School of Life Sciences, University of Dundee, Dow St., Dundee DD3 5EH, UK.
Dev Biol. 2010 Mar 15;339(2):390-7. doi: 10.1016/j.ydbio.2009.12.045. Epub 2010 Jan 18.
The mature fruiting body of Dictyostelium consists of stalk and spore cells but its construction, and the migration of the preceding slug stage, requires a number of specialized sub-types of prestalk cell whose nature and function are not well understood. The prototypic prestalk-specific gene, ecmA, is inducible by the polyketide DIF-1 in a monolayer assay and requires the DimB and MybE transcription factors for full inducibility. We perform genome-wide microarray analyses, on parental, mybE- and dimB- cells, and identify many additional genes that depend on MybE and DimB for their DIF-1 inducibility. Surprisingly, an even larger number of genes are only DIF inducible in mybE- cells, some genes are only inducible in DimB- cells and some are inducible when either transcription factor is absent. Thus in assay conditions where MybE and DimB function as inducers of ecmA these genes fall under negative control by the same two transcription factors. We have studied in detail rtaA, one of the MybE and DimB repressed genes. One especially enigmatic group of prestalk cells is the anterior-like cells (ALCs), which exist intermingled with prespore cells in the slug. A promoter fusion reporter gene, rtaA:gal(u), is expressed in a subset of the ALCs that is distinct from the ALC population detected by a reporter construct containing ecmA and ecmB promoter fragments. At culmination, when the ALC sort out from the prespore cells and differentiate to form three ancillary stalk cell structures: the upper cup, the lower cup and the outer basal disk, the rtaA:gal(u) expressing cells preferentially populate the upper cup region. This fact, and their virtual absence from the anterior and posterior regions of the slug, identifies them as a new prestalk sub-type: the pstU cells. PstU cell differentiation is, as expected, increased in a dimB- mutant during normal development but, surprisingly, they differentiate normally in a mutant lacking DIF. Thus genetic removal of MybE or DimB reveals an alternate DIF-1 activation pathway, for pstU differentiation, that functions under monolayer assay conditions but that is not essential during multicellular development.
Dictyostelium 的成熟生殖体由柄细胞和孢子细胞组成,但它的结构和前 slug 阶段的迁移需要许多专门的前柄细胞亚型,其性质和功能尚未完全理解。原型前柄特异性基因 ecmA 在单层测定中可被聚酮 DIF-1 诱导,并且完全诱导需要 DimB 和 MybE 转录因子。我们对亲本、mybE-和 dimB-细胞进行全基因组微阵列分析,并鉴定出许多其他依赖 MybE 和 DimB 才能对 DIF-1 诱导的基因。令人惊讶的是,甚至更多的基因仅在 mybE-细胞中才对 DIF 有诱导作用,一些基因仅在 DimB-细胞中诱导,而一些基因在两个转录因子缺失时才诱导。因此,在 MybE 和 DimB 作为 ecmA 诱导物起作用的测定条件下,这些基因受到相同两个转录因子的负调控。我们详细研究了 MybE 和 DimB 抑制的基因之一 rtaA。前柄细胞中一个特别神秘的群体是类似前体细胞 (ALCs),它们与 slug 中的前孢子细胞混合存在。rtaA:gal(u)启动子融合报告基因在一个与包含 ecmA 和 ecmB 启动子片段的报告构建体检测到的 ALC 群体不同的亚群 ALCs 中表达。在 culmination 时,当 ALC 从前孢子细胞中分离出来并分化形成三个辅助柄细胞结构:上杯、下杯和外基底盘时,rtaA:gal(u)表达细胞优先填充在上杯区域。这一事实以及它们在前部和后部 slug 中几乎不存在,将它们鉴定为一种新的前柄细胞亚型:pstU 细胞。pstU 细胞分化在正常发育过程中在 dimB-突变体中增加,如预期的那样,但令人惊讶的是,它们在缺乏 DIF 的突变体中正常分化。因此,MybE 或 DimB 的遗传缺失揭示了 pstU 分化的另一种 DIF-1 激活途径,该途径在单层测定条件下起作用,但在多细胞发育过程中并非必不可少。