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Cloning and expression of a porcine zona pellucida gene: an approach to immunocontraception

dc.contributor.authorFontenot, Gregory Kenneth, author
dc.contributor.authorBowen, R. A., advisor
dc.contributor.authorJonathan Carlson, committee member
dc.contributor.authorNiswender, Gordon, committee member
dc.date.accessioned2021-12-15T18:13:26Z
dc.date.available2021-12-15T18:13:26Z
dc.date.issued1991
dc.descriptionCovers not scanned.
dc.descriptionPrint version deaccessioned 2021.
dc.description.abstractImmunization with native porcine zona pellucida (ZP) proteins has been shown to induce infertility in females of several species and is thus a potentially valuable method of contraception. However, more extensive testing and commercialization of such a vaccine has been hampered by the limited availability of ZP proteins from natural sources. Availability of recombinant ZP proteins should simplify production of a practical ZP vaccine. The objective of this research was to clone a porcine ZP gene and use it to develop a recombinant ZP vaccine for use in pet animals. Polyadenylated RNA isolated from swine ovary was used to generate a cDNA library in the bacteriophage lambda gt11. This library was screened immunologically for ZP sequences using a polyclonal antiserum raised against solubilized porcine ZP. One immunoreactive clone, PZP, contained an insert of approximately 2.6 kb and was characterized further. The three Eco RI fragments constituting PZP were isolated and subcloned into a plasmid vector. The amino acid sequence deduced from the nucleotide sequence of PZP is considered to represent 305 residues from the carboxyterminal end of the ZP protein. A putative N-glycosylation site is present at residue 288 of this polypeptide. Comparison of the deduced amino acid sequence of PZP with deduced protein sequences from all of the other ZP proteins published to date failed to reveal significant homology. To confirm that PZP represented a ZP mRNA, a 418 bp fragment of the cDNA was expressed as a fusion protein in E. coli and used to hyperimmunize a rabbit. Antibodies to the PZP fusion protein bound to ZP surrounding porcine oocytes, stained ZP in sections of porcine ovary and immunoprecipitated a porcine ZP protein that was tentatively identified as ZP2. The PZP fusion protein was preliminarily evaluated as a vaccine in rabbits. Two groups of four adult rabbits were immunized three or four times with PZP2 fusion protein emulsified in either one of two adjuvants. Reproductive function was evaluated eight and sixteen weeks after initial immunization. In comparison to control rabbits, no effect of vaccination on reproductive function was observed.
dc.format.mediumdoctoral dissertations
dc.identifier.urihttps://hdl.handle.net/10217/234118
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relationCatalog record number (MMS ID): 991017970239703361
dc.relationQL965 .F65 1991
dc.relation.ispartof1980-1999
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.subjectZona pellucida
dc.subjectMolecular cloning
dc.subjectContraception, Immunological
dc.titleCloning and expression of a porcine zona pellucida gene: an approach to immunocontraception
dc.typeText
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplinePhysiology
thesis.degree.grantorColorado State University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy (Ph.D)

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