PUBLICATION

Versatile Synthesis and Rational Design of Caged Morpholinos

Authors
Ouyang, X., Shestopalov, I.A., Sinha, S., Zheng, G., Pitt, C.L., Li, W.H., Olson, A.J., and Chen, J.K.
ID
ZDB-PUB-090828-28
Date
2009
Source
Journal of the American Chemical Society   131(37): 13255-13269 (Journal)
Registered Authors
Chen, James K., Shestopalov, Ilya, Sinha, Surajit
Keywords
none
MeSH Terms
  • Animals
  • Base Sequence
  • Cross-Linking Reagents/chemistry
  • Drug Design*
  • Gene Silencing
  • Hydroxyquinolines/chemistry
  • Inverted Repeat Sequences
  • Nitrobenzenes/chemistry
  • Oligonucleotides/chemical synthesis*
  • Oligonucleotides/chemistry*
  • Oligonucleotides/genetics
  • Oligonucleotides/metabolism
  • Photons
  • T-Box Domain Proteins/metabolism
  • Zebrafish/embryology
  • Zebrafish/genetics
PubMed
19708646 Full text @ J. Am. Chem. Soc.
Abstract
Embryogenesis is regulated by genetic programs that are dynamically executed in a stereotypic manner, and deciphering these molecular mechanisms requires the ability to control embryonic gene function with similar spatial and temporal precision. Chemical technologies can enable such genetic manipulations, as exemplified by the use of caged morpholino (cMO) oligonucleotides to inactivate genes in zebrafish and other optically transparent organisms with spatiotemporal control. Here we report optimized methods for the design and synthesis of hairpin cMOs incorporating a dimethoxynitrobenzyl (DMNB)-based bifunctional linker that permits cMO assembly in only three steps from commercially available reagents. Using this simplified procedure, we have systematically prepared cMOs with differing structural configurations and investigated how the in vitro thermodynamic properties of these reagents correlate with their in vivo activities. Through these studies, we have established general principles for cMO design and successfully applied them to several developmental genes. Our optimized synthetic and design methodologies have also enabled us to prepare a next-generation cMO that contains a bromohydroxyquinoline (BHQ)-based linker for two-photon uncaging. Collectively, these advances establish the generality of cMO technologies and will facilitate the application of these chemical probes in vivo for functional genomic studies.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping