FLCCR是一种荧光报告系统,在单细胞水平上量化分裂酵母不同细胞周期阶段的持续时间。

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI:10.1371/journal.pbio.3002969
Guillem Murciano-Julià, Marina Francos-Cárdenas, Clàudia Salat-Canela, Elena Hidalgo, José Ayté
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引用次数: 0

摘要

裂变酵母是一种优良的模型系统,已被广泛用于研究细胞周期进程的调控机制。然而,缺乏能够高精度测量单个细胞中细胞周期不同阶段持续时间的工具。为了避免这个问题,我们开发了一种荧光报告器,可以在大多数遗传背景下在单细胞水平上定量细胞周期的不同阶段。为了证明该荧光报告因子的准确性,我们在已知G1/S或G2/M过渡有延迟的菌株中测试了报告因子,证实了该系统的强度和通用性。这种方法的一个优点是,它消除了培养同步的需要,避免了对细胞的压力。利用这个报告基因,我们发现缺乏Sty1的未受干扰的细胞具有标准的细胞周期长度和分布,并且这些细胞的长度延长是由于细胞生长速度的增加,而不是由于细胞周期进程的改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FLCCR is a fluorescent reporter system that quantifies the duration of different cell cycle phases at the single-cell level in fission yeast.

Fission yeast is an excellent model system that has been widely used to study the mechanism that control cell cycle progression. However, there is a lack of tools that allow to measure with high precision the duration of the different phases of the cell cycle in individual cells. To circumvent this problem, we have developed a fluorescent reporter that allows the quantification of the different phases of the cell cycle at the single-cell level in most genetic backgrounds. To prove the accuracy of this fluorescent reporter, we have tested the reporter in strains known to have a delay in the G1/S or G2/M transitions, confirming the strength and versatility of the system. An advantage of this reporter is that it eliminates the need for culture synchronization, avoiding stressing the cells. Using this reporter, we show that unperturbed cells lacking Sty1 have a standard cell cycle length and distribution and that the extended length of these cells is due to their increased cell growth rate but not to alterations in their cell cycle progression.

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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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