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印记控制区域中的多个YY1和CTCF结合位点。

Multiple YY1 and CTCF binding sites in imprinting control regions.

作者信息

Kim Joomyeong

机构信息

Department of Biological Sciences; Louisiana State University, Baton Rouge, Louisiana, USA.

出版信息

Epigenetics. 2008 May-Jun;3(3):115-8. doi: 10.4161/epi.3.3.6176.

Abstract

Known imprinting control regions (ICRs) contain unusual tandem arrays of DNA-binding sites for transcription factors, including YY1 for the Peg3, Gnas, and Xist/Tsix domains and CTCF for the H19/Igf2 domain. These multiple DNA-binding sites are known to be the only functionally shared and evolutionarily selected feature among these ICRs. However, it is not well understood why the imprinting control regions tend to maintain a high density of a particular transcription factor-binding site. We hypothesize that the multiplicity associated with the YY1 and CTCF binding sites may be designed for attracting and maintaining the relatively high levels of YY1 and CTCF proteins or for covering the relatively large genomic sizes of the associated ICRs. This idea remains to be tested in the near future, but it is one of the most likely explanations for all those unusual features that are associated with the functionally critical regions (ICRs) of genomic imprinting.

摘要

已知的印记控制区域(ICR)包含转录因子的异常串联DNA结合位点阵列,包括Peg3、Gnas和Xist/Tsix结构域的YY1以及H19/Igf2结构域的CTCF。这些多个DNA结合位点是这些ICR中唯一功能共享且经过进化选择的特征。然而,目前尚不清楚为什么印记控制区域倾向于维持特定转录因子结合位点的高密度。我们假设,与YY1和CTCF结合位点相关的多重性可能是为了吸引和维持相对高水平的YY1和CTCF蛋白,或者是为了覆盖相关ICR相对较大的基因组区域。这个想法有待在不久的将来进行验证,但它是对与基因组印记功能关键区域(ICR)相关的所有这些异常特征最有可能的解释之一。

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