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Ciba Foundation Symposium 98 - Molecular Biology of Egg

Chapter 1 creation (pages 1–5): J. R. Tata
Chapter 2 Poly(A) RNA of the Egg Cytoplasm: Structural Resemblance to the Nuclear RNA of Somatic Cells (pages 6–24): Eric H. Davidson, Howard T. Jacobs, Terry L. Thomas, Barbara R. Hough?Evans and Roy J. Britten
Chapter three Induction of Chromosome Replication in the course of Maturation of Amphibian Oocytes (pages 25–43): Ronald A. Laskey, Richard M. Harland and Marcel Mechali
Chapter four Retroviruses and Mouse Embryos: A version approach during which to review Gene Expression in improvement and Differentiation (pages 44–62): Rudolf Jaenisch
Chapter five The law of Yolk Protein Gene Expression in Drosophila melanogaster (pages 63–79): Mary Bownes, Maureen Dempster and Mairearad Blair
Chapter 6 Higher?Order Structural Determinants for Expression of the Ovalbumin Gene family members (pages 80–95): William E. Stumph, Melvyn Baez, George M. Lawson, Ming?Jer Tsai and Bert W. O'Malley
Chapter 7 Hormonal law and Expression of Vitellogenin Multigene family members (pages 96–110): Jamshed R. Tata, Tharappel C. James, Cheryl S. Watson, John L. Williams and Alan P. Wolffe
Chapter eight nutrition service Proteins in the course of Embryonic improvement in Birds and Mammals (pages 111–136): P. R. Adiga and C. V. Ramana Murty
Chapter nine Steroid and Peptide keep watch over Mechanisms in Membrane of Xenopus zaevis Oocytes Resuming Meiotic department (pages 137–158): Etienne?Emile Baulieu and Sabine Schorderet?Slatkine
Chapter 10 Nature and motion of the Mediators Inducing Maturation of the Starfish Oocyte (pages 159–177): Haruo Kanatani
Chapter eleven Somatic regulate of Protein Synthesis in Mammalian Oocytes in the course of Maturation (pages 178–196): R. M. Moor and J. C. Osborn
Chapter 12 The Legacy from the Oocyte and its position in Controlling Early improvement of the Mouse Embryo (pages 197–227): Hester P.M. Pratt, Virginia N. Bolton and Katy A. Gudgeon
Chapter thirteen The Oocyte as an Endocytic mobilephone (pages 228–248): R. A. Wallace, Lee Opresko, H. S. Wiley and Kelly Selman
Chapter 14 The Oocyte as a Secretory phone (pages 249–267): A. Colman, D. Cutler, P. Krieg and G. Valle
Chapter 15 The Molecular foundation of Sperm?Egg interplay within the Sea Urchin (pages 268–296): Daniel P. Rossignol and William J. Lennarz
Chapter sixteen ultimate comments (pages 297–299):

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Extra info for Ciba Foundation Symposium 98 - Molecular Biology of Egg Maturation

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Nor can one say that the cell has to constrain initiation to specific sites to prevent reinitiation within one cell cycle, because it can be prevented without specific sequence constraints. In asking why sequence constraints exist, it is striking that the time at which the distance between initiation events elongates to be approximately the same as the distribution of domains in the chromosome, is approximately the time when transcription switches on in the early embryos of Drosophila melanogaster or amphibians.

Cell 24:283-284 Laskey RA, Harland RM, Earnshaw WE, Dingwall C 1981 Chromatin assembly and the coordination of DNA replication in the eukaryotic genome. In: Schweiger GH (ed) International cell biology 1980-1981. Springer-Verlag. Berlin, p 161-167 McKnight SL, Bustin M, Miller OL Jr 1978 Electron microscopic analysis of chromosome metabolism in the Drosophila rnelanoguster embryo. Cold Spring Harbor Symp Quant Biol 42:741-754 McTiernan CF, Stambrook PJ 1980 Replication of DNA templates injected into frog eggs.

I didn’t mean to suggest that no bona fide mRNAs have repeat sequences on them. There certainly are examples of this. However, the presence of repeats in apparently internal locations, and also the quantitative extent of the interspersion, is far greater than what one finds on polysomal messages in the sea urchin embryo. Tutu: Can you rule out the possibility that the poly(A) non-messenger RNA fulfils the role of the nuclear inhibitory substance of Newport & Kirschner (1982), by being diluted out over several cell divisions?

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