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Changes in cathepsin gene expression and relative enzymatic activity during gilthead sea bream oogenesis
Author(s) -
Carnevali O.,
Cionna C.,
Tosti L.,
Cerdà J.,
Gioacchini G.
Publication year - 2008
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/mrd.20768
Subject(s) - biology , cathepsin , cathepsin l , cathepsin b , cathepsin d , gene expression , cathepsin h , cathepsin l1 , cathepsin e , gene , cathepsin o , cathepsin s , yolk , microbiology and biotechnology , enzyme , biochemistry , ecology
The aim of this study was to provide evidence on the modulation of lysosomal enzymes in terms of both gene expression and enzymatic activity during follicle maturation. For this purpose three lysosomal enzymes, cathepsins B, D, and L, were studied in relation to yolk formation and degradation, during the main phases of ovarian follicle growth in the pelagophil species, the sea bream Sparus aurata . Specific attention was focused on the gene expression quantification method, on the assay of enzymatic activities, and on the relationship between the proteolytic cleavage of yolk proteins (YPs), cathepsin gene expression and cathepsin activities. For the gene expression study, the cathepsins B‐like and L‐like mRNAs were isolated and partially or fully characterized, respectively; the sequences were used as design specific primers for the quantification of cathepsin gene expression by real‐time PCR, in follicles at different stages of maturation. The enzymatic assays for cathepsins B, D, and L were optimized in terms of specificity, sensitivity and reliability, using specific substrates and inhibitors. In ovulated eggs, the lipovitellin I (LV I) was degraded and the changes in electrophoretic pattern were preceded by an increase in the activity of a cysteine proteinase, cathepsin L, and its mRNA. Cathepsin B did not appear to be involved in YP changes during the final maturation stage. Mol. Reprod. Dev. 75: 97–104, 2008. © 2007 Wiley‐Liss, Inc.