Evidence map›Paper›PMID 32051613›Full record

ArticleNature protocols2020

Superresolution imaging of chromatin fibers to visualize epigenetic information on replicative DNA.

Matthew Wooten, Yingying Li, Jonathan Snedeker, Zehra F Nizami, Joseph G Gall, Xin Chen

Open access · greenAbstract read
In one paragraph

Article in Nature protocols, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Reduced Levels of Lagging Strand Polymerases Shape Stem Cell Chromatin.bioRxiv : the preprint server for biology · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Mitotic drive in asymmetric epigenetic inheritance.Biochemical Society transactions · 2022
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
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

6 authors at 2 institutions in 1 country.

Matthew WootenDepartment of Biology, The Johns Hopkins University, Baltimore, MD, USA.
Yingying Li *Department of Biology, The Johns Hopkins University, Baltimore, MD, USA.
Jonathan Snedeker *Department of Biology, The Johns Hopkins University, Baltimore, MD, USA.
Zehra F NizamiDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD, USA.
Joseph G GallDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD, USA.
Xin ChenDepartment of Biology, The Johns Hopkins University, Baltimore, MD, USA. xchen32@jhu.edu.ORCID http://orcid.org/0000-0002-6990-0926
Johns Hopkins University · USCarnegie Institution for Science · US

Funding

CELLULAR AND MOLECULAR BIOLOGYT32GM007231 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI VAN DOREN, MARK B · 1985 to 2020
$18.4M
THE ORGANIZATION OF ANIMAL CELL NUCLEIR01GM033397 · NIGMS · CARNEGIE INSTITUTION OF WASHINGTON, D.C. · PI GALL, JOSEPH G. · 1985 to 2019
$8.4M
Study epigenetic inheritance during development, homeostasis and regenerationR35GM127075 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Xin Chen · 2018 to 2026
$3.2M
Molecular and cellular mechanisms underlying asymmetric histone inheritanceR01GM112008 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CHEN, XIN, XIAO, JIE · 2014 to 2017
$1.6M
Investigating the mechanisms and generality of asymmetric histone inheritance in multiple stem cell systemsF31GM115149 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI WOOTEN, MATTHEW · 2016 to 2017
$88k
NIGMS NIH HHS F31 GM115149NIGMS NIH HHS R01 GM033397NIGMS NIH HHS R01 GM112008NIGMS NIH HHS R35 GM127075NIGMS NIH HHS T32 GM007231U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) 5T32GM007231U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) F31GM115149-01A1U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM112008U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM33397U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM127075
6 · The paper itself

Abstract

During DNA replication, the genetic information of a cell is copied. Subsequently, identical genetic information is segregated reliably to the two daughter cells through cell division. Meanwhile, DNA replication is intrinsically linked to the process of chromatin duplication, which is required for regulating gene expression and establishing cell identities. Understanding how chromatin is established, maintained or changed during DNA replication represents a fundamental question in biology. Recently, we developed a method to directly visualize chromatin components at individual replication forks undergoing DNA replication. This method builds upon the existing chromatin fiber technique and combines it with cell type-specific chromatin labeling and superresolution microscopy. In this method, a short pulse of nucleoside analog labels replicative regions in the cells of interest. Chromatin fibers are subsequently isolated and attached to a glass slide, after which a laminar flow of lysis buffer extends the lysed chromatin fibers parallel with the direction of the flow. Fibers are then immunostained for different chromatin-associated proteins and mounted for visualization using superresolution microscopy. Replication foci, or 'bubbles,' are identified by the presence of the incorporated nucleoside analog. For researchers experienced in molecular biology and superresolution microscopy, this protocol typically takes 2-3 d from sample preparation to data acquisition, with an additional day for data processing and quantification.

Indexed as

ChromatinAnimalsCell LineDNADNA ReplicationDrosophila melanogasterEpigenesis, GeneticMicroscopy, FluorescenceOptical ImagingSingle Molecule ImagingChromatinDNA

Identifiers

PMID32051613
PMCPMC7255620
OpenAlexW3006294054

What OpenQuestion holds

Textmetadata
LicenceTDM
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.