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      A proteomic approach to identifying spermatozoa proteins in Indonesian native Madura bulls

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          Abstract

          Proteins assist sperm mature, transit the female reproductive tract, and recognise sperm oocytes. Indigenous Indonesian bulls, Madura bulls, have not been studied for reproductive proteomics. As local Indonesian beef livestock, Madura cattle assist in achieving food security; hence, their number must be improved. Thus, the identification of molecular proteomics-based bull fertility biomarkers is needed. This study aimed to characterise the sperm fertility function of the superior Madura bull ( Bos indicus × Bos Javanicus) spermatozoa proteome. Frozen semen from eight Madura superior bulls ( Bos indicus × Bos javanicus) aged 4–8 years was obtained from the artificial insemination centre (AIC) in Singosari and Lembang. Madura superior bulls are those that have passed the bull breeding soundness evaluation. Frozen sperm were thawed and centrifuged at 3000 × g for 30 min. Proteins in sperm were characterised through proteomic analysis using liquid chromatography–tandem mass spectrometry (LC–MS/MS). The resulting gene symbols for each protein were then subjected to bioinformatics tools, including UniProt, DAVID, and STRING databases. Regarding sperm fertility, the analysis revealed that 15 proteins were identified in the sperm of Madura bulls. Amongst the identified proteins, the superior Madura bull sperm contained several motilities, energy-related proteins, and chaperone proteins. A substantial portion of characterised proteins are linked to metabolic pathways and the tricarboxylic acid (TCA) cycle, contributing to sperm energy production. In conclusion, the first in-depth proteome identification of sperm related to sperm quality and bull fertility of a unique indigenous Madura breed of Indonesia was performed using the LC–MS/MS proteomic method. These findings may serve as a reference point for further studies related to the functions of bovine sperm and biomarkers of fertility and sperm quality.

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          A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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            Comprehensive proteomic analysis of bovine spermatozoa of varying fertility rates and identification of biomarkers associated with fertility

            Background Male infertility is a major problem for mammalian reproduction. However, molecular details including the underlying mechanisms of male fertility are still not known. A thorough understanding of these mechanisms is essential for obtaining consistently high reproductive efficiency and to ensure lower cost and time-loss by breeder. Results Using high and low fertility bull spermatozoa, here we employed differential detergent fractionation multidimensional protein identification technology (DDF-Mud PIT) and identified 125 putative biomarkers of fertility. We next used quantitative Systems Biology modeling and canonical protein interaction pathways and networks to show that high fertility spermatozoa differ from low fertility spermatozoa in four main ways. Compared to sperm from low fertility bulls, sperm from high fertility bulls have higher expression of proteins involved in: energy metabolism, cell communication, spermatogenesis, and cell motility. Our data also suggests a hypothesis that low fertility sperm DNA integrity may be compromised because cell cycle: G2/M DNA damage checkpoint regulation was most significant signaling pathway identified in low fertility spermatozoa. Conclusion This is the first comprehensive description of the bovine spermatozoa proteome. Comparative proteomic analysis of high fertility and low fertility bulls, in the context of protein interaction networks identified putative molecular markers associated with high fertility phenotype.
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              Outer dense fibers stabilize the axoneme to maintain sperm motility

              Abstract Outer dense fibers (ODFs), as unique accessory structures in mammalian sperm, are considered to play a role in the protection of the sperm tail against shear forces. However, the role and relevant mechanisms of ODFs in modulating sperm motility and its pathological involvement in asthenozoospermia were unknown. Here, we found that the percentage of ODF defects was higher in asthenozoospermic samples than that in control samples and was significantly correlated with the percentage of axoneme defects and non‐motile sperm. Furthermore, the expression levels of ODF major components (Odf1, 2, 3, 4) were frequently down‐regulated in asthenozoospermic samples. Intriguingly, the positive relationship between ODF size and sperm motility existed across species. The conditional disruption of Odf2 expression in mice led to reduced sperm motility and the characteristics of asthenozoospermia. Meanwhile, the expression of acetylated α‐tubulin was decreased in sperm from both Odf2 conditional knockout (cKO) mice and asthenozoospermic men. Immunofluorescence and biochemistry analyses showed that Odf2 could bind to acetylated α‐tubulin and protect the acetylation level of α‐tubulin in HEK293T cells in a cold environment. Finally, we found that lithium elevated the expression levels of Odf family proteins and acetylated α‐tubulin, elongated the midpiece length and increased the percentage of rapidly moving sperm in mice. Our results demonstrate that ODFs are beneficial for sperm motility via stabilization of the axoneme and that hypo‐expression of Odf family proteins is involved in the pathogenesis of asthenozoospermia. The lithium administration assay will provide valuable insights into the development of new treatments for asthenozoospermia.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2563977/overviewRole: Role: Role: Role: Role: Role: Role:
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                Role:
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                URI : https://loop.frontiersin.org/people/1884724/overviewRole: Role: Role:
                URI : https://loop.frontiersin.org/people/2397383/overviewRole: Role: Role: Role: Role: Role: Role: Role:
                Journal
                Front Vet Sci
                Front Vet Sci
                Front. Vet. Sci.
                Frontiers in Veterinary Science
                Frontiers Media S.A.
                2297-1769
                04 December 2023
                2023
                : 10
                : 1287676
                Affiliations
                [1] 1Division of Reproduction and Obstetrics, School of Veterinary Medicine and Biomedical Sciences, IPB University , Bogor, Indonesia
                [2] 2Research Center for Applied Zoology, National Research and Innovation Agency (BRIN) , Bogor, Indonesia
                [3] 3Division of Veterinary Anatomy, Faculty of Veterinary Medicine, Universitas Airlangga , Surabaya, Indonesia
                [4] 4Department of Biology, Faculty of Science, IPB University , Bogor, Indonesia
                Author notes

                Edited by: Lucas Lima Verardo, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Brazil

                Reviewed by: Mahak Singh, The ICAR Research Complex for North Eastern Hill Region (ICAR RC NEH), India; Mustafa Hitit, Kastamonu University, Türkiye

                *Correspondence: Bambang Purwantara, purwantara@ 123456apps.ipb.ac.id ; Zulfi Nur Amrina Rosyada, nur.amrina@ 123456fkh.unair.ac.id
                Article
                10.3389/fvets.2023.1287676
                10725959
                38111731
                39b49810-d263-49ee-a509-8267dd1ebc42
                Copyright © 2023 Rosyada, Pardede, Kaiin, Gunawan, Maulana, Said, Tumbelaka, Solihin, Ulum and Purwantara.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 02 September 2023
                : 06 November 2023
                Page count
                Figures: 5, Tables: 1, Equations: 0, References: 49, Pages: 10, Words: 6693
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was financially supported by the Indonesian Ministry of Education, Culture, Research, and Technology through Fundamental Research grant number 18789/IT3.D10/PT.01.02/M/T/2023.
                Categories
                Veterinary Science
                Original Research
                Custom metadata
                Livestock Genomics

                fertility,food security,lc–ms/ms,madura bulls,sperm proteins fertility,proteomic,sperm proteins

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