Suppr超能文献

使用 APEX-染色质纤维进行着丝粒蛋白关联的高分辨率作图。

High-resolution mapping of centromeric protein association using APEX-chromatin fibers.

机构信息

Max-Planck Institute of Immunobiology and Epigenetics, Freiburg im Breisgau, Germany.

Faculty of Biology, Albert-Ludwigs Universität Freiburg, Freiburg im Breisgau, Germany.

出版信息

Epigenetics Chromatin. 2018 Nov 16;11(1):68. doi: 10.1186/s13072-018-0237-6.

Abstract

BACKGROUND

The centromere is a specialized chromosomal locus that forms the basis for the assembly of a multi-protein complex, the kinetochore and ensures faithful chromosome segregation during every cell division. The repetitive nature of the underlying centromeric sequence represents a major obstacle for high-resolution mapping of protein binding using methods that rely on annotated genomes. Here, we present a novel microscopy-based approach called "APEX-chromatin fibers" for localizing protein binding over the repetitive centromeric sequences at kilobase resolution.

RESULTS

By fusing centromere factors of interest to ascorbate peroxidase, we were able to label their binding profiles on extended chromatin fibers with biotin marks. We applied APEX-chromatin fibers to at least one member of each CCAN complex, most of which show a localization pattern different from CENP-A but within the CENP-A delineated centromeric domain. Interestingly, we describe here a novel characteristic of CENP-I and CENP-B that display extended localization beyond the CENP-A boundaries.

CONCLUSIONS

Our approach was successfully applied for mapping protein association over centromeric chromatin, revealing previously undescribed localization patterns. In this study, we focused on centromeric factors, but we believe that this approach could be useful for mapping protein binding patterns in other repetitive regions.

摘要

背景

着丝粒是一种特殊的染色体位置,它构成了多蛋白复合物——动粒的基础,并确保在每次细胞分裂中染色体的正确分离。其下的着丝粒序列的重复性质代表了使用依赖于注释基因组的方法进行高分辨率蛋白质结合作图的主要障碍。在这里,我们提出了一种新的基于显微镜的方法,称为“APEX-染色质纤维”,用于在千碱基分辨率上定位重复着丝粒序列上的蛋白质结合。

结果

通过将感兴趣的着丝粒因子与抗坏血酸过氧化物酶融合,我们能够在延伸的染色质纤维上用生物素标记标记它们的结合谱。我们将 APEX-染色质纤维应用于至少每个 CCAN 复合物的一个成员,其中大多数显示与 CENP-A 不同的定位模式,但在 CENP-A 划定的着丝粒域内。有趣的是,我们在这里描述了 CENP-I 和 CENP-B 的一个新特征,它们在 CENP-A 边界之外显示出延伸的定位。

结论

我们的方法成功地应用于在着丝粒染色质上绘制蛋白质关联图谱,揭示了以前未描述的定位模式。在这项研究中,我们专注于着丝粒因子,但我们相信这种方法在绘制其他重复区域的蛋白质结合模式方面可能很有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75d/6238281/703f2f91f4b1/13072_2018_237_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验