Evidence map›Paper›PMID 24873880›Full record

ReviewFEBS letters2014

Poly(A) polymerase (PAP) diversity in gene expression--star-PAP vs canonical PAP.

Rakesh S Laishram

Open access · hybridAbstract readComparative StudyReview
In one paragraph

Review in FEBS letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

36 citing papers in PubMed, 51 citations in OpenAlex.

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  19. Regulation of RNA stability at the 3' end.Biological chemistry · 2021
    Review
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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

1 author at 1 institution in 1 country.

Rakesh S LaishramCancer Research Program, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram 695014, India. Electronic address: laishram@rgcb.res.in.
Rajiv Gandhi Centre for Biotechnology · IN

Funding

Wellcome TrustWellcome Trust IA/I/1/505008
6 · The paper itself

Abstract

Almost all eukaryotic mRNAs acquire a poly(A) tail at the 3'-end by a concerted RNA processing event: cleavage and polyadenylation. The canonical PAP, PAPα, was considered the only nuclear PAP involved in general polyadenylation of mRNAs. A phosphoinositide-modulated nuclear PAP, Star-PAP, was then reported to regulate a select set of mRNAs in the cell. In addition, several non-canonical PAPs have been identified with diverse cellular functions. Further, canonical PAP itself exists in multiple isoforms thus illustrating the diversity of PAPs. In this review, we compare two nuclear PAPs, Star-PAP and PAPα with a general overview of PAP diversity in the cell. Emerging evidence suggests distinct niches of target pre-mRNAs for the two PAPs and that modulation of these PAPs regulates distinct cellular functions.

Indexed as

Gene Expression RegulationAnimalsBase SequenceBinding SitesConsensus SequenceHumansNucleotidyltransferasesPolyadenylationPolynucleotide AdenylyltransferaseProtein BindingProtein IsoformsRNA, MessengerNucleotidyltransferasesPolynucleotide AdenylyltransferaseProtein IsoformsRNA, MessengerTUT1 protein, human3′-end processingCanonical PAPCKIOxidative stressPAP isoformsPAPαPI4,5P(2)PIPKIαPolyadenylationPoly(A) polymerase (PAP)Star-PAPUridylation

Identifiers

PMID24873880
PMCPMC6309179
OpenAlexW2122327377

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.