Zuker (1994) This ancestral "eye" may have been just a single or a few photoreceptive cells, the development of which was controlled by genetic cascade from Pax-6.
There are however arguments against the hypothesis that Pax-6 illustrates the monophyly of extant eyes. Firstly there is evidence that Pax-6 homologues are expressed in sea urchins and nematodes, neither of which has eyes. Other evidence is that Pax-6 also plays a role in the development of other tissues in the brain and is not exclusively involved in eye development (Fernald,1997). Many homologous developmental patterns have been found between invertebrates and vertebrates, for example the hom/hox genes.Although there are homolgous molecules in the developmental cascades of diverse eyes, Fernald, 1997 argues that this does not mean that the structures themselves are. It is interesting to note that the evolutionary conservation of Pax genes is higher than for Hox genes (Quiring et al, 1994). The model of eye evolution that argues against the common origin of metazoan eyes, must therefore propose the independent recruitment of the Pax-6gene, after the eyes diversified. However (Sheng et al,1997) suggest that the model of a common ancestor of eyes is more parsimonous, since recruitment of Pax-6 would only have had to occur once. It is suggested that Pax-6 may be "locked in" to the regulation of eye development because of its ancient function of directly targetting photoreceptor molecule genes such as rh. It would be interesting now to see where if at all flatworms with primitive eye spots express Pax-6 (Sheng et al,1997, Zuker, 1994).