|
|
|
|
|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
|
Fig. 6. Disruption of the DeltaD-MAGI interaction causes mislocalization of
Rohon-Beard neurons. (A-D) Dorsal views of embryos at 16 hpf stained by in
situ hybridization for islet1 (black) to mark Rohon-Beard
neurons (as well as other primary neurons below the plane of focus).
myoD (brown) expression serves as a reference for somite number and
position. aei embryos (C,D) show a 1.6-fold increase in the number of
Rohon-Beard cells compared to wild-type embryos (A), whereas the number of
these cells is only slightly increased in wild-type embryos injected with
MO[dlD-V] (B). The MO[dlD-V] embryos are abnormal, however, in that many of
the Rohon-Beard cells stray into the midline region. The proportion of such
mislocalized cells is not affected by the morpholino in aei embryos,
where DeltaD is missing (C,D). (E,F) Cell counts. The distribution of the
neurons was quantified for a region corresponding approximately to somites 5
to 10; 10-13 embryos were analysed for each condition. Error bars represent
s.e.m. Scale bar: 50 mm for A-D.
|
