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EFCAB2 is a novel calcium-binding protein in mouse testis and sperm

Calcium-binding proteins regulate ion metabolism and the necessary signaling pathways for the maturational events of sperm. Our aim is to identify the novel calcium-binding proteins in testis. The gene EFCAB2 (GenBank NM_026626.3, NP_080902.1) was not previously examined, and its properties and exac...

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Autores principales: Shawki, Hossam H., Ishikawa-Yamauchi, Yu, Kawashima, Akihiro, Katoh, Yuki, Matsuda, Manabu, Al-Soudy, Al-Sayed, Minisy, Fatma M., Kuno, Akihiro, Gulibaikelamu, Xiafukaiti, Hirokawa, Takatsugu, Takahashi, Satoru, Oishi, Hisashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443151/
https://www.ncbi.nlm.nih.gov/pubmed/30933994
http://dx.doi.org/10.1371/journal.pone.0214687
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author Shawki, Hossam H.
Ishikawa-Yamauchi, Yu
Kawashima, Akihiro
Katoh, Yuki
Matsuda, Manabu
Al-Soudy, Al-Sayed
Minisy, Fatma M.
Kuno, Akihiro
Gulibaikelamu, Xiafukaiti
Hirokawa, Takatsugu
Takahashi, Satoru
Oishi, Hisashi
author_facet Shawki, Hossam H.
Ishikawa-Yamauchi, Yu
Kawashima, Akihiro
Katoh, Yuki
Matsuda, Manabu
Al-Soudy, Al-Sayed
Minisy, Fatma M.
Kuno, Akihiro
Gulibaikelamu, Xiafukaiti
Hirokawa, Takatsugu
Takahashi, Satoru
Oishi, Hisashi
author_sort Shawki, Hossam H.
collection PubMed
description Calcium-binding proteins regulate ion metabolism and the necessary signaling pathways for the maturational events of sperm. Our aim is to identify the novel calcium-binding proteins in testis. The gene EFCAB2 (GenBank NM_026626.3, NP_080902.1) was not previously examined, and its properties and exact mechanisms of action are unknown. In this study, we performed phylogenetic and structure prediction analyses of EFCAB2, which displays definitive structural features. Additionally, the distribution, localization, and calcium binding ability of mouse EFCAB2 were investigated. Results revealed extensive conservation of EFCAB2 among different eukaryotic orthologs. The constructed 3D model predicted that mouse EFCAB2 contains seven α-helices and two EF-hand motifs. The first EF-hand motif is located in N-terminal, while the second is located in C-terminal. By aligning the 3D structure of Ca(2+)-binding loops from EFCAB2 with calmodulin, we predicted six residues that might be involved in Ca(2+) binding. The distribution of the Efcab2 mRNA, as determined by northern blotting, was detected only in the testis among mouse tissues. Native and recombinant EFCAB2 protein were detected by western blotting as one band at 20 kDa. In situ hybridization and immunohistochemical analyses showed its localization specifically in spermatogenic cells from primary spermatocytes to elongate spermatids within the seminiferous epithelium, but neither spermatogonia nor somatic cells were expressed. Moreover, EFCAB2 was specifically localized to the principal piece of cauda epididymal sperm flagellum. Furthermore, the analyses of purified recombinant EFCAB2 by Stains-all, ruthenium red staining, and by applying in vitro autoradiography assay showed that the physiological function of this protein is Ca(2+) binding. These results suggested that EFCAB2 might be involved in the control of sperm flagellar movement. Altogether, here we describe about EFCAB2 as a novel calcium-binding protein in mouse testis and sperm.
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spelling pubmed-64431512019-04-17 EFCAB2 is a novel calcium-binding protein in mouse testis and sperm Shawki, Hossam H. Ishikawa-Yamauchi, Yu Kawashima, Akihiro Katoh, Yuki Matsuda, Manabu Al-Soudy, Al-Sayed Minisy, Fatma M. Kuno, Akihiro Gulibaikelamu, Xiafukaiti Hirokawa, Takatsugu Takahashi, Satoru Oishi, Hisashi PLoS One Research Article Calcium-binding proteins regulate ion metabolism and the necessary signaling pathways for the maturational events of sperm. Our aim is to identify the novel calcium-binding proteins in testis. The gene EFCAB2 (GenBank NM_026626.3, NP_080902.1) was not previously examined, and its properties and exact mechanisms of action are unknown. In this study, we performed phylogenetic and structure prediction analyses of EFCAB2, which displays definitive structural features. Additionally, the distribution, localization, and calcium binding ability of mouse EFCAB2 were investigated. Results revealed extensive conservation of EFCAB2 among different eukaryotic orthologs. The constructed 3D model predicted that mouse EFCAB2 contains seven α-helices and two EF-hand motifs. The first EF-hand motif is located in N-terminal, while the second is located in C-terminal. By aligning the 3D structure of Ca(2+)-binding loops from EFCAB2 with calmodulin, we predicted six residues that might be involved in Ca(2+) binding. The distribution of the Efcab2 mRNA, as determined by northern blotting, was detected only in the testis among mouse tissues. Native and recombinant EFCAB2 protein were detected by western blotting as one band at 20 kDa. In situ hybridization and immunohistochemical analyses showed its localization specifically in spermatogenic cells from primary spermatocytes to elongate spermatids within the seminiferous epithelium, but neither spermatogonia nor somatic cells were expressed. Moreover, EFCAB2 was specifically localized to the principal piece of cauda epididymal sperm flagellum. Furthermore, the analyses of purified recombinant EFCAB2 by Stains-all, ruthenium red staining, and by applying in vitro autoradiography assay showed that the physiological function of this protein is Ca(2+) binding. These results suggested that EFCAB2 might be involved in the control of sperm flagellar movement. Altogether, here we describe about EFCAB2 as a novel calcium-binding protein in mouse testis and sperm. Public Library of Science 2019-04-01 /pmc/articles/PMC6443151/ /pubmed/30933994 http://dx.doi.org/10.1371/journal.pone.0214687 Text en © 2019 Shawki et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shawki, Hossam H.
Ishikawa-Yamauchi, Yu
Kawashima, Akihiro
Katoh, Yuki
Matsuda, Manabu
Al-Soudy, Al-Sayed
Minisy, Fatma M.
Kuno, Akihiro
Gulibaikelamu, Xiafukaiti
Hirokawa, Takatsugu
Takahashi, Satoru
Oishi, Hisashi
EFCAB2 is a novel calcium-binding protein in mouse testis and sperm
title EFCAB2 is a novel calcium-binding protein in mouse testis and sperm
title_full EFCAB2 is a novel calcium-binding protein in mouse testis and sperm
title_fullStr EFCAB2 is a novel calcium-binding protein in mouse testis and sperm
title_full_unstemmed EFCAB2 is a novel calcium-binding protein in mouse testis and sperm
title_short EFCAB2 is a novel calcium-binding protein in mouse testis and sperm
title_sort efcab2 is a novel calcium-binding protein in mouse testis and sperm
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443151/
https://www.ncbi.nlm.nih.gov/pubmed/30933994
http://dx.doi.org/10.1371/journal.pone.0214687
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