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G1/S 转录因子拷贝数是酵母细胞周期启动的生长依赖性决定因素。

G1/S Transcription Factor Copy Number Is a Growth-Dependent Determinant of Cell Cycle Commitment in Yeast.

机构信息

Department of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.

Institute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC H3T 1J4, Canada; Wellcome Trust Centre for Cell Biology, Institute of Cell Biology, School of Biological Sciences, The University of Edinburgh, Edinburgh EH9 3JR, UK.

出版信息

Cell Syst. 2018 May 23;6(5):539-554.e11. doi: 10.1016/j.cels.2018.04.012.

Abstract

To understand how commitment to cell division in late G1 phase (Start) is controlled by growth and nutrients in budding yeast, we determined the absolute concentrations of the G1/S transcription factors SBF (composed of Swi4 and Swi6) and MBF (composed of Mbp1 and Swi6), the transcriptional repressor Whi5, and the G1 cyclins, Cln1 and Cln2, in single live yeast cells using scanning number and brightness (sN&B) microscopy. In rich medium, Whi5, Mbp1, and Swi6 concentrations were independent of cell size, whereas Swi4 concentration doubled in G1 phase, leading to a size-dependent decrease in the Whi5/Swi4 ratio. In small cells, SBF and MBF copy numbers were insufficient to saturate target G1/S promoters, but this restriction diminished as cells grew in size. In poor medium, SBF and MBF subunits, as well as Cln1, were elevated, consistent with a smaller cell size at Start. A mathematical model constrained by sN&B data suggested that size- and nutrient-dependent occupancy of G1/S promoters by SBF/MBF helps set the cell size threshold for Start activation.

摘要

为了理解芽殖酵母中细胞分裂在 G1 晚期(起始点)的分裂是如何被生长和营养物质控制的,我们使用扫描数字和亮度(sN&B)显微镜,在单个活酵母细胞中测定了 G1/S 转录因子 SBF(由 Swi4 和 Swi6 组成)和 MBF(由 Mbp1 和 Swi6 组成)、转录抑制因子 Whi5 以及 G1 周期蛋白 Cln1 和 Cln2 的绝对浓度。在丰富的培养基中,Whi5、Mbp1 和 Swi6 的浓度与细胞大小无关,而 Swi4 的浓度在 G1 期增加了一倍,导致 Whi5/Swi4 比值随细胞大小而下降。在小细胞中,SBF 和 MBF 的拷贝数不足以使靶 G1/S 启动子饱和,但随着细胞体积的增大,这种限制会减小。在贫培养基中,SBF 和 MBF 亚基以及 Cln1 升高,与起始点的细胞体积较小一致。受 sN&B 数据约束的数学模型表明,SBF/MBF 对 G1/S 启动子的大小和营养依赖性占据有助于确定起始激活的细胞大小阈值。

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