Evidence map›Paper›PMID 25047835›Full record

ArticleMolecular and cellular biology2014

Role of the mTORC1 complex in satellite cell activation by RNA-induced mitochondrial restoration: dual control of cyclin D1 through microRNAs.

Sukanta Jash, Gunjan Dhar, Utpalendu Ghosh, Samit Adhya

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

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

14 citing papers in PubMed.

  1. Article
  2. The Importance of mTORC1-Autophagy Axis for Skeletal Muscle Diseases.International journal of molecular sciences · 2022
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
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

4 authors.

Sukanta JashGenetic Engineering Laboratory, CSIR-Indian Institute of Chemical Biology, Calcutta, India.
Gunjan DharGenetic Engineering Laboratory, CSIR-Indian Institute of Chemical Biology, Calcutta, India.
Utpalendu GhoshGenetic Engineering Laboratory, CSIR-Indian Institute of Chemical Biology, Calcutta, India.
Samit AdhyaGenetic Engineering Laboratory, CSIR-Indian Institute of Chemical Biology, Calcutta, India nilugrandson@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During myogenesis, satellite stem cells (SCs) are induced to proliferate and differentiate to myogenic precursors. The role of energy sensors such as the AMP-activated protein kinase (AMPK) and the mammalian Target of Rapamycin (mTOR) in SC activation is unclear. We previously observed that upregulation of ATP through RNA-mediated mitochondrial restoration (MR) accelerates SC activation following skeletal muscle injury. We show here that during regeneration, the AMPK-CRTC2-CREB and Raptor-mTORC-4EBP1 pathways were rapidly activated. The phosho-CRTC2-CREB complex was essential for myogenesis and activated transcription of the critical cell cycle regulator cyclin D1 (Ccnd1). Knockdown (KD) of either mTORC or its subunit Raptor delayed SC activation without influencing the differentiation program. KD of 4EBP1 had no effect on SC activation but enhanced myofiber size. mTORC1 positively regulated Ccnd1 translation but destabilized Ccnd1 mRNA. These antithetical effects of mTORC1 were mediated by two microRNAs (miRs) targeted to the 3' untranslated region (UTR) of Ccnd1 mRNA: miR-1 was downregulated in mTORC-KD muscle, and depletion of miR-1 resulted in increased levels of mRNA without any effect on Ccnd1 protein. In contrast, miR-26a was upregulated upon mTORC depletion, while anti-miR-26a oligonucleotide specifically stimulated Ccnd1 protein expression. Thus, mTORC may act as a timer of satellite cell proliferation during myogenesis.

Indexed as

AMP-Activated Protein KinasesAnimalsCell ProliferationCyclic AMP Response Element-Binding ProteinCyclin D1Gene Expression RegulationGene Knockdown TechniquesHumansMaleMicroRNAsMuscle DevelopmentMuscle, SkeletalRatsRats, Sprague-DawleyRNARNA, MitochondrialAMP-Activated Protein KinasesCRTC2 protein, ratCyclic AMP Response Element-Binding ProteinCyclin D1MicroRNAsMIRN1 microRNA, ratMIRN26 microRNA, ratRNARNA, MitochondrialTOR Serine-Threonine KinasesTrans-Activators

Identifiers

PMID25047835
PMCPMC4187730

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.