Evidence map›Paper›PMID 39223634›Full record

ArticleBMC research notes2024

Cleavage and polyadenylation factors are potential regulators of adipogenesis.

Salwa Mohd Mostafa, Claire Moore

Abstract read
In one paragraph

Article in BMC research notes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Salwa Mohd MostafaGraduate School of Biomedical Sciences, Department of Developmental, Molecular, and Chemical Biology, Tufts University School of Medicine, Boston, MA, 02111, USA.
Claire MooreGraduate School of Biomedical Sciences, Department of Developmental, Molecular, and Chemical Biology, Tufts University School of Medicine, Boston, MA, 02111, USA. claire.moore@tufts.edu.

Funding

Defining the Role of Alternative Polyadenylation in Macrophage Differentiation and FunctionR01AI152337 · NIAID · TUFTS UNIVERSITY BOSTON · PI MOORE, CLAIRE L · 2020 to 2024
$2.9M
NIAID NIH HHS R01 AI152337NIH HHS 1R01AI152337
6 · The paper itself

Abstract

objectiveAlternative polyadenylation (APA) is a co-transcriptional process that leads to isoform diversity in the 3' ends of mRNAs. APA is known to occur during differentiation, and its dysregulation is observed in diseases like cancer and autoimmune disorders. It has been previously reported that differentiation of 3T3-L1 cells to adipocytes leads to an overall lengthening of mRNAs, but the proteins involved in this regulation have not been identified. The expression levels of subunits of the cleavage and polyadenylation (C/P) complex can regulate the choice of poly(A) site, which in turn can affect different cellular activities. In this paper, we studied the change in levels of C/P proteins during 3T3-L1 differentiation.

resultsWe observed that while the RNA expression of these proteins is unchanged during differentiation, the protein levels of some subunits do change, including a decrease in levels of CPSF73, the nuclease that cuts at the poly(A) site. However, overexpression of CPSF73 alone does not affect the efficiency and rate of differentiation.

Indexed as

3T3-L1 CellsAdipogenesisCell DifferentiationAdipocytesAnimalsCleavage And Polyadenylation Specificity FactorMicePolyadenylationRNA, MessengerCleavage And Polyadenylation Specificity FactorRNA, Messenger3T3-L1AdipogenesisCleavage and polyadenylation

Identifiers

PMID39223634
PMCPMC11370009

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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.