Evidence map›Paper›PMID 23189207›Full record

ArticlePloS one2012

Heterogeneous expression of the core circadian clock proteins among neuronal cell types in mouse retina.

Xiaoqin Liu, Zhijing Zhang, Christophe P Ribelayga

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

47 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
  2. Circadian clock disruption promotes retinal photoreceptor degeneration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Localisation of cryptochrome 2 in the avian retina.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2022
    Article
  10. Photoreceptor Degeneration in Homozygous Male Per2Journal of biological rhythms · 2021
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Circadian regulation in the retina: From molecules to network.The European journal of neuroscience · 2020
    Review
  17. Review
  18. Article
  19. The circadian clock geneFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  20. Review
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 1 country.

Xiaoqin LiuDepartment of Ophthalmology and Visual Science, The University of Texas Health Science Center at Houston, Medical School, Houston, Texas, United States of America.
Zhijing Zhang
Christophe P Ribelayga
The University of Texas Health Science Center at Houston · US

Funding

VISION RESEARCHP30EY010608 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MASSEY, STEPHEN C · 1994 to 2014
$7.9M
Circadian Clock Function in the Mammalian RetinaR01EY018640 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI RIBELAYGA, CHRISTOPHE P. · 2009 to 2015
$2.0M
NEI NIH HHS P30 EY010608NEI NIH HHS R01 EY018640
6 · The paper itself

Abstract

Circadian rhythms in metabolism, physiology, and behavior originate from cell-autonomous circadian clocks located in many organs and structures throughout the body and that share a common molecular mechanism based on the clock genes and their protein products. In the mammalian neural retina, despite evidence supporting the presence of several circadian clocks regulating many facets of retinal physiology and function, the exact cellular location and genetic signature of the retinal clock cells remain largely unknown. Here we examined the expression of the core circadian clock proteins CLOCK, BMAL1, NPAS2, PERIOD 1(PER1), PERIOD 2 (PER2), and CRYPTOCHROME2 (CRY2) in identified neurons of the mouse retina during daily and circadian cycles. We found concurrent clock protein expression in most retinal neurons, including cone photoreceptors, dopaminergic amacrine cells, and melanopsin-expressing intrinsically photosensitive ganglion cells. Remarkably, diurnal and circadian rhythms of expression of all clock proteins were observed in the cones whereas only CRY2 expression was found to be rhythmic in the dopaminergic amacrine cells. Only a low level of expression of the clock proteins was detected in the rods at any time of the daily or circadian cycle. Our observations provide evidence that cones and not rods are cell-autonomous circadian clocks and reveal an important disparity in the expression of the core clock components among neuronal cell types. We propose that the overall temporal architecture of the mammalian retina does not result from the synchronous activity of pervasive identical clocks but rather reflects the cellular and regional heterogeneity in clock function within retinal tissue.

Indexed as

AnimalsARNTL Transcription FactorsCircadian ClocksCircadian RhythmCLOCK ProteinsCryptochromesDopaminergic NeuronsGene Expression ProfilingMiceMice, KnockoutPeriod Circadian ProteinsRetinaRetinal NeuronsARNTL Transcription FactorsCLOCK ProteinsCry2 protein, mouseCryptochromesPeriod Circadian Proteins

Identifiers

PMID23189207
PMCPMC3506613
OpenAlexW2042227355

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.