Evidence map›Paper›PMID 23564456›Full record

ArticleThe Journal of biological chemistry2013

MicroRNA-322 (miR-322) and its target protein Tob2 modulate Osterix (Osx) mRNA stability.

Beatriz Gámez, Edgardo Rodríguez-Carballo, Ramon Bartrons, José Luis Rosa, Francesc Ventura

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 78 citations in OpenAlex.

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  15. Downregulation of miR-322 promotes apoptosis of GC-2 cell by targeting Ddx3x.Reproductive biology and endocrinology : RB&E · 2019
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  17. MICROmanagement of Runx2 Function in Skeletal Cells.Current molecular biology reports · 2019
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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

5 authors at 1 institution in 1 country.

Beatriz GámezDepartament de Ciències Fisiològiques II, Universitat de Barcelona, and L'Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), E-08907 L'Hospitalet de Llobregat, Barcelona, Spain.
Edgardo Rodríguez-CarballoDepartament de Ciències Fisiològiques II, Universitat de Barcelona, and L'Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), E-08907 L'Hospitalet de Llobregat, Barcelona, Spain.
Ramon BartronsDepartament de Ciències Fisiològiques II, Universitat de Barcelona, and L'Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), E-08907 L'Hospitalet de Llobregat, Barcelona, Spain.
José Luis RosaDepartament de Ciències Fisiològiques II, Universitat de Barcelona, and L'Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), E-08907 L'Hospitalet de Llobregat, Barcelona, Spain.
Francesc VenturaDepartament de Ciències Fisiològiques II, Universitat de Barcelona, and L'Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), E-08907 L'Hospitalet de Llobregat, Barcelona, Spain. Electronic address: fventura@ub.edu.
Universitat de Barcelona · ES

Funding

Diseases of Public Health Importance Training GrantT32AI007509 · NIAID · UNIVERSITY OF WASHINGTON · PI LUND, JENNIFER M · 1997 to 2024
$6.3M
Genome wide assessment of essential genes in Trypanosoma bruceiR01AI078962 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI STUART, KENNETH D · 2010 to 2012
$2.5M
NIAID NIH HHS 5T32AI007509-12NIAID NIH HHS R01 AI078962
6 · The paper itself

Abstract

Osteogenesis depends on a coordinated network of signals and transcription factors such as Runx2 and Osterix. Recent evidence indicates that microRNAs (miRNAs) act as important post-transcriptional regulators in a large number of processes, including osteoblast differentiation. In this study, we performed miRNA expression profiling and identified miR-322, a BMP-2-down-regulated miRNA, as a regulator of osteoblast differentiation. We report miR-322 gain- and loss-of-function experiments in C2C12 and MC3T3-E1 cells and primary cultures of murine bone marrow-derived mesenchymal stem cells. We demonstrate that overexpression of miR-322 enhances BMP-2 response, increasing the expression of Osx and other osteogenic genes. Furthermore, we identify Tob2 as a target of miR-322, and we characterize the specific Tob2 3'-UTR sequence bound by miR-322 by reporter assays. We demonstrate that Tob2 is a negative regulator of osteogenesis that binds and mediates degradation of Osx mRNA. Our results demonstrate a new molecular mechanism controlling osteogenesis through the specific miR-322/Tob2 regulation of specific target mRNAs. This regulatory circuit provides a clear example of a complex miRNA-transcription factor network for fine-tuning the osteoblast differentiation program.

Indexed as

Gene Expression Regulation3T3 CellsAnimalsBase SequenceCell Cycle ProteinsCell DifferentiationCell LineCell ProliferationGene Expression ProfilingHeLa CellsHumansMiceMicroRNAsMolecular Sequence DataOsteoblastsOsteogenesisCell Cycle ProteinsMicroRNAsMIRN322 microRNA, mouseRNA, MessengerSp7 protein, mouseSp7 Transcription FactorTob2 protein, mouseTranscription FactorsBoneBone Morphogenetic Protein (BMP)MicroRNAmRNA DecaymRNA DegradationOsteoblast DifferentiationOsteoblastsOsterixPolyadenylationTob2

Identifiers

PMID23564456
PMCPMC3656283
OpenAlexW2021386254

What OpenQuestion holds

Textmetadata
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.