Evidence map›Paper›PMID 25917881›Full record

ArticleTheriogenology2015

Germline transmission in transgenic Huntington's disease monkeys.

Sean Moran, Tim Chi, Melinda S Prucha, Kwang Sung Ahn, Fawn Connor-Stroud, Sherrie Jean, Kenneth Gould, Anthony W S Chan

Abstract read
In one paragraph

Article in Theriogenology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Mending a broken heart:Disease models & mechanisms · 2021
    Review
  6. Article
  7. Review
  8. Review
  9. Progress in developing transgenic monkey model for Huntington's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2018
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Cryotolerance of Sperm from Transgenic Rhesus Macaques (Macaca mulatta).Journal of the American Association for Laboratory Animal Science : JAALAS · 2016
    Article
  18. 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

8 authors at 1 institution in 1 country.

Sean MoranDepartment of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA; Division of Neuropharmacology and Neurologic Diseases, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Tim ChiDepartment of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA; Division of Neuropharmacology and Neurologic Diseases, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Melinda S PruchaDepartment of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA; Division of Neuropharmacology and Neurologic Diseases, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Kwang Sung AhnDepartment of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA; Division of Neuropharmacology and Neurologic Diseases, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Fawn Connor-StroudDivision of Animal Resources, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Sherrie JeanDivision of Animal Resources, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Kenneth GouldDivision of Animal Resources, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Anthony W S ChanDepartment of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA; Division of Neuropharmacology and Neurologic Diseases, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA. Electronic address: awchan@emory.edu.
Emory University · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI ALTMAN, JOHN DAVID · 1985 to 2011
$114.0M
Establishment of a transgenic monkey of Huntingtons's dieseaseR24RR018827 · NCRR · EMORY UNIVERSITY · PI CHAN, ANTHONY WING SANG · 2004 to 2011
$6.2M
Transgenic Huntington's disease monkey resourceR24OD010930 · OD · EMORY UNIVERSITY · PI CHAN, ANTHONY WING SANG · 2012 to 2018
$6.1M
NCRR NIH HHS P51 RR000165NCRR NIH HHS P51RR165NCRR NIH HHS R24 RR018827NCRR NIH HHS RR018827NIH HHS P51 OD011132NIH HHS P51OD11132NIH HHS R24 OD010930
6 · The paper itself

Abstract

Transgenic nonhuman primate models are an increasingly popular model for neurologic and neurodegenerative disease because their brain functions and neural anatomies closely resemble those of humans. Transgenic Huntington's disease monkeys (HD monkeys) developed clinical features similar to those seen in HD patients, making the monkeys suitable for a preclinical study of HD. However, until HD monkey colonies can be readily expanded, their use in preclinical studies will be limited. In the present study, we confirmed germline transmission of the mutant huntingtin (mHTT) transgene in both embryonic stem cells generated from three male HD monkey founders (F0) and in second-generation offspring (F1) produced via artificial insemination by using intrauterine insemination technique. A total of five offspring were produced from 15 females that were inseminated by intrauterine insemination using semen collected from the three HD founders (5 of 15, 33%). Thus far, sperm collected from the HD founder (rHD8) has led to two F1 transgenic HD monkeys with germline transmission rate at 100% (2 of 2). mHTT expression was confirmed by quantitative real-time polymerase chain reaction using skin fibroblasts from the F1 HD monkeys and induced pluripotent stem cells established from one of the F1 HD monkeys (rHD8-2). Here, we report the stable germline transmission and expression of the mHTT transgene in HD monkeys, which suggest possible expansion of HD monkey colonies for preclinical and biomedical research studies.

Indexed as

Animals, Genetically ModifiedMacaca mulattaSpermatozoaAnimalsCell DifferentiationDisease Models, AnimalEmbryonic Stem CellsFemaleGenotypeGerm CellsHuntingtin ProteinHuntington DiseaseInduced Pluripotent Stem CellsInsemination, ArtificialMaleNerve Tissue ProteinsHTT protein, humanHuntingtin ProteinNerve Tissue ProteinsGermline transmissionSecond generationTransgenic Huntington's disease monkeyUltrasound-guided intrauterine insemination

Identifiers

PMID25917881
PMCPMC4631054
OpenAlexW2005306869

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.