Evidence map›Paper›PMID 38189925›Full record

ArticleJournal of molecular evolution2024

Deep Conservation and Unexpected Evolutionary History of Neighboring lncRNAs MALAT1 and NEAT1.

Forrest Weghorst, Martí Torres Marcén, Garrison Faridi, Yuh Chwen G Lee, Karina S Cramer

Open access · hybridAbstract read
In one paragraph

Article in Journal of molecular evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Metamorphosis and lncRNAs: A Close Relationship.Genesis (New York, N.Y. : 2000) · 2026
    Review
  3. Article
  4. Article
  5. RNA Triple Helices: From Structures and Mechanisms to Therapeutic Targets.International journal of biological sciences · 2026
    Review
  6. Mapping rat lncRNA Bdnf-as.Molecular biology reports · 2025
    Article
  7. Review
  8. Article
  9. Long noncoding RNAs in ubiquitination, protein degradation, and human diseases.Biochimica et biophysica acta. Gene regulatory mechanisms · 2024
    Review
  10. 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

5 authors at 1 institution in 1 country.

Forrest WeghorstDepartment of Neurobiology and Behavior, University of California, Irvine, USA.
Martí Torres MarcénDepartment of Neurobiology and Behavior, University of California, Irvine, USA.
Garrison FaridiDepartment of Neurobiology and Behavior, University of California, Irvine, USA.
Yuh Chwen G LeeDepartment of Ecology and Evolutionary Biology, University of California, Irvine, USA.
Karina S CramerDepartment of Neurobiology and Behavior, University of California, Irvine, USA. cramerk@uci.edu.ORCID 0000-0003-3793-4862
University of California, Irvine · US

Funding

NIDCD T32 Interdisciplinary Training Program in Hearing ResearchT32DC010775 · NIDCD · UNIVERSITY OF CALIFORNIA-IRVINE · PI Karina S Cramer, Raju Metherate · 2010 to 2026
$3.5M
Non-apoptotic functions of caspase-3 in neural developmentR56DC020246 · NIDCD · UNIVERSITY OF CALIFORNIA-IRVINE · PI CRAMER, KARINA S · 2023 to 2023
$473k
Mechanisms of non-apoptotic caspase-3 regulation of auditory brainstem developmentF31DC019548 · NIDCD · UNIVERSITY OF CALIFORNIA-IRVINE · PI WEGHORST, FORREST · 2021 to 2022
$72k
NIDCD NIH HHS F31 DC019548NIDCD NIH HHS R56 DC020246NIDCD NIH HHS T32 DC010775
6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) have begun to receive overdue attention for their regulatory roles in gene expression and other cellular processes. Although most lncRNAs are lowly expressed and tissue-specific, notable exceptions include MALAT1 and its genomic neighbor NEAT1, two highly and ubiquitously expressed oncogenes with roles in transcriptional regulation and RNA splicing. Previous studies have suggested that NEAT1 is found only in mammals, while MALAT1 is present in all gnathostomes (jawed vertebrates) except birds. Here we show that these assertions are incomplete, likely due to the challenges associated with properly identifying these two lncRNAs. Using phylogenetic analysis and structure-aware annotation of publicly available genomic and RNA-seq coverage data, we show that NEAT1 is a common feature of tetrapod genomes except birds and squamates. Conversely, we identify MALAT1 in representative species of all major gnathostome clades, including birds. Our in-depth examination of MALAT1, NEAT1, and their genomic context in a wide range of vertebrate species allows us to reconstruct the series of events that led to the formation of the locus containing these genes in taxa from cartilaginous fish to mammals. This evolutionary history includes the independent loss of NEAT1 in birds and squamates, since NEAT1 is found in the closest living relatives of both clades (crocodilians and tuataras, respectively). These data clarify the origins and relationships of MALAT1 and NEAT1 and highlight an opportunity to study the change and continuity in lncRNA structure and function over deep evolutionary time.

Indexed as

RNA, Long NoncodingAnimalsBiological EvolutionGene Expression RegulationMammalsPhylogenyRNA, Long NoncodingBirdsComparative genomicsLong non-coding RNAMALAT1NEAT1

Identifiers

PMID38189925
PMCPMC10869381
OpenAlexW4390673434

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.