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在体外和体内与CTCF结合的DNA片段能够阻断增强子活性。

DNA fragments binding CTCF in vitro and in vivo are capable of blocking enhancer activity.

作者信息

Didych Dmitry A, Kotova Elena S, Akopov Segey B, Nikolaev Lev G, Sverdlov Eugene D

机构信息

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 16/10 Miklukho-Maklaya, Moscow 117997, Russia.

出版信息

BMC Res Notes. 2012 Apr 5;5:178. doi: 10.1186/1756-0500-5-178.

Abstract

BACKGROUND

Earlier we identified ten 100-300-bp long CTCF-binding DNA fragments selected earlier from a 1-Mb human chromosome 19 region. Here the positive-negative selection technique was used to check the ability of CTCF-binding human genomic fragments to block enhancer-promoter interaction when inserted into the genome.

RESULTS

Ten CTCF-binding DNA fragments were inserted between the CMV enhancer and CMV minimal promoter driving the herpes simplex virus thymidine kinase (HSV-tk) gene in a vector expressing also the neoR gene under a separate promoter. The constructs were then integrated into the genome of CHO cells, and the cells resistant to neomycin and ganciclovir (positive-negative selection) were picked up, and their DNAs were PCR analyzed to confirm the presence of the fragments between the enhancer and promoter in both orientations.

CONCLUSIONS

We demonstrated that all sequences identified by their CTCF binding both in vitro and in vivo had enhancer-blocking activity when inserted between the CMV minimal promoter and enhancer in stably transfected CHO cells.

摘要

背景

此前我们从人类1号染色体的1兆碱基区域中筛选出了10个长度为100 - 300碱基对的CTCF结合DNA片段。在此,我们运用正反向选择技术,来检测插入基因组后,CTCF结合的人类基因组片段阻断增强子-启动子相互作用的能力。

结果

将10个CTCF结合DNA片段插入到载体中,该载体在独立启动子的驱动下表达新霉素抗性基因(neoR),同时其巨细胞病毒(CMV)增强子与驱动单纯疱疹病毒胸苷激酶(HSV-tk)基因的CMV最小启动子之间存在上述片段。然后将构建体整合到中国仓鼠卵巢(CHO)细胞的基因组中,挑选出对新霉素和更昔洛韦具有抗性的细胞(正反向选择),并对其DNA进行PCR分析,以确认增强子和启动子之间在两个方向上均存在这些片段。

结论

我们证明,在稳定转染的CHO细胞中,所有在体外和体内通过CTCF结合鉴定出的序列,插入到CMV最小启动子和增强子之间时均具有增强子阻断活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96f0/3369819/16930d531788/1756-0500-5-178-1.jpg

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