Evidence map›Paper›PMID 24026178›Full record

ArticleGenome research2013

Analysis of variable retroduplications in human populations suggests coupling of retrotransposition to cell division.

Alexej Abyzov, Rebecca Iskow, Omer Gokcumen, David W Radke, Suganthi Balasubramanian, Baikang Pei, Lukas Habegger, 1000 Genomes Project Consortium, Charles Lee, Mark Gerstein

Abstract read
In one paragraph

Article in Genome research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
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

37 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. The mutational load in natural populations is significantly affected by high primary rates of retroposition.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Cancer, Retrogenes, and Evolution.Life (Basel, Switzerland) · 2021
    Review
  10. Pseudogene Profiling for Cancer Subtype Classification.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  11. Article
  12. MultipleGenes · 2020
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

10 authors.

Alexej AbyzovProgram in Computational Biology and Bioinformatics.
Rebecca Iskow
Omer Gokcumen
David W Radke
Suganthi Balasubramanian
Baikang Pei
Lukas Habegger
1000 Genomes Project Consortium
Charles Lee
Mark Gerstein

Funding

YALE BIOMEDICAL SUPERCOMPUTER: NEUROSCIENCES10RR019895 · NCRR · YALE UNIVERSITY · PI WILLIAMS, KENNETH ROBERT · 2004 to 2004
$1.6M
The Role of Somatic Copy Number Changes in AgingF32AG039979 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI TORENE, REBECCA I · 2011 to 2013
$76k
NCRR NIH HHS RR19895NCRR NIH HHS S10 RR019895NIA NIH HHS F32 AG039979NIA NIH HHS F32AG039979Wellcome Trust 085532
6 · The paper itself

Abstract

In primates and other animals, reverse transcription of mRNA followed by genomic integration creates retroduplications. Expressed retroduplications are either "retrogenes" coding for functioning proteins, or expressed "processed pseudogenes," which can function as noncoding RNAs. To date, little is known about the variation in retroduplications in terms of their presence or absence across individuals in the human population. We have developed new methodologies that allow us to identify "novel" retroduplications (i.e., those not present in the reference genome), to find their insertion points, and to genotype them. Using these methods, we catalogued and analyzed 174 retroduplication variants in almost one thousand humans, which were sequenced as part of Phase 1 of The 1000 Genomes Project Consortium. The accuracy of our data set was corroborated by (1) multiple lines of sequencing evidence for retroduplication (e.g., depth of coverage in exons vs. introns), (2) experimental validation, and (3) the fact that we can reconstruct a correct phylogenetic tree of human subpopulations based solely on retroduplications. We also show that parent genes of retroduplication variants tend to be expressed at the M-to-G1 transition in the cell cycle and that M-to-G1 expressed genes have more copies of fixed retroduplications than genes expressed at other times. These findings suggest that cell division is coupled to retrotransposition and, perhaps, is even a requirement for it.

Indexed as

Gene DuplicationCell DivisionComputational BiologyEvolution, MolecularGenome, HumanGenotypeHumansPhylogenyPseudogenesReproducibility of ResultsRetroelementsSequence Analysis, DNARetroelements

Identifiers

PMID24026178
PMCPMC3847774

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.