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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Kiani, Samira Beal, Jacob Ebrahimkhani, Mohammad R. Huh, Jin Hall, Richard N. Xie, Zhen Li, Yinqing Weiss, Ron |
| Description | Country affiliation: United States Author Affiliation: Kiani S ( 1] Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA. [2] Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.); Beal J ( Raytheon BBN Technologies, Cambridge, Massachusetts, USA.); Ebrahimkhani MR ( Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.); Huh J ( 1] Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA. [2] Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA. [3] Institute for the BioCentury, Korea Advanced Institute of Science and Technology, Dae); Hall RN ( 1] Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA. [2] Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.); Xie Z ( 1] Bioinformatics Division, Center for Synthetic & Systems Biology, Tsinghua National Laboratory for Information Science and Technology, Beijing, China. [2] Department of Automation, Tsinghua University, Beijing, China.); Li Y ( Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.); Weiss R ( 1] Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA. [2] Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA. [3] Department of Electrical Engineering and Computer Science, Massachusetts Institute of) |
| Abstract | A key obstacle to creating sophisticated genetic circuits has been the lack of scalable device libraries. Here we present a modular transcriptional repression architecture based on clustered regularly interspaced palindromic repeats (CRISPR) system and examine approaches for regulated expression of guide RNAs in human cells. Subsequently we demonstrate that CRISPR regulatory devices can be layered to create functional cascaded circuits, which provide a valuable toolbox for engineering purposes. |
| File Format | HTM / HTML |
| ISSN | 15487091 |
| e-ISSN | 15487105 |
| DOI | 10.1038/nmeth.2969 |
| Journal | Nature Methods |
| Issue Number | 7 |
| Volume Number | 11 |
| Language | English |
| Publisher | Nature Publishing Group |
| Publisher Date | 2014-07-01 |
| Publisher Place | United States |
| Access Restriction | Open |
| Subject Keyword | Discipline Clinical Laboratory Techniques Clustered Regularly Interspaced Short Palindromic Repeats Genetics Genetic Engineering Instrumentation Rna, Guide Biosynthesis Gene Expression Regulation Gene Targeting Hek293 Cells Promoter Regions, Genetic Rna Polymerase Ii Rna Polymerase Iii Metabolism Transcription, Genetic Drug Effects Research Support, N.i.h., Extramural Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article |
| Subject | Cell Biology Biochemistry Molecular Biology Biotechnology |
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