Evidence map›Paper›PMID 36979066›Full record

ReviewBiology2023

On the Advent of Super-Resolution Microscopy in the Realm of Polycomb Proteins.

Irene Nepita, Simonluca Piazza, Martina Ruglioni, Sofia Cristiani, Emanuele Bosurgi, Tiziano Salvadori, Giuseppe Vicidomini, Alberto Diaspro, Marco Castello, Andrea Cerase and 3 more

Open access · goldFull text readReview
In one paragraph

Review in Biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Irene NepitaNanoscopy, Istituto Italiano di Tecnologia, Via E. Melen 83, 16152 Genova, Italy.ORCID 0000-0002-4343-0006
Simonluca PiazzaMolecular Microscopy and Spectroscopy, Istituto Italiano di Tecnologia, Via E. Melen 83, 16152 Genova, Italy.
Martina RuglioniDepartment of Surgical, Medical and Molecular Pathology, and Critical Care Medicine, University of Pisa, Via Roma 65, 56126 Pisa, Italy.
Sofia CristianiDepartment of Surgical, Medical and Molecular Pathology, and Critical Care Medicine, University of Pisa, Via Roma 65, 56126 Pisa, Italy.
Emanuele BosurgiDepartment of Surgical, Medical and Molecular Pathology, and Critical Care Medicine, University of Pisa, Via Roma 65, 56126 Pisa, Italy.
Tiziano SalvadoriDepartment of Surgical, Medical and Molecular Pathology, and Critical Care Medicine, University of Pisa, Via Roma 65, 56126 Pisa, Italy.
Giuseppe VicidominiMolecular Microscopy and Spectroscopy, Istituto Italiano di Tecnologia, Via E. Melen 83, 16152 Genova, Italy.
Alberto DiasproNanoscopy, Istituto Italiano di Tecnologia, Via E. Melen 83, 16152 Genova, Italy.ORCID 0000-0002-4916-5928
Marco CastelloNanoscopy, Istituto Italiano di Tecnologia, Via E. Melen 83, 16152 Genova, Italy.ORCID 0000-0002-4472-6968
Andrea CeraseUnit of Cell and Developmental Biology, Department of Biology, University of Pisa, Strada Statale dell'Abetone Brennero 4, 56123 Pisa, Italy.ORCID 0000-0002-1985-2049
Paolo BianchiniNanoscopy, Istituto Italiano di Tecnologia, Via E. Melen 83, 16152 Genova, Italy.ORCID 0000-0001-6457-751X
Barbara StortiNEST, Scuola Normale Superiore and Istituto Nanoscienze-CNR, Piazza San Silvestro 12, 56127 Pisa, Italy.ORCID 0000-0002-2758-0426
Ranieri BizzarriNanoscopy, Istituto Italiano di Tecnologia, Via E. Melen 83, 16152 Genova, Italy.ORCID 0000-0002-8222-2672
Italian Institute of Technology · ITUniversity of Pisa · ITIstituto Nanoscienze · IT

Funding

University of Pisa PRA_2020_77
6 · The paper itself

Abstract

The genomes of metazoans are organized at multiple spatial scales, ranging from the double helix of DNA to whole chromosomes. The intermediate genomic scale of kilobases to megabases, which corresponds to the 50-300 nm spatial scale, is particularly interesting, as the 3D arrangement of chromatin is implicated in multiple regulatory mechanisms. In this context, polycomb group (PcG) proteins stand as major epigenetic modulators of chromatin function, acting prevalently as repressors of gene transcription by combining chemical modifications of target histones with physical crosslinking of distal genomic regions and phase separation. The recent development of super-resolution microscopy (SRM) has strongly contributed to improving our comprehension of several aspects of nano-/mesoscale (10-200 nm) chromatin domains. Here, we review the current state-of-the-art SRM applied to PcG proteins, showing that the application of SRM to PcG activity and organization is still quite limited and mainly focused on the 3D assembly of PcG-controlled genomic loci. In this context, SRM approaches have mostly been applied to multilabel fluorescence in situ hybridization (FISH). However, SRM data have complemented the maps obtained from chromosome capture experiments and have opened a new window to observe how 3D chromatin topology is modulated by PcGs.

Indexed as

3D-SIMchromatin organizationFISHoligopaintpolycomb proteinsPRC1PRC2STORMsuper-resolution microscopyXist RNA

Identifiers

PMID36979066
PMCPMC10044799
OpenAlexW4322501597

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read6
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.