The nucleolus and its modifications during oogenesis of Torpedo marmorata

The structural organisation of the nucleolar apparatus during oogenesis of the spotted ray Torpedo marmorata was investigated. The observations showed that unlike other cartilaginous fishes, in T. marmorata the nucleolar apparatus was always represented by one or two conspicuous nucleoli, whose organization significantly changed during oocyte development. In the smallest follicles (follicles <300 μm in diameter) the nucleolus was made up of granular and fibrillar components, and actively incorporated 3 H uridine; later it becomes more and more electron-dense so in follicles of 400μm in diameter its components and 3 H uridine incorporation were no longer evident. These results indicate that in T. marmorata the nucleolar apparatus significantly changes and undergoes a possible impairment in rRNA synthesis. After nucleolus inactivation, the synthesis of rRNA may be substained by granulosa.

[1]  D. Treré,et al.  Relationship between interphase AgNOR distribution and nucleolar size in cancer cells , 1992, The Histochemical Journal.

[2]  J. S. Balsano,et al.  Nucleoprotein cytochemistry during oogenesis in a unisexual fish,Poecilia formosa , 1981, The Histochemical Journal.

[3]  M. Prisco,et al.  Distribution of terminal sugar residues in the testis of the spotted ray Torpedo marmorata , 2004, Molecular reproduction and development.

[4]  P. Marina,et al.  Ovarian follicle cells in torpedo marmorata synthesize vitellogenin , 2004, Molecular reproduction and development.

[5]  P. Marina,et al.  α and β spectrin distribution during the differentiation of pyriform cells in follicles of lizard Podarcis sicula , 2004 .

[6]  E. Raikova,et al.  Amplified ribosomal DNA in meiotic prophase oocyte nuclei of acipenserid fishes , 1979, Wilhelm Roux's archives of developmental biology.

[7]  M. Vlad Nucleolar DNA in oocytes of Salmo irideus (Gibbons) , 1976, Cell and Tissue Research.

[8]  M. Prisco,et al.  Developing follicles of the spotted ray Torpedo marmorata express different glycoside residues in relation to granulosa differentiation and vitelline envelope formation. , 2003, Histology and histopathology.

[9]  C. Migné,et al.  Chromatin configuration and transcriptional control in human and mouse oocytes , 2003, Molecular reproduction and development.

[10]  P. Marina,et al.  Spherical bodies present within the germinal vesicle of Podarcis sicula previtellogenic oocyte derive from the temporaneous inactivation of ribosomal genes , 2003, Molecular reproduction and development.

[11]  M. Prisco,et al.  Apoptosis during spermatogenesis in the spotted ray Torpedo marmorata , 2003, Molecular reproduction and development.

[12]  M. I. Vera,et al.  An increased expression of nucleolin is associated with a physiological nucleolar segregation. , 2003, Biochemical and biophysical research communications.

[13]  P. Marina,et al.  Fine structure of leydig and sertoli cells in the testis of immature and mature spotted ray Torpedo marmorata , 2002, Molecular reproduction and development.

[14]  M. Prisco,et al.  An ultrastructural study on the vitellogenesis in the spotted ray Torpedo marmorata. , 2002, General and comparative endocrinology.

[15]  M. Prisco,et al.  Ultrastructural studies on developing follicles of the spotted ray Torpedo marmorata , 2002, Molecular reproduction and development.

[16]  S. Bucci,et al.  TAFII70 protein in Cajal bodies of the amphibian germinal vesicle. , 2001, Genome.

[17]  M. Prisco,et al.  An ultrastructural study of germ cells during ovarian differentiation in Torpedo marmorata , 2001, The Anatomical record.

[18]  J. Laurinčík,et al.  Nucleolar Proteins and Ultrastructure in Preimplantation Porcine Embryos Developed In Vivo1 , 2000, Biology of reproduction.

[19]  S. Fakan,et al.  Nucleoli undergo structural and molecular modifications during hibernation , 2000, Chromosoma.

[20]  J. Gall,et al.  Cajal bodies: the first 100 years. , 2000, Annual review of cell and developmental biology.

[21]  M. Prisco,et al.  Intercellular bridges between granulosa cells and the oocyte in the elasmobranch Raya asterias , 1999, The Anatomical record.

[22]  R. Spieler,et al.  Ultrastructural analysis of folliculogenesis in the ovary of the yellow spotted stingray, Urolophus jamaicensis. , 1999, Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft.

[23]  M. Prisco,et al.  Structural and functional modifications of the nucleolus during previtellogenic oocyte growth in the lizard Podarcis sicula , 1998, Molecular reproduction and development.

[24]  J. Fléchon,et al.  The nature of the ‘nucleolus precursor body’ in early preimplantation embryos: a review of fine-structure cytochemical, immunocytochemical and autoradiographic data related to nucleolar function , 1998, Zygote.

[25]  A. Lamond,et al.  Structure and function in the nucleus. , 1998, Science.

[26]  P. Hyttel,et al.  Nucleus structure and transcriptional activity in relation to oocyte diameter in cattle , 1996 .

[27]  P. Andreuccetti,et al.  Role of pyriform cells during the growth of oocytes in the lizard Podarcis sicula , 1995 .

[28]  M. Thiry Nucleic acid compartmentalization within the cell nucleus by in situ transferase‐immunogold techniques , 1995, Microscopy research and technique.

[29]  V. De Smedt,et al.  Morphological and functional changes accompanying the acquisition of meiotic competence in ovarian goat oocyte. , 1994, The Journal of experimental zoology.

[30]  R. Tuma,et al.  Identification and characterization of a sphere organelle protein , 1993, The Journal of cell biology.

[31]  M. Derenzini,et al.  Ultrastructural cytochemistry of the mammalian cell nucleolus. , 1990, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[32]  P. Andreuccetti,et al.  Structural modifications of the nuclear components during lizard oogenesis in relation to the differentiation of the follicular epithelium. , 1990, Cell differentiation and development : the official journal of the International Society of Developmental Biologists.

[33]  J. Gall,et al.  The sphere organelle contains small nuclear ribonucleoproteins. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[34]  V. Parfenov,et al.  Human antral follicles: oocyte nucleus and the karyosphere formation (electron microscopic and autoradiographic data). , 1989, Gamete research.

[35]  J. Fulka,et al.  Nucleolar fine structure and RNA synthesis in bovine oocytes from antral follicles , 1986 .

[36]  J. Fulka,et al.  Factors affecting meiotic competence in pig oocytes , 1986 .

[37]  P. Andreuccetti,et al.  Intercellular bridges between follicle cells and oocyte during the differentiation of follicular epithelium in Lacerta sicula Raf. , 1978, Journal of cell science.

[38]  W. Franke,et al.  Regulation of transcription of genes of ribosomal rna during amphibian oogenesis. A biochemical and morphological study , 1976, The Journal of cell biology.

[39]  J. S. Bisht,et al.  Seasonal histological changes in the ovaries of a mountain stream teleost, Schizothorax richardsonii (Gray and Hard). , 1975, Acta anatomica.

[40]  C. Taddei Significance of pyriform cells in ovarian follicle of Lacerta sicula. , 1972, Experimental cell research.

[41]  L. Chouinard A light- and electron-microscope study of the nucleolus during growth of the oocyte in the prepubertal mouse. , 1971, Journal of cell science.

[42]  D. D. Brown,et al.  VARIATIONS IN THE SYNTHESIS OF STABLE RNA'S DURING OOGENESIS AND DEVELOPMENT OF XENOPUS LAEVIS. , 1964, Journal of molecular biology.