Sliva Anna, Kuang Zheng, Meluh Pamela B, Boeke Jef D
Institute for Systems Genetics, New York University Langone School of Medicine, New York 10016 Human Genetics Program, Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Institute for Systems Genetics, New York University Langone School of Medicine, New York 10016.
G3 (Bethesda). 2016 Apr 7;6(4):881-92. doi: 10.1534/g3.115.026757.
The yeast pheromone response pathway serves as a valuable model of eukaryotic mitogen-activated protein kinase (MAPK) pathways, and transcription of their downstream targets. Here, we describe application of a screening method combining two technologies: fluorescence-activated cell sorting (FACS), and barcode analysis by sequencing (Bar-Seq). Using this screening method, and pFUS1-GFP as a reporter for MAPK pathway activation, we readily identified mutants in known mating pathway components. In this study, we also include a comprehensive analysis of the FUS1 induction properties of known mating pathway mutants by flow cytometry, featuring single cell analysis of each mutant population. We also characterized a new source of false positives resulting from the design of this screen. Additionally, we identified a deletion mutant, sub1Δ, with increased basal expression of pFUS1-GFP. Here, in the first ChIP-Seq of Sub1, our data shows that Sub1 binds to the promoters of about half the genes in the genome (tripling the 991 loci previously reported), including the promoters of several pheromone-inducible genes, some of which show an increase upon pheromone induction. Here, we also present the first RNA-Seq of a sub1Δ mutant; the majority of genes have no change in RNA, but, of the small subset that do, most show decreased expression, consistent with biochemical studies implicating Sub1 as a positive transcriptional regulator. The RNA-Seq data also show that certain pheromone-inducible genes are induced less in the sub1Δ mutant relative to the wild type, supporting a role for Sub1 in regulation of mating pathway genes. The sub1Δ mutant has increased basal levels of a small subset of other genes besides FUS1, including IMD2 and FIG1, a gene encoding an integral membrane protein necessary for efficient mating.
酵母信息素反应途径是真核细胞丝裂原活化蛋白激酶(MAPK)途径及其下游靶标转录的重要模型。在此,我们描述了一种结合两种技术的筛选方法的应用:荧光激活细胞分选(FACS)和测序条形码分析(Bar-Seq)。使用这种筛选方法,并以pFUS1-GFP作为MAPK途径激活的报告基因,我们很容易地鉴定出已知交配途径成分中的突变体。在本研究中,我们还通过流式细胞术对已知交配途径突变体的FUS1诱导特性进行了全面分析,对每个突变群体进行了单细胞分析。我们还对该筛选设计产生的假阳性新来源进行了表征。此外,我们鉴定出一个缺失突变体sub1Δ,其pFUS1-GFP的基础表达增加。在此,在Sub1的首次染色质免疫沉淀测序(ChIP-Seq)中,我们的数据表明Sub1与基因组中约一半的基因启动子结合(使先前报道的991个位点增加了两倍),包括几个信息素诱导基因的启动子,其中一些在信息素诱导后表达增加。在此,我们还展示了sub1Δ突变体的首次RNA测序(RNA-Seq);大多数基因的RNA没有变化,但在少数有变化的基因中,大多数表达下降,这与将Sub1作为正转录调节因子的生化研究一致。RNA-Seq数据还表明,某些信息素诱导基因在sub1Δ突变体中相对于野生型的诱导程度较低,这支持了Sub1在交配途径基因调控中的作用。除了FUS1之外,sub1Δ突变体中一小部分其他基因的基础水平也有所增加,包括IMD2和FIG1,FIG1是一种编码高效交配所需的整合膜蛋白的基因。