The Histone Demethylase FBXL10 Regulates the Proliferation of Spermatogonia and Ensures Long-Term Sustainable Spermatogenesis in Mice1
The F-box and leucine-rich repeat protein 10 (Fbxl10) gene encodes a protein that catalyzes demethylation of H3K4 and H3K36. In this study, we show the important roles of FBXL10 as a histone demethylase in sustainable sperm production using mice in which the JmjC domain of Fbxl10 was deleted (Fbxl10...
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Veröffentlicht in: | Biology of reproduction 2016-04, Vol.94 (4) |
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creator | Ozawa, Manabu Fukuda, Tsuyoshi Sakamoto, Reiko Honda, Hiroaki Yoshida, Nobuaki |
description | The F-box and leucine-rich repeat protein 10 (Fbxl10) gene encodes a protein that catalyzes demethylation of H3K4 and H3K36. In this study, we show the important roles of FBXL10 as a histone demethylase in sustainable sperm production using mice in which the JmjC domain of Fbxl10 was deleted (Fbxl10DeltaJ/DeltaJ). In histological analysis, testis sections from 10-wk-old Fbxl10DeltaJ/DeltaJ mice appeared normal. On the other hand, testes from 7-mo-old Fbxl10DeltaJ/DeltaJ mice contained a greater ratio of seminiferous tubules exhibiting degeneration of spermatogenesis. Further analysis using an in vitro spermatogonia culture system, that is, germline stem cells (GSCs), revealed that Fbxl10DeltaJ/DeltaJ GSCs expressed a significantly higher level of P21 and P19 mRNA, cyclin-dependent kinase inhibitors and also known as cellular senescence markers, than wild-type (WT) GSCs. Furthermore, the ratio of Fbxl10DeltaJ/DeltaJ GSCs in G0/G1 phase was higher and the ratios in S and G2/M phases were lower than the corresponding ratios of WT GSCs, and the doubling speed of Fbxl10DeltaJ/DeltaJ GSCs was significantly slower than that of WT GSCs. In addition to these in vitro results, an in vivo study indicated that recovery of spermatogenesis after a transient reduction in the number of testicular germ cells by busulfan treatment was significantly slower in Fbxl10DeltaJ/DeltaJ mice than in WT mice. These data suggest that Fbxl10 plays important roles in long-term sustainable spermatogenesis via regulating cell cycle. |
doi_str_mv | 10.1095/biolreprod.115.135988 |
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In this study, we show the important roles of FBXL10 as a histone demethylase in sustainable sperm production using mice in which the JmjC domain of Fbxl10 was deleted (Fbxl10DeltaJ/DeltaJ). In histological analysis, testis sections from 10-wk-old Fbxl10DeltaJ/DeltaJ mice appeared normal. On the other hand, testes from 7-mo-old Fbxl10DeltaJ/DeltaJ mice contained a greater ratio of seminiferous tubules exhibiting degeneration of spermatogenesis. Further analysis using an in vitro spermatogonia culture system, that is, germline stem cells (GSCs), revealed that Fbxl10DeltaJ/DeltaJ GSCs expressed a significantly higher level of P21 and P19 mRNA, cyclin-dependent kinase inhibitors and also known as cellular senescence markers, than wild-type (WT) GSCs. Furthermore, the ratio of Fbxl10DeltaJ/DeltaJ GSCs in G0/G1 phase was higher and the ratios in S and G2/M phases were lower than the corresponding ratios of WT GSCs, and the doubling speed of Fbxl10DeltaJ/DeltaJ GSCs was significantly slower than that of WT GSCs. In addition to these in vitro results, an in vivo study indicated that recovery of spermatogenesis after a transient reduction in the number of testicular germ cells by busulfan treatment was significantly slower in Fbxl10DeltaJ/DeltaJ mice than in WT mice. These data suggest that Fbxl10 plays important roles in long-term sustainable spermatogenesis via regulating cell cycle.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1095/biolreprod.115.135988</identifier><language>eng</language><publisher>Society for the Study of Reproduction, Inc</publisher><subject>cell cycle ; epigenetics ; spermatogenesis ; spermatogonia ; spermatogonial stem cells</subject><ispartof>Biology of reproduction, 2016-04, Vol.94 (4)</ispartof><rights>2016 by the Society for the Study of Reproduction, Inc. This is an Open Access article, freely available through Biology of Reproduction's Authors' Choice option, and is available under a Creative Commons License 4.0 (Attribution-Non-Commercial), as described at http://creativecommons.org/licenses/by-nc/4.0/.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b2558-15f5578869580832de03182b79728e073648b8edab8ee958182562e4ff6e3d3d3</citedby><cites>FETCH-LOGICAL-b2558-15f5578869580832de03182b79728e073648b8edab8ee958182562e4ff6e3d3d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Ozawa, Manabu</creatorcontrib><creatorcontrib>Fukuda, Tsuyoshi</creatorcontrib><creatorcontrib>Sakamoto, Reiko</creatorcontrib><creatorcontrib>Honda, Hiroaki</creatorcontrib><creatorcontrib>Yoshida, Nobuaki</creatorcontrib><title>The Histone Demethylase FBXL10 Regulates the Proliferation of Spermatogonia and Ensures Long-Term Sustainable Spermatogenesis in Mice1</title><title>Biology of reproduction</title><description>The F-box and leucine-rich repeat protein 10 (Fbxl10) gene encodes a protein that catalyzes demethylation of H3K4 and H3K36. In this study, we show the important roles of FBXL10 as a histone demethylase in sustainable sperm production using mice in which the JmjC domain of Fbxl10 was deleted (Fbxl10DeltaJ/DeltaJ). In histological analysis, testis sections from 10-wk-old Fbxl10DeltaJ/DeltaJ mice appeared normal. On the other hand, testes from 7-mo-old Fbxl10DeltaJ/DeltaJ mice contained a greater ratio of seminiferous tubules exhibiting degeneration of spermatogenesis. Further analysis using an in vitro spermatogonia culture system, that is, germline stem cells (GSCs), revealed that Fbxl10DeltaJ/DeltaJ GSCs expressed a significantly higher level of P21 and P19 mRNA, cyclin-dependent kinase inhibitors and also known as cellular senescence markers, than wild-type (WT) GSCs. Furthermore, the ratio of Fbxl10DeltaJ/DeltaJ GSCs in G0/G1 phase was higher and the ratios in S and G2/M phases were lower than the corresponding ratios of WT GSCs, and the doubling speed of Fbxl10DeltaJ/DeltaJ GSCs was significantly slower than that of WT GSCs. In addition to these in vitro results, an in vivo study indicated that recovery of spermatogenesis after a transient reduction in the number of testicular germ cells by busulfan treatment was significantly slower in Fbxl10DeltaJ/DeltaJ mice than in WT mice. These data suggest that Fbxl10 plays important roles in long-term sustainable spermatogenesis via regulating cell cycle.</description><subject>cell cycle</subject><subject>epigenetics</subject><subject>spermatogenesis</subject><subject>spermatogonia</subject><subject>spermatogonial stem cells</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkM1KAzEURoMoWKuPIOQFpuanyWSWWlsrjCi2grsh07lpI9OkJOmiL-BzG6nQrVy4d_Gd7y4OQreUjCipxF1rfR9gF3w3olSMKBeVUmdoQAWripJJdY4GhBBZcC75JbqK8YsQOuaMD9D3cgN4bmPyDvAjbCFtDr2OgGcPnzUl-B3W-14niDhl8C343hoIOlnvsDd4sYOw1cmvvbMaa9fhqYv7kPHau3WxzCle7GPS1um2hxMPDqKN2Dr8YldAr9GF0X2Em787RB-z6XIyL-rXp-fJfV20TAhVUGGEKJWSlVBEcdYB4VSxtqxKpoCUXI5Vq6DTeUFmciYkg7ExEniXZ4jE8e8q-BgDmGYX7FaHQ0NJ8yuzOclssszmKDP3-LGX42zqn60fzTV9dg</recordid><startdate>201604</startdate><enddate>201604</enddate><creator>Ozawa, Manabu</creator><creator>Fukuda, Tsuyoshi</creator><creator>Sakamoto, Reiko</creator><creator>Honda, Hiroaki</creator><creator>Yoshida, Nobuaki</creator><general>Society for the Study of Reproduction, Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201604</creationdate><title>The Histone Demethylase FBXL10 Regulates the Proliferation of Spermatogonia and Ensures Long-Term Sustainable Spermatogenesis in Mice1</title><author>Ozawa, Manabu ; Fukuda, Tsuyoshi ; Sakamoto, Reiko ; Honda, Hiroaki ; Yoshida, Nobuaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b2558-15f5578869580832de03182b79728e073648b8edab8ee958182562e4ff6e3d3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>cell cycle</topic><topic>epigenetics</topic><topic>spermatogenesis</topic><topic>spermatogonia</topic><topic>spermatogonial stem cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ozawa, Manabu</creatorcontrib><creatorcontrib>Fukuda, Tsuyoshi</creatorcontrib><creatorcontrib>Sakamoto, Reiko</creatorcontrib><creatorcontrib>Honda, Hiroaki</creatorcontrib><creatorcontrib>Yoshida, Nobuaki</creatorcontrib><collection>CrossRef</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ozawa, Manabu</au><au>Fukuda, Tsuyoshi</au><au>Sakamoto, Reiko</au><au>Honda, Hiroaki</au><au>Yoshida, Nobuaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Histone Demethylase FBXL10 Regulates the Proliferation of Spermatogonia and Ensures Long-Term Sustainable Spermatogenesis in Mice1</atitle><jtitle>Biology of reproduction</jtitle><date>2016-04</date><risdate>2016</risdate><volume>94</volume><issue>4</issue><issn>0006-3363</issn><eissn>1529-7268</eissn><abstract>The F-box and leucine-rich repeat protein 10 (Fbxl10) gene encodes a protein that catalyzes demethylation of H3K4 and H3K36. In this study, we show the important roles of FBXL10 as a histone demethylase in sustainable sperm production using mice in which the JmjC domain of Fbxl10 was deleted (Fbxl10DeltaJ/DeltaJ). In histological analysis, testis sections from 10-wk-old Fbxl10DeltaJ/DeltaJ mice appeared normal. On the other hand, testes from 7-mo-old Fbxl10DeltaJ/DeltaJ mice contained a greater ratio of seminiferous tubules exhibiting degeneration of spermatogenesis. Further analysis using an in vitro spermatogonia culture system, that is, germline stem cells (GSCs), revealed that Fbxl10DeltaJ/DeltaJ GSCs expressed a significantly higher level of P21 and P19 mRNA, cyclin-dependent kinase inhibitors and also known as cellular senescence markers, than wild-type (WT) GSCs. Furthermore, the ratio of Fbxl10DeltaJ/DeltaJ GSCs in G0/G1 phase was higher and the ratios in S and G2/M phases were lower than the corresponding ratios of WT GSCs, and the doubling speed of Fbxl10DeltaJ/DeltaJ GSCs was significantly slower than that of WT GSCs. In addition to these in vitro results, an in vivo study indicated that recovery of spermatogenesis after a transient reduction in the number of testicular germ cells by busulfan treatment was significantly slower in Fbxl10DeltaJ/DeltaJ mice than in WT mice. These data suggest that Fbxl10 plays important roles in long-term sustainable spermatogenesis via regulating cell cycle.</abstract><pub>Society for the Study of Reproduction, Inc</pub><doi>10.1095/biolreprod.115.135988</doi><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals Current; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | cell cycle epigenetics spermatogenesis spermatogonia spermatogonial stem cells |
title | The Histone Demethylase FBXL10 Regulates the Proliferation of Spermatogonia and Ensures Long-Term Sustainable Spermatogenesis in Mice1 |
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