Evidence map›Paper›PMID 25662466›Full record

ArticleMethods in enzymology2015

Analysis of circadian regulation of poly(A)-tail length.

Shihoko Kojima, Carla B Green

Abstract read
In one paragraph

Article in Methods in enzymology, 2015. 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
–field-weighted citation impact
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.

  1. Review
  2. Article
  3. OverexpressingMarine drugs · 2022
    Article
  4. Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

2 authors.

Shihoko KojimaDepartment of Biological Sciences, Virginia Tech, Blacksburg, VA, USA. Electronic address: skojima@vt.edu.
Carla B GreenDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Funding

Transcriptional Architecture and Chromatin Landscape of Circadian Clocks in AgingR01AG045795 · NIA · UT SOUTHWESTERN MEDICAL CENTER · PI GREEN, CARLA B., TAKAHASHI, JOSEPH S · 2013 to 2017
$1.5M
Structure/Function Studies of Mammalian Circadian Clock ProteinsR01GM090247 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI GREEN, CARLA B. · 2011 to 2014
$1.3M
Circadian regulation of mitochondrial RNA polyadenylationR01GM111387 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI GREEN, CARLA B. · 2014 to 2017
$1.2M
Analysis of a new circadian mutantR21NS079986 · NINDS · UNIVERSITY OF VIRGINIA · PI GREEN, CARLA B., MENAKER, MICHAEL · 2012 to 2013
$436k
NIA NIH HHS R01 AG045795NIA NIH HHS R01AG045795NIGMS NIH HHS R01 GM090247NIGMS NIH HHS R01GM090247NIGMS NIH HHS R01 GM111387NINDS NIH HHS R21 NS079986NINDS NIH HHS R21NS079986
6 · The paper itself

Abstract

The poly(A) tail is found on the 3'-end of most eukaryotic mRNAs, and its length significantly contributes to the mRNAs half-life and translational competence. Circadian regulation of poly(A)-tail length is a powerful mechanism to confer rhythmicity in gene expression posttranscriptionally and provides a means to regulate protein levels independent of rhythmic transcription in the nucleus. Therefore, analysis of circadian poly(A)-tail length regulation is important for a complete understanding of rhythmic physiology, since rhythmically expressed proteins are the ultimate mediators of rhythmic function. Nevertheless, it has previously been challenging to measure changes in poly(A)-tail length, especially at a global level, due to technical constraints. However, new methodology depending on differential fractionation of mRNAs depending on the length of their tails has recently been developed. In this chapter, we describe these methods as used for examining the circadian regulation of poly(A)-tail length and provide detailed experimental procedures to measure poly(A)-tail length both at a the single mRNA level and the global level. Although this chapter concentrates on methods we used for analyzing poly(A)-tail length in the mammalian circadian system, the methods described here can be applicable to any organisms and any biological processes.

Indexed as

Circadian ClocksPolyadenylationAnimalsBase SequenceChromatography, AffinityHumansReverse Transcriptase Polymerase Chain ReactionRNA, MessengerRNA, MessengerCircadianLM-PATOligo(dT) chromatographyPoly(A)denylomePoly(A)-tail lengthPoly(A) tail (PAT) assayPosttranscriptional

Identifiers

PMID25662466
PMCPMC4415494

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.