In the nematode Caenorhabditis elegans, a well-established model organism f
or the analysis of nervous system development and function, nerve processes
can be labelled in the intact animal with markers based on the "Green Fluo
rescent Protein" (GFP). The generation of GFP variants with improved bright
ness and modified emission spectra potentiated the use of this marker for i
n vivo labelling of subcellular structures. This made it possible to label
different groups of neurons and their axons in the same animal with GFP var
iants of different spectral characteristics. Here I show with double labell
ing experiments that spatial relationships of axons in small axon bundles c
an now be resolved at the light microscopic level. In the future this will
largely circumvent the need for time-consuming electron microscopic reconst
ructions to detect local defects in axon outgrowth. Furthermore, I demonstr
ate that neuronal processes can now be traced even in the head ganglia, an
area of the nervous system that was previously-almost inaccessible for anal
ysis due to the compact arrangement of cell bodies and axons. (C) 2000 Wile
y-Liss, Inc.