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GLI1 Localization in the Germinal Epithelial Cells Alternates Between Cytoplasm and Nucleus: Upregulation in Transgenic Mice Blocks Spermatogenesis in Pachytene
The zinc finger transcription factor GLI1 is the mediator of signaling by members of the Hedgehog (Hh) family. Male mice in which Desert hedgehog (Dhh), an Hh homologue expressed in Sertoli cells of the testis, was knocked out are sterile, suggesting that the Dhh/GLI1 pathway plays a role in spermat...
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Published in: | Biology of reproduction 2001-12, Vol.65 (6), p.1663-1671 |
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container_end_page | 1671 |
container_issue | 6 |
container_start_page | 1663 |
container_title | Biology of reproduction |
container_volume | 65 |
creator | KROFT, Tim L PATTERSON, John JOON WON YOON DOGLIO, Lynn WALTERHOUSE, David O IANNACCONE, Phillip M GOLDBERG, Erwin |
description | The zinc finger transcription factor GLI1 is the mediator of signaling by members of the Hedgehog (Hh) family. Male mice in
which Desert hedgehog (Dhh), an Hh homologue expressed in Sertoli cells of the testis, was knocked out are sterile, suggesting
that the Dhh/GLI1 pathway plays a role in spermatogenesis. Using an antiserum raised against human GLI1, we found that during
the first round of spermatogenesis, GLI1 expression is initially cytoplasmic, then shifts to the nuclei of Sertoli and germ
cells, and finally shifts back to the cytoplasm. In the adult mouse testis, GLI1 expression localized to the nuclei of germ
cells, beginning with pachytene cells and persisting through round spermatids. Localization of GLI1 in elongating spermatids
shifted from the nucleus to the cytoplasm and became associated with microtubules. We also examined a line of transgenic mice
that overexpressed human GLI1. Male mice in this line were sterile. Spermatogenesis was blocked at the pachytene stage, and
a subset of the morphologically indistinguishable pachytene cells underwent apoptosis. Patched-2, which is a Dhh receptor,
and Fused, another component of the signal transduction pathway, are expressed in Leydig cells and in primary and secondary
spermatocytes. Expression of GLI1 in the same cell types as Patched-2 and Fused and the disruption of spermatogenesis by GLI1
overexpression suggest that GLI1 is the mediator of the Dhh signal in the testis, and that it may be a regulator of spermatogenesis. |
doi_str_mv | 10.1095/biolreprod65.6.1663 |
format | article |
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which Desert hedgehog (Dhh), an Hh homologue expressed in Sertoli cells of the testis, was knocked out are sterile, suggesting
that the Dhh/GLI1 pathway plays a role in spermatogenesis. Using an antiserum raised against human GLI1, we found that during
the first round of spermatogenesis, GLI1 expression is initially cytoplasmic, then shifts to the nuclei of Sertoli and germ
cells, and finally shifts back to the cytoplasm. In the adult mouse testis, GLI1 expression localized to the nuclei of germ
cells, beginning with pachytene cells and persisting through round spermatids. Localization of GLI1 in elongating spermatids
shifted from the nucleus to the cytoplasm and became associated with microtubules. We also examined a line of transgenic mice
that overexpressed human GLI1. Male mice in this line were sterile. Spermatogenesis was blocked at the pachytene stage, and
a subset of the morphologically indistinguishable pachytene cells underwent apoptosis. Patched-2, which is a Dhh receptor,
and Fused, another component of the signal transduction pathway, are expressed in Leydig cells and in primary and secondary
spermatocytes. Expression of GLI1 in the same cell types as Patched-2 and Fused and the disruption of spermatogenesis by GLI1
overexpression suggest that GLI1 is the mediator of the Dhh signal in the testis, and that it may be a regulator of spermatogenesis.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1095/biolreprod65.6.1663</identifier><identifier>PMID: 11717126</identifier><identifier>CODEN: BIREBV</identifier><language>eng</language><publisher>Madison, WI: Society for the Study of Reproduction</publisher><subject>Animals ; Apoptosis ; Biological and medical sciences ; Cell Nucleus - chemistry ; Cytoplasm - chemistry ; Epithelial Cells - chemistry ; Epithelial Cells - ultrastructure ; Gene Expression ; Hedgehog Proteins ; Isoenzymes - analysis ; L-Lactate Dehydrogenase - analysis ; Male ; Mice ; Mice, Knockout ; Mice, Transgenic ; Microtubules - chemistry ; Mitosis ; Oncogene Proteins - analysis ; Oncogene Proteins - genetics ; Sertoli Cells - ultrastructure ; Spermatogenesis ; Spermatozoa - enzymology ; Testis - ultrastructure ; Trans-Activators - genetics ; Transcription Factors - analysis ; Transcription Factors - genetics ; Zinc Finger Protein GLI1 ; Zinc Fingers</subject><ispartof>Biology of reproduction, 2001-12, Vol.65 (6), p.1663-1671</ispartof><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13538583$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11717126$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KROFT, Tim L</creatorcontrib><creatorcontrib>PATTERSON, John</creatorcontrib><creatorcontrib>JOON WON YOON</creatorcontrib><creatorcontrib>DOGLIO, Lynn</creatorcontrib><creatorcontrib>WALTERHOUSE, David O</creatorcontrib><creatorcontrib>IANNACCONE, Phillip M</creatorcontrib><creatorcontrib>GOLDBERG, Erwin</creatorcontrib><title>GLI1 Localization in the Germinal Epithelial Cells Alternates Between Cytoplasm and Nucleus: Upregulation in Transgenic Mice Blocks Spermatogenesis in Pachytene</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description>The zinc finger transcription factor GLI1 is the mediator of signaling by members of the Hedgehog (Hh) family. Male mice in
which Desert hedgehog (Dhh), an Hh homologue expressed in Sertoli cells of the testis, was knocked out are sterile, suggesting
that the Dhh/GLI1 pathway plays a role in spermatogenesis. Using an antiserum raised against human GLI1, we found that during
the first round of spermatogenesis, GLI1 expression is initially cytoplasmic, then shifts to the nuclei of Sertoli and germ
cells, and finally shifts back to the cytoplasm. In the adult mouse testis, GLI1 expression localized to the nuclei of germ
cells, beginning with pachytene cells and persisting through round spermatids. Localization of GLI1 in elongating spermatids
shifted from the nucleus to the cytoplasm and became associated with microtubules. We also examined a line of transgenic mice
that overexpressed human GLI1. Male mice in this line were sterile. Spermatogenesis was blocked at the pachytene stage, and
a subset of the morphologically indistinguishable pachytene cells underwent apoptosis. Patched-2, which is a Dhh receptor,
and Fused, another component of the signal transduction pathway, are expressed in Leydig cells and in primary and secondary
spermatocytes. Expression of GLI1 in the same cell types as Patched-2 and Fused and the disruption of spermatogenesis by GLI1
overexpression suggest that GLI1 is the mediator of the Dhh signal in the testis, and that it may be a regulator of spermatogenesis.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Biological and medical sciences</subject><subject>Cell Nucleus - chemistry</subject><subject>Cytoplasm - chemistry</subject><subject>Epithelial Cells - chemistry</subject><subject>Epithelial Cells - ultrastructure</subject><subject>Gene Expression</subject><subject>Hedgehog Proteins</subject><subject>Isoenzymes - analysis</subject><subject>L-Lactate Dehydrogenase - analysis</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Mice, Transgenic</subject><subject>Microtubules - chemistry</subject><subject>Mitosis</subject><subject>Oncogene Proteins - analysis</subject><subject>Oncogene Proteins - genetics</subject><subject>Sertoli Cells - ultrastructure</subject><subject>Spermatogenesis</subject><subject>Spermatozoa - enzymology</subject><subject>Testis - ultrastructure</subject><subject>Trans-Activators - genetics</subject><subject>Transcription Factors - analysis</subject><subject>Transcription Factors - genetics</subject><subject>Zinc Finger Protein GLI1</subject><subject>Zinc Fingers</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNpFkdtu1DAQhi0EokvhCZCQb-Auiw-xk3DXrsq20rYg0V5HE2eyMTgH2V5F26fhUeuqhWouZn7Np380M4R85GzNWaW-NnZyHmc_tVqt9ZprLV-RFVeiygqhy9dkxRjTmZRanpB3IfxmjOdSyLfkhPMihdAr8ne7u-J0Nxlw9h6inUZqRxp7pFv0gx3B0YvZJu1sKjfoXKBnLqIfIWKg5xgXxJFujnGaHYSBwtjSm4NxeAjf6N3scX9w_31vPYxhj6M19NoapOduMn8C_TWnWRCn1MFgwyP5E0x_jEm_J286cAE_POdTcvf94nZzme1-bK82Z7usl1LErCpzUXWixRygzXmhGAMtCymaThmtVdMI0ZkcDFfcqNJ0IIQRRVNWqimZLOUp-fTkOx-aAdt69nYAf6z_nSoBn58BCOlaXVrF2PDCSSVLVcrEfXniervvF-uxDgM4l2xlvSyLVrWuH38lHwASmYqC</recordid><startdate>20011201</startdate><enddate>20011201</enddate><creator>KROFT, Tim L</creator><creator>PATTERSON, John</creator><creator>JOON WON YOON</creator><creator>DOGLIO, Lynn</creator><creator>WALTERHOUSE, David O</creator><creator>IANNACCONE, Phillip M</creator><creator>GOLDBERG, Erwin</creator><general>Society for the Study of Reproduction</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20011201</creationdate><title>GLI1 Localization in the Germinal Epithelial Cells Alternates Between Cytoplasm and Nucleus: Upregulation in Transgenic Mice Blocks Spermatogenesis in Pachytene</title><author>KROFT, Tim L ; PATTERSON, John ; JOON WON YOON ; DOGLIO, Lynn ; WALTERHOUSE, David O ; IANNACCONE, Phillip M ; GOLDBERG, Erwin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h332t-98429f2de4aad417500a63732bf5c665bb22fc4ac151c58cfa22c27b895b80383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Biological and medical sciences</topic><topic>Cell Nucleus - chemistry</topic><topic>Cytoplasm - chemistry</topic><topic>Epithelial Cells - chemistry</topic><topic>Epithelial Cells - ultrastructure</topic><topic>Gene Expression</topic><topic>Hedgehog Proteins</topic><topic>Isoenzymes - analysis</topic><topic>L-Lactate Dehydrogenase - analysis</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Mice, Transgenic</topic><topic>Microtubules - chemistry</topic><topic>Mitosis</topic><topic>Oncogene Proteins - analysis</topic><topic>Oncogene Proteins - genetics</topic><topic>Sertoli Cells - ultrastructure</topic><topic>Spermatogenesis</topic><topic>Spermatozoa - enzymology</topic><topic>Testis - ultrastructure</topic><topic>Trans-Activators - genetics</topic><topic>Transcription Factors - analysis</topic><topic>Transcription Factors - genetics</topic><topic>Zinc Finger Protein GLI1</topic><topic>Zinc Fingers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KROFT, Tim L</creatorcontrib><creatorcontrib>PATTERSON, John</creatorcontrib><creatorcontrib>JOON WON YOON</creatorcontrib><creatorcontrib>DOGLIO, Lynn</creatorcontrib><creatorcontrib>WALTERHOUSE, David O</creatorcontrib><creatorcontrib>IANNACCONE, Phillip M</creatorcontrib><creatorcontrib>GOLDBERG, Erwin</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KROFT, Tim L</au><au>PATTERSON, John</au><au>JOON WON YOON</au><au>DOGLIO, Lynn</au><au>WALTERHOUSE, David O</au><au>IANNACCONE, Phillip M</au><au>GOLDBERG, Erwin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GLI1 Localization in the Germinal Epithelial Cells Alternates Between Cytoplasm and Nucleus: Upregulation in Transgenic Mice Blocks Spermatogenesis in Pachytene</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>2001-12-01</date><risdate>2001</risdate><volume>65</volume><issue>6</issue><spage>1663</spage><epage>1671</epage><pages>1663-1671</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><coden>BIREBV</coden><abstract>The zinc finger transcription factor GLI1 is the mediator of signaling by members of the Hedgehog (Hh) family. Male mice in
which Desert hedgehog (Dhh), an Hh homologue expressed in Sertoli cells of the testis, was knocked out are sterile, suggesting
that the Dhh/GLI1 pathway plays a role in spermatogenesis. Using an antiserum raised against human GLI1, we found that during
the first round of spermatogenesis, GLI1 expression is initially cytoplasmic, then shifts to the nuclei of Sertoli and germ
cells, and finally shifts back to the cytoplasm. In the adult mouse testis, GLI1 expression localized to the nuclei of germ
cells, beginning with pachytene cells and persisting through round spermatids. Localization of GLI1 in elongating spermatids
shifted from the nucleus to the cytoplasm and became associated with microtubules. We also examined a line of transgenic mice
that overexpressed human GLI1. Male mice in this line were sterile. Spermatogenesis was blocked at the pachytene stage, and
a subset of the morphologically indistinguishable pachytene cells underwent apoptosis. Patched-2, which is a Dhh receptor,
and Fused, another component of the signal transduction pathway, are expressed in Leydig cells and in primary and secondary
spermatocytes. Expression of GLI1 in the same cell types as Patched-2 and Fused and the disruption of spermatogenesis by GLI1
overexpression suggest that GLI1 is the mediator of the Dhh signal in the testis, and that it may be a regulator of spermatogenesis.</abstract><cop>Madison, WI</cop><pub>Society for the Study of Reproduction</pub><pmid>11717126</pmid><doi>10.1095/biolreprod65.6.1663</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford Journals Online |
subjects | Animals Apoptosis Biological and medical sciences Cell Nucleus - chemistry Cytoplasm - chemistry Epithelial Cells - chemistry Epithelial Cells - ultrastructure Gene Expression Hedgehog Proteins Isoenzymes - analysis L-Lactate Dehydrogenase - analysis Male Mice Mice, Knockout Mice, Transgenic Microtubules - chemistry Mitosis Oncogene Proteins - analysis Oncogene Proteins - genetics Sertoli Cells - ultrastructure Spermatogenesis Spermatozoa - enzymology Testis - ultrastructure Trans-Activators - genetics Transcription Factors - analysis Transcription Factors - genetics Zinc Finger Protein GLI1 Zinc Fingers |
title | GLI1 Localization in the Germinal Epithelial Cells Alternates Between Cytoplasm and Nucleus: Upregulation in Transgenic Mice Blocks Spermatogenesis in Pachytene |
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