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A variant of Runx2 that differs from the bone isoform in its splicing is expressed in spermatogenic cells

Background. Members of the Runx gene family encode transcription factors that bind to DNA in a sequence-specific manner. Among the three Runx proteins, Runx2 comprises 607 amino acid (aa) residues, is expressed in bone, and plays crucial roles in osteoblast differentiation and bone development. We e...

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Autores principales: Kanto, Satoru, Grynberg, Marcin, Kaneko, Yoshiyuki, Fujita, Jun, Satake, Masanobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824880/
https://www.ncbi.nlm.nih.gov/pubmed/27069802
http://dx.doi.org/10.7717/peerj.1862
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author Kanto, Satoru
Grynberg, Marcin
Kaneko, Yoshiyuki
Fujita, Jun
Satake, Masanobu
author_facet Kanto, Satoru
Grynberg, Marcin
Kaneko, Yoshiyuki
Fujita, Jun
Satake, Masanobu
author_sort Kanto, Satoru
collection PubMed
description Background. Members of the Runx gene family encode transcription factors that bind to DNA in a sequence-specific manner. Among the three Runx proteins, Runx2 comprises 607 amino acid (aa) residues, is expressed in bone, and plays crucial roles in osteoblast differentiation and bone development. We examined whether the Runx2 gene is also expressed in testes. Methods. Murine testes from 1-, 2-, 3-, 4-, and 10-week-old male mice of the C57BL/6J strain and W∕W(v) strain were used throughout the study. Northern Blot Analyses were performed using extracts form the murine testes. Sequencing of cDNA clones and 5′-rapid amplification of cDNA ends were performed to determine the full length of the transcripts, which revealed that the testicular Runx2 comprises 106 aa residues coding novel protein. Generating an antiserum using the amino-terminal 15 aa of Runx2 (Met(1) to Gly(15)) as an antigen, immunoblot analyses were performed to detect the predicted polypeptide of 106 aa residues with the initiating Met(1). With the affinity-purified anti-Runx2 antibody, immunohistochemical analyses were performed to elucidate the localization of the protein. Furthermore, bioinformatic analyses were performed to predict the function of the protein. Results. A Runx2 transcript was detected in testes and was specifically expressed in germ cells. Determination of the transcript structure indicated that the testicular Runx2 is a splice isoform. The predicted testicular Runx2 polypeptide is composed of only 106 aa residues, lacks a Runt domain, and appears to be a basic protein with a predominantly alpha-helical conformation. Immunoblot analyses with an anti-Runx2 antibody revealed that Met(1) in the deduced open reading frame of Runx2 is used as the initiation codon to express an 11 kDa protein. Furthermore, immunohistochemical analyses revealed that the Runx2 polypeptide was located in the nuclei, and was detected in spermatocytes at the stages of late pachytene, diplotene and second meiotic cells as well as in round spermatids. Bioinformatic analyses suggested that the testicular Runx2 is a histone-like protein. Discussion. A variant of Runx2 that differs from the bone isoform in its splicing is expressed in pachytene spermatocytes and round spermatids in testes, and encodes a histone-like, nuclear protein of 106 aa residues. Considering its nuclear localization and differentiation stage-dependent expression, Runx2 may function as a chromatin-remodeling factor during spermatogenesis. We thus conclude that a single Runx2 gene can encode two different types of nuclear proteins, a previously defined transcription factor in bone and cartilage and a short testicular variant that lacks a Runt domain.
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spelling pubmed-48248802016-04-11 A variant of Runx2 that differs from the bone isoform in its splicing is expressed in spermatogenic cells Kanto, Satoru Grynberg, Marcin Kaneko, Yoshiyuki Fujita, Jun Satake, Masanobu PeerJ Andrology Background. Members of the Runx gene family encode transcription factors that bind to DNA in a sequence-specific manner. Among the three Runx proteins, Runx2 comprises 607 amino acid (aa) residues, is expressed in bone, and plays crucial roles in osteoblast differentiation and bone development. We examined whether the Runx2 gene is also expressed in testes. Methods. Murine testes from 1-, 2-, 3-, 4-, and 10-week-old male mice of the C57BL/6J strain and W∕W(v) strain were used throughout the study. Northern Blot Analyses were performed using extracts form the murine testes. Sequencing of cDNA clones and 5′-rapid amplification of cDNA ends were performed to determine the full length of the transcripts, which revealed that the testicular Runx2 comprises 106 aa residues coding novel protein. Generating an antiserum using the amino-terminal 15 aa of Runx2 (Met(1) to Gly(15)) as an antigen, immunoblot analyses were performed to detect the predicted polypeptide of 106 aa residues with the initiating Met(1). With the affinity-purified anti-Runx2 antibody, immunohistochemical analyses were performed to elucidate the localization of the protein. Furthermore, bioinformatic analyses were performed to predict the function of the protein. Results. A Runx2 transcript was detected in testes and was specifically expressed in germ cells. Determination of the transcript structure indicated that the testicular Runx2 is a splice isoform. The predicted testicular Runx2 polypeptide is composed of only 106 aa residues, lacks a Runt domain, and appears to be a basic protein with a predominantly alpha-helical conformation. Immunoblot analyses with an anti-Runx2 antibody revealed that Met(1) in the deduced open reading frame of Runx2 is used as the initiation codon to express an 11 kDa protein. Furthermore, immunohistochemical analyses revealed that the Runx2 polypeptide was located in the nuclei, and was detected in spermatocytes at the stages of late pachytene, diplotene and second meiotic cells as well as in round spermatids. Bioinformatic analyses suggested that the testicular Runx2 is a histone-like protein. Discussion. A variant of Runx2 that differs from the bone isoform in its splicing is expressed in pachytene spermatocytes and round spermatids in testes, and encodes a histone-like, nuclear protein of 106 aa residues. Considering its nuclear localization and differentiation stage-dependent expression, Runx2 may function as a chromatin-remodeling factor during spermatogenesis. We thus conclude that a single Runx2 gene can encode two different types of nuclear proteins, a previously defined transcription factor in bone and cartilage and a short testicular variant that lacks a Runt domain. PeerJ Inc. 2016-04-04 /pmc/articles/PMC4824880/ /pubmed/27069802 http://dx.doi.org/10.7717/peerj.1862 Text en ©2016 Kanto 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, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Andrology
Kanto, Satoru
Grynberg, Marcin
Kaneko, Yoshiyuki
Fujita, Jun
Satake, Masanobu
A variant of Runx2 that differs from the bone isoform in its splicing is expressed in spermatogenic cells
title A variant of Runx2 that differs from the bone isoform in its splicing is expressed in spermatogenic cells
title_full A variant of Runx2 that differs from the bone isoform in its splicing is expressed in spermatogenic cells
title_fullStr A variant of Runx2 that differs from the bone isoform in its splicing is expressed in spermatogenic cells
title_full_unstemmed A variant of Runx2 that differs from the bone isoform in its splicing is expressed in spermatogenic cells
title_short A variant of Runx2 that differs from the bone isoform in its splicing is expressed in spermatogenic cells
title_sort variant of runx2 that differs from the bone isoform in its splicing is expressed in spermatogenic cells
topic Andrology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824880/
https://www.ncbi.nlm.nih.gov/pubmed/27069802
http://dx.doi.org/10.7717/peerj.1862
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