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聚焦HOX基因座的CRISPR/sgRNA文库筛选鉴定关键的CTCF边界

HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries.

作者信息

Luo Huacheng, Sobh Amin, Vulpe Christopher D, Brewer Edmond, Dovat Sinisa, Qiu Yi, Huang Suming

机构信息

Department of Pediatrics, Pennsylvania State University College of Medicine;

Department of Physiological Sciences, University of Florida.

出版信息

J Vis Exp. 2019 Mar 31(145). doi: 10.3791/59382.

Abstract

CCCTC-binding factor (CTCF)-mediated stable topologically associating domains (TADs) play a critical role in constraining interactions of DNA elements that are located in neighboring TADs. CTCF plays an important role in regulating the spatial and temporal expression of HOX genes that control embryonic development, body patterning, hematopoiesis, and leukemogenesis. However, it remains largely unknown whether and how HOX loci associated CTCF boundaries regulate chromatin organization and HOX gene expression. In the current protocol, a specific sgRNA pooled library targeting all CTCF binding sites in the HOXA/B/C/D loci has been generated to examine the effects of disrupting CTCF-associated chromatin boundaries on TAD formation and HOX gene expression. Through CRISPR-Cas9 genetic screening, the CTCF binding site located between HOXA7/HOXA9 genes (CBS7/9) has been identified as a critical regulator of oncogenic chromatin domain, as well as being important for maintaining ectopic HOX gene expression patterns in MLL-rearranged acute myeloid leukemia (AML). Thus, this sgRNA library screening approach provides novel insights into CTCF mediated genome organization in specific gene loci and also provides a basis for the functional characterization of the annotated genetic regulatory elements, both coding and noncoding, during normal biological processes in the post-human genome project era.

摘要

CCCTC结合因子(CTCF)介导的稳定拓扑相关结构域(TAD)在限制位于相邻TAD中的DNA元件的相互作用中起关键作用。CTCF在调节控制胚胎发育、身体模式形成、造血和白血病发生的HOX基因的时空表达中起重要作用。然而,HOX基因座相关的CTCF边界是否以及如何调节染色质组织和HOX基因表达在很大程度上仍然未知。在当前方案中,已经生成了一个针对HOXA/B/C/D基因座中所有CTCF结合位点的特定sgRNA汇集文库,以研究破坏与CTCF相关的染色质边界对TAD形成和HOX基因表达的影响。通过CRISPR-Cas9基因筛选,已确定位于HOXA7/HOXA9基因之间的CTCF结合位点(CBS7/9)是致癌染色质结构域的关键调节因子,并且对于维持MLL重排急性髓细胞白血病(AML)中异位HOX基因表达模式也很重要。因此,这种sgRNA文库筛选方法为CTCF介导的特定基因座中的基因组组织提供了新见解,也为在后人类基因组计划时代正常生物学过程中注释的遗传调控元件(包括编码和非编码元件)的功能表征提供了基础。

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