Evidence map›Paper›PMID 33734444›Full record

ReviewImmunological reviews2021

In search of lost time: Enhancers as modulators of timing in lymphocyte development and differentiation.

Jonathan M Chu, Nicholas A Pease, Hao Yuan Kueh

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Antigen perception in T cells by long-term Erk and NFAT signaling dynamics.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

3 authors at 1 institution in 2 countries.

Jonathan M ChuDepartment of Bioengineering, University of Washington, Seattle, WA, USA.ORCID 0000-0002-8520-1439
Nicholas A PeaseDepartment of Bioengineering, University of Washington, Seattle, WA, USA.ORCID 0000-0001-6140-1949
Hao Yuan KuehDepartment of Bioengineering, University of Washington, Seattle, WA, USA.ORCID 0000-0001-6272-6673
California Institute for Regenerative Medicine · US

Funding

A chromatin-based timer controlling T-cell developmentR01HL146478 · NHLBI · UNIVERSITY OF WASHINGTON · PI KUEH, HAO YUAN · 2020 to 2024
$1.9M
Single-cell analysis of immune cell fate decision makingR00HL119638 · NHLBI · UNIVERSITY OF WASHINGTON · PI KUEH, HAO YUAN · 2016 to 2018
$747k
Single cell analysis of hematopoietic cell fate determinationK99HL119638 · NHLBI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI KUEH, HAO YUAN · 2014 to 2015
$180k
Regulation of hematopoiesis by epigenetic timing controlF31HL151090 · NHLBI · UNIVERSITY OF WASHINGTON · PI PEASE, NICHOLAS · 2020 to 2020
$38k
NHLBI NIH HHS F31 HL151090NHLBI NIH HHS K99 HL119638NHLBI NIH HHS R00 HL119638NHLBI NIH HHS R01 HL146478NIH HHS 5R00HL119638
6 · The paper itself

Abstract

Proper timing of gene expression is central to lymphocyte development and differentiation. Lymphocytes often delay gene activation for hours to days after the onset of signaling components, which act on the order of seconds to minutes. Such delays play a prominent role during the intricate choreography of developmental events and during the execution of an effector response. Though a number of mechanisms are sufficient to explain timing at short timescales, it is not known how timing delays are implemented over long timescales that may span several cell generations. Based on the literature, we propose that a class of cis-regulatory elements, termed "timing enhancers," may explain how timing delays are controlled over these long timescales. By considering chromatin as a kinetic barrier to state switching, the timing enhancer model explains experimentally observed dynamics of gene expression where other models fall short. In this review, we elaborate on features of the timing enhancer model and discuss the evidence for its generality throughout development and differentiation. We then discuss potential molecular mechanisms underlying timing enhancer function. Finally, we explore recent evidence drawing connections between timing enhancers and genetic risk for immunopathology. We argue that the timing enhancer model is a useful framework for understanding how cis-regulatory elements control the central dimension of timing in lymphocyte biology.

Indexed as

ChromatinEnhancer Elements, GeneticCell DifferentiationChromatinchromatin regulationenhancersgene regulation processeslymphocytesnon-coding regulatory mutationstranscription

Identifiers

PMID33734444
PMCPMC8005465
OpenAlexW3136322670

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.