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Dynamics of Notch pathway expression during mouse testis post-natal development and along the spermatogenic cycle
The transcription and expression patterns of Notch pathway components (Notch 1-3, Delta1 and 4, Jagged1) and effectors (Hes1, Hes2, Hes5 and Nrarp) were evaluated (through RT-PCR and IHC) in the mouse testis at key moments of post-natal development, and along the adult spermatogenic cycle. Notch pat...
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Published in: | PloS one 2013-08, Vol.8 (8), p.e72767-e72767 |
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description | The transcription and expression patterns of Notch pathway components (Notch 1-3, Delta1 and 4, Jagged1) and effectors (Hes1, Hes2, Hes5 and Nrarp) were evaluated (through RT-PCR and IHC) in the mouse testis at key moments of post-natal development, and along the adult spermatogenic cycle. Notch pathway components and effectors are transcribed in the testis and expressed in germ, Sertoli and Leydig cells, and each Notch component shows a specific cell-type and time-window expression pattern. This expression at key testis developmental events prompt for a role of Notch signaling in pre-pubertal spermatogonia quiescence, onset of spermatogenesis, and regulation of the spermatogenic cycle. |
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Notch pathway components and effectors are transcribed in the testis and expressed in germ, Sertoli and Leydig cells, and each Notch component shows a specific cell-type and time-window expression pattern. This expression at key testis developmental events prompt for a role of Notch signaling in pre-pubertal spermatogonia quiescence, onset of spermatogenesis, and regulation of the spermatogenic cycle.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0072767</identifier><identifier>PMID: 24015274</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Drosophila ; Effectors ; Gene expression ; Gene Expression Regulation - physiology ; Genetic engineering ; Infertility ; Insects ; Jagged1 protein ; Leydig cells ; Ligands ; Male ; Mammals ; Medical research ; Mice ; Notch protein ; Notch1 protein ; Obstetrics ; Polymerase chain reaction ; Puberty ; Receptors, Notch - genetics ; Receptors, Notch - metabolism ; Rodents ; Signal Transduction - physiology ; Signaling ; Spermatogenesis ; Spermatogenesis - physiology ; Spermatogonia ; Studies ; Testis - cytology ; Testis - growth & development ; Testis - metabolism ; Testosterone ; Transcription ; Transcription, Genetic - physiology ; Veterinary medicine ; Windows (intervals)</subject><ispartof>PloS one, 2013-08, Vol.8 (8), p.e72767-e72767</ispartof><rights>2013 Murta et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Murta et al 2013 Murta et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c619t-965be7bd52e761ff766b16724d2699f728f8f46baccd5f262c2bbc59703352113</citedby><cites>FETCH-LOGICAL-c619t-965be7bd52e761ff766b16724d2699f728f8f46baccd5f262c2bbc59703352113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1428549768/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1428549768?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24015274$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Lobaccaro, Jean-Marc A.</contributor><creatorcontrib>Murta, Daniel</creatorcontrib><creatorcontrib>Batista, Marta</creatorcontrib><creatorcontrib>Silva, Elisabete</creatorcontrib><creatorcontrib>Trindade, Alexandre</creatorcontrib><creatorcontrib>Henrique, Domingos</creatorcontrib><creatorcontrib>Duarte, António</creatorcontrib><creatorcontrib>Lopes-da-Costa, Luís</creatorcontrib><title>Dynamics of Notch pathway expression during mouse testis post-natal development and along the spermatogenic cycle</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The transcription and expression patterns of Notch pathway components (Notch 1-3, Delta1 and 4, Jagged1) and effectors (Hes1, Hes2, Hes5 and Nrarp) were evaluated (through RT-PCR and IHC) in the mouse testis at key moments of post-natal development, and along the adult spermatogenic cycle. Notch pathway components and effectors are transcribed in the testis and expressed in germ, Sertoli and Leydig cells, and each Notch component shows a specific cell-type and time-window expression pattern. This expression at key testis developmental events prompt for a role of Notch signaling in pre-pubertal spermatogonia quiescence, onset of spermatogenesis, and regulation of the spermatogenic cycle.</description><subject>Animals</subject><subject>Drosophila</subject><subject>Effectors</subject><subject>Gene expression</subject><subject>Gene Expression Regulation - physiology</subject><subject>Genetic engineering</subject><subject>Infertility</subject><subject>Insects</subject><subject>Jagged1 protein</subject><subject>Leydig cells</subject><subject>Ligands</subject><subject>Male</subject><subject>Mammals</subject><subject>Medical research</subject><subject>Mice</subject><subject>Notch protein</subject><subject>Notch1 protein</subject><subject>Obstetrics</subject><subject>Polymerase chain reaction</subject><subject>Puberty</subject><subject>Receptors, Notch - genetics</subject><subject>Receptors, Notch - metabolism</subject><subject>Rodents</subject><subject>Signal Transduction - physiology</subject><subject>Signaling</subject><subject>Spermatogenesis</subject><subject>Spermatogenesis - 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Notch pathway components and effectors are transcribed in the testis and expressed in germ, Sertoli and Leydig cells, and each Notch component shows a specific cell-type and time-window expression pattern. This expression at key testis developmental events prompt for a role of Notch signaling in pre-pubertal spermatogonia quiescence, onset of spermatogenesis, and regulation of the spermatogenic cycle.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24015274</pmid><doi>10.1371/journal.pone.0072767</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Drosophila Effectors Gene expression Gene Expression Regulation - physiology Genetic engineering Infertility Insects Jagged1 protein Leydig cells Ligands Male Mammals Medical research Mice Notch protein Notch1 protein Obstetrics Polymerase chain reaction Puberty Receptors, Notch - genetics Receptors, Notch - metabolism Rodents Signal Transduction - physiology Signaling Spermatogenesis Spermatogenesis - physiology Spermatogonia Studies Testis - cytology Testis - growth & development Testis - metabolism Testosterone Transcription Transcription, Genetic - physiology Veterinary medicine Windows (intervals) |
title | Dynamics of Notch pathway expression during mouse testis post-natal development and along the spermatogenic cycle |
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