Evidence map›Paper›PMID 41252438›Full record

ArticlePLoS genetics2025

Identification of an innexin required for termination of the asexual state in planarian reproductive switching.

Nobuyoshi Kumagai, Michio Kuroda, Tosei Hanai, Masaki Fujita, Takaaki Hino, Shunta Yorimoto, Sayaka Manta, Shuzo Nakagawa, Moe Yokoyama, Leon Tajima and 9 more

Abstract read
In one paragraph

Article in PLoS genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Nobuyoshi KumagaiDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Michio KurodaDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Tosei HanaiDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Masaki FujitaDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Takaaki HinoDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Shunta YorimotoLife Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA), University of Tsukuba, Tsukuba, Japan.ORCID https://orcid.org/0000-0002-8178-3574
Sayaka MantaDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Shuzo NakagawaDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Moe YokoyamaDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Leon TajimaDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Riku ItoDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Hikaru YamadaDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Kota MiuraDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.
Makoto KashimaDepartment of Biomolecular Science, Faculty of Science, Toho University, Funabashi, Chiba, Japan.
Katsushi YamaguchiNIBB Core Facility, National Institute for Basic Biology, Okazaki Japan.
Shuji ShigenobuLife Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA), University of Tsukuba, Tsukuba, Japan.
Ryohei FurukawaDepartment of Biology, Research and Education Center for Natural Sciences, Keio University, Yokohama, Kanagawa, Japan.ORCID https://orcid.org/0000-0002-0020-6231
Kiyono SekiiFaculty of Business and Commerce, Keio University, Yokohama, Kanagawa, Japan.ORCID https://orcid.org/0000-0001-5825-2129
Kazuya KobayashiDepartment of Biology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki, Aomori Japan.ORCID https://orcid.org/0000-0001-5839-0337

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many metazoans switch between asexual and sexual reproduction based on environmental changes, life cycle phases, or both. This reproductive strategy enables them to benefit from the features of both reproductive modes. In general, asexual reproduction is broadly divided into parthenogenesis and vegetative reproduction. As in parthenogenesis, individuals develop ovaries and lay eggs, the most significant event in switching from parthenogenesis to sexual reproduction is the production of testes. Meanwhile, in vegetative reproduction, individuals do not need germ cells themselves. Thus, they must post-embryonically develop and maintain germ cells derived from pluripotent cells as they switch from vegetative to sexual reproduction. The complicated mechanisms for controlling the postembryonic reproductive development remain unknown. The planarian Dugesia ryukyuensis can switch from vegetative to sexual reproduction by stimulating bioactive compounds called sex-inducing substances, which are widely conserved in Platyhelminthes, including parasitic flatworms. The two reproductive modes are facilitated by the presence of adult pluripotent stem cells, which generate any type of somatic tissue in the asexual state and produce and maintain hermaphroditic reproductive organs in the sexual state. In this study, using RNA sequencing analysis in experimental sexualization by sex-inducing substances, we identified four essential genes for sexualization. A common feature following the knockdown of the four essential genes was a blockage of testicular differentiation. One of the four essential genes was a gap junction gene, Dr-siri (Dugesia ryukyuensis-sexual induction-related innexin). We suggest that the establishment of a testicular stem cell niche supported by Dr-siri protein is responsible for the breakthrough of dormancy in postembryonic reproductive development in planarian reproductive switching. Our findings suggest that the production of testes might be crucial for even switching from vegetative to sexual reproduction.

Indexed as

ConnexinsHelminth ProteinsHermaphroditic OrganismsPlanariansReproduction, AsexualSexual DevelopmentTestisAnimalsFemaleGenes, EssentialGerm CellsMalePluripotent Stem CellsRNA-SeqConnexinsHelminth Proteins

Identifiers

PMID41252438
PMCPMC12654950

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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.