Ll. Wang et Jc. Way, ACTIVATION OF THE MEC-3 PROMOTER IN 2 CLASSES OF STEREOTYPED LINEAGESIN CAENORHABDITIS-ELEGANS, Mechanisms of development, 56(1-2), 1996, pp. 165-181
The mec-3 gene of Caenorhabditis elegans encodes a homeodomain protein
and is expressed in one of two cells upon asymmetric cell division. A
s a result of asymmetric mec-3 expression, the two sister cells expres
s different fates, so mec-3 is a likely target for the machinery that
mediates asymmetric cell division. The unc-86 gene encodes a homeodoma
in protein of the POU family, which activates mec-3 by binding to its
promoter. The ten mec3-expressing cells are a subset of the anterior d
aughters of UNC-86-containing cells. Posterior daughters of UNC-86-con
taining cells do not express mec-3, even though the UNC-86 protein is
distributed into both daughter cells. Lineages that express the unc-86
and mec-3 genes can be grouped into two types: in Type I lineages, UN
C-86 protein is first made in the immediate parent of the terminal mec
-3-expressing cell, while in Type II lineages, UNC-86 is first made in
the grandparent of the terminal mec-3-expressing cell. The purpose of
experiments presented here is to understand the relationship between
the mec-3 expression patterns in each type of lineage, and to determin
e the fundamental activity pattern of the mec-3 promoter. We find that
in the Type I V5.pa lineage, mec-3-lacZ is first synthesized in the t
erminal PVDR neuron, one cell division after unc-86 is expressed. mec-
3 expression in PVDR can occur by transcriptional regulation alone; se
gregation of the mec-3 RNA or protein is not required to explain the a
symmetric expression of mec-3. In the Type: II Q lineage, the mec-3 pr
omoter activity can be detected in the immediate anterior daughter of
the first unc-86-expressing cell, but when this cell divides, mec-3 is
expressed in only one of its daughters at later times. It seems likel
y that, in the short-lived immediate anterior daughter cell in Type II
lineages, mec-3 product does not accumulate to levels that can influe
nce subsequent events. Our results suggest that the mec-3 promoter is
activated in all anterior daughters of unc-86-expressing cells.