The sites of microtubule assembly in neurites of cultured chick retina
l neurons were assessed by double indirect immunofluorescence using an
tibodies specific for tyrosinated and detyrosinated tubulin. Tyrosinat
ed microtubules were distributed all over the neuron while detyrosinat
ed microtubules were found only in long neurites. When cultures were i
ncubated with nocodazole, the tyrosinated but not the detyrosinated mi
crotubules were disassembled. The sites of appearance of tyrosinated m
icrotubules after a reversible depolymerization by nocodazole were exa
mined in neurons bearing one unique and long neurite. One minute after
releasing the drug, tyrosinated microtubules quickly appeared as a sh
ort segment at the neurite tip and as spots periodically distributed a
long the neurite length. At longer times, the tyrosinated microtubules
depicted a segmented pattern along the neurite reaching a continuous
pattern at about 60 min. Our results suggest that the neurite cytoskel
eton is composed by microtubules of low (detyrosinated) and high (tyro
sinated) dynamism. Dynamic tyrosinated microtubules could be formed al
ong the entire length and at the tip of the axon-like neurite using de
tyrosinated microtubules as primers.