posted on 2016-02-19, 05:44authored byHongzhou Gu, Kazuhiro Furukawa, Zasha Weinberg, Daniel
F. Berenson, Ronald R. Breaker
DNA phosphoester bonds are exceedingly
resistant to hydrolysis in the absence of chemical or enzymatic catalysts.
This property is particularly important for organisms with large genomes,
as resistance to hydrolytic degradation permits the long-term storage
of genetic information. Here we report the creation and analysis of
two classes of engineered deoxyribozymes that selectively and rapidly
hydrolyze DNA. Members of class I deoxyribozymes carry a catalytic
core composed of only 15 conserved nucleotides and attain an observed
rate constant (kobs) of ∼1 min–1 when incubated near neutral pH in the presence of
Zn2+. Natural DNA sequences conforming to the class I consensus
sequence and structure were found that undergo hydrolysis under selection
conditions (2 mM Zn2+, pH 7), which demonstrates that the
inherent structure of certain DNA regions might promote catalytic
reactions, leading to genomic instability.