Affiliation:
1. Laboratoire de Biochimie, URA 1970 CNRS, Ecole Polytechnique, 91128 Palaiseau Cedex, France
Abstract
ABSTRACT
The putative human tumor suppressor gene
FHIT
(fragile histidine triad) (M. Ohta et al., Cell 84:587–597, 1996) encodes a protein behaving in vitro as a dinucleoside 5′,5′′′-P
1
,P
3
-triphosphate (Ap
3
A) hydrolase. In this report, we show that the
Saccharomyces cerevisiae APH1
gene product, which resembles human Fhit protein, also hydrolyzes dinucleoside 5′,5′-polyphosphates, with Ap
3
A being the preferred substrate. Accordingly, disruption of the
APH1
gene produced viable
S. cerevisiae
cells containing reduced Ap
3
A-hydrolyzing activity and a 30-fold-elevated Ap
3
N concentration.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
23 articles.
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