The third egg envelope subunit in fish: cDNA cloning and analysis, and gene expression

The inner layer of the egg envelope of a teleost fish, the medaka, Oryzias latipes, consists of two major subunit groups, Zl‐1,2 and Zl‐3. On SDS‐PAGE, the Zl‐1,2 group presents three glycoprotein bands that were considered to be composed of a common polypeptide moiety derived from their precursor,...

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Veröffentlicht in:Development, growth & differentiation growth & differentiation, 1998-02, Vol.40 (1), p.35-45
Hauptverfasser: Sugiyama, Hitoshi, Yasumasu, Shigeki, Murata, Kenji, Iuchi, Ichiro, Yamagami, Kenjiro
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container_end_page 45
container_issue 1
container_start_page 35
container_title Development, growth & differentiation
container_volume 40
creator Sugiyama, Hitoshi
Yasumasu, Shigeki
Murata, Kenji
Iuchi, Ichiro
Yamagami, Kenjiro
description The inner layer of the egg envelope of a teleost fish, the medaka, Oryzias latipes, consists of two major subunit groups, Zl‐1,2 and Zl‐3. On SDS‐PAGE, the Zl‐1,2 group presents three glycoprotein bands that were considered to be composed of a common polypeptide moiety derived from their precursor, choriogenin H (Chg H). Zl‐3 is a single glycoprotein derived from the precursor, choriogenin L (Chg L). In the present study, a fraction of a novel subunit protein was found in the V8 protease digest of Zl‐1,2 that was partially purified from oocyte envelopes. This protein fraction was not present in the purified precursor, Chg H. By RT‐PCR employing the primers based on the amino acid sequence of this fraction, a cDNA for the novel subunit was amplified, and a full‐length clone of the cDNA was obtained by screening a cDNA library constructed from the spawning female liver. The clone consisted of 2025 b.p. and contained an open reading frame encoding the novel protein of 634 amino acids. This protein included Pro‐X‐Y repeat sequences in two‐fifths of the whole length from its N‐terminus. Northern blot analysis revealed that the gene expression for this protein occurred in the liver but not in the ovary of spawning female fish. This protein is considered as the third major subunit of the inner layer of the egg envelope of medaka.
doi_str_mv 10.1046/j.1440-169X.1998.t01-5-00005.x
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On SDS‐PAGE, the Zl‐1,2 group presents three glycoprotein bands that were considered to be composed of a common polypeptide moiety derived from their precursor, choriogenin H (Chg H). Zl‐3 is a single glycoprotein derived from the precursor, choriogenin L (Chg L). In the present study, a fraction of a novel subunit protein was found in the V8 protease digest of Zl‐1,2 that was partially purified from oocyte envelopes. This protein fraction was not present in the purified precursor, Chg H. By RT‐PCR employing the primers based on the amino acid sequence of this fraction, a cDNA for the novel subunit was amplified, and a full‐length clone of the cDNA was obtained by screening a cDNA library constructed from the spawning female liver. The clone consisted of 2025 b.p. and contained an open reading frame encoding the novel protein of 634 amino acids. This protein included Pro‐X‐Y repeat sequences in two‐fifths of the whole length from its N‐terminus. 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On SDS‐PAGE, the Zl‐1,2 group presents three glycoprotein bands that were considered to be composed of a common polypeptide moiety derived from their precursor, choriogenin H (Chg H). Zl‐3 is a single glycoprotein derived from the precursor, choriogenin L (Chg L). In the present study, a fraction of a novel subunit protein was found in the V8 protease digest of Zl‐1,2 that was partially purified from oocyte envelopes. This protein fraction was not present in the purified precursor, Chg H. By RT‐PCR employing the primers based on the amino acid sequence of this fraction, a cDNA for the novel subunit was amplified, and a full‐length clone of the cDNA was obtained by screening a cDNA library constructed from the spawning female liver. The clone consisted of 2025 b.p. and contained an open reading frame encoding the novel protein of 634 amino acids. This protein included Pro‐X‐Y repeat sequences in two‐fifths of the whole length from its N‐terminus. Northern blot analysis revealed that the gene expression for this protein occurred in the liver but not in the ovary of spawning female fish. 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Yasumasu, Shigeki ; Murata, Kenji ; Iuchi, Ichiro ; Yamagami, Kenjiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5015-51d4041a358370a3ba4200c184e81d606c690dea76bf929f07b0df7d85c0e6943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>cDNA cloning</topic><topic>Chorion - chemistry</topic><topic>Cloning, Molecular - methods</topic><topic>DNA, Complementary - genetics</topic><topic>egg envelope</topic><topic>Egg Proteins - chemistry</topic><topic>Egg Proteins - genetics</topic><topic>Egg Proteins - isolation &amp; purification</topic><topic>Female</topic><topic>fish</topic><topic>Fish Proteins</topic><topic>Freshwater</topic><topic>gene expression</topic><topic>Gene Expression Regulation, Developmental - physiology</topic><topic>Liver - chemistry</topic><topic>Molecular Sequence Data</topic><topic>Molecular Weight</topic><topic>Oryzias - genetics</topic><topic>Oryzias latipes</topic><topic>Peptide Mapping</topic><topic>Pro‐X‐Y repeat</topic><topic>RNA, Messenger - analysis</topic><topic>Sequence Analysis</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Homology, Amino Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sugiyama, Hitoshi</creatorcontrib><creatorcontrib>Yasumasu, Shigeki</creatorcontrib><creatorcontrib>Murata, Kenji</creatorcontrib><creatorcontrib>Iuchi, Ichiro</creatorcontrib><creatorcontrib>Yamagami, Kenjiro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science &amp; 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On SDS‐PAGE, the Zl‐1,2 group presents three glycoprotein bands that were considered to be composed of a common polypeptide moiety derived from their precursor, choriogenin H (Chg H). Zl‐3 is a single glycoprotein derived from the precursor, choriogenin L (Chg L). In the present study, a fraction of a novel subunit protein was found in the V8 protease digest of Zl‐1,2 that was partially purified from oocyte envelopes. This protein fraction was not present in the purified precursor, Chg H. By RT‐PCR employing the primers based on the amino acid sequence of this fraction, a cDNA for the novel subunit was amplified, and a full‐length clone of the cDNA was obtained by screening a cDNA library constructed from the spawning female liver. The clone consisted of 2025 b.p. and contained an open reading frame encoding the novel protein of 634 amino acids. This protein included Pro‐X‐Y repeat sequences in two‐fifths of the whole length from its N‐terminus. 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subjects Amino Acid Sequence
Animals
Base Sequence
cDNA cloning
Chorion - chemistry
Cloning, Molecular - methods
DNA, Complementary - genetics
egg envelope
Egg Proteins - chemistry
Egg Proteins - genetics
Egg Proteins - isolation & purification
Female
fish
Fish Proteins
Freshwater
gene expression
Gene Expression Regulation, Developmental - physiology
Liver - chemistry
Molecular Sequence Data
Molecular Weight
Oryzias - genetics
Oryzias latipes
Peptide Mapping
Pro‐X‐Y repeat
RNA, Messenger - analysis
Sequence Analysis
Sequence Analysis, DNA
Sequence Homology, Amino Acid
title The third egg envelope subunit in fish: cDNA cloning and analysis, and gene expression
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