Evidence map›Paper›PMID 17653270›Full record

ArticlePloS one2007

The cis-regulatory logic of the mammalian photoreceptor transcriptional network.

Timothy H-C Hsiau, Claudiu Diaconu, Connie A Myers, Jongwoo Lee, Constance L Cepko, Joseph C Corbo

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

101 citing papers in PubMed, 149 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Enhanced Transcriptional Activation in Developing Mouse Photoreceptors.Investigative ophthalmology & visual science · 2025
    Article
  5. AnFrontiers in genetics · 2025
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  8. Germline knockout ofProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Mutations inScience advances · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Retinoschisin and Cardiac Glycoside Crosstalk at the Retinal Na/K-ATPase.Investigative ophthalmology & visual science · 2020
    Article

41 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

6 authors at 2 institutions in 1 country.

Timothy H-C HsiauDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Claudiu Diaconu
Connie A Myers
Jongwoo Lee
Constance L Cepko
Joseph C Corbo
Washington University in St. Louis · USHarvard University · US

Funding

DETERMINATION OF RETINAL CELL FATER01EY009676 · NEI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI CEPKO, CONSTANCE L · 1992 to 2010
$3.9M
Gene Regulatory Networks in Rod Photoreceptor CellsK08EY014822 · NEI · WASHINGTON UNIVERSITY · PI CORBO, JOSEPH C · 2003 to 2007
$756k
Howard Hughes Medical InstituteNEI NIH HHS K08 EY014822NEI NIH HHS K08EY014822NEI NIH HHS R01 EY009676NEI NIH HHS R01EY009676
6 · The paper itself

Abstract

The photoreceptor cells of the retina are subject to a greater number of genetic diseases than any other cell type in the human body. The majority of more than 120 cloned human blindness genes are highly expressed in photoreceptors. In order to establish an integrative framework in which to understand these diseases, we have undertaken an experimental and computational analysis of the network controlled by the mammalian photoreceptor transcription factors, Crx, Nrl, and Nr2e3. Using microarray and in situ hybridization datasets we have produced a model of this network which contains over 600 genes, including numerous retinal disease loci as well as previously uncharacterized photoreceptor transcription factors. To elucidate the connectivity of this network, we devised a computational algorithm to identify the photoreceptor-specific cis-regulatory elements (CREs) mediating the interactions between these transcription factors and their target genes. In vivo validation of our computational predictions resulted in the discovery of 19 novel photoreceptor-specific CREs near retinal disease genes. Examination of these CREs permitted the definition of a simple cis-regulatory grammar rule associated with high-level expression. To test the generality of this rule, we used an expanded form of it as a selection filter to evolve photoreceptor CREs from random DNA sequences in silico. When fused to fluorescent reporters, these evolved CREs drove strong, photoreceptor-specific expression in vivo. This study represents the first systematic identification and in vivo validation of CREs in a mammalian neuronal cell type and lays the groundwork for a systems biology of photoreceptor transcriptional regulation.

Indexed as

Transcription, GeneticAlgorithmsAnimalsBasic-Leucine Zipper Transcription FactorsBlindnessConsensus SequenceEye ProteinsHomeodomain ProteinsHumansIn Situ HybridizationMammalsOligonucleotide Array Sequence AnalysisOrphan Nuclear ReceptorsPhotoreceptor Cells, VertebrateRegulatory Sequences, Nucleic AcidRetinal DiseasesBasic-Leucine Zipper Transcription Factorscone rod homeobox proteinEye ProteinsHomeodomain ProteinsNR2E3 protein, humanNRL protein, humanOrphan Nuclear ReceptorsTrans-ActivatorsTranscription Factors

Identifiers

PMID17653270
PMCPMC1916400
OpenAlexW2125716773

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.