Frameworks for Programming Biological Function through RNA Parts and Devices

被引:93
作者
Win, Maung Nyan [1 ]
Liang, Joe C. [1 ]
Smolke, Christina D. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
来源
CHEMISTRY & BIOLOGY | 2009年 / 16卷 / 03期
关键词
DUAL GENETIC SELECTION; RIBOSOME ENTRY SITES; MESSENGER-RNA; HAMMERHEAD RIBOZYMES; MAMMALIAN-CELLS; IN-VIVO; ESCHERICHIA-COLI; SACCHAROMYCES-CEREVISIAE; SYNTHETIC RIBOSWITCHES; TRANSLATION INITIATION;
D O I
10.1016/j.chembiol.2009.02.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
One of the long-term goals of synthetic biology is to reliably engineer biological systems that perform human-defined functions. Currently, researchers face several scientific and technical challenges in designing and building biological systems, one of which is associated with our limited ability to access, transmit, and control molecular information through the design of functional biomolecules exhibiting novel properties. The fields of RNA biology and nucleic acid engineering, along with the tremendous interdisciplinary growth of synthetic biology, are fueling advances in the emerging field of RNA programming in living systems. Researchers are designing functional RNA molecules that exhibit increasingly complex functions and integrating these molecules into cellular circuits to program higher-level biological functions. The continued integration and growth of RNA design and synthetic biology presents exciting potential to transform how we interact with and program biology.
引用
收藏
页码:298 / 310
页数:13
相关论文
共 117 条
[21]   THE USE OF RNAS COMPLEMENTARY TO SPECIFIC MESSENGER-RNAS TO REGULATE THE EXPRESSION OF INDIVIDUAL BACTERIAL GENES [J].
COLEMAN, J ;
GREEN, PJ ;
INOUYE, M .
CELL, 1984, 37 (02) :429-436
[22]   Selected classes of minimised hammerhead ribozyme have very high cleavage rates at low Mg2+ concentration [J].
Conaty, J ;
Hendry, P ;
Lockett, T .
NUCLEIC ACIDS RESEARCH, 1999, 27 (11) :2400-2407
[23]  
Cox JC, 2002, COMB CHEM HIGH T SCR, V5, P289
[24]   Progress in antisense technology [J].
Crooke, ST .
ANNUAL REVIEW OF MEDICINE, 2004, 55 :61-95
[25]   A tunable genetic switch based on RNAi and repressor proteins for regulating gene expression in mammalian cells [J].
Deans, Tara L. ;
Cantor, Charles R. ;
Collins, James J. .
CELL, 2007, 130 (02) :363-372
[26]   Genetic screens and selections for small molecules based on a synthetic riboswitch that activates protein translation [J].
Desai, SK ;
Gallivan, JP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (41) :13247-13254
[27]   The chemical repertoire of natural ribozymes [J].
Doudna, JA ;
Cech, TR .
NATURE, 2002, 418 (6894) :222-228
[28]   Selection of smart aptamers by equilibrium capillary electrophoresis of equilibrium mixtures (ECEEM) [J].
Drabovich, A ;
Berezovski, M ;
Krylov, SN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (32) :11224-11225
[29]   Killing the messenger: Short RNAs that silence gene expression [J].
Dykxhoorn, DM ;
Novina, CD ;
Sharp, PA .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (06) :457-467
[30]   INVITRO SELECTION OF RNA MOLECULES THAT BIND SPECIFIC LIGANDS [J].
ELLINGTON, AD ;
SZOSTAK, JW .
NATURE, 1990, 346 (6287) :818-822