Evidence map›Paper›PMID 38019864›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Generation of de novo miRNAs from template switching during DNA replication.

Heli A M Mönttinen, Mikko J Frilander, Ari Löytynoja

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

3 authors at 1 institution in 1 country.

Heli A M MönttinenInstitute of Biotechnology, Helsinki Institute of Life Science, University of Helsinki, Helsinki FI-000, Finland.ORCID 0000-0003-2461-0690
Mikko J FrilanderInstitute of Biotechnology, Helsinki Institute of Life Science, University of Helsinki, Helsinki FI-000, Finland.ORCID 0000-0002-1732-4808
Ari LöytynojaInstitute of Biotechnology, Helsinki Institute of Life Science, University of Helsinki, Helsinki FI-000, Finland.ORCID 0000-0001-5389-6611
University of Helsinki · FI

Funding

Academy of Finland (AKA) 322681Academy of Finland (AKA) 341477Emil Aaltosen Säätiö (Emil Aaltonen Foundation) NA
6 · The paper itself

Abstract

The mechanisms generating novel genes and genetic information are poorly known, even for microRNA (miRNA) genes with an extremely constrained design. All miRNA primary transcripts need to fold into a stem-loop structure to yield short gene products ([Formula: see text]22 nt) that bind and repress their mRNA targets. While a substantial number of miRNA genes are ancient and highly conserved, short secondary structures coding for entirely novel miRNA genes have been shown to emerge in a lineage-specific manner. Template switching is a DNA-replication-related mutation mechanism that can introduce complex changes and generate perfect base pairing for entire hairpin structures in a single event. Here, we show that the template-switching mutations (TSMs) have participated in the emergence of over 6,000 suitable hairpin structures in the primate lineage to yield at least 18 new human miRNA genes, that is 26% of the miRNAs inferred to have arisen since the origin of primates. While the mechanism appears random, the TSM-generated miRNAs are enriched in introns where they can be expressed with their host genes. The high frequency of TSM events provides raw material for evolution. Being orders of magnitude faster than other mechanisms proposed for de novo creation of genes, TSM-generated miRNAs enable near-instant rewiring of genetic information and rapid adaptation to changing environments.

Indexed as

MicroRNAsAnimalsDNA ReplicationHumansIntronsPrimatesMicroRNAsde novo emergencegenetic informationmicroRNA genestemplate switching mutations

Identifiers

PMID38019864
PMCPMC10710096
OpenAlexW4389128610

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.