Evidence map›Paper›PMID 29738469›Full record

ReviewJournal of cardiovascular development and disease2018

The Role of scaRNAs in Adjusting Alternative mRNA Splicing in Heart Development.

Chloe Nagasawa, Allison Ogren, Nataliya Kibiryeva, Jennifer Marshall, James E O'Brien, Naoya Kenmochi, Douglas C Bittel

Open access · goldAbstract readReview
In one paragraph

Review in Journal of cardiovascular development and disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 2'-RNA (New York, N.Y.) · 2024
    Review
  5. Article
  6. Review
  7. Identification of mClinical epigenetics · 2023
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Epitranscriptomics of cardiovascular diseases (Review).International journal of molecular medicine · 2022
    Review
  14. The Potential Role of Small Nucleolar RNAs in Cancers - An Evidence Map.International journal of general medicine · 2022
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. 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

7 authors at 4 institutions in 2 countries.

Chloe NagasawaCollege of Biosciences, Kansas City University, Kansas City, MO 64106, USA. cnagasawa94@kcumb.edu.
Allison OgrenCollege of Biosciences, Kansas City University, Kansas City, MO 64106, USA. allison.ogren@kcumb.edu.
Nataliya KibiryevaWard Family Heart Center, Children's Mercy Hospital, University of Missouri-Kansas City School of Medicine, Kansas City, MO 64108, USA. nkibiryeva@cmh.edu.
Jennifer MarshallWard Family Heart Center, Children's Mercy Hospital, University of Missouri-Kansas City School of Medicine, Kansas City, MO 64108, USA. jamarshall@cmh.edu.
James E O'BrienWard Family Heart Center, Children's Mercy Hospital, University of Missouri-Kansas City School of Medicine, Kansas City, MO 64108, USA. jobrien@cmh.edu.
Naoya KenmochiFrontier Science Research Center, University of Miyazaki, Miyazaki 889-1692, Japan. kenmochi@med.miyazaki-u.ac.jp.
Douglas C BittelCollege of Biosciences, Kansas City University, Kansas City, MO 64106, USA. dbittel@kcumb.edu.
Kansas City University · USChildren's Mercy Hospital · USUniversity of Missouri–Kansas City · USUniversity of Miyazaki · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital heart disease (CHD) is a leading cause of death in children <1 year of age. Despite intense effort in the last 10 years, most CHDs (~70%) still have an unknown etiology. Conotruncal based defects, such as Tetralogy of Fallot (TOF), a common complex of devastating heart defects, typically requires surgical intervention in the first year of life. We reported that the noncoding transcriptome in myocardial tissue from children with TOF is characterized by significant variation in levels of expression of noncoding RNAs, and more specifically, a significant reduction in 12 small cajal body-associated RNAs (scaRNAs) in the right ventricle. scaRNAs are essential for the biochemical modification and maturation of small nuclear RNAs (spliceosomal RNAs), which in turn are critical components of the spliceosome. This is particularly important because we also documented that splicing of mRNAs that are critical for heart development was dysregulated in the heart tissue of infants with TOF. Furthermore, we went on to show, using the zebrafish model, that altering the expression of these same scaRNAs led to faulty mRNA processing and heart defects in the developing embryo. This review will examine how scaRNAs may influence spliceosome fidelity in exon retention during heart development and thus contribute to regulation of heart development.

Indexed as

alternative mRNA splicingcongenital heart defectsscaRNAssmall cajal body-associated RNAstetralogy of Fallot

Identifiers

PMID29738469
PMCPMC6023535
OpenAlexW2801876616

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.