Evidence map›Paper›PMID 41020479›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2026

Multiple gene knockouts in newts reveal novel functions of 5' Hox genes in limb development along the anterior-posterior and proximal-distal axes.

Kohei Urakawa, Yu Ito, Haruka Matsubara, Ken-Ichi T Suzuki, Masatoshi Matsunami, Shuji Shigenobu, Toshinori Hayashi, Gembu Abe, Takashi Takeuchi

Abstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

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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

2 citing papers in PubMed.

  1. Editorial highlights.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  2. Penile Length can be Estimated by the Foot-Length? Study in Human Fetuses with Neural Tube Defects.International braz j urol : official journal of the Brazilian Society of Urology
    Article
4 · The record

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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

9 authors.

Kohei UrakawaGraduate School of Medical Sciences, Tottori University, Yonago, Tottori, Japan.
Yu ItoGraduate School of Medical Sciences, Tottori University, Yonago, Tottori, Japan.
Haruka MatsubaraDivision of Developmental Biology, School of Life Sciences, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Ken-Ichi T SuzukiTrans-Scale Biology Center, National Institute for Basic Biology, Okazaki, Aichi, Japan.
Masatoshi MatsunamiGraduate School of Medicine, University of the Ryukyus, Ginowan, Okinawa, Japan.
Shuji ShigenobuTrans-Scale Biology Center, National Institute for Basic Biology, Okazaki, Aichi, Japan.
Toshinori HayashiGraduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Hiroshima, Japan.ORCID https://orcid.org/0000-0003-3676-5710
Gembu AbeGraduate School of Medical Sciences, Tottori University, Yonago, Tottori, Japan.
Takashi TakeuchiGraduate School of Medical Sciences, Tottori University, Yonago, Tottori, Japan.ORCID https://orcid.org/0000-0001-9308-1302

Funding

Japan Society for the Promotion of Science 23K05783Japan Society for the Promotion of Science JP20K06656
6 · The paper itself

Abstract

background5' Hox genes play crucial roles in limb patterning along the proximal-distal and anterior-posterior axes in mice. However, their functional conservation across tetrapods remains unclear. We previously found that newt Hox13 is essential for digit formation during both development and regeneration. In contrast, the functions of other 5' Hox genes (Hox9-Hox12) in newts remain u[WLYJ-108]nknown. Therefore, we generated 5' Hox knockout newts (Pleurodeles waltl) using CRISPR-Cas9.

resultsIndividual knockouts of Hox9, Hox10, and Hox12 disrupted all respective paralogs; however, these newts displayed no apparent abnormalities in limb skeletons. In contrast, Hox11 knockout newts exhibited skeletal defects in the posterior zeugopod and autopod of both the forelimbs and hindlimbs. Moreover, compound knockouts of Hox9 and Hox10 caused substantial loss of stylopod and anterior zeugopod/autopod elements specifically in the hindlimbs.

conclusionThese findings indicate that Hox9 and Hox10 redundantly regulate stylopod formation in the hindlimbs. Furthermore, Hox9/Hox10 and Hox11 contribute to the development of the anterior and posterior regions of the zeugopod/autopod in the hindlimbs, respectively. These novel roles of 5' Hox genes identified in newts suggest the functional diversification of 5' Hox genes in tetrapod limb development.

Indexed as

Body PatterningExtremitiesGenes, HomeoboxHomeodomain ProteinsAnimalsGene Expression Regulation, DevelopmentalGene Knockout TechniquesHomeodomain Proteinsdigit formationlimb‐bud formationlimb evolutionPleurodeles waltlskeletal formation

Identifiers

PMID41020479
PMCPMC13448364

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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.