Evidence map›Paper›PMID 25607544›Full record

ArticlePloS one2015

Effects of different per translational kinetics on the dynamics of a core circadian clock model.

Paula S Nieto, Jorge A Revelli, Eduardo Garbarino-Pico, Carlos A Condat, Mario E Guido, Francisco A Tamarit

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Circadian Posttranscriptional Regulatory Mechanisms in Mammals.Cold Spring Harbor perspectives in biology · 2018
    Review
  3. Review
  4. Circadian systems biology: When time matters.Computational and structural biotechnology journal · 2015
    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

6 authors at 2 institutions in 1 country.

Paula S NietoInstituto de Física Enrique Gaviola (IFEG-CONICET) and Facultad de Matemática, Astronomía y Física (FaMAF), Universidad Nacional de Córdoba (UNC). Ciudad Universitaria, CP:X5000HUA Córdoba, Argentina.
Jorge A RevelliInstituto de Física Enrique Gaviola (IFEG-CONICET) and Facultad de Matemática, Astronomía y Física (FaMAF), Universidad Nacional de Córdoba (UNC). Ciudad Universitaria, CP:X5000HUA Córdoba, Argentina.
Eduardo Garbarino-PicoCentro de Investigaciones en Química Biológica de Córdoba (CIQUIBIC-CONICET) and Departamento de Química Biológica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba (UNC). Ciudad Universitaria, CP:X5000HUA Córdoba, Argentina.
Carlos A CondatInstituto de Física Enrique Gaviola (IFEG-CONICET) and Facultad de Matemática, Astronomía y Física (FaMAF), Universidad Nacional de Córdoba (UNC). Ciudad Universitaria, CP:X5000HUA Córdoba, Argentina.
Mario E GuidoCentro de Investigaciones en Química Biológica de Córdoba (CIQUIBIC-CONICET) and Departamento de Química Biológica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba (UNC). Ciudad Universitaria, CP:X5000HUA Córdoba, Argentina.
Francisco A TamaritInstituto de Física Enrique Gaviola (IFEG-CONICET) and Facultad de Matemática, Astronomía y Física (FaMAF), Universidad Nacional de Córdoba (UNC). Ciudad Universitaria, CP:X5000HUA Córdoba, Argentina.
Universidad Nacional de Córdoba · ARConsejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Living beings display self-sustained daily rhythms in multiple biological processes, which persist in the absence of external cues since they are generated by endogenous circadian clocks. The period (per) gene is a central player within the core molecular mechanism for keeping circadian time in most animals. Recently, the modulation PER translation has been reported, both in mammals and flies, suggesting that translational regulation of clock components is important for the proper clock gene expression and molecular clock performance. Because translational regulation ultimately implies changes in the kinetics of translation and, therefore, in the circadian clock dynamics, we sought to study how and to what extent the molecular clock dynamics is affected by the kinetics of PER translation. With this objective, we used a minimal mathematical model of the molecular circadian clock to qualitatively characterize the dynamical changes derived from kinetically different PER translational mechanisms. We found that the emergence of self-sustained oscillations with characteristic period, amplitude, and phase lag (time delays) between per mRNA and protein expression depends on the kinetic parameters related to PER translation. Interestingly, under certain conditions, a PER translation mechanism with saturable kinetics introduces longer time delays than a mechanism ruled by a first-order kinetics. In addition, the kinetic laws of PER translation significantly changed the sensitivity of our model to parameters related to the synthesis and degradation of per mRNA and PER degradation. Lastly, we found a set of parameters, with realistic values, for which our model reproduces some experimental results reported recently for Drosophila melanogaster and we present some predictions derived from our analysis.

Indexed as

Models, BiologicalAnimalsCircadian ClocksDrosophila melanogasterDrosophila ProteinsGene Expression RegulationPeriod Circadian ProteinsProtein BiosynthesisRNA, MessengerDrosophila ProteinsPeriod Circadian ProteinsPER protein, DrosophilaRNA, Messenger

Identifiers

PMID25607544
PMCPMC4301915
OpenAlexW2077566027

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.