Evidence map›Paper›PMID 38418700›Full record

ArticleCommunications biology2024

Ror homolog nhr-23 is essential for both developmental clock and circadian clock in C. elegans.

Shingo Hiroki, Hikari Yoshitane

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Role of the clock gene homologFrontiers in neuroscience · 2025
    Article
  6. 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

2 authors at 1 institution in 1 country.

Shingo HirokiTokyo Metropolitan Institute of Medical Sciences, Tokyo, Japan. s.hiroki.phd.work2022@gmail.com.ORCID 0009-0003-7545-7646
Hikari YoshitaneTokyo Metropolitan Institute of Medical Sciences, Tokyo, Japan. yoshitane-hk@igakuken.or.jp.ORCID 0000-0001-6319-3354
Tokyo Metropolitan Institute of Medical Science · JP

Funding

Japan Agency for Medical Research and Development (AMED) 20gm6110010h0004Japan Agency for Medical Research and Development (AMED) 22gm4010019h0001MEXT | Japan Science and Technology Agency (JST) JPMJFR2150MEXT | Japan Society for the Promotion of Science (JSPS) JP21H05130MEXT | Japan Society for the Promotion of Science (JSPS) JP21K18231
6 · The paper itself

Abstract

Animals have internal clocks that generate biological rhythms. In mammals, clock genes such as Period form the circadian clock to generate approximately 24-h biological rhythms. In C. elegans, the clock gene homologs constitute the "developmental clock", which has an 8-h period during larval development to determine the timing of molting. Thus, the ancestral circadian clock has been believed to evolve into the oscillator with a shorter period in C. elegans. However, circadian rhythms have also been observed in adult C. elegans, albeit relatively weak. This prompts the question: if the clock gene homologs drive the developmental rhythm with 8-h period, which genes generate the circadian rhythms in C. elegans? In this study, we discovered that nhr-23, a homolog of the mammalian circadian clock gene Ror, is essential for circadian transcriptional rhythms in adult C. elegans. Interestingly, nhr-23 was also known to be essential for the molting clock. The bilaterian ancestral circadian clock genes might have evolved to function over multiple periods depending on developmental contexts rather than a single 8-h period in C. elegans.

Indexed as

Circadian ClocksAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCircadian RhythmMammalsTranscription FactorsCaenorhabditis elegans ProteinsNHR-23 protein, C elegansTranscription Factors

Identifiers

PMID38418700
PMCPMC10902330
OpenAlexW4392230107

What OpenQuestion holds

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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.