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miR-206 and -486 Induce Myoblast Differentiation by Downregulating Pax7

2010· article· en· 421 citations· W2062427797 on OpenAlex· 10.1128/mcb.01009-10

Why is this work in the frame?

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.

No Canadian affiliation. An affiliation-only frame — the usual design — would never have seen this work. It is one of the works that make the case for inverting the frame.

Machine scores (provisional)

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Opus teacher head0.003
GPT teacher head0.201
Teacher spread
0.198 · how far apart the two teachers sit on this one work
Validation status
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Abstract

The Pax7 transcription factor is required for muscle satellite cell biogenesis and specification of the myogenic precursor lineage. Pax7 is expressed in proliferating myoblasts but is rapidly downregulated during differentiation. Here we report that miR-206 and -486 are induced during myoblast differentiation and downregulate Pax7 by directly targeting its 3' untranslated region (UTR). Expression of either of these microRNAs in myoblasts accelerates differentiation, whereas inhibition of these microRNAs causes persistence of Pax7 protein and delays differentiation. A microRNA-resistant form of Pax7 is sufficient to inhibit differentiation. Since both these microRNAs are induced by MyoD and since Pax7 promotes the expression of Id2, an inhibitor of MyoD, our results revealed a bistable switch that exists either in a Pax7-driven myoblast state or a MyoD-driven myotube state.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

The record

Venue
Molecular and Cellular Biology
Topic
Muscle Physiology and Disorders
Field
Biochemistry, Genetics and Molecular Biology
Canadian institutions
Funders
National Institute of Arthritis and Musculoskeletal and Skin DiseasesOhio State UniversityNational Institute of General Medical SciencesHeart and Stroke Foundation of Canada
Keywords
MyoDBiologyMyocyteCell biologyCellular differentiationMyoD ProteinmicroRNAMyogenesisMyogenic regulatory factorsMyogeninTranscription factorPITX2Molecular biologyGeneticsGeneHomeobox
Has abstract in OpenAlex
yes