Department of Molecular Genetics, The Ohio State University, Columbus, OH, 43210, USA.
Department of Human Nutrition, The Ohio State University, Columbus, OH, 43210, USA.
Mol Microbiol. 2019 Dec;112(6):1701-1717. doi: 10.1111/mmi.14384. Epub 2019 Sep 24.
In Schizosaccharomyces pombe, the expression of the zrt1 zinc uptake gene is tightly regulated by zinc status. When intracellular zinc levels are low, zrt1 is highly expressed. However, when zinc levels are high, transcription of zrt1 is blocked in a manner that is dependent upon the transcription factor Loz1. To gain additional insight into the mechanism by which Loz1 inhibits gene expression in high zinc, we used RNA-seq to identify Loz1-regulated genes, and ChIP-seq to analyze the recruitment of Loz1 to target gene promoters. We find that Loz1 is recruited to the promoters of 27 genes that are also repressed in high zinc in a Loz1-dependent manner. We also find that the recruitment of Loz1 to the majority of target gene promoters is dependent upon zinc and the motif 5'-CGN(A/C)GATCNTY-3', which we have named the Loz1 response element (LRE). Using reporter assays, we show that LREs are both required and sufficient for Loz1-mediated gene repression, and that the level of gene repression is dependent upon the number and sequence of LREs. Our results elucidate the Loz1 regulon in fission yeast and provide new insight into how eukaryotic cells are able to respond to changes in zinc availability in the environment.
在裂殖酵母中,zrt1 锌摄取基因的表达受到锌状态的严格调控。当细胞内锌水平较低时,zrt1 高度表达。然而,当锌水平较高时,zrt1 的转录被依赖于转录因子 Loz1 的方式阻断。为了更深入地了解 Loz1 如何在高锌条件下抑制基因表达,我们使用 RNA-seq 鉴定了 Loz1 调控的基因,并通过 ChIP-seq 分析了 Loz1 向靶基因启动子的募集情况。我们发现,Loz1 被募集到 27 个基因的启动子上,这些基因在高锌条件下也受到 Loz1 依赖的抑制。我们还发现,Loz1 对大多数靶基因启动子的募集依赖于锌和 5'-CGN(A/C)GATCNTY-3' 基序,我们将其命名为 Loz1 反应元件 (LRE)。通过报告基因实验,我们表明 LRE 对于 Loz1 介导的基因抑制是必需和充分的,并且基因抑制的程度取决于 LRE 的数量和序列。我们的研究结果阐明了裂殖酵母中的 Loz1 调控组,并为真核细胞如何能够响应环境中锌可用性的变化提供了新的见解。