Evidence map›Paper›PMID 35217597›Full record

ArticleRNA (New York, N.Y.)2022

Oppositional poly(A) tail length regulation by FMRP and CPEB1.

Jihae Shin, Ki Young Paek, Lies Chikhaoui, Suna Jung, SitharaRaju Ponny, Yutaka Suzuki, Kiran Padmanabhan, Joel D Richter

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

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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

8 authors at 3 institutions in 3 countries.

Jihae Shin *Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.ORCID 0000-0001-6034-2027
Ki Young Paek *Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Lies Chikhaoui *Institut de Genomique Fonctionnelle de Lyon, Univ Lyon, CNRS UMR 5242, Ecole Normale Superieure de Lyon, Universite Claude Bernard Lyon 1, F-69364 Lyon, France.
Suna JungProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
SitharaRaju PonnyProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Yutaka SuzukiUniversity of Tokyo, Kashiwa II campus, Kashiwa-Shi 2770882, Japan.
Kiran PadmanabhanInstitut de Genomique Fonctionnelle de Lyon, Univ Lyon, CNRS UMR 5242, Ecole Normale Superieure de Lyon, Universite Claude Bernard Lyon 1, F-69364 Lyon, France.
Joel D RichterProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
University of Massachusetts Chan Medical School · USUniversité Claude Bernard Lyon 1 · FRKaichi International University · JP

Funding

POLYADENYLATION AND TRANSLATIONAL CONTROLR01GM046779 · NIGMS · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI RICHTER, JOEL D · 1992 to 2022
$7.7M
FMRP Regulation of Gene ExpressionR01GM135087 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HUBER, KIMBERLY M., RICHTER, JOEL D · 2020 to 2023
$2.4M
NIGMS NIH HHS R01 GM046779NIGMS NIH HHS R01 GM135087
6 · The paper itself

Abstract

Poly(A) tail length is regulated in both the nucleus and cytoplasm. One factor that controls polyadenylation in the cytoplasm is CPEB1, an RNA binding protein that associates with specific mRNA 3'UTR sequences to tether enzymes that add and remove poly(A). Two of these enzymes, the noncanonical poly(A) polymerases GLD2 (TENT2, PAPD4, Wispy) and GLD4 (TENT4B, PAPD5, TRF4, TUT3), interact with CPEB1 to extend poly(A). To identify additional RNA binding proteins that might anchor GLD4 to RNA, we expressed double tagged GLD4 in U87MG cells, which was used for sequential immunoprecipitation and elution followed by mass spectrometry. We identified several RNA binding proteins that coprecipitated with GLD4, among which was FMRP. To assess whether FMRP regulates polyadenylation, we performed TAIL-seq from WT and FMRP-deficient HEK293 cells. Surprisingly, loss of FMRP resulted in an overall increase in poly(A), which was also observed for several specific mRNAs. Conversely, loss of CPEB1 elicited an expected decrease in poly(A), which was examined in cultured neurons. We also examined polyadenylation in wild type (WT) and FMRP-deficient mouse brain cortex by direct RNA nanopore sequencing, which identified RNAs with both increased and decreased poly(A). Our data show that FMRP has a role in mediating poly(A) tail length, which adds to its repertoire of RNA regulation.

Indexed as

mRNA Cleavage and Polyadenylation FactorsPolyadenylationAnimalsHEK293 CellsHumansMicePoly APolynucleotide AdenylyltransferaseRNA-Binding ProteinsRNA, MessengerTranscription FactorsCPEB1 protein, humanmRNA Cleavage and Polyadenylation FactorsPoly APolynucleotide AdenylyltransferaseRNA-Binding ProteinsRNA, MessengerTranscription FactorsCPEB1FMRPGLD4nanopore RNA-seqpolyadenylation

Identifiers

PMID35217597
PMCPMC9014880
OpenAlexW4214578211

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.