Evidence map›Paper›PMID 29447160›Full record

ArticlePLoS computational biology2018

Modeling the interactions of sense and antisense Period transcripts in the mammalian circadian clock network.

Dorjsuren Battogtokh, Shihoko Kojima, John J Tyson

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Natural antisense transcript ofGenes & development · 2021
    Article
  4. Article
  5. 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

3 authors at 2 institutions in 1 country.

Dorjsuren BattogtokhDepartment of Biological Sciences, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.
Shihoko KojimaDepartment of Biological Sciences, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.ORCID 0000-0001-9579-7830
John J TysonDepartment of Biological Sciences, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.ORCID 0000-0001-7560-6013
Biocom · USVirginia Tech · US

Funding

Functional analysis of a non-coding RNA in the mammalian circadian clock systemR01GM126223 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI KOJIMA, SHIHOKO · 2018 to 2022
$1.7M
NIGMS NIH HHS R01 GM126223
6 · The paper itself

Abstract

In recent years, it has become increasingly apparent that antisense transcription plays an important role in the regulation of gene expression. The circadian clock is no exception: an antisense transcript of the mammalian core-clock gene PERIOD2 (PER2), which we shall refer to as Per2AS RNA, oscillates with a circadian period and a nearly 12 h phase shift from the peak expression of Per2 mRNA. In this paper, we ask whether Per2AS plays a regulatory role in the mammalian circadian clock by studying in silico the potential effects of interactions between Per2 and Per2AS RNAs on circadian rhythms. Based on the antiphasic expression pattern, we consider two hypotheses about how Per2 and Per2AS mutually interfere with each other's expression. In our pre-transcriptional model, the transcription of Per2AS RNA from the non-coding strand represses the transcription of Per2 mRNA from the coding strand and vice versa. In our post-transcriptional model, Per2 and Per2AS transcripts form a double-stranded RNA duplex, which is rapidly degraded. To study these two possible mechanisms, we have added terms describing our alternative hypotheses to a published mathematical model of the molecular regulatory network of the mammalian circadian clock. Our pre-transcriptional model predicts that transcriptional interference between Per2 and Per2AS can generate alternative modes of circadian oscillations, which we characterize in terms of the amplitude and phase of oscillation of core clock genes. In our post-transcriptional model, Per2/Per2AS duplex formation dampens the circadian rhythm. In a model that combines pre- and post-transcriptional controls, the period, amplitude and phase of circadian proteins exhibit non-monotonic dependencies on the rate of expression of Per2AS. All three models provide potential explanations of the observed antiphasic, circadian oscillations of Per2 and Per2AS RNAs. They make discordant predictions that can be tested experimentally in order to distinguish among these alternative hypotheses.

Indexed as

Gene Expression RegulationAnimalsCell CycleCircadian ClocksCircadian RhythmCytoplasmGene ExpressionLiverMiceModels, TheoreticalOligonucleotides, AntisenseOscillometryPeriod Circadian ProteinsPhosphorylationRNA, MessengerTranscription FactorsOligonucleotides, AntisensePer2 protein, mousePeriod Circadian ProteinsRNA, MessengerTranscription Factors

Identifiers

PMID29447160
PMCPMC5831635
OpenAlexW2786747691

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.