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Controlling gene loss of function in newts with emphasis on lens regeneration

Authors: 
Tsonis PA, Haynes T, Maki N, Nakamura K, Casco-Robles MM, Yamada S, Miura T, Chiba C, Del Rio-Tsonis K
Citation: 
Nature Protocols. 2011;6:593–599 doi:10.1038/nprot.2011.341
Abstract: 
Here we describe a protocol for gene loss of function during regeneration in newts, specifically applied to lens regeneration. Knockdown with the use of morpholinos can be achieved both in vitro and in vivo, depending on the experimental design. These methods achieve desirable levels of gene knockdown, and thus can be compared with methods developed for use in other animals, such as zebrafish. The technology has been applied to study molecular mechanisms during the process of lens regeneration by knocking down genes at specific stages and examining their effects on other genes and lens differentiation. The protocol can take a few days or up to 20 d to complete, depending on the duration of the experiment.
Organism or Cell Type: 
Notophthalmus viridescens (newt), cell cutlures and in vivo
Delivery Method: 
Vivo-Morpholino in vivo, Morpholinos and Endo-Porter in cultures