Evidence map›Paper›PMID 34795249›Full record

ArticleNature communications2021

Hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals.

Christopher P Arnold, Analí Migueles Lozano, Frederick G Mann, Stephanie H Nowotarski, Julianna O Haug, Jeffrey J Lange, Chris W Seidel, Alejandro Sánchez Alvarado

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Backward scrunching: planarians escape from noxious stimuli, cannibalism, and predation.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Investigating the Functions of Hox Genes Using Planarian Asexual Reproduction.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  6. Review
  7. The role ofbioRxiv : the preprint server for biology · 2024
    Article
  8. Article
  9. The Role ofIntegrative organismal biology (Oxford, England) · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Hox genes in development and beyond.Development (Cambridge, England) · 2023
    Article
  16. Article
  17. Review
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 2 institutions in 1 country.

Christopher P ArnoldStowers Institute, Kansas City, MO, USA.
Analí Migueles LozanoUniversity of Chicago, Chicago, IL, USA.
Frederick G MannStowers Institute, Kansas City, MO, USA.ORCID http://orcid.org/0000-0002-6234-0081
Stephanie H NowotarskiStowers Institute, Kansas City, MO, USA.
Julianna O HaugStowers Institute, Kansas City, MO, USA.ORCID http://orcid.org/0000-0001-8093-0221
Jeffrey J LangeStowers Institute, Kansas City, MO, USA.
Chris W SeidelStowers Institute, Kansas City, MO, USA.
Alejandro Sánchez AlvaradoStowers Institute, Kansas City, MO, USA. asa@stowers.org.ORCID http://orcid.org/0000-0002-1966-6959
Stowers Institute for Medical Research · USUniversity of Illinois Chicago · US

Funding

The molecular basis of planarian regenerationR37GM057260 · NIGMS · UNIVERSITY OF UTAH · PI SANCHEZ ALVARADO, ALEJANDRO · 2009 to 2018
$2.8M
Howard Hughes Medical InstituteNIGMS NIH HHS R37 GM057260
6 · The paper itself

Abstract

Hox genes are highly conserved transcription factors renowned for their roles in the segmental patterning of the embryonic anterior-posterior (A/P) axis. We report functions for Hox genes in A/P tissue segmentation and transverse fission behavior underlying asexual reproduction in adult planarian flatworms, Schmidtea mediterranea. Silencing of each of the Hox family members identifies 5 Hox genes required for asexual reproduction. Among these, silencing of hox3 genes results in supernumerary fission segments, while silencing of post2b eliminates segmentation altogether. The opposing roles of hox3 and post2b in segmentation are paralleled in their respective regulation of fission behavior. Silencing of hox3 increases the frequency of fission behavior initiation while silencing of post2b eliminates fission behavior entirely. Furthermore, we identify a network of downstream effector genes mediating Hox gene functions, providing insight into their respective mechanisms of action. In particular, we resolve roles for post2b and effector genes in the functions of the marginal adhesive organ in fission behavior regulation. Collectively, our study establishes adult stage roles for Hox genes in the regulation of tissue segmentation and behavior associated with asexual reproduction.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBody PatterningGenes, HelminthGenes, HomeoboxHomeodomain ProteinsIn Situ Hybridization, FluorescenceMicroscopy, ConfocalMicroscopy, Electron, ScanningPlanariansReproduction, AsexualRNA InterferenceRNA-SeqTranscription FactorsHomeodomain ProteinsTranscription Factors

Identifiers

PMID34795249
PMCPMC8602322
OpenAlexW3213678675

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.