Attendance sheet for the lecture.
Organismal complexity in animal development.
Differentiation and body plans of organisms.
Experimental model systems of development.
Definition: The capacity of a cell to generate different types of specialized cells.
Totipotent: Cells that can develop into all types of cells in an organism.
Pluripotent: Cells that can become many types but not all.
Terminally differentiated: Cells that are specialized and cannot become other types (e.g., muscle cells, neurons, hepatocytes).
Differentiation: The process through which a cell becomes specialized.
Zygote: 1 cell.
Adult: Approximately 100 trillion cells (10^14).
Achieved through 47 rounds of cell division.
Differentiation: Formation of distinct cell types (neurons, muscle cells, etc.).
Morphogenesis: Development of shape, pattern, and form.
Example: Adult sponges vs. complex animals.
Complex animals exhibit distinct anterior/posterior and dorsal/ventral orientations with bilateral symmetry, unlike simpler forms like sponges.
Zygote - Totipotent.
Blood Stem Cells, Muscle Cells, Neurons, Liver Cells, Lung Cells, Intestinal Cells.
Adult cells are terminally differentiated, meaning they perform specific functions.
Differentiation occurs in stages, progressively restricting potentials of cells.
Cells can form all parts of an organism.
When is totipotency lost? This occurs at specific developmental stages.
In mammals, single cells from 2, 4, and 8-cell stages can form an embryo.
Totipotency remains until the early blastocyst stage.
After the 8-cell stage, blastomeres may diminish in size restrictively, limiting their ability to develop into functional embryos.
Evolution and classification based on symmetry:
Monoblastic: No true tissues (e.g., sponges).
Diploblastic: Two layers of cells (e.g., jellyfish) - radial symmetry.
Triploblastic: Three layers, bilateral symmetry (e.g., humans).
Monoblasts: Sponges with only one layer of cells, no true tissues.
Diploblasts: Cnidarians with ectoderm and endoderm.
Triploblasts: Animals with ectoderm, mesoderm, and endoderm, allowing for a more complex anatomy.
Gastrulation: The process that forms three distinct layers from the embryonic cells.
All bilaterians have bilateral symmetry and organizational complexity from three cellular layers.
Diploblasts have basic dorsal/ventral sides without anterior/posterior.
Bilaterians introduce anterior/posterior distinctions alongside gut structures.
Gastrulation contributes to the formation of complex body plans.
All complex animals share a three-layered body derived from embryonic layers.
This body plan exists in adult tissues, highlighting evolutionary continuity.
Major groups:
Metazoa: All animals.
Eumetazoa: True tissues.
Triploblastic vs. Diploblastic Animals: Providing insights into animal evolution.
Notochord: A precursor to the vertebrate spine.
Ectoderm: Skin.
Endoderm: Digestive system.
Mesoderm: Muscle and skeleton.
This structure is typical in sea urchins, illustrating triploblastic organization.
The evolution of land-dwelling animals requires adaptations in embryogenesis for survival (e.g., amniotic sac, placenta).
Epiblast migration through the primitive streak to form endoderm cells.
Mesodermal cells develop between endoderm and epiblast.
Ectodermal layer remains uppermost.
Amnion: Fluid-filled sac.
Placenta: Formed from trophoblast and extra-embryonic mesoderm.
Yolk Sac and Allantois: Structures aiding in nourishment and connection.
Utilizing model organisms for understanding genetic principles of development (e.g., Drosophila, Caenorhabditis elegans).
Drosophila melanogaster: The fruit fly (5mm).
Caenorhabditis elegans: The nematode worm (1mm).
Both are favored due to their short life cycles and prolific offspring.
Edward B. Lewis discovered homeotic mutants in Drosophila.
Homeotic genes determine anatomical identity in organisms and play a key role in segment development.
Homeotic genes specify body segment identity and influence structure production.
These genes produce transcription factors that guide embryonic development.
Homeotic genes contain the Homeobox motif.
Regulates developmental gene expression and functions as a global positioning system for anatomical identity.
Four Hox clusters observed in mammals signify the diversity of anatomical structures developed through evolution.
Mutation in human homeotic gene HOXD13 leads to anatomical misconfigurations.
Highlights the role of homeotic genes in controlling differentiation.
Diploblasts (e.g., Cnidaria): Two tissue types, limited anatomical structures.
Triploblasts: Introduces a more complex body plan with anterior/posterior orientation.
Amplification of HOX gene families in Bilaterians leads to diversified morphologies and the Cambrian explosion.
Gastrulation and HOX complexity are integral to the evolution of modern animal forms.