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Differential Expression of PRAMEL1, a Cancer/Testis Antigen, during Spermatogenesis in the Mouse

PRAME belongs to a group of cancer/testis antigens (CTAs) that are characterized by their restricted expression in normal gametogenic tissues and a variety of tumors. The PRAME family is one of the most amplified gene families in the mouse and other mammalian genomes. Members of the PRAME gene famil...

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Autores principales: Mistry, Bhavesh V., Zhao, Yaqi, Chang, Ti-Cheng, Yasue, Hiroshi, Chiba, Mitsuru, Oatley, Jon, Diaz, Francisco, Liu, Wan-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614976/
https://www.ncbi.nlm.nih.gov/pubmed/23565261
http://dx.doi.org/10.1371/journal.pone.0060611
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author Mistry, Bhavesh V.
Zhao, Yaqi
Chang, Ti-Cheng
Yasue, Hiroshi
Chiba, Mitsuru
Oatley, Jon
Diaz, Francisco
Liu, Wan-Sheng
author_facet Mistry, Bhavesh V.
Zhao, Yaqi
Chang, Ti-Cheng
Yasue, Hiroshi
Chiba, Mitsuru
Oatley, Jon
Diaz, Francisco
Liu, Wan-Sheng
author_sort Mistry, Bhavesh V.
collection PubMed
description PRAME belongs to a group of cancer/testis antigens (CTAs) that are characterized by their restricted expression in normal gametogenic tissues and a variety of tumors. The PRAME family is one of the most amplified gene families in the mouse and other mammalian genomes. Members of the PRAME gene family encode leucine-rich repeat (LRR) proteins functioning as transcription regulators in cancer cells. However, the role of PRAME in normal gonads is unknown. The objective of this study is to characterize the temporal and spatial expression of the mouse Pramel1 gene, and to determine the cellular localization of the PRAMEL1 protein during the mouse spermatogenesis. Our results indicated that the mouse Pramel1 was expressed in testis only. The mRNA and protein expression level was low in the newborn testes, and gradually increased from 1- to 3-week-old testes, and then remained constant after three weeks of age. Immunofluorescent staining on testis sections with the mouse PRAMEL1 antibody revealed that PRAMEL1 was localized in the cytoplasm of spermatocytes and the acrosomal region of round, elongating and elongated spermatids. Further analyses on the testis squash preparation and spermatozoa at a subcellular level indicated that the protein localization patterns of PRAMEL1 were coordinated with morphological alterations during acrosome formation in spermatids, and were significantly different in connecting piece, middle piece and principal piece of the flagellum between testicular and epididymal spermatozoa. Collectively, our results suggest that PRAMEL1 may play a role in acrosome biogenesis and sperm motility.
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spelling pubmed-36149762013-04-05 Differential Expression of PRAMEL1, a Cancer/Testis Antigen, during Spermatogenesis in the Mouse Mistry, Bhavesh V. Zhao, Yaqi Chang, Ti-Cheng Yasue, Hiroshi Chiba, Mitsuru Oatley, Jon Diaz, Francisco Liu, Wan-Sheng PLoS One Research Article PRAME belongs to a group of cancer/testis antigens (CTAs) that are characterized by their restricted expression in normal gametogenic tissues and a variety of tumors. The PRAME family is one of the most amplified gene families in the mouse and other mammalian genomes. Members of the PRAME gene family encode leucine-rich repeat (LRR) proteins functioning as transcription regulators in cancer cells. However, the role of PRAME in normal gonads is unknown. The objective of this study is to characterize the temporal and spatial expression of the mouse Pramel1 gene, and to determine the cellular localization of the PRAMEL1 protein during the mouse spermatogenesis. Our results indicated that the mouse Pramel1 was expressed in testis only. The mRNA and protein expression level was low in the newborn testes, and gradually increased from 1- to 3-week-old testes, and then remained constant after three weeks of age. Immunofluorescent staining on testis sections with the mouse PRAMEL1 antibody revealed that PRAMEL1 was localized in the cytoplasm of spermatocytes and the acrosomal region of round, elongating and elongated spermatids. Further analyses on the testis squash preparation and spermatozoa at a subcellular level indicated that the protein localization patterns of PRAMEL1 were coordinated with morphological alterations during acrosome formation in spermatids, and were significantly different in connecting piece, middle piece and principal piece of the flagellum between testicular and epididymal spermatozoa. Collectively, our results suggest that PRAMEL1 may play a role in acrosome biogenesis and sperm motility. Public Library of Science 2013-04-02 /pmc/articles/PMC3614976/ /pubmed/23565261 http://dx.doi.org/10.1371/journal.pone.0060611 Text en © 2013 Mistry 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mistry, Bhavesh V.
Zhao, Yaqi
Chang, Ti-Cheng
Yasue, Hiroshi
Chiba, Mitsuru
Oatley, Jon
Diaz, Francisco
Liu, Wan-Sheng
Differential Expression of PRAMEL1, a Cancer/Testis Antigen, during Spermatogenesis in the Mouse
title Differential Expression of PRAMEL1, a Cancer/Testis Antigen, during Spermatogenesis in the Mouse
title_full Differential Expression of PRAMEL1, a Cancer/Testis Antigen, during Spermatogenesis in the Mouse
title_fullStr Differential Expression of PRAMEL1, a Cancer/Testis Antigen, during Spermatogenesis in the Mouse
title_full_unstemmed Differential Expression of PRAMEL1, a Cancer/Testis Antigen, during Spermatogenesis in the Mouse
title_short Differential Expression of PRAMEL1, a Cancer/Testis Antigen, during Spermatogenesis in the Mouse
title_sort differential expression of pramel1, a cancer/testis antigen, during spermatogenesis in the mouse
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614976/
https://www.ncbi.nlm.nih.gov/pubmed/23565261
http://dx.doi.org/10.1371/journal.pone.0060611
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