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Originally published In Press as doi:10.1074/jbc.M006589200 on December 4, 2000
J. Biol. Chem., Vol. 276, Issue 13, 10320-10329, March 30, 2001
Possible Roles of Protein Kinase A in Cell Motility and
Excystation of the Early Diverging Eukaryote Giardia
lamblia*
Erika S.
Abel ,
Barbara J.
Davids§,
Liza D.
Robles ,
Clarence
E.
Loflin ,
Frances D.
Gillin§, and
Ratna
Chakrabarti ¶
From the Department of Molecular Biology and
Microbiology, University of Central Florida, Orlando, Florida 32826 and the § Department of Pathology, Division of Infectious
Diseases, University of California, School of Medicine,
San Diego, California 92103
Since little is known of how the primitive
protozoan parasite, Giardia lamblia, senses and responds to
its changing environment, we characterized a giardial protein kinase A
(gPKA) catalytic subunit with unusual subcellular localization.
Sequence analysis of the 1080-base pair open reading frame shows 48%
amino acid identity with the cyclic AMP-dependent kinase
from Euglena gracilis. Northern analysis
indicated a 1.28- kilobase pair transcript at relatively constant
concentrations during growth and encystation. gPKA is
autophosphorylated, although amino acid residues
corresponding to Thr-197 and Ser-338 of human protein kinase A
(PKA) that are important for autophosphorylation are absent. Kinetic
analysis of the recombinant PKA showed that ATP and magnesium are
preferred over GTP and manganese. Kinase activity of the native PKA has also been detected in crude extracts using kemptide as a substrate. A
myristoylated PKA inhibitor, amide 14-22, inhibited excystation with an
IC50 of 3 µM, suggesting an important role of
gPKA during differentiation from the dormant cyst form into the active
trophozoite. gPKA localizes independently of cell density to the eight
flagellar basal bodies between the two nuclei together with centrin, a
basal body/centrosome-specific protein. However, localization of gPKA to marginal plates along the intracellular portions of the anterior and
caudal pairs of flagella was evident only at low cell density and
higher endogenous cAMP concentrations or after refeeding with fresh
medium. These data suggest an important role of PKA in trophozoite motility during vegetative growth and the cellular activation of excystation.
*
This work was supported by Grants GM53835, AI42488, and
DK35108 from the National Institutes of Health and funds from the College of Health and Public Affairs, University of Central Florida.The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
AF181097.
¶
To whom correspondence should be addressed: Dept. of Molecular
Biology and Microbiology, Biomolecular Research Annex, University of
Central Florida, 12722 Research Pkwy., Orlando, FL 32826-2362. Tel.:
407-384-2187; Fax: 407-384-2062; E-mail:
rchak@pegasus.cc.ucf.edu.
Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 2001 by the American Society for Biochemistry and Molecular Biology.
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