4.7 Review

Studying Chromatin Epigenetics with Fluorescence Microscopy

Journal

Publisher

MDPI
DOI: 10.3390/ijms23168988

Keywords

epigenetics; histone modification; fluorescent proteins; genetically encoded probes

Funding

  1. Russian Science Foundation [22-14-00141]

Ask authors/readers for more resources

This review focuses on fluorescent probes for histone modification detection, discussing various live-cell imaging epigenetic sensors suitable for different types of fluorescence microscopy. It also highlights the problems and future perspectives in the development of fluorescent probes for epigenetics.
Epigenetic modifications of histones (methylation, acetylation, phosphorylation, etc.) are of great importance in determining the functional state of chromatin. Changes in epigenome underlay all basic biological processes, such as cell division, differentiation, aging, and cancerous transformation. Post-translational histone modifications are mainly studied by immunoprecipitation with high-throughput sequencing (ChIP-Seq). It enables an accurate profiling of target modifications along the genome, but suffers from the high cost of analysis and the inability to work with living cells. Fluorescence microscopy represents an attractive complementary approach to characterize epigenetics. It can be applied to both live and fixed cells, easily compatible with high-throughput screening, and provide access to rich spatial information down to the single cell level. In this review, we discuss various fluorescent probes for histone modification detection. Various types of live-cell imaging epigenetic sensors suitable for conventional as well as super-resolution fluorescence microscopy are described. We also focus on problems and future perspectives in the development of fluorescent probes for epigenetics.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available