Evidence map›Paper›PMID 39092789›Full record

ArticleJournal of cell science2024

MYCBPAP is a central apparatus protein required for centrosome-nuclear envelope docking and sperm tail biogenesis in mice.

Haoting Wang, Hiroko Kobayashi, Keisuke Shimada, Seiya Oura, Yuki Oyama, Hiroaki Kitakaze, Taichi Noda, Norikazu Yabuta, Haruhiko Miyata, Masahito Ikawa

Abstract read
In one paragraph

Article in Journal of cell science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

10 authors.

Haoting WangGraduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871, Japan.
Hiroko KobayashiGraduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871, Japan.
Keisuke ShimadaResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan.ORCID 0000-0003-3739-7163
Seiya OuraGraduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871, Japan.
Yuki OyamaGraduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871, Japan.ORCID 0000-0003-4579-5487
Hiroaki KitakazeResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan.
Taichi NodaResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan.ORCID 0000-0003-0260-7861
Norikazu YabutaResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan.
Haruhiko MiyataResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan.ORCID 0000-0003-4758-5803
Masahito IkawaGraduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871, Japan.ORCID 0000-0001-9859-6217

Funding

Targeting sperm-specific proteins during meiosis and sperm morphogenesisP01HD087157 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI MATZUK, MARTIN M. · 2017 to 2021
$6.2M
Functional analysis of novel testis-expressed secreted and transmembrane proteinsR01HD088412 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI MARTIN M. MATZUK · 2016 to 2026
$4.5M
Eunice Kennedy Shriver National Institute of Child Health and Human Development P01HD087157Fusion Oriented REsearch for disruptive Science and Technology JPMJFR211FInamori FoundationJapan Science and Technology Agency JPMJFR211FJapan Society for the Promotion of Science JP22H03214NICHD NIH HHS P01 HD087157NICHD NIH HHS R01 HD088412Senri Life Science FoundationTakeda Science FoundationThe Mochida Memorial Foundation for Medical and Pharmaceutical Research
6 · The paper itself

Abstract

The structure of the sperm flagellar axoneme is highly conserved across species and serves the essential function of generating motility to facilitate the meeting of spermatozoa with the egg. During spermiogenesis, the axoneme elongates from the centrosome, and subsequently the centrosome docks onto the nuclear envelope to continue tail biogenesis. Mycbpap is expressed predominantly in mouse and human testes and conserved in Chlamydomonas as FAP147. A previous cryo-electron microscopy analysis has revealed the localization of FAP147 to the central apparatus of the axoneme. Here, we generated Mycbpap-knockout mice and demonstrated the essential role of Mycbpap in male fertility. Deletion of Mycbpap led to disrupted centrosome-nuclear envelope docking and abnormal flagellar biogenesis. Furthermore, we generated transgenic mice with tagged MYCBPAP, which restored the fertility of Mycbpap-knockout males. Interactome analyses of MYCBPAP using Mycbpap transgenic mice unveiled binding partners of MYCBPAP including central apparatus proteins, such as CFAP65 and CFAP70, which constitute the C2a projection, and centrosome-associated proteins, such as CCP110. These findings provide insights into a MYCBPAP-dependent regulation of the centrosome-nuclear envelope docking and sperm tail biogenesis.

Indexed as

CentrosomeMice, KnockoutNuclear EnvelopeSperm TailAnimalsAxonemeFertilityMaleMiceMice, TransgenicSpermatogenesisSpermatozoaCentral pairCentrioleFlagellum formationGenome editingKnockout mice

Identifiers

PMID39092789
PMCPMC11385322

What OpenQuestion holds

Textmetadata
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.