MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital, Edinburgh, UK.
RILD Building, University of Exeter, Royal Devon and Exeter Hospital, Exeter, Devon, UK.
Methods Mol Biol. 2024;2818:249-270. doi: 10.1007/978-1-0716-3906-1_17.
Prophase I is a remarkable stage of meiotic division during which homologous chromosomes pair together and exchange DNA by meiotic recombination. Fluorescence microscopy of meiotic chromosome spreads is a central tool in the study of this process, with chromosome axis proteins being visualized as extended filaments upon which recombination proteins localize in focal patterns.Chromosome pairing and recombination are dynamic processes, and hundreds of recombination foci can be present in some meiotic nuclei. As meiotic nuclei can exhibit significant variations in staining patterns within and between nuclei, particularly in mutants, manual analysis of images presents challenges for consistency, documentation, and reproducibility. Here we share a combination of complementary computational tools that can be used to partially automate the quantitative analysis of meiotic images. (1) The segmentation of axial and focal staining patterns to automatically measure chromosome axis length and count axis-associated (and non-axis associated) recombination foci; (2) Quantification of focus position along chromosome axes to investigate spatial regulation; (3) Simulation of random distributions of foci within the nucleus or along the chromosome axes to statistically investigate observed foci-axis associations and foci-foci associations; (4) Quantification of chromosome axis proximity to investigate relationships with chromosome synapsis/asynapsis; (5) Quantification of and orientation of focus-axis distances. Together, these tools provide a framework to perform routine documentation and analysis of meiotic images, as well as opening up routes to build on this initial output and perform more detailed analyses.
前期 I 是减数分裂过程中一个显著的阶段,在此期间同源染色体配对并通过减数重组交换 DNA。对减数分裂染色体展开的荧光显微镜观察是研究这一过程的核心工具,染色体轴蛋白在重组蛋白以焦点模式定位的情况下被可视化成长度的丝状结构。染色体配对和重组是动态过程,在一些减数分裂核中可以存在数百个重组焦点。由于减数分裂核在核内和核间表现出显著的染色模式变化,特别是在突变体中,图像的手动分析在一致性、文档记录和可重复性方面提出了挑战。在这里,我们分享了一系列互补的计算工具,可以部分自动化减数分裂图像的定量分析。(1)轴和焦点染色模式的分割,以自动测量染色体轴长度并计数轴相关(和非轴相关)重组焦点;(2)焦点沿染色体轴位置的定量分析,以研究空间调节;(3)在核内或沿染色体轴模拟焦点的随机分布,以统计研究观察到的焦点-轴关联和焦点-焦点关联;(4)染色体轴接近程度的量化,以研究与染色体联会/不联会的关系;(5)焦点-轴距离的量化和取向。这些工具共同提供了一个框架,用于对减数分裂图像进行常规的文档记录和分析,并为在初始输出的基础上进行更详细的分析开辟了途径。