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Vol. 9, Issue 8, 2093-2106, August 1998

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and
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*Department of Biochemistry and Cell Biology, Rice University,
Houston Texas 77005;
The cellular slime mold Dictyostelium discoideum is
an attractive system for studying the roles of microtubule-based
motility in cell development and differentiation. In this work, we
report the first molecular characterization of kinesin-related proteins (KRPs) in Dictyostelium. A PCR-based strategy was used
to isolate DNA fragments encoding six KRPs, several of which are
induced during the developmental program that is initiated by
starvation. The complete sequence of one such developmentally regulated
KRP (designated K7) was determined and found to be a novel member of
the kinesin superfamily. The motor domain of K7 is most similar to that
of conventional kinesin, but unlike conventional kinesin, K7 is not
predicted to have an extensive
Department of Molecular and
Cellular Pharmacology and
¶Howard Hughes Medical
Institute, University of California, San Francisco, California 94143;
and
Department of Biochemistry, Baylor College of
Medicine, Houston Texas 77030
-helical coiled-coil domain. The
nonmotor domain is unusual and is rich in Asn, Gln, and Thr residues;
similar sequences are found in other developmentally regulated genes in
Dictyostelium. K7, expressed in Escherichia coli, supports plus end-directed microtubule motility in vitro at a speed of 0.14 µm/s, indicating that it is a bona fide motor protein. The K7 motor is found only in developing cells and reaches a
peak level of expression between 12 and 16 h after starvation. By
immunofluorescence microscopy, K7 localizes to a membranous perinuclear
structure. To examine K7 function, we prepared a null cell line but
found that these cells show no gross developmental abnormalities.
However, when cultivated in the presence of wild-type cells, the
K7-null cells are mostly absent from the prestalk zone of the slug.
This result suggests that in a population composed largely of wild-type
cells, the absence of the K7 motor protein interferes either with the
ability of the cells to localize to the prestalk zone or to
differentiate into prestalk cells.
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