核小体转录过程中关键中间体的结构分析。

Trends in cell & molecular biology Pub Date : 2013-01-01
H-W Chang, A K Shaytan, F-K Hsieh, O I Kulaeva, M P Kirpichnikov, V M Studitsky
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引用次数: 0

摘要

不同RNA聚合酶通过染色质转录产生不同的生物学结果,并伴随着核小体在原始位置的存活(Pol ii型机制)或核小体沿DNA的反向易位(Pol iii型机制)。有人提出,转录过程中形成的关键中间体结构的差异决定了核小体的命运。为了评估这种可能性,我们利用DNase I足迹和分子模型研究了Pol iii型机制转录过程中形成的关键中间体的结构。Pol iii型机制的特点是核小体存活所需的关键中间体的形成效率较低(Ø-loop, Pol ii型机制),很可能是由于Ø-loop中RNA聚合酶和DNA之间的空间干扰。这些数据表明,在转录过程中,较低的Ø-loop形成效率通过Pol iii型机制诱导核小体屏障的形成和核小体易位。
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Structural Analysis of the Key Intermediate Formed during Transcription through a Nucleosome.

Transcription through chromatin by different RNA polymerases produces different biological outcomes and is accompanied by either nucleosome survival at the original location (Pol II-type mechanism) or backward nucleosome translocation along DNA (Pol III-type mechanism). It has been proposed that differences in the structure of the key intermediates formed during transcription dictate the fate of the nucleosomes. To evaluate this possibility, structure of the key intermediate formed during transcription by Pol III-type mechanism was studied by DNase I footprinting and molecular modeling. The Pol III-type mechanism is characterized by less efficient formation of the key intermediate required for nucleosome survival (Ø-loop, Pol II-type mechanism), most likely due to steric interference between the RNA polymerase and DNA in the Ø-loop. The data suggest that the lower efficiency of Ø-loop formation induces formation of a lower nucleosomal barrier and nucleosome translocation during transcription by Pol III-type mechanism.

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