Evidence map›Paper›PMID 32559457›Full record

ArticleStem cell reports2020

Human Stem Cell Resources Are an Inroad to Neandertal DNA Functions.

Michael Dannemann, Zhisong He, Christian Heide, Benjamin Vernot, Leila Sidow, Sabina Kanton, Anne Weigert, Barbara Treutlein, Svante Pääbo, Janet Kelso and 1 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Large-scale functional screen identifies genetic variants with splicing effects in modern and archaic humans.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Article
  6. Review
  7. Predicting Archaic Hominin Phenotypes from Genomic Data.Annual review of genomics and human genetics · 2022
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 3 countries.

Michael DannemannMax Planck Institute for Evolutionary Anthropology, Leipzig, Germany; Institute of Genomics, University of Tartu, Tartu, Estonia.
Zhisong HeDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.
Christian HeideMax Planck Institute for Evolutionary Anthropology, Leipzig, Germany.
Benjamin VernotMax Planck Institute for Evolutionary Anthropology, Leipzig, Germany.
Leila SidowMax Planck Institute for Evolutionary Anthropology, Leipzig, Germany.
Sabina KantonMax Planck Institute for Evolutionary Anthropology, Leipzig, Germany.
Anne WeigertMax Planck Institute for Evolutionary Anthropology, Leipzig, Germany.
Barbara TreutleinMax Planck Institute for Evolutionary Anthropology, Leipzig, Germany; Department of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.
Svante PääboMax Planck Institute for Evolutionary Anthropology, Leipzig, Germany.
Janet KelsoMax Planck Institute for Evolutionary Anthropology, Leipzig, Germany.
J Gray CampMax Planck Institute for Evolutionary Anthropology, Leipzig, Germany; Institute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland; Department of Ophthalmology, University of Basel, Basel, Switzerland. Electronic address: grayson.camp@iob.ch.
Max Planck Institute for Evolutionary Anthropology · DEETH Zurich · CHUniversity of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Induced pluripotent stem cells (iPSCs) from diverse humans offer the potential to study human functional variation in controlled culture environments. A portion of this variation originates from an ancient admixture between modern humans and Neandertals, which introduced alleles that left a phenotypic legacy on individual humans today. Here, we show that a large iPSC repository harbors extensive Neandertal DNA, including alleles that contribute to human phenotypes and diseases, encode hundreds of amino acid changes, and alter gene expression in specific tissues. We provide a database of the inferred introgressed Neandertal alleles for each individual iPSC line, together with the annotation of the predicted functional variants. We also show that transcriptomic data from organoids generated from iPSCs can be used to track Neandertal-derived RNA over developmental processes. Human iPSC resources provide an opportunity to experimentally explore Neandertal DNA function and its contribution to present-day phenotypes, and potentially study Neandertal traits.

Indexed as

AllelesAnimalsBrainCell LineDNAHaplotypesHumansNeanderthalsPhenotypePluripotent Stem CellsRNAStem CellsDNARNAarchaic introgressioncerebral organoidsinduced pluripotent stem cellsNeandertal genomicssingle-cell transcriptomics

Identifiers

PMID32559457
PMCPMC7363959
OpenAlexW3036132644

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.