Evidence map›Paper›PMID 20693478›Full record

ArticleGenome research2010

CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors.

Joseph C Corbo, Karen A Lawrence, Marcus Karlstetter, Connie A Myers, Musa Abdelaziz, William Dirkes, Karin Weigelt, Martin Seifert, Vladimir Benes, Lars G Fritsche and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

141 citing papers in PubMed, 1 synthesis or guideline pooled it, 235 citations in OpenAlex.

  1. Pooled it
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  13. Mutational scanning ofGenome research · 2024
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  15. Mutational scanning ofbioRxiv : the preprint server for biology · 2024
    Article
  16. Pathogenic variants inGenome research · 2024
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81 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 3 countries.

Joseph C CorboDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, Missouri 63110-1024, USA. jcorbo@pathology.wustl.edu
Karen A Lawrence
Marcus Karlstetter
Connie A Myers
Musa Abdelaziz
William Dirkes
Karin Weigelt
Martin Seifert
Vladimir Benes
Lars G Fritsche
Bernhard H F Weber
Thomas Langmann
Washington University in St. Louis · USErasmus MC · NLEuropean Molecular Biology Laboratory · DE

Funding

QUANTITATIVE ANALYSIS AND ENGINEERING OF THE PHOTORECEPTOR TRANSCRIPTION NETWORKR01EY018826 · NEI · WASHINGTON UNIVERSITY · PI CORBO, JOSEPH · 2008 to 2012
$1.9M
ELUCIDATING THE CIS-REGULATORY ARCHITECTURE OF RETINAL BIPOLAR CELLSF32EY029571 · NEI · WASHINGTON UNIVERSITY · PI MURPHY, DANIEL P · 2018 to 2019
$123k
NEI NIH HHS EY018826NEI NIH HHS F32 EY029571NEI NIH HHS R01 EY018826
6 · The paper itself

Abstract

Approximately 98% of mammalian DNA is noncoding, yet we understand relatively little about the function of this enigmatic portion of the genome. The cis-regulatory elements that control gene expression reside in noncoding regions and can be identified by mapping the binding sites of tissue-specific transcription factors. Cone-rod homeobox (CRX) is a key transcription factor in photoreceptor differentiation and survival, but its in vivo targets are largely unknown. Here, we used chromatin immunoprecipitation with massively parallel sequencing (ChIP-seq) on CRX to identify thousands of cis-regulatory regions around photoreceptor genes in adult mouse retina. CRX directly regulates downstream photoreceptor transcription factors and their target genes via a network of spatially distributed regulatory elements around each locus. CRX-bound regions act in a synergistic fashion to activate transcription and contain multiple CRX binding sites which interact in a spacing- and orientation-dependent manner to fine-tune transcript levels. CRX ChIP-seq was also performed on Nrl(-/-) retinas, which represent an enriched source of cone photoreceptors. Comparison with the wild-type ChIP-seq data set identified numerous rod- and cone-specific CRX-bound regions as well as many shared elements. Thus, CRX combinatorially orchestrates the transcriptional networks of both rods and cones by coordinating the expression of photoreceptor genes including most retinal disease genes. In addition, this study pinpoints thousands of noncoding regions of relevance to both Mendelian and complex retinal disease.

Indexed as

Sequence Analysis, DNAAnimalsBase SequenceBinding SitesChromatin ImmunoprecipitationChromosome MappingHigh-Throughput Nucleotide SequencingHomeodomain ProteinsMiceMice, Inbred C57BLMice, KnockoutMolecular Sequence DataPhylogenyProtein BindingRegulatory Sequences, Nucleic AcidRetinal Cone Photoreceptor Cellscone rod homeobox proteinHomeodomain ProteinsTrans-Activators

Identifiers

PMID20693478
PMCPMC2963815
OpenAlexW2114715558

What OpenQuestion holds

Textmetadata
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.