Evidence map›Paper›PMID 40598224›Full record

ArticleCell communication and signaling : CCS2025

A novel mechanism of sperm midpiece epididymal maturation and the role of CCDC112 in sperm midpiece formation and establishing an optimal flagella waveform.

Maddison L Graffeo, Joseph Nguyen, Farin Yazdan Parast, Jessica E M Dunleavy, Denis Korneev, Hongyi Yang, Hidenobu Okuda, Anne E O'Connor, Donald F Conrad, Reza Nosrati and 2 more

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Maddison L GraffeoSchool of Bio Sciences and Bio 21 Molecular Science and Biotechnology Institute, Faculty of Science, The University of Melbourne, Parkville, VIC, 3010, Australia.
Joseph NguyenSchool of Bio Sciences and Bio 21 Molecular Science and Biotechnology Institute, Faculty of Science, The University of Melbourne, Parkville, VIC, 3010, Australia.
Farin Yazdan ParastDepartment of Mechanical and Aerospace Engineering, Monash University, Clayton, VIC, 3800, Australia.
Jessica E M DunleavySchool of Bio Sciences and Bio 21 Molecular Science and Biotechnology Institute, Faculty of Science, The University of Melbourne, Parkville, VIC, 3010, Australia.
Denis KorneevDepartment of Biochemistry and Molecular Biology, Monash University, Clayton, VIC, 3800, Australia.
Hongyi YangSchool of Bio Sciences and Bio 21 Molecular Science and Biotechnology Institute, Faculty of Science, The University of Melbourne, Parkville, VIC, 3010, Australia.
Hidenobu OkudaDepartment of Nephrology and Dialysis, Moriguchi Keijinkai Hospital, Osaka, Japan.
Anne E O'ConnorSchool of Bio Sciences and Bio 21 Molecular Science and Biotechnology Institute, Faculty of Science, The University of Melbourne, Parkville, VIC, 3010, Australia.
Donald F ConradDivision of Genetics, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR, USA.
Reza NosratiDepartment of Mechanical and Aerospace Engineering, Monash University, Clayton, VIC, 3800, Australia.
Brendan J HoustonSchool of Bio Sciences and Bio 21 Molecular Science and Biotechnology Institute, Faculty of Science, The University of Melbourne, Parkville, VIC, 3010, Australia. brendan.houston@unimelb.edu.au.
Moira K O'BryanSchool of Bio Sciences and Bio 21 Molecular Science and Biotechnology Institute, Faculty of Science, The University of Melbourne, Parkville, VIC, 3010, Australia. moira.obryan@unimelb.edu.au.

Funding

Australian Research Council DP230100747National Health and Medical Research Council 2017370The Gates Foundation INV-050872
6 · The paper itself

Abstract

backgroundThe mitochondrial sheath is a defining feature of mammalian sperm with proposed functions in structural support and energy production for flagella movement. Recently, coiled coil domain containing (CCDC) protein 112 (CCDC112) was suggested to play a role in the regulation of ciliogenesis. CCDC112 is a poorly characterised protein and there is virtually no knowledge of its in vivo function.

methodsHere, we define CCDC112 as crucial for male fertility using a Ccdc112 loss-of-function mouse line. To characterize and analyze male fertility, and to identify a novel process of epididymal midpiece maturation, we utilized a range of assays including fertility testing, scanning electron microscopy, high-resolution sperm motility and power output analysis, in vitro fertilization, intracytoplasmic sperm injection, mitochondria stress test assays and glycolytic flux assays. Localization of CCDC112 in cilia was assessed via the transfection of IMCD-3 cells with a CCDC112-eGFP vector and subsequent immunofluorescent staining.

resultsResults reveal CCDC112 as a requirement for male fertility in the mouse with an essential role in mitochondrial sheath formation. Our data reveal the critical role of CCDC112 in mitochondrial morphogenesis during midpiece formation, with the lack of CCDC112 leading to significantly reduced respiration capacity, irregular flagellar waveforms, diminished progressive motility and ultimately male sterility. In the absence of CCDC112, sperm are unable to traverse the female reproductive tract to the site of fertilization and in vitro have a poor capacity to penetrate the zonae pellucidae of oocytes or fuse with the oocyte. We further unveil a previously unrecognized process of epididymal mitochondrial sheath maturation. We show the sperm midpiece is structurally immature upon exiting the testis and maturation continues during transit from the caput to the cauda epididymis. Finally, we identify CCDC112 as a component of the distal appendages of the mother centriole in IMCD-3 cells suggestive of a facilitative role for CCDC112 in protein entry into the ciliary compartment within germ cells.

conclusionCollectively, we establish CCDC112 as a key regulator of sperm midpiece assembly and function while further expanding our understanding on functional sperm production, energy generation and flagella kinematics.

Indexed as

EpididymisFlagellaSpermatozoaSperm MaturationSperm MidpieceSperm TailAnimalsMaleMiceMitochondriaSperm MotilityEpididymal maturationMale fertilityMidpieceMitochondrial sheathSpermatogenesisSperm motility

Identifiers

PMID40598224
PMCPMC12218091

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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.