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使用反基因肽核酸抑制染色体DNA转录。

Inhibiting transcription of chromosomal DNA with antigene peptide nucleic acids.

作者信息

Janowski Bethany A, Kaihatsu Kunihiro, Huffman Kenneth E, Schwartz Jacob C, Ram Rosalyn, Hardy Daniel, Mendelson Carole R, Corey David R

机构信息

Department of Pharmacology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390, USA.

出版信息

Nat Chem Biol. 2005 Sep;1(4):210-5. doi: 10.1038/nchembio724. Epub 2005 Jul 31.

Abstract

Synthetic molecules that recognize specific sequences within cellular DNA are potentially powerful tools for investigating chromosome structure and function. Here, we designed antigene peptide nucleic acids (agPNAs) to target the transcriptional start sites for the human progesterone receptor B (hPR-B) and A (hPR-A) isoforms at sequences predicted to be single-stranded within the open complex of chromosomal DNA. We found that the agPNAs were potent inhibitors of transcription, showing for the first time that synthetic molecules can recognize transcription start sites inside cells. Breast cancer cells treated with agPNAs showed marked changes in morphology and an unexpected relationship between the strictly regulated levels of hPR-B and hPR-A. We confirmed these phenotypes using siRNAs and antisense PNAs, demonstrating the power of combining antigene and antisense strategies for gene silencing. agPNAs provide a general approach for controlling transcription initiation and a distinct option for target validation and therapeutic development.

摘要

能够识别细胞DNA内特定序列的合成分子,有可能成为研究染色体结构和功能的强大工具。在此,我们设计了反基因肽核酸(agPNA),以染色体DNA开放复合物中预测为单链的序列为靶点,作用于人类孕激素受体B(hPR-B)和A(hPR-A)亚型的转录起始位点。我们发现,agPNA是强效转录抑制剂,首次表明合成分子能够识别细胞内的转录起始位点。用agPNA处理的乳腺癌细胞在形态上出现显著变化,并且hPR-B和hPR-A严格调控水平之间呈现出意想不到的关系。我们使用小干扰RNA(siRNA)和反义PNA证实了这些表型,证明了将反基因和反义策略相结合用于基因沉默的强大作用。agPNA为控制转录起始提供了一种通用方法,也是用于靶点验证和治疗开发的独特选择。

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