Evidence map›Paper›PMID 25886262›Full record

ArticleGenome biology2015

Expansion of a novel endogenous retrovirus throughout the pericentromeres of modern humans.

Joseph Zahn, Mark H Kaplan, Sabrina Fischer, Manhong Dai, Fan Meng, Anjan Kumar Saha, Patrick Cervantes, Susana M Chan, Derek Dube, Gilbert S Omenn and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Genome biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.2field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  17. Mobile elements contribute to the uniqueness of human genome with 15,000 human-specific insertions and 14 Mbp sequence increase.DNA research : an international journal for rapid publication of reports on genes and genomes · 2018
    Article
  18. Article
  19. Transposable elements: genome innovation, chromosome diversity, and centromere conflict.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2018
    Review
  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

12 authors at 1 institution in 1 country.

Joseph ZahnDepartment of Internal Medicine, Division of Infectious Diseases and Programs in Immunology, Cancer Biology, and Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI, 48109, USA. jazahn@med.umich.edu.
Mark H KaplanDepartment of Internal Medicine, Division of Infectious Diseases and Programs in Immunology, Cancer Biology, and Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI, 48109, USA. mhkaplan@med.umich.edu.
Sabrina FischerDepartment of Internal Medicine, Division of Infectious Diseases and Programs in Immunology, Cancer Biology, and Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI, 48109, USA. sfischee@cin.edu.uy.
Manhong DaiMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI, 48109, USA. daimh@umich.edu.
Fan MengMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI, 48109, USA. mengf@umich.edu.
Anjan Kumar SahaDepartment of Internal Medicine, Division of Infectious Diseases and Programs in Immunology, Cancer Biology, and Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI, 48109, USA. aksaha@med.umich.edu.
Patrick CervantesDepartment of Internal Medicine, Division of Infectious Diseases and Programs in Immunology, Cancer Biology, and Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI, 48109, USA. pcervant@umich.edu.
Susana M ChanDepartment of Internal Medicine, Division of Infectious Diseases and Programs in Immunology, Cancer Biology, and Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI, 48109, USA. susanac@umich.edu.
Derek DubeDepartment of Internal Medicine, Division of Infectious Diseases and Programs in Immunology, Cancer Biology, and Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI, 48109, USA. ddube@usj.edu.
Gilbert S OmennDepartments of Computational Medicine and Bioinformatics, Internal Medicine, and Human Genetics, and School of Public Health, University of Michigan, Ann Arbor, MI, 48109, USA. gomenn@med.umich.edu.
David M MarkovitzDepartment of Internal Medicine, Division of Infectious Diseases and Programs in Immunology, Cancer Biology, and Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI, 48109, USA. dmarkov@med.umich.edu.
Rafael Contreras-GalindoDepartment of Internal Medicine, Division of Infectious Diseases and Programs in Immunology, Cancer Biology, and Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI, 48109, USA. rafaelc@med.umich.edu.
University of Michigan–Ann Arbor · US

Funding

MICHIGAN INSTITUTE FOR CLINICAL AND HEALTH RESEARCH (MICHR) (UL1): (BPCA)UL1RR024986 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHANLEY, THOMAS P. · 2007 to 2011
$51.2M
MICHIGAN MEDICAL SCIENTIST TRAINING PROGRAMT32GM007863 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COLLINS, KATHLEEN L. · 1985 to 2024
$38.3M
Strategic Vision & Impact on Environmental HealthP30ES017885 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Dana Dolinoy · 2011 to 2026
$21.3M
CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
Molecular Mechanisms of Microbial Pathogenesis Training ProgramT32AI007528 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CARRUTHERS, VERNON BRUCE · 1998 to 2024
$6.8M
Replication of Human Endogenous Retroviruses in Modern HumansR01CA144043 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MARKOVITZ, DAVID MICHAEL · 2009 to 2013
$6.4M
University of Michigan Postbaccalaureate Research Education Program (UM PREP)R25GM086262 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ALLEN, BENJAMIN · 2009 to 2024
$6.1M
Cellular Biotechnology Training Program (CBTP) - Years 31-35T32GM145304 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Guizhi Zhu · 2022 to 2026
$2.6M
Human Endogenous Retroviral Sequences, a Tool to Study the Role of Centromeres inK22CA177824 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CONTRERAS, RAFAEL ALEJANDRO · 2013 to 2015
$346k
The Viral Life Cycle of Human Endogenous Retrovirus Type KF32AI106189 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DUBE, DEREK · 2013 to 2014
$66k
NCI NIH HHS 3R01CA144043-03S1NCI NIH HHS K22 CA177824NCI NIH HHS R01 CA144043NCRR NIH HHS UL1 RR024986NCRR NIH HHS UL1RR24986NIAID NIH HHS 1F32AI106189-01NIAID NIH HHS 5T32AI007528-13NIAID NIH HHS F32 AI106189NIAID NIH HHS T32 AI007528NIEHS NIH HHS P30 ES017885NIEHS NIH HHS P30U54ES017885NIGMS NIH HHS R25 GM086262NIGMS NIH HHS R25GM086262-07NIGMS NIH HHS T32 GM007315NIGMS NIH HHS T32-GM007315NIGMS NIH HHS T32 GM007863NIGMS NIH HHS T32 GM145304RMOD NIH HHS RM-08-029
6 · The paper itself

Abstract

backgroundApproximately 8% of the human genome consists of sequences of retroviral origin, a result of ancestral infections of the germ line over millions of years of evolution. The most recent of these infections is attributed to members of the human endogenous retrovirus type-K (HERV-K) (HML-2) family. We recently reported that a previously undetected, large group of HERV-K (HML-2) proviruses, which are descendants of the ancestral K111 infection, are spread throughout human centromeres.

resultsStudying the genomes of certain cell lines and the DNA of healthy individuals that seemingly lack K111, we discover new HERV-K (HML-2) members hidden in pericentromeres of several human chromosomes. All are related through a common ancestor, termed K222, which is a virus that infected the germ line approximately 25 million years ago. K222 exists as a single copy in the genomes of baboons and high order primates, but not New World monkeys, suggesting that progenitor K222 infected the primate germ line after the split between New and Old World monkeys. K222 exists in modern humans at multiple loci spread across the pericentromeres of nine chromosomes, indicating it was amplified during the evolution of modern humans.

conclusionsCopying of K222 may have occurred through recombination of the pericentromeres of different chromosomes during human evolution. Evidence of recombination between K111 and K222 suggests that these retroviral sequences have been templates for frequent cross-over events during the process of centromere recombination in humans.

Indexed as

Evolution, MolecularBase SequenceCentromereChromosomes, HumanComputational BiologyDNA PrimersDNA, ViralEndogenous RetrovirusesGenome, HumanHigh-Throughput Nucleotide SequencingHumansMolecular Sequence DataSequence AlignmentSequence Analysis, DNADNA PrimersDNA, Viral

Identifiers

PMID25886262
PMCPMC4425911
OpenAlexW1974449258

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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.