Evidence map›Paper›PMID 26836402›Full record

ArticleBiochemistry2016

Quantitative Measurement of Histone Tail Acetylation Reveals Stage-Specific Regulation and Response to Environmental Changes during Drosophila Development.

Ryan A Henry, Tanu Singh, Yin-Ming Kuo, Alison Biester, Abigail O'Keefe, Sandy Lee, Andrew J Andrews, Alana M O'Reilly

Abstract read
In one paragraph

Article in Biochemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Proteomic-based approaches to cardiac development and disease.Current opinion in chemical biology · 2019
    Review
  3. Article
  4. 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

8 authors at 3 institutions in 1 country.

Ryan A HenryDepartment of Cancer Biology, Fox Chase Cancer Center , Philadelphia, Pennsylvania 19111, United States.
Tanu SinghDepartment of Cancer Biology, Fox Chase Cancer Center , Philadelphia, Pennsylvania 19111, United States.
Yin-Ming KuoDepartment of Cancer Biology, Fox Chase Cancer Center , Philadelphia, Pennsylvania 19111, United States.
Alison BiesterImmersion Science Program, Fox Chase Cancer Center , Philadelphia, Pennsylvania 19111, United States.
Abigail O'KeefeImmersion Science Program, Fox Chase Cancer Center , Philadelphia, Pennsylvania 19111, United States.
Sandy LeeImmersion Science Program, Fox Chase Cancer Center , Philadelphia, Pennsylvania 19111, United States.
Andrew J AndrewsDepartment of Cancer Biology, Fox Chase Cancer Center , Philadelphia, Pennsylvania 19111, United States.
Alana M O'ReillyDepartment of Cancer Biology, Fox Chase Cancer Center , Philadelphia, Pennsylvania 19111, United States.
Fox Chase Cancer Center · USImmersion (United States) · USDrexel University · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
TRAINING PROGRAM IN CANCER RESEARCHT32CA009035 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI CHERNOFF, JONATHAN · 1985 to 2020
$10.5M
The Role of Histone Chaperones in Histone Acetylation and Nucleosome DynamicsR01GM102503 · NIGMS · UNIVERSITY OF NORTH CAROLINA WILMINGTON · PI ANDREWS, ANDREW JOSEPH · 2014 to 2023
$3.9M
Mechanisms Controlling Epithelial HomeostasisR01HD065800 · NICHD · RESEARCH INST OF FOX CHASE CAN CTR · PI O'REILLY, ALANA M · 2010 to 2020
$3.9M
NCI NIH HHS CA06927NCI NIH HHS P30 CA006927NCI NIH HHS T32 CA009035NCI NIH HHS T32 CA009035-36A1NICHD NIH HHS HD065800NICHD NIH HHS R01 HD065800NIGMS NIH HHS GM102503NIGMS NIH HHS R01 GM102503
6 · The paper itself

Abstract

Histone modification plays a major role in regulating gene transcription and ensuring the healthy development of an organism. Numerous studies have suggested that histones are dynamically modified during developmental events to control gene expression levels in a temporal and spatial manner. However, the study of histone acetylation dynamics using currently available techniques is hindered by the difficulty of simultaneously measuring acetylation of the numerous potential sites of modification present in histones. Here, we present a methodology that allows us to combine mass spectrometry-based histone analysis with Drosophila developmental genetics. Using this system, we characterized histone acetylation patterns during multiple developmental stages of the fly. Additionally, we utilized this analysis to characterize how treatments with pharmacological agents or environmental changes such as γ-irradiation altered histone acetylation patterns. Strikingly, γ-irradiation dramatically increased the level of acetylation at H3K18, a site linked to DNA repair via nonhomologous end joining. In mutant fly strains deficient in DNA repair proteins, however, this increase in the level of H3K18 acetylation was lost. These results demonstrate the efficacy of our combined mass spectrometry system with a Drosophila model system and provide interesting insight into the changes in histone acetylation during development, as well as the effects of both pharmacological and environmental agents on global histone acetylation.

Indexed as

DNA RepairGamma RaysAcetylationAnimalsDrosophila melanogasterDrosophila ProteinsHistonesMutationTranscription, GeneticDrosophila ProteinsHistones

Identifiers

PMID26836402
PMCPMC4821013
OpenAlexW2262182111

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.