Bioengineering of noncoding RNAs for research agents and therapeutics

被引:64
作者
Ho, Pui Yan [1 ]
Yu, Ai-Ming [1 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Biochem & Mol Med, Sacramento, CA USA
关键词
DOUBLE-STRANDED-RNA; ESCHERICHIA-COLI; RECOMBINANT RNA; RECOGNITION; INTERFERENCE; PURIFICATION; POLYMERASE; EXPRESSION; MICRORNAS; THERAPY;
D O I
10.1002/wrna.1324
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The discovery of functional small noncoding RNAs (ncRNAs), such as microRNAs and small interfering RNAs, in the control of human cellular processes has opened new avenues to develop RNA-based therapies for various diseases including viral infections and cancers. However, studying ncRNA functions and developing RNA-based therapeutics relies on access to large quantities of affordable ncRNA agents. Currently, synthetic RNAs account for the major source of agents for RNA research and development, yet carry artificial modifications on the ribose ring and phosphate backbone in sharp contrast to posttranscriptional modifications present on the nucleobases or unmodified natural RNA molecules produced within cells. Therefore, large efforts have been made in recent years to develop recombinant RNA techniques to cost-effectively produce biological RNA agents that may better capture the structure, function, and safety properties of natural RNAs. In this article, we summarize and compare current in vitro and in vivo methods for the production of RNA agents including chemical synthesis, in vitro transcription, and bioengineering approaches. We highlight the latest recombinant RNA approaches using transfer RNA (tRNA), ribosomal RNA (rRNA), and optimal ncRNA scaffold (OnRS), and discuss the applications of bioengineered ncRNA agents (BERAs) that should facilitate RNA research and development. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:186 / 197
页数:12
相关论文
共 69 条
  • [1] Current and future treatment of amyloid neuropathies
    Adams, David
    Cauquil, Cecile
    Theaudin, Marie
    Rousseau, Antoine
    Algalarrondo, Vincent
    Slama, Michel S.
    [J]. EXPERT REVIEW OF NEUROTHERAPEUTICS, 2014, 14 (12) : 1437 - 1451
  • [2] Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3
    Alexopoulou, L
    Holt, AC
    Medzhitov, R
    Flavell, RA
    [J]. NATURE, 2001, 413 (6857) : 732 - 738
  • [3] The functions of animal microRNAs
    Ambros, V
    [J]. NATURE, 2004, 431 (7006) : 350 - 355
  • [4] Bader Andreas G., 2012, Frontiers in Genetics, V3, P120, DOI 10.3389/fgene.2012.00120
  • [5] MicroRNAs: Target Recognition and Regulatory Functions
    Bartel, David P.
    [J]. CELL, 2009, 136 (02) : 215 - 233
  • [6] Beckert B, 2011, METHODS MOL BIOL, V703, P29, DOI 10.1007/978-1-59745-248-9_3
  • [7] RNA Targeting Therapeutics: Molecular Mechanisms of Antisense Oligonucleotides as a Therapeutic Platform
    Bennett, C. Frank
    Swayze, Eric E.
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2010, 50 : 259 - 293
  • [8] RNA-Based Therapeutics: Current Progress and Future Prospects
    Burnett, John C.
    Rossi, John J.
    [J]. CHEMISTRY & BIOLOGY, 2012, 19 (01): : 60 - 71
  • [9] The RNA modification database, RNAMDB: 2011 update
    Cantara, William A.
    Crain, Pamela F.
    Rozenski, Jef
    McCloskey, James A.
    Harris, Kimberly A.
    Zhang, Xiaonong
    Vendeix, Franck A. P.
    Fabris, Daniele
    Agris, Paul F.
    [J]. NUCLEIC ACIDS RESEARCH, 2011, 39 : D195 - D201
  • [10] A general approach to high-yield biosynthesis of chimeric RNAs bearing various types of functional small RNAs for broad applications
    Chen, Qiu-Xia
    Wang, Wei-Peng
    Zeng, Su
    Urayama, Shiro
    Yu, Ai-Ming
    [J]. NUCLEIC ACIDS RESEARCH, 2015, 43 (07) : 3857 - 3869