Wasserstrom Lisa, Lengeler Klaus, Walther Andrea, Wendland Jürgen
Carlsberg Laboratory, Yeast Genetics, Copenhagen, Denmark.
Carlsberg Laboratory, Yeast Genetics, Copenhagen, Denmark
Eukaryot Cell. 2015 Jun;14(6):593-601. doi: 10.1128/EC.00045-15. Epub 2015 Apr 10.
Sporulation in Ashbya gossypii is induced by nutrient-limited conditions and leads to the formation of haploid spores. Using RNA-seq, we have determined a gene set induced upon sporulation, which bears considerable overlap with that of Saccharomyces cerevisiae but also contains A. gossypii-specific genes. Addition of cyclic AMP (cAMP) to nutrient-limited media blocks sporulation and represses the induction of sporulation specific genes. Deletion of the protein kinase A (PKA) catalytic subunits encoded by TPK1 and TPK2 showed reduced growth in tpk1 but enhanced growth in the tpk2 strain; however, both mutants sporulated well. Sporulation can be blocked by cAMP in tpk1 but not in tpk2 strains. Similarly, TPK2 acts at a second developmental switch promoting the break in spore dormancy. In S. cerevisiae, PKA phosphorylates and inhibits Msn2/4. The transcript profiles of the tpk1 and msn2/4 mutants were very similar to that of the wild type under sporulation conditions. However, deletion of the single A. gossypii MSN2/4 homolog generated a specific sporulation defect. We identified a set of genes involved in spore wall assembly that was downregulated in the msn2/4 mutant, particularly DIT2, suggesting that poor spore viability may be due to lysis of spores. Our results reveal specific functional differences between the two catalytic PKA subunits in A. gossypii and identified Tpk2 as the key A kinase that transduces developmental decisions of growth. Our data also suggest that Msn2/4 is involved only at a late step of sporulation in A. gossypii and is not a major regulator of IME1.
棉阿舒囊霉(Ashbya gossypii)中的孢子形成由营养受限条件诱导,并导致单倍体孢子的形成。利用RNA测序,我们确定了一组在孢子形成时被诱导的基因,该基因集与酿酒酵母(Saccharomyces cerevisiae)的基因集有相当大的重叠,但也包含棉阿舒囊霉特有的基因。向营养受限的培养基中添加环磷酸腺苷(cAMP)可阻断孢子形成,并抑制孢子形成特异性基因的诱导。由TPK1和TPK2编码的蛋白激酶A(PKA)催化亚基的缺失显示,tpk1菌株的生长受到抑制,而tpk2菌株的生长增强;然而,这两个突变体都能很好地形成孢子。cAMP可在tpk1菌株中阻断孢子形成,但在tpk2菌株中则不能。同样,TPK2在促进孢子休眠打破的第二个发育转换中起作用。在酿酒酵母中,PKA磷酸化并抑制Msn2/4。在孢子形成条件下,tpk1和msn2/4突变体的转录谱与野生型非常相似。然而,棉阿舒囊霉单个Msn2/4同源物的缺失产生了特定的孢子形成缺陷。我们鉴定出一组参与孢子壁组装的基因,这些基因在msn2/4突变体中表达下调,特别是DIT2,这表明孢子活力差可能是由于孢子裂解所致。我们的结果揭示了棉阿舒囊霉中两个催化PKA亚基之间的特定功能差异,并确定Tpk2是转导生长发育决定的关键A激酶。我们的数据还表明,Msn2/4仅在棉阿舒囊霉孢子形成的后期参与,并且不是IME1的主要调节因子。