Design, synthesis and biochemical investigation, by in vitro luciferase reporter system, of peptide nucleic acids as new inhibitors of miR-509-3p involved in the regulation of cystic fibrosis diseasegene expression

被引:20
作者
Amato, Felice [1 ,2 ]
Tomaiuolo, Rossella [1 ,2 ]
Borbone, Nicola [3 ]
Elce, Ausilia [1 ,2 ,4 ]
Amato, Jussara [3 ]
D'Errico, Stefano [3 ]
De Rosa, Giuseppe [3 ]
Mayol, Laura [3 ]
Piccialli, Gennaro [3 ]
Oliviero, Giorgia [3 ]
Castaldo, Giuseppe [1 ,2 ]
机构
[1] Dipartimento Med Mol & Biotecnol Med, I-80131 Naples, Italy
[2] CEINGE Biotecnol Avanzate, Naples, Italy
[3] Univ Naples Federico II, Dipartimento Farm, I-80131 Naples, Italy
[4] Univ Telemat Pegaso, Naples, Italy
关键词
TRANSMEMBRANE CONDUCTANCE REGULATOR; PNA; OLIGONUCLEOTIDES; HYBRIDIZATION; DNA;
D O I
10.1039/c3md00257h
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Recently, microRNAs (miRNAs) were identified as being able to inhibit the expression of the Cystic Fibrosis Transmembrane Regulator (CFTR) disease-gene of Cystic Fibrosis (CF) and CFTR-Related Disorders (CFTRRD). This study shows the use of peptide nucleic acids (PNAs) as inhibitors of miR-509-3p, one of the CFTR regulating miRNAs, by reverting the expression of the luciferase gene containing the 30'UTR of CFTR gene.
引用
收藏
页码:68 / 71
页数:4
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