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Vol. 11, Issue 1, 201-215, January 2000
Department of Genetics, Cell Biology, and Development, University
of Minnesota, Minneapolis, Minnesota 55455
Ciliary and flagellar microtubules contain a specialized set of
three protofilaments, termed ribbons, that are composed of tubulin and
several associated proteins. Previous studies of sea urchin sperm
flagella identified three of the ribbon proteins as
tektins, which form coiled-coil filaments in doublet
microtubules and which are associated with basal bodies and centrioles.
To study the function of tektins and other ribbon proteins in the assembly of flagella and basal bodies, we have begun an analysis of
ribbons from the unicellular biflagellate, Chlamydomonas
reinhardtii, and report here the molecular characterization of
the ribbon protein rib43a. Using antibodies against rib43a to screen an
expression library, we recovered a full-length cDNA clone that encodes
a 42,657-Da polypeptide. On Northern blots, the rib43a cDNA hybridized to a 1.7-kb transcript, which was up-regulated upon deflagellation, consistent with a role for rib43a in flagellar assembly. The cDNA was
used to isolate RIB43a, an ~4.6-kb genomic clone
containing the complete rib43a coding region, and restriction fragment
length polymorphism analysis placed the RIB43a
gene on linkage group III. Sequence analysis of the
RIB43a gene indicates that the substantially coiled-coil
rib43a protein shares a high degree of sequence identity with clones
from Trypanosoma cruzi and Homo sapiens
(genomic, normal fetal kidney, and endometrial and germ cell tumors)
but little sequence similarity to other proteins including tektins. Affinity-purified antibodies against native and bacterially expressed rib43a stained both flagella and basal bodies by immunofluorescence microscopy and stained isolated flagellar ribbons by immuno-electron microscopy. The structure of rib43a and its association with the specialized protofilament ribbons and with basal bodies is relevant to
the proposed role of ribbons in forming and stabilizing doublet and
triplet microtubules and in organizing their three-dimensional structure.
Corresponding author. E-mail address:
linck{at}lenti.med.umn.edu.
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