Institute of Biology, Leiden University, Leiden, the Netherlands.
Institute of Biology, Leiden University, Leiden, the Netherlands.
Biochim Biophys Acta Gene Regul Mech. 2021 Jun-Jul;1864(6-7):194714. doi: 10.1016/j.bbagrm.2021.194714. Epub 2021 May 7.
Dependent on phosphate availability the yeast Saccharomyces cerevisiae expresses either low or high affinity phosphate transporters. In the presence of phosphate yeast cells still express low levels of the high affinity phosphate transporter Pho84. The regulator Spl2 is expressed in approximately 90% of the cells, and is not expressed in the remaining cells. Here we report that deletion of RRP6, encoding an exonuclease degrading non-coding RNA, or BMH1, encoding the major 14-3-3 isoform, resulted in less cells expressing SPL2 and in increased levels of RNA transcribed from sequences upstream of the SPL2 coding region. SPL2 stimulates its own expression and that of PHO84 ensuing a positive feedback. Upon deletion of the region responsible for upstream SPL2 transcription almost all cells express SPL2. These results indicate that the cell-to-cell variation in PHO84 and SPL2 expression is dependent on a specific part of the SPL2 promoter and is controlled by Bmh1 and Spl2.
依赖于磷酸盐的可用性,酵母酿酒酵母表达低亲和力或高亲和力的磷酸盐转运蛋白。在磷酸盐存在的情况下,酵母细胞仍然表达低水平的高亲和力磷酸盐转运蛋白 Pho84。调节剂 Spl2 在大约 90%的细胞中表达,而在其余的细胞中不表达。在这里,我们报告说,编码外切核酸酶降解非编码 RNA 的 RRP6 或编码主要 14-3-3 同工型的 BMH1 的缺失导致表达 SPL2 的细胞减少,并且来自 SPL2 编码区域上游序列的转录 RNA 水平增加。SPL2 刺激其自身的表达和 PHO84 的表达,从而产生正反馈。当删除负责 SPL2 转录上游的区域时,几乎所有的细胞都表达 SPL2。这些结果表明,PHO84 和 SPL2 表达的细胞间变化依赖于 SPL2 启动子的特定部分,并受 Bmh1 和 Spl2 控制。