Following passage through the oviduct, the coelomic envelope of Discoglossus pictus (amphibia) acquires fertilizability upon reorganization, conversion of gp 42 to gp 40, extensive glycosylation, and formation of a specific layer

This paper describes the morphological and biochemical changes in Discoglossus pictus coelomic oocyte envelope (CE) following passage through the oviduct. As in other anurans, in this species, the transformation of the envelope into vitelline envelope (VE) leads to the acquisition of fertilizability...

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Veröffentlicht in:Molecular reproduction and development 2001-03, Vol.58 (3), p.318-329
Hauptverfasser: Caputo, Mariangela, Infante, Vincenzo, Talevi, Riccardo, Vaccaro, Maria Carmen, Carotenuto, Rosa, Campanella, Chiara
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container_issue 3
container_start_page 318
container_title Molecular reproduction and development
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creator Caputo, Mariangela
Infante, Vincenzo
Talevi, Riccardo
Vaccaro, Maria Carmen
Carotenuto, Rosa
Campanella, Chiara
description This paper describes the morphological and biochemical changes in Discoglossus pictus coelomic oocyte envelope (CE) following passage through the oviduct. As in other anurans, in this species, the transformation of the envelope into vitelline envelope (VE) leads to the acquisition of fertilizability and involves the cleavage of a glycoprotein. In addition, several features, typical of Discoglossus pictus, were observed. A new layer, VE‐D, forms underneath the VE region facing the site of sperm entrance, the dimple. In the VE, arrowhead‐like bundles of fibrils are perpendicularly oriented toward the dimple. Ultrastructural observations and staining with UEA‐I suggested that VE‐D might have a role in supporting sperm penetration into the dimple by orienting VE bundles and exposing sugar residues such as fucose. In ‘in vitro’ tests, VE binding of sperm occurs only if sperm are exposed to A23187, in agreement with previous data (Campanella et al., 1997: Mol Reprod Dev 47:323–333). Sperm binding occurs all over the VE. Accordingly, extracts of the VE covering the animal or the vegetal hemisphere have the same affinity to lectins (DBA, DSA, GNA, MAA, SBA, SNA, UEA‐I, WGA). The CE contains six main glycoproteins. Peptide mapping indicated that during CE transformation into VE, gp 42 shifts to an apparent Mr of 40 and gp 61 is converted to an apparent Mr of 63 kDa. Lectin blot analyses showed extensive changes in cross‐reactivity of most glycoproteins during the CE→VE transition. The fact that DBA and UEA‐I stain gp 63 rather than gp 61 and that this change is related only to gp 63, suggested that O‐glycosylation and terminal fucose might be acquired by gp 63 in preparation of fertilization. Gp 63 has recently been cloned (Vaccaro et al., submitted) and shown to exhibit high homology to Xenopus gp 69/64, a VE sperm ligand (Tian et al., 1997a: J. Cell Biol. 136: 1099–1108; Tian et al., 1997b: Dev Biol 187:143–153), and to ZP2 of mammals. Mol. Reprod. Dev. 58:318–329, 2001. © 2001 Wiley‐Liss, Inc.
doi_str_mv 10.1002/1098-2795(200103)58:3<318::AID-MRD10>3.0.CO;2-8
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As in other anurans, in this species, the transformation of the envelope into vitelline envelope (VE) leads to the acquisition of fertilizability and involves the cleavage of a glycoprotein. In addition, several features, typical of Discoglossus pictus, were observed. A new layer, VE‐D, forms underneath the VE region facing the site of sperm entrance, the dimple. In the VE, arrowhead‐like bundles of fibrils are perpendicularly oriented toward the dimple. Ultrastructural observations and staining with UEA‐I suggested that VE‐D might have a role in supporting sperm penetration into the dimple by orienting VE bundles and exposing sugar residues such as fucose. In ‘in vitro’ tests, VE binding of sperm occurs only if sperm are exposed to A23187, in agreement with previous data (Campanella et al., 1997: Mol Reprod Dev 47:323–333). Sperm binding occurs all over the VE. Accordingly, extracts of the VE covering the animal or the vegetal hemisphere have the same affinity to lectins (DBA, DSA, GNA, MAA, SBA, SNA, UEA‐I, WGA). The CE contains six main glycoproteins. Peptide mapping indicated that during CE transformation into VE, gp 42 shifts to an apparent Mr of 40 and gp 61 is converted to an apparent Mr of 63 kDa. Lectin blot analyses showed extensive changes in cross‐reactivity of most glycoproteins during the CE→VE transition. The fact that DBA and UEA‐I stain gp 63 rather than gp 61 and that this change is related only to gp 63, suggested that O‐glycosylation and terminal fucose might be acquired by gp 63 in preparation of fertilization. Gp 63 has recently been cloned (Vaccaro et al., submitted) and shown to exhibit high homology to Xenopus gp 69/64, a VE sperm ligand (Tian et al., 1997a: J. Cell Biol. 136: 1099–1108; Tian et al., 1997b: Dev Biol 187:143–153), and to ZP2 of mammals. Mol. Reprod. 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Reprod. Dev</addtitle><description>This paper describes the morphological and biochemical changes in Discoglossus pictus coelomic oocyte envelope (CE) following passage through the oviduct. As in other anurans, in this species, the transformation of the envelope into vitelline envelope (VE) leads to the acquisition of fertilizability and involves the cleavage of a glycoprotein. In addition, several features, typical of Discoglossus pictus, were observed. A new layer, VE‐D, forms underneath the VE region facing the site of sperm entrance, the dimple. In the VE, arrowhead‐like bundles of fibrils are perpendicularly oriented toward the dimple. Ultrastructural observations and staining with UEA‐I suggested that VE‐D might have a role in supporting sperm penetration into the dimple by orienting VE bundles and exposing sugar residues such as fucose. 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Psychology</subject><subject>Glycoproteins - metabolism</subject><subject>Lectins - metabolism</subject><subject>Male</subject><subject>Non mammalian vertebrate reproduction</subject><subject>oligosaccharide chains</subject><subject>Oviducts - metabolism</subject><subject>Ovum - physiology</subject><subject>Ovum - ultrastructure</subject><subject>Peptide Mapping</subject><subject>sperm binding</subject><subject>Spermatozoa - metabolism</subject><subject>Vertebrates: reproduction</subject><subject>vitelline envelope</subject><subject>Vitelline Membrane - chemistry</subject><subject>Vitelline Membrane - metabolism</subject><issn>1040-452X</issn><issn>1098-2795</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFUtFu0zAUjRCIjcEvIEtIaJOWch0ndTIQ0mjZmDRWMcHYm-U6N6nBjTM76VaeeOU3eeMvcNdSXnzPuT732LJPFHEKAwqQvKJQ5HHCi2w_AaDADrL8iL1hND86Oj4bxx8vxxTesgEMRpPXSZw_iHa3Ew9XOIU4zZLrneiJ998AoChyeBztUEo5JJztRn9OrDH2Vjc1aaX3skbSzZzt61moSOxCl73qDu-JsmjsXCuCzSKgNmxXZKy9srWx3veetFp1oezLeTvTUy0PiFQ3vXboSYWu00b_kNOwdkvSt7YhDq2rZRO6nbbNYTghODsf8Mq6bn___JUmpLMbCIcE7zpsvF4gqc1SWb80m1HZlKSybn5PV9OS-BaVrsJ9jVyiexo9qqTx-GxT96IvJ-8_jz7E55PTs9HxeaxZyiGWPOOUTkvG5FCpXKVlWiS84jQrpoGliicpQlGWEpMqLRVHTKeUlhmjiGWRs73o5dq3dfamR9-JeXgiNEY2aHsvOGQF5AkNwucbYT-dYylap-fSLcW_zwmCFxuB9EqayslGab_V5QUMUwiqT2vVrTa4_O8CYpUgscqDWOVBrBMkslwwERIkQoDEfYACBzGaiETk60bwjNee2nd4t_WU7rsYcsYz8fXiVFxcXl1fwbtcnLK_WobT0w</recordid><startdate>200103</startdate><enddate>200103</enddate><creator>Caputo, Mariangela</creator><creator>Infante, Vincenzo</creator><creator>Talevi, Riccardo</creator><creator>Vaccaro, Maria Carmen</creator><creator>Carotenuto, Rosa</creator><creator>Campanella, Chiara</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley-Liss</general><scope>BSCLL</scope><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>200103</creationdate><title>Following passage through the oviduct, the coelomic envelope of Discoglossus pictus (amphibia) acquires fertilizability upon reorganization, conversion of gp 42 to gp 40, extensive glycosylation, and formation of a specific layer</title><author>Caputo, Mariangela ; Infante, Vincenzo ; Talevi, Riccardo ; Vaccaro, Maria Carmen ; Carotenuto, Rosa ; Campanella, Chiara</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3470-a75711bd33a6cc8c4d4927f7159b8c44c724e09ddae2f4dc7ee4b11d531eed983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>amphibian oocytes</topic><topic>Animals</topic><topic>Anura - physiology</topic><topic>Biological and medical sciences</topic><topic>Cell Polarity</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Female</topic><topic>Fertilization - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glycoproteins - metabolism</topic><topic>Lectins - metabolism</topic><topic>Male</topic><topic>Non mammalian vertebrate reproduction</topic><topic>oligosaccharide chains</topic><topic>Oviducts - metabolism</topic><topic>Ovum - physiology</topic><topic>Ovum - ultrastructure</topic><topic>Peptide Mapping</topic><topic>sperm binding</topic><topic>Spermatozoa - metabolism</topic><topic>Vertebrates: reproduction</topic><topic>vitelline envelope</topic><topic>Vitelline Membrane - chemistry</topic><topic>Vitelline Membrane - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Caputo, Mariangela</creatorcontrib><creatorcontrib>Infante, Vincenzo</creatorcontrib><creatorcontrib>Talevi, Riccardo</creatorcontrib><creatorcontrib>Vaccaro, Maria Carmen</creatorcontrib><creatorcontrib>Carotenuto, Rosa</creatorcontrib><creatorcontrib>Campanella, Chiara</creatorcontrib><collection>Istex</collection><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>Molecular reproduction and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Caputo, Mariangela</au><au>Infante, Vincenzo</au><au>Talevi, Riccardo</au><au>Vaccaro, Maria Carmen</au><au>Carotenuto, Rosa</au><au>Campanella, Chiara</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Following passage through the oviduct, the coelomic envelope of Discoglossus pictus (amphibia) acquires fertilizability upon reorganization, conversion of gp 42 to gp 40, extensive glycosylation, and formation of a specific layer</atitle><jtitle>Molecular reproduction and development</jtitle><addtitle>Mol. Reprod. Dev</addtitle><date>2001-03</date><risdate>2001</risdate><volume>58</volume><issue>3</issue><spage>318</spage><epage>329</epage><pages>318-329</pages><issn>1040-452X</issn><eissn>1098-2795</eissn><coden>MREDEE</coden><abstract>This paper describes the morphological and biochemical changes in Discoglossus pictus coelomic oocyte envelope (CE) following passage through the oviduct. As in other anurans, in this species, the transformation of the envelope into vitelline envelope (VE) leads to the acquisition of fertilizability and involves the cleavage of a glycoprotein. In addition, several features, typical of Discoglossus pictus, were observed. A new layer, VE‐D, forms underneath the VE region facing the site of sperm entrance, the dimple. In the VE, arrowhead‐like bundles of fibrils are perpendicularly oriented toward the dimple. Ultrastructural observations and staining with UEA‐I suggested that VE‐D might have a role in supporting sperm penetration into the dimple by orienting VE bundles and exposing sugar residues such as fucose. In ‘in vitro’ tests, VE binding of sperm occurs only if sperm are exposed to A23187, in agreement with previous data (Campanella et al., 1997: Mol Reprod Dev 47:323–333). Sperm binding occurs all over the VE. Accordingly, extracts of the VE covering the animal or the vegetal hemisphere have the same affinity to lectins (DBA, DSA, GNA, MAA, SBA, SNA, UEA‐I, WGA). The CE contains six main glycoproteins. Peptide mapping indicated that during CE transformation into VE, gp 42 shifts to an apparent Mr of 40 and gp 61 is converted to an apparent Mr of 63 kDa. Lectin blot analyses showed extensive changes in cross‐reactivity of most glycoproteins during the CE→VE transition. The fact that DBA and UEA‐I stain gp 63 rather than gp 61 and that this change is related only to gp 63, suggested that O‐glycosylation and terminal fucose might be acquired by gp 63 in preparation of fertilization. Gp 63 has recently been cloned (Vaccaro et al., submitted) and shown to exhibit high homology to Xenopus gp 69/64, a VE sperm ligand (Tian et al., 1997a: J. Cell Biol. 136: 1099–1108; Tian et al., 1997b: Dev Biol 187:143–153), and to ZP2 of mammals. Mol. Reprod. Dev. 58:318–329, 2001. © 2001 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>11170273</pmid><doi>10.1002/1098-2795(200103)58:3&lt;318::AID-MRD10&gt;3.0.CO;2-8</doi><tpages>12</tpages></addata></record>
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subjects amphibian oocytes
Animals
Anura - physiology
Biological and medical sciences
Cell Polarity
Electrophoresis, Polyacrylamide Gel
Female
Fertilization - physiology
Fundamental and applied biological sciences. Psychology
Glycoproteins - metabolism
Lectins - metabolism
Male
Non mammalian vertebrate reproduction
oligosaccharide chains
Oviducts - metabolism
Ovum - physiology
Ovum - ultrastructure
Peptide Mapping
sperm binding
Spermatozoa - metabolism
Vertebrates: reproduction
vitelline envelope
Vitelline Membrane - chemistry
Vitelline Membrane - metabolism
title Following passage through the oviduct, the coelomic envelope of Discoglossus pictus (amphibia) acquires fertilizability upon reorganization, conversion of gp 42 to gp 40, extensive glycosylation, and formation of a specific layer
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