covalent ion and hydrogen bonds. They appear to be a vast protein group involved in numerous intranuclear processes. The TBPs fraction co-purified with DNA deproteinized by mild procedures is extremely heterogeneous, tissue and species-specific. The protein fraction co-purified with DNA after harsh deproteinization procedures appears to be formed from few polypeptides common to different species and tissues. Interaction sites between DNA and TBPs depend on the physiological status of the cell. The binding sites of TBPs to DNA do not co-localize with the nuclear matrix attachment regions. We hypothesize that TBPs form a universal substrate for intranuclear processes. (C) 2011 Elsevier B.V. All rights reserved.

 
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