The GATA transcription factor gene gtaG is required for terminal differentiation in Dictyostelium

被引:4
|
作者
Katoh-Kurasawa, Mariko [1 ]
Santhanam, Balaji [1 ]
Shaulsky, Gad [1 ]
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
GtaG; Dictyostelium; Terminal differentiation; c-di-GMP; SDF-1; ENZYME-MEDIATED INTEGRATION; STALK CELL-DIFFERENTIATION; SPORE DIFFERENTIATION; PRESTALK CELLS; DD-STATA; DISCOIDEUM; EXPRESSION; FAMILY; CULMINATION; MATURATION;
D O I
10.1242/jcs.181545
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The GATA transcription factor GtaG is conserved in Dictyostelids and is 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 (Dd-STATa is also known as DstA) as well as Dd-STATa target-genes, including extracellular matrix genes. We show that GtaG might be involved in the production of two culmination-signaling molecules, cyclic di-GMP (c-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.
引用
收藏
页码:1722 / 1733
页数:12
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