Evidence map›Paper›PMID 38918373›Full record

ArticleNature communications2024

A newly identified gene Ahed plays essential roles in murine haematopoiesis.

Ritsuko Nakai, Takafumi Yokota, Masahiro Tokunaga, Mikiro Takaishi, Tomomasa Yokomizo, Takao Sudo, Henyun Shi, Yoshiaki Yasumizu, Daisuke Okuzaki, Chikara Kokubu and 10 more

Erratum issuedAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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

5 · Who and what money

Authors and funding

20 authors.

Ritsuko NakaiDepartment of Haematology and Oncology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.ORCID 0000-0002-7891-4879
Takafumi YokotaDepartment of Haematology and Oncology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan. yokotat@oici.jp.ORCID 0000-0001-9358-8947
Masahiro TokunagaDepartment of Haematology, Suita Municipal Hospital, Suita, Osaka, 564-0018, Japan.
Mikiro TakaishiDepartment of Dermatology, Kochi Medical School, Kochi University, Nankoku, Kochi, 783-8505, Japan.
Tomomasa YokomizoDepartment of Microscopic and Developmental Anatomy, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, 162-8666, Japan.
Takao SudoDepartment of Haematology and Oncology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.
Henyun ShiDepartment of Haematology and Oncology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.
Yoshiaki YasumizuDepartment of Experimental Immunology, Immunology Frontier Research Centre, Osaka University, Suita, Osaka, 565-0871, Japan.ORCID 0000-0002-9872-4909
Daisuke OkuzakiIntegrated Frontier Research for Medical Science Division, Institute for Open and Transdisciplinary Research Initiatives, Osaka University, Suita, Osaka, 565-0871, Japan.ORCID 0000-0002-4552-783X
Chikara KokubuDepartment of Genome Biology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.
Sachiyo TanakaDepartment of Genome Biology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.
Katsuyoshi TakaokaDevelopmental Genetics Group, Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, 565-0871, Japan.
Ayako YamanishiDepartment of Genome Biology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.
Junko YoshidaDepartment of Genome Biology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.ORCID 0009-0006-5748-2567
Hitomi WatanabeLaboratory of Animal Experiments for Regeneration, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, Kyoto, 606-8507, Japan.
Gen KondohLaboratory of Animal Experiments for Regeneration, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, Kyoto, 606-8507, Japan.
Kyoji HorieDepartment of Genome Biology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.ORCID 0000-0001-9036-8180
Naoki HosenDepartment of Haematology and Oncology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.ORCID 0000-0001-9570-0947
Shigetoshi SanoDepartment of Dermatology, Kochi Medical School, Kochi University, Nankoku, Kochi, 783-8505, Japan.ORCID 0000-0002-9812-0216
Junji TakedaResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka, 565-0871, Japan. jjjtakeda@biken.osaka-u.ac.jp.ORCID 0000-0001-6321-0898

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 20K17379MEXT | Japan Society for the Promotion of Science (JSPS) 21K08415MEXT | Japan Society for the Promotion of Science (JSPS) 24790972MEXT | Japan Society for the Promotion of Science (JSPS) 26860731
6 · The paper itself

Abstract

The development of haematopoiesis involves the coordinated action of numerous genes, some of which are implicated in haematological malignancies. However, the biological function of many genes remains elusive and unknown functional genes are likely to remain to be uncovered. Here, we report a previously uncharacterised gene in haematopoiesis, identified by screening mutant embryonic stem cells. The gene, 'attenuated haematopoietic development (Ahed)', encodes a nuclear protein. Conditional knockout (cKO) of Ahed results in anaemia from embryonic day 14.5 onward, leading to prenatal demise. Transplantation experiments demonstrate the incapacity of Ahed-deficient haematopoietic cells to reconstitute haematopoiesis in vivo. Employing a tamoxifen-inducible cKO model, we further reveal that Ahed deletion impairs the intrinsic capacity of haematopoietic cells in adult mice. Ahed deletion affects various pathways, and published databases present cancer patients with somatic mutations in Ahed. Collectively, our findings underscore the fundamental roles of Ahed in lifelong haematopoiesis, implicating its association with malignancies.

Indexed as

HematopoiesisMice, KnockoutAnemiaAnimalsEmbryonic Stem CellsFemaleHematopoietic Stem CellsHumansMaleMiceMice, Inbred C57BLMutation

Identifiers

PMID38918373
PMCPMC11199565

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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.