Evidence map›Paper›PMID 31751568›Full record

ArticleJournal of molecular and cellular cardiology2020

Transcriptional control of a novel long noncoding RNA Mymsl in smooth muscle cells by a single Cis-element and its initial functional characterization in vessels.

Mihyun Choi, Yao Wei Lu, Jinjing Zhao, Mingfu Wu, Wei Zhang, Xiaochun Long

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Long Non-Coding RNA Function in Smooth Muscle Cell Plasticity and Atherosclerosis.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
  3. Review
  4. Article
  5. Circulation · 2023
    Article
  6. Of mice and human-specific long noncoding RNAs.Mammalian genome : official journal of the International Mammalian Genome Society · 2022
    Review
  7. Article
  8. Review
  9. Circulation · 2021
    Article
  10. Review
  11. Article
  12. Article
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

6 authors at 1 institution in 1 country.

Mihyun ChoiDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, NY, United States of America.
Yao Wei LuDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, NY, United States of America.
Jinjing ZhaoDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, NY, United States of America.
Mingfu WuDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, NY, United States of America.
Wei ZhangDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, NY, United States of America.
Xiaochun LongDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, NY, United States of America. Electronic address: Xlong@augusta.edu.
Albany Medical Center Hospital · US

Funding

Signaling by beta 1 integrins regulates ventricular wall morphogenesis and compactionR01HL121700 · NHLBI · UNIVERSITY OF HOUSTON · PI Mingfu Wu, YANG Kevin XIANG · 2015 to 2026
$5.4M
Novel Role of MAPK14 in Regulation of VSMC Contractile PhenotypeR01HL122686 · NHLBI · AUGUSTA UNIVERSITY · PI LONG, XIAOCHUN · 2014 to 2022
$4.0M
Function and Regulation of TSPAN2 in Vascular DiseaseR01HL139794 · NHLBI · AUGUSTA UNIVERSITY · PI LONG, XIAOCHUN · 2019 to 2023
$2.7M
NHLBI NIH HHS R01 HL121700NHLBI NIH HHS R01 HL122686NHLBI NIH HHS R01 HL139794
6 · The paper itself

Abstract

Differentiated vascular smooth muscle cells (VSMCs) are crucial in maintaining vascular homeostasis. While the coding transcriptome of the differentiated VSMC phenotype has been defined, we know little about its noncoding signature. Herein, we identified a Myocardin-induced muscle specific long noncoding RNA (lncRNA) (Mymsl) downregulated upon VSMC phenotypic modulation. We demonstrated an essential role of a proximal consensus CArG element in response to MYOCD/SRF in vitro. To validate the in vivo role of this CArG element, we generated CArG mutant mice via CRISPR-Cas9 genome editing. While the CArG mutation had no impact on the expression of surrounding genes, it abolished Mymsl expression in SMCs, but not skeletal and cardiac muscle. Chromatin immunoprecipitation assays (ChIPs) showed decreased SRF binding to CArG region in mutants whereas the enrichment of H3K79Me2 remained the same. RNA-seq analysis showed a downregulation of matrix genes in aortas from Mymsl knockout mice, which was further validated in injured carotid arteries. Our study defined the transcriptional control of a novel lncRNA in SMCs via a single transcription factor binding site, which may offer a new strategy for generating SMC-specific knockout mouse models. We also provided in vivo evidence supporting the potential importance of Mymsl in vascular pathophysiology.

Indexed as

Transcription, GeneticAnimalsAortaBlood VesselsCell DifferentiationDown-RegulationExtracellular MatrixGene EditingGenomeMice, Inbred C57BLMice, KnockoutMutationMyocardinMyocytes, CardiacMyocytes, Smooth MuscleNuclear ProteinsMyocardinNuclear ProteinsRNA, Long NoncodingSerum Response FactorTrans-ActivatorsCRISPR genome editingLong noncoding RNATranscription factorVascular smooth muscle

Identifiers

PMID31751568
PMCPMC7036038
OpenAlexW2985965616

What OpenQuestion holds

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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.