Equatorial Segment Protein Defines a Discrete Acrosomal Subcompartment Persisting Throughout Acrosomal Biogenesis
The equatorial segment of the acrosome underlies the domain of the sperm that fuses with the egg membrane during fertilization. Equatorial segment protein (ESP), a novel 349-amino acid concanavalin-A-binding protein encoded by a two-exon gene ( SP-ESP ) located on chromosome 15 at q22, has been loca...
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Veröffentlicht in: | Biology of reproduction 2003-09, Vol.69 (3), p.735-745 |
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container_title | Biology of reproduction |
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creator | WOLKOWICZ, Michael J SHETTY, Jagathpala WESTBROOK, Anne KLOTZ, Ken JAYES, Frederike MANDAL, Arabinda FLICKINGER, Charles J HERR, John C |
description | The equatorial segment of the acrosome underlies the domain of the sperm that fuses with the egg membrane during fertilization.
Equatorial segment protein (ESP), a novel 349-amino acid concanavalin-A-binding protein encoded by a two-exon gene ( SP-ESP ) located on chromosome 15 at q22, has been localized to the equatorial segment of ejaculated human sperm. Light microscopic
immunofluorescent observations revealed that during acrosome biogenesis ESP first appears in the nascent acrosomal vesicle
in early round spermatids and subsequently segregates to the periphery of the expanding acrosomal vesicle, thereby defining
a peripheral equatorial segment compartment within flattened acrosomal vesicles and in the acrosomes of early and late cap
phase, elongating, and mature spermatids. Electron microscopic examination revealed that ESP segregates to an electron-lucent
subdomain of the condensing acrosomal matrix in Golgi phase round spermatids and persists in a similar electron-lucent subdomain
within cap phase spermatids. Subsequently, ESP was localized to electron-dense regions of the equatorial segment and the expanded
equatorial bulb in elongating spermatids and mature sperm. ESP is the earliest known protein to be recognized as a marker
for the specification of the equatorial segment, and it allows this region to be traced through all phases of acrosomal biogenesis.
Based on these observations, we propose a new model of acrosome biogenesis in which the equatorial segment is defined as a
discrete domain within the acrosomal vesicle as early as the Golgi phase of acrosome biogenesis. |
doi_str_mv | 10.1095/biolreprod.103.016675 |
format | Article |
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Equatorial segment protein (ESP), a novel 349-amino acid concanavalin-A-binding protein encoded by a two-exon gene ( SP-ESP ) located on chromosome 15 at q22, has been localized to the equatorial segment of ejaculated human sperm. Light microscopic
immunofluorescent observations revealed that during acrosome biogenesis ESP first appears in the nascent acrosomal vesicle
in early round spermatids and subsequently segregates to the periphery of the expanding acrosomal vesicle, thereby defining
a peripheral equatorial segment compartment within flattened acrosomal vesicles and in the acrosomes of early and late cap
phase, elongating, and mature spermatids. Electron microscopic examination revealed that ESP segregates to an electron-lucent
subdomain of the condensing acrosomal matrix in Golgi phase round spermatids and persists in a similar electron-lucent subdomain
within cap phase spermatids. Subsequently, ESP was localized to electron-dense regions of the equatorial segment and the expanded
equatorial bulb in elongating spermatids and mature sperm. ESP is the earliest known protein to be recognized as a marker
for the specification of the equatorial segment, and it allows this region to be traced through all phases of acrosomal biogenesis.
Based on these observations, we propose a new model of acrosome biogenesis in which the equatorial segment is defined as a
discrete domain within the acrosomal vesicle as early as the Golgi phase of acrosome biogenesis.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1095/biolreprod.103.016675</identifier><identifier>PMID: 12773409</identifier><identifier>CODEN: BIREBV</identifier><language>eng</language><publisher>Madison, WI: Society for the Study of Reproduction</publisher><subject>Acrosome - metabolism ; Amino Acid Sequence ; Base Sequence ; Biological and medical sciences ; Blotting, Western ; Carrier Proteins - genetics ; Carrier Proteins - metabolism ; Cell Membrane - metabolism ; Chromosomes, Human, Pair 15 - genetics ; Fundamental and applied biological sciences. Psychology ; Hormone metabolism and regulation ; Humans ; Immunohistochemistry ; Male ; Mammalian male genital system ; Molecular Sequence Data ; Receptors, Concanavalin A - metabolism ; Seminal Plasma Proteins - genetics ; Seminal Plasma Proteins - metabolism ; Spermatogenesis - genetics ; Subcellular Fractions ; Testis - metabolism ; Tissue Distribution ; Vertebrates: reproduction</subject><ispartof>Biology of reproduction, 2003-09, Vol.69 (3), p.735-745</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15454000$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12773409$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WOLKOWICZ, Michael J</creatorcontrib><creatorcontrib>SHETTY, Jagathpala</creatorcontrib><creatorcontrib>WESTBROOK, Anne</creatorcontrib><creatorcontrib>KLOTZ, Ken</creatorcontrib><creatorcontrib>JAYES, Frederike</creatorcontrib><creatorcontrib>MANDAL, Arabinda</creatorcontrib><creatorcontrib>FLICKINGER, Charles J</creatorcontrib><creatorcontrib>HERR, John C</creatorcontrib><title>Equatorial Segment Protein Defines a Discrete Acrosomal Subcompartment Persisting Throughout Acrosomal Biogenesis</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description>The equatorial segment of the acrosome underlies the domain of the sperm that fuses with the egg membrane during fertilization.
Equatorial segment protein (ESP), a novel 349-amino acid concanavalin-A-binding protein encoded by a two-exon gene ( SP-ESP ) located on chromosome 15 at q22, has been localized to the equatorial segment of ejaculated human sperm. Light microscopic
immunofluorescent observations revealed that during acrosome biogenesis ESP first appears in the nascent acrosomal vesicle
in early round spermatids and subsequently segregates to the periphery of the expanding acrosomal vesicle, thereby defining
a peripheral equatorial segment compartment within flattened acrosomal vesicles and in the acrosomes of early and late cap
phase, elongating, and mature spermatids. Electron microscopic examination revealed that ESP segregates to an electron-lucent
subdomain of the condensing acrosomal matrix in Golgi phase round spermatids and persists in a similar electron-lucent subdomain
within cap phase spermatids. Subsequently, ESP was localized to electron-dense regions of the equatorial segment and the expanded
equatorial bulb in elongating spermatids and mature sperm. ESP is the earliest known protein to be recognized as a marker
for the specification of the equatorial segment, and it allows this region to be traced through all phases of acrosomal biogenesis.
Based on these observations, we propose a new model of acrosome biogenesis in which the equatorial segment is defined as a
discrete domain within the acrosomal vesicle as early as the Golgi phase of acrosome biogenesis.</description><subject>Acrosome - metabolism</subject><subject>Amino Acid Sequence</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - metabolism</subject><subject>Cell Membrane - metabolism</subject><subject>Chromosomes, Human, Pair 15 - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hormone metabolism and regulation</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Mammalian male genital system</subject><subject>Molecular Sequence Data</subject><subject>Receptors, Concanavalin A - metabolism</subject><subject>Seminal Plasma Proteins - genetics</subject><subject>Seminal Plasma Proteins - metabolism</subject><subject>Spermatogenesis - genetics</subject><subject>Subcellular Fractions</subject><subject>Testis - metabolism</subject><subject>Tissue Distribution</subject><subject>Vertebrates: reproduction</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpN0M1KxDAUBeAgio6jj6B0o7tqmrTJZOm_woCCui637U0baZuZJGXw7Y04oqsQ-O5JziXkJKMXGVXFZWVs73DlbBPv_IJmQshih8yygqlUMrHYJTNKqUg5F_yAHHr_QWmWc8b3yUHGpOQ5VTOyvltPEKwz0Cev2A44huTF2YBmTG5RmxF9Asmt8bXDgMlV7ay3wzeeqtoOK3DhZwadNz6YsU3eOmentrNT-MevjW0xhhl_RPY09B6Pt-ecvN_fvd08psvnh6ebq2XaMSFDKgAqVFQvQGqp8pwVOWs0KtVIttAsVgNJUYEWHOtcU60Kjpw2EkArhIrPyflPbtzRekIfyiG2wL6HEe3kS8mLhWSSRni6hVM1YFOunBnAfZa_S4rgbAvA19BrB2Nt_J8r8iKP__lznWm7jXFY-li9j7G83Gw2QpX8-1X-BUmGiPg</recordid><startdate>20030901</startdate><enddate>20030901</enddate><creator>WOLKOWICZ, Michael J</creator><creator>SHETTY, Jagathpala</creator><creator>WESTBROOK, Anne</creator><creator>KLOTZ, Ken</creator><creator>JAYES, Frederike</creator><creator>MANDAL, Arabinda</creator><creator>FLICKINGER, Charles J</creator><creator>HERR, John C</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><scope>7X8</scope></search><sort><creationdate>20030901</creationdate><title>Equatorial Segment Protein Defines a Discrete Acrosomal Subcompartment Persisting Throughout Acrosomal Biogenesis</title><author>WOLKOWICZ, Michael J ; SHETTY, Jagathpala ; WESTBROOK, Anne ; KLOTZ, Ken ; JAYES, Frederike ; MANDAL, Arabinda ; FLICKINGER, Charles J ; HERR, John C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h267t-6aabe90f8a7f79442542dfe99d728f2000a70e9af63ec4f0f953e30d7aaf9eab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Acrosome - metabolism</topic><topic>Amino Acid Sequence</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Carrier Proteins - genetics</topic><topic>Carrier Proteins - metabolism</topic><topic>Cell Membrane - metabolism</topic><topic>Chromosomes, Human, Pair 15 - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hormone metabolism and regulation</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Mammalian male genital system</topic><topic>Molecular Sequence Data</topic><topic>Receptors, Concanavalin A - metabolism</topic><topic>Seminal Plasma Proteins - genetics</topic><topic>Seminal Plasma Proteins - metabolism</topic><topic>Spermatogenesis - genetics</topic><topic>Subcellular Fractions</topic><topic>Testis - metabolism</topic><topic>Tissue Distribution</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WOLKOWICZ, Michael J</creatorcontrib><creatorcontrib>SHETTY, Jagathpala</creatorcontrib><creatorcontrib>WESTBROOK, Anne</creatorcontrib><creatorcontrib>KLOTZ, Ken</creatorcontrib><creatorcontrib>JAYES, Frederike</creatorcontrib><creatorcontrib>MANDAL, Arabinda</creatorcontrib><creatorcontrib>FLICKINGER, Charles J</creatorcontrib><creatorcontrib>HERR, John C</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WOLKOWICZ, Michael J</au><au>SHETTY, Jagathpala</au><au>WESTBROOK, Anne</au><au>KLOTZ, Ken</au><au>JAYES, Frederike</au><au>MANDAL, Arabinda</au><au>FLICKINGER, Charles J</au><au>HERR, John C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Equatorial Segment Protein Defines a Discrete Acrosomal Subcompartment Persisting Throughout Acrosomal Biogenesis</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>2003-09-01</date><risdate>2003</risdate><volume>69</volume><issue>3</issue><spage>735</spage><epage>745</epage><pages>735-745</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><coden>BIREBV</coden><abstract>The equatorial segment of the acrosome underlies the domain of the sperm that fuses with the egg membrane during fertilization.
Equatorial segment protein (ESP), a novel 349-amino acid concanavalin-A-binding protein encoded by a two-exon gene ( SP-ESP ) located on chromosome 15 at q22, has been localized to the equatorial segment of ejaculated human sperm. Light microscopic
immunofluorescent observations revealed that during acrosome biogenesis ESP first appears in the nascent acrosomal vesicle
in early round spermatids and subsequently segregates to the periphery of the expanding acrosomal vesicle, thereby defining
a peripheral equatorial segment compartment within flattened acrosomal vesicles and in the acrosomes of early and late cap
phase, elongating, and mature spermatids. Electron microscopic examination revealed that ESP segregates to an electron-lucent
subdomain of the condensing acrosomal matrix in Golgi phase round spermatids and persists in a similar electron-lucent subdomain
within cap phase spermatids. Subsequently, ESP was localized to electron-dense regions of the equatorial segment and the expanded
equatorial bulb in elongating spermatids and mature sperm. ESP is the earliest known protein to be recognized as a marker
for the specification of the equatorial segment, and it allows this region to be traced through all phases of acrosomal biogenesis.
Based on these observations, we propose a new model of acrosome biogenesis in which the equatorial segment is defined as a
discrete domain within the acrosomal vesicle as early as the Golgi phase of acrosome biogenesis.</abstract><cop>Madison, WI</cop><pub>Society for the Study of Reproduction</pub><pmid>12773409</pmid><doi>10.1095/biolreprod.103.016675</doi><tpages>11</tpages></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; BioOne Complete |
subjects | Acrosome - metabolism Amino Acid Sequence Base Sequence Biological and medical sciences Blotting, Western Carrier Proteins - genetics Carrier Proteins - metabolism Cell Membrane - metabolism Chromosomes, Human, Pair 15 - genetics Fundamental and applied biological sciences. Psychology Hormone metabolism and regulation Humans Immunohistochemistry Male Mammalian male genital system Molecular Sequence Data Receptors, Concanavalin A - metabolism Seminal Plasma Proteins - genetics Seminal Plasma Proteins - metabolism Spermatogenesis - genetics Subcellular Fractions Testis - metabolism Tissue Distribution Vertebrates: reproduction |
title | Equatorial Segment Protein Defines a Discrete Acrosomal Subcompartment Persisting Throughout Acrosomal Biogenesis |
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