1. Cleavage follows fertilization. Functions of cleavage: Multicellular for differentiation The zygote is partitioned into blastomeres. Each blastomere contains different regions of the undivided cytoplasm and thus different cytoplasmic determinants. Restores Somatic Nuclear to Cytoplasmic Ratio 1:500 -> ->-> 1:6 sea urchin fertilized egg at end of cleavage - somatic cell Controls on # of cleavage divisions? 2n = 6 divisions 4n = ? n = ?

2. Holoblastic unequal where there is more yolk at the vegetal pole. Cleavage occurs more rapidly in the animal pole than in the vegetal pole. first two cleavages are vertical. The third division is horizontal. The result is an eight-celled embryo with two tiers of four cells Yolk is most concentrated at the vegetal pole and least concentrated at the animal pole. In animals with less yolk there is complete division of the egg: holoblastic cleavage. Holoblastic equal

5. A blastocoel forms within the morula  blastula

6. In birds the yolk is so plentiful that it restricts cleavage to the animal pole: meroblastic cleavage.

7. What Controls Cleavage? Information in Cytoplasm – Source? Spiral Cleavage in Snails Rt = Dextral (dominant) Left= recessive Female dd X male DD F1 genotype vs. phenotype F1 cross dD X dD Prediction? Genotype Phenotype

10.  Gastrulation rearranges the embryo into a triploblastic gastrula. –The embryonic germ layers are the ectoderm, mesoderm, and endoderm. Gastrulation rearranges the blastula to form a three-layered embryo with a primitive gut Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings

11. Fate map

14. Ability of the micromeres to induce presumptive ectodermal cells to acquire other fates

15. 8.10 Ability of the micromeres to induce a secondary axis in sea urchin embryos

16. Normal sea urchin development

18. Fate map – vital stain Invagination

19. Involution Epiboly

20. Avian Development. Cleavage is meroblastic, or incomplete. Cell division is restricted to a small cap of cytoplasm at the animal pole. Produces a blastodisc, which becomes arranged into the epiblast and hypoblast that bound the blastocoel, the avian version of a blastula.

21. During gastrulation some cells of the epiblast migrate (arrows) towards the interior of the embryo through the primitive streak. The primitive knot is where the future notochoral mesoderm forms. Ingression (immigration)

24. Once again, the embryonic membranes – homologous with those of shelled eggs. Chorion: completely surrounds the embryo and other embryonic membranes. Amnion: encloses the embryo in a fluid-filled amniotic cavity. Yolk sac: found below the developing embryo. Develops from the hypoblast. Site of early formation of blood cells which later migrate to the embryo. Allantois: develops as an outpocketing of the embryo’s rudimentary gut. Incorporated into the umbilical cord, where it forms blood vessels.

25. Activation of embryonic genome Mexican axolotl o-mutant strain The “o” gene is a recessive gene “O” gene is the normal, dominant gene In embryos obtained from female axolotls homozygous for gene “o”, development is always arrested during gastrulation. WHY? “O” protein is necessary to activate the embryonic genome. PROOF?

26. The eggs can be rescued by injecting eggs of o/o females with cytoplasm from normal eggs. Where is the "corrective component" (O protein) produced? Rescue Experiments Cytoplasm from Egg vs. Primary Oocytes Cytoplasm vs. Primary Oocyte fluid from germinal vesicle

27. What is the “O” protein doing?

28. activation of the embryonic genome. How can we prove it?

29. When is mammalian embryonic genome activated? Two-cell stage determined by radioactive labeling experiments Imprinting of mammalian gamete’s nucleus Experiments combining: Female pronucleus combined with Female pronucleus Male pronucleus combined with Male pronucleus