V. Nguyen et al., Morphogenesis of the optic tectum in the medaka (Oryzias latipes): A morphological and molecular study, with special emphasis on cell proliferation, J COMP NEUR, 413(3), 1999, pp. 385-404
We analyzed the medaka optic tectum (OT) morphogenesis by using 5-bromo-2'-
deoxyuridine (BrdU) immunohistochemistry (with a new method we developed fo
r pulse-labeling embryos) and in situ hybridization with three probes, two
for recently cloned homeobox genes (Ol-Prx3 [Paired-Related-Homeobox3] and
Ol-Gsh1 [Genetic-Screen-Homeobox1:]) and one for Ol-tailless. The tectal an
lage first appears as a sheet of proliferating cells expressing Ol-Gsh1 and
Ol-tailless but not Ol-Prx3. Cells subsequently cease to proliferate in a
superficial and rostral zone and begin to express Ol-Prx3. When tectal lami
nation begins, the proliferative zone (mpz) becomes restricted to a crescen
t at the OT medial, caudal, and lateral margin. This mpz functions througho
ut the fish's entire life. It produces cells that are added at the OT's edg
e as radial rows, spanning every layer of the OT. The cells of the mpz cont
inue to express Ol tailless in the adult, whereas Ol-Gsh1 expression is tur
ned off. When superficial layers form, Ol-Prx3 expression becomes restricte
d to the underlying deep layer, where it persists in the adult. Ol-Prx3 see
ms to be a marker for the differentiation of a subset of deep cells and all
ows analysis of tectal lamination, whereas Ol-tailless and Ol-Gsh1 could be
involved in the control of tectal cell proliferation. This study constitut
es a first step toward molecular approach to OT development in anamniotes.
We compare and discuss the expression patterns of the homologs of the genes
studied, and more generally the morphogenetic patterns of the medaka tectu
m, with those encountered in other cortical structures and in other vertebr
ate groups. (C) 1999 Wiley-Liss, Inc.