Katoh-Kurasawa Mariko, Santhanam Balaji, Shaulsky Gad
Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston TX 77030, USA
Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston TX 77030, USA.
J Cell Sci. 2016 Apr 15;129(8):1722-1733. doi: 10.1242/jcs.181545.
The GATA transcription factor GtaG is conserved in Dictyostelids and essential for terminal differentiation in Dictyostelium discoideum, but its function is not well understood. Here we show that gtaG is expressed in prestalk cells at the anterior region of fingers and in the extending stalk during culmination. The gtaG phenotype is cell-autonomous in prestalk cells and non-cell-autonomous in prespore cells. Transcriptome analyses reveal that GtaG regulates prestalk gene expression during cell differentiation before culmination and is required for progression into culmination. GtaG-dependent genes include genetic suppressors of the Dd-STATa-defective phenotype as well as Dd-STATa target-genes, including extra cellular matrix genes. We show that GtaG may be involved in the production of two culmination-signaling molecules, cyclic di-GMP and the spore differentiation factor SDF-1 and that addition of c-di-GMP rescues the gtaG culmination and spore formation deficiencies. We propose that GtaG is a regulator of terminal differentiation that functions in concert with Dd-STATa and controls culmination through regulating c-di-GMP and SDF-1 production in prestalk cells.
GATA转录因子GtaG在盘基网柄菌中保守,对其终末分化至关重要,但其功能尚不清楚。我们在此表明,gtaG在指状结构前部的前柄细胞以及发育成熟过程中延伸的柄中表达。gtaG表型在前柄细胞中是细胞自主的,而在孢子前体细胞中是非细胞自主的。转录组分析表明,GtaG在发育成熟前的细胞分化过程中调节前柄基因表达,并且是发育成熟所必需的。GtaG依赖的基因包括Dd-STATa缺陷表型的遗传抑制因子以及Dd-STATa靶基因,包括细胞外基质基因。我们表明,GtaG可能参与两种发育成熟信号分子环二鸟苷酸和孢子分化因子SDF-1的产生,并且添加环二鸟苷酸可挽救gtaG发育成熟和孢子形成缺陷。我们提出,GtaG是终末分化的调节因子,与Dd-STATa协同发挥作用,并通过调节前柄细胞中环二鸟苷酸和SDF-1的产生来控制发育成熟。