Evidence map›Paper›PMID 23877069›Full record

ArticleNature2013

Optical control of mammalian endogenous transcription and epigenetic states.

Silvana Konermann, Mark D Brigham, Alexandro Trevino, Patrick D Hsu, Matthias Heidenreich, Le Cong, Randall J Platt, David A Scott, George M Church, Feng Zhang

Open access · greenAbstract read
In one paragraph

Article in Nature, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 455 papers.

0numbers the graph read from it
0cells of the map it votes in
455citing papers in PubMed
171.9field-weighted citation impact, top 1% 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

455 citing papers in PubMed, 805 citations in OpenAlex.

  1. Review
  2. Advances and clinical potential of epigenome editing.Cellular and molecular life sciences : CMLS · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Epigenetic editing: from concept to clinic.Nature reviews. Drug discovery · 2026
    Review
  8. Article
  9. Article
  10. Review
  11. Review
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  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
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  20. Article

395 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Silvana Konermann *Broad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.
Mark D Brigham *Broad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.
Alexandro TrevinoBroad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.
Patrick D HsuBroad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.
Matthias HeidenreichBroad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.
Le CongBroad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.
Randall J PlattBroad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.
David A ScottBroad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.
George M ChurchBroad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.
Feng ZhangBroad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.
Harvard University · USMcGovern Institute for Brain Research · USBroad Institute · USMassachusetts Institute of Technology · US

Funding

Causal Transcriptional Consequences of Human Genetic VariationP50HG005550 · NHGRI · HARVARD MEDICAL SCHOOL · PI CHURCH, GEORGE M · 2010 to 2014
$19.0M
Isogenic Human Pluripotent Stem Cell-Based Models of Human Disease MutationsR01DK097768 · NIDDK · BROAD INSTITUTE, INC. · PI COWAN, CHAD ALBERT, ZHANG, FENG · 2012 to 2016
$11.0M
Probing Neuropsychiatric Diseases Using Targeted Epigenome and Genome EngineeringDP1MH100706 · NIMH · BROAD INSTITUTE, INC. · PI ZHANG, FENG · 2012 to 2016
$4.3M
Genome-wide Light-inducible Tuning of Transcriptional Network DynamicR01NS073124 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI ARLOTTA, PAOLA, JOUNG, J. KEITH · 2010 to 2014
$3.3M
NCCDPHP CDC HHS DP1-MH100706NHGRI NIH HHS P50 HG005550NHGRI NIH HHS P50-HG005550NIDDK NIH HHS R01 DK097768NIMH NIH HHS DP1 MH100706NINDS NIH HHS R01 NS073124NINDS NIH HHS R01-NS073124
6 · The paper itself

Abstract

The dynamic nature of gene expression enables cellular programming, homeostasis and environmental adaptation in living systems. Dissection of causal gene functions in cellular and organismal processes therefore necessitates approaches that enable spatially and temporally precise modulation of gene expression. Recently, a variety of microbial and plant-derived light-sensitive proteins have been engineered as optogenetic actuators, enabling high-precision spatiotemporal control of many cellular functions. However, versatile and robust technologies that enable optical modulation of transcription in the mammalian endogenous genome remain elusive. Here we describe the development of light-inducible transcriptional effectors (LITEs), an optogenetic two-hybrid system integrating the customizable TALE DNA-binding domain with the light-sensitive cryptochrome 2 protein and its interacting partner CIB1 from Arabidopsis thaliana. LITEs do not require additional exogenous chemical cofactors, are easily customized to target many endogenous genomic loci, and can be activated within minutes with reversibility. LITEs can be packaged into viral vectors and genetically targeted to probe specific cell populations. We have applied this system in primary mouse neurons, as well as in the brain of freely behaving mice in vivo to mediate reversible modulation of mammalian endogenous gene expression as well as targeted epigenetic chromatin modifications. The LITE system establishes a novel mode of optogenetic control of endogenous cellular processes and enables direct testing of the causal roles of genetic and epigenetic regulation in normal biological processes and disease states.

Indexed as

LightAnimalsArabidopsis ProteinsBasic Helix-Loop-Helix ProteinsCells, CulturedChromatinCryptochromesEpigenesis, GeneticGene Expression RegulationGenetic VectorsMaleMiceMice, Inbred C57BLNeuronsOptogeneticsTime FactorsArabidopsis ProteinsBasic Helix-Loop-Helix ProteinsChromatinCIB1 protein, ArabidopsisCryptochromes

Identifiers

PMID23877069
PMCPMC3856241
OpenAlexW2111648798

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.