Evidence map›Paper›PMID 12391306›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Production of transgenic rats by lentiviral transduction of male germ-line stem cells.

F Kent Hamra, Joel Gatlin, Karen M Chapman, Dana M Grellhesl, J Victor Garcia, Robert E Hammer, David L Garbers

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
9.3field-weighted citation impact, top 2% 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

82 citing papers in PubMed, 242 citations in OpenAlex.

  1. Article
  2. Male germ cell technologies in large animals.The Journal of reproduction and development · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Viral Transduction of Mammalian Spermatogonial Stem Cells.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  9. Rattus norvegicus Spermatogenesis Colony-Forming Assays.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  10. Article
  11. Article
  12. Review
  13. Targeted Gene Editing in Porcine Germ Cells.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Role of stem cells in fertility preservation: current insights.Stem cells and cloning : advances and applications · 2019
    Article
  20. Laser-assisted Lentiviral Gene Delivery to Mouse Fertilized Eggs.Journal of visualized experiments : JoVE · 2018
    Article

22 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

F Kent HamraCecil H. and Ida Green Center for Reproductive Biology Sciences, Dallas, TX 75390, USA.
Joel Gatlin
Karen M Chapman
Dana M Grellhesl
J Victor Garcia
Robert E Hammer
David L Garbers
The University of Texas Southwestern Medical Center · USHoward Hughes Medical Institute · USSouthwestern Medical Center · US

Funding

GENE TRANSFER SYSTEM FOR AIDS THERAPYR01AI039416 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI GARCIA-MARTINEZ, J. VICTOR · 1996 to 2008
$2.5M
NIAID NIH HHS AI39416NIAID NIH HHS R01 AI039416
6 · The paper itself

Abstract

Primary cultures of rat spermatogenic cells that did not bind to collagen matrices were able to colonize and form mature spermatozoa when transferred to testes of recipient males. Up to 73% of the progeny from matings with recipient males were derived from the transferred spermatogenic cells. Subsequently, two populations of germ cells were obtained by selection on laminin matrices. Both populations expressed the spermatogenic cell marker, DAZL, but not the somatic cell marker, vimentin. The cells that bound to laminin represented approximately 5% of the total population and were greatly enriched in ability to colonize a recipient testis, suggesting an enrichment in germ-line stem cells. The colonization potential was maintained for at least 7 days in culture. These cells were subsequently transduced with a lentiviral enhanced GFP reporter vector and then transferred to WT recipient males. After mating, 26 of 44 pups were derived from the cultured donor germ cells, and 13 pups carried the lentiviral transgene. Based on Southern analysis, the transgene was integrated at a different genetic locus in each animal and was transmitted to approximately 50% of pups in the F(2) generation. Thus, by using these procedures, approximately 30% of pups in the F(1) generation inherited and stably transmitted a lentiviral transgene that integrated at various genomic sites.

Indexed as

RNA-Binding ProteinsAmino Acid SequenceAnimalsAnimals, Genetically Modifiedbeta-GalactosidaseCell TransplantationFertilizationGenetic VectorsGerm CellsGreen Fluorescent ProteinsHomozygoteImmunohistochemistryLentivirusLuminescent ProteinsMaleMicebeta-GalactosidaseDAZL protein, humanGreen Fluorescent ProteinsLuminescent ProteinsPeptide FragmentsProteinsRNA-Binding Proteins

Identifiers

PMID12391306
PMCPMC137522
OpenAlexW2170881245

What OpenQuestion holds

Textmetadata
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.