Evidence map›Paper›PMID 23171859›Full record

ArticleMolecular biology and evolution2013

Human microRNAs originated from two periods at accelerated rates in mammalian evolution.

Hisakazu Iwama, Kiyohito Kato, Hitomi Imachi, Koji Murao, Tsutomu Masaki

Abstract read
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Article in Molecular biology and evolution, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

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23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Primate-specific Long Non-coding RNAs and MicroRNAs.Genomics, proteomics & bioinformatics · 2017
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Evolutionary Transitions of MicroRNA-Target Pairs.Genome biology and evolution · 2016
    Article
  16. Article
  17. ncRNA orthologies in the vertebrate lineage.Database : the journal of biological databases and curation · 2016
    Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Hisakazu IwamaLife Science Research Center, Kagawa University, Kita-gun, Kagawa, Japan. iwama@med.kagawa-u.ac.jp
Kiyohito Kato
Hitomi Imachi
Koji Murao
Tsutomu Masaki

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are short, noncoding RNAs that modulate genes posttranscriptionally. Frequent gains and losses of miRNA genes have been reported to occur during evolution. However, little is known systematically about the periods of evolutionary origin of the present miRNA gene repertoire of an extant mammalian species. Thus, in this study, we estimated the evolutionary periods during which each of 1,433 present human miRNA genes originated within 15 periods, from human to platypus-human common ancestral branch and a class "conserved beyond theria," primarily using multiple genome alignments of 38 species, plus the pairwise genome alignments of five species. The results showed two peak periods in which the human miRNA genes originated at significantly accelerated rates. The most accelerated rate appeared in the period of the initial phase of hominoid lineage, and the second appeared shortly before Laurasiatherian divergence. Approximately 53% of the present human miRNA genes have originated within the simian lineage to human. In particular, approximately 28% originated within the hominoid lineage. The early phase of placental mammal radiation comprises approximately 28%, while no more than 15% of human miRNAs have been conserved beyond placental mammals. We also clearly showed a general trend, in which the miRNA expression level decreases as the miRNA becomes younger. Intriguingly, amid this decreasing trend of expression, we found one significant rise in the expression level that corresponded to the initial phase of the hominoid lineage, suggesting that increased functional acquisitions of miRNAs originated at this particular period.

Indexed as

Evolution, MolecularModels, GeneticAnimalsChromosomes, HumanComputer SimulationGene ExpressionGenetic SpeciationGenomeHominidaeHumansMammalsMicroRNAsMolecular Sequence AnnotationMultigene FamilyMicroRNAs

Identifiers

PMID23171859
PMCPMC3563971

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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.