Identification and structural characterization of the 75-kDa rabbit zona pellucida protein
| Autor: | V H, Lee, E, Schwoebel, S, Prasad, P, Cheung, T M, Timmons, R, Cook, B S, Dunbar |
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| Rok vydání: | 1993 |
| Předmět: |
Aging
Membrane Glycoproteins Base Sequence Sequence Homology Amino Acid Egg Proteins Molecular Sequence Data Ovary Receptors Cell Surface DNA Blotting Northern Zona Pellucida Glycoproteins Protein Structure Secondary Recombinant Proteins Molecular Weight Animals RNA Female Amino Acid Sequence RNA Messenger Rabbits Cloning Molecular Zona Pellucida |
| Zdroj: | The Journal of biological chemistry. 268(17) |
| ISSN: | 0021-9258 |
| Popis: | A cDNA (rc75) encoding a 75-kDa rabbit zona pellucida (ZP) glycoprotein (R75) has been cloned and sequenced. The predicted amino acid sequence consists of 676 amino acids including seven potential N-glycosylation sites. The cDNA hybridizes to a 2.4-kilobase mRNA in ovary that is not detectable in other rabbit tissues. The R75 mRNA was also found to be expressed during the early stages of rabbit ovarian development (2-6 weeks of age) when the ovary contains primordial, primary, and early secondary follicles. The deduced amino acid sequence of rc75 has 77% similarity to the mouse ZP2 protein but no similarity to mouse ZP3. R75 also contains regions with 35-55% similarity to a previously cloned rabbit 55-kDa ZP protein. Monte Carlo simulation comparison confirmed that R75 has a significant probability of homology with mouse ZP2 and the rabbit 55-kDa ZP protein. Antibodies were developed against a fragment of R75 (rc75a cDNA) expressed in the pEX expression vector. These antibodies were used to confirm that the expressed protein contained epitopes found in the native rabbit ZP glycoprotein. These data suggest that some, but not all, ZP proteins may be conserved among different species and that within a species ZP proteins may share similar regions. |
| Databáze: | OpenAIRE |
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