Lineage-specific regulators couple cell lineage asymmetry to the transcription of the Caenorhabditis elegans POU gene unc-86 during neurogenesis

被引:72
作者
Baumeister, R
Liu, YX
Ruvkun, G
机构
[1] HARVARD UNIV, MASSACHUSETTS GEN HOSP, SCH MED, DEPT BIOL MOLEC, BOSTON, MA 02114 USA
[2] HARVARD UNIV, SCH MED, DEPT GENET, BOSTON, MA 02114 USA
关键词
POU homeo domain protein; C-elegans; neurogenesis; unc-86; asymmetric cell division; transcriptional regulation;
D O I
10.1101/gad.10.11.1395
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The POU homeo box gene unc-86 specifies neuroblast and neural identities in the developing Caenorhabditis elegans nervous system. After an asymmetric neuroblast division, unc-86 is expressed in one of two daughter cells in 27 lineage classes that are not obviously related by function or position. We show here that unc-86 transcriptional regulatory regions detect cell lineage asymmetry to activate unc-86 expression in one of two neuroblast daughter cells. Distinct regulatory regions activate unc-86 expression in particular sets of sublineages. Therefore the unc-86 regulatory region integrates distinct cell lineage asymmetry cues to activate unc-86 expression in the many classes of neuroblast cell lineages. In agreement with such lineage-specific regulation of unc-86 asymmetric activation, mutations in lin-11 (LIM homeo box), ham-1, and lin-17 affect the asymmetry of unc-86 expression in particular cell lineages, and mutations in lin-32 (achaete/scute family), vab-3 (Pax-G homolog) and egl-5 (Abd-B homolog) affect the establishment of unc-86 expression in other cell lineages. Homologs of unc-86 and many of these unc-86 regulators have been implicated in control of neurogenesis in vertebrates and invertebrates. These data suggest that unc-86 acts in a phylogenetically conserved pathway that couples neuroblast cell lineage asymmetry to the generation of diverse neural types.
引用
收藏
页码:1395 / 1410
页数:16
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