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33 Cards in this Set

  • Front
  • Back

Aster

sperm with two centrioles - centrosome - microtubules extend from this

Fusion of genetic material

Aster forms


Sperm mitochondria and flagellum disintegrate


Dissolution of sperm nuclear envelope


Decondensation of male chromatin, swap packaging for egg proteins


Difference between mammal and sea urchin is timing

Sea urchin fusion

Sperm enters perpendicular to egg, Contributes nucleus and centriole, Female pronucleus is eccentric, Fusion initiates cortical granule exocytosis, Sperm enters, centrosome activated, microtubules move pronucleuses together, fuse to diploid, DNA replication, centrosome duplicates, organizes mitosis

Mammal fusion

Takes longer, M2, sperm enters sideways, several Ca2+ waves, one starts meiosis, DNA is uncompacted, DNA replication in both pronuclei while migrating, centrosome duplicates, almost two cells before diploid nucleus

What is determined during cleavage and gastrulation

Cell fate and embro axis

Cleavage

Rapid cell division


NOT accompanied by cell growth - more cells (blastomeres), less volume


Cleavage furrow determined by sperm entry


Egg protein and RNA control this

maternal mRNA test

Shows that maternal RNA is used for translation


Actinomycin D added to inhibit transcription but translation is till happening

Mitosis promoting factor

Drives cleavage


Subunits Cyclin B and cdc 2


Cyclin B upregulates cdc2 (protein kinase)


Cdc2 phosphorylates several factors - chromatin condensation, organization of mitotic spindle


Cyclin B regulated by remaining factors

Mid Blastula Transition

aka maternal to zygotic transition


embryonic genome starts to get utilized


maternal factors in cytoplasm are used up

Karyokinesis

Mitotic division of nucleus

Cytokinesis

Physical division of the cell

Contractile ring

actin filaments perpendicular to mitotic spindle aka tubulin microtubules


Create cleavage furrow

Cleavage pattern is determined by

1. Amount and distribution of yolk - where cleavage can occur and size of blastomeres


2. Factors in the egg cytoplasm - angle of mitotic spindle

Based on whether daughter cells are completely seperated

Holoblastic - complete separate cells, not much yolk


Meroblastic - incomplete separation - massive yolk

Based on position or amount of yolk

Isolecithal - uniform yolk distribution - holo


Mesolecital - moderate yolk - holo


Telolecithal - one end - mero


Centrolecitahal - centre - mero

Based on positioning of mitotic spindle

Radial


Spiral


Bilateral


Rotational


Discoidal


Superficial

Holoblasic - Isolecithal


--> Raidal, spiral, bilateral, rotational


Holobalstic - Mesolecithal


--> Displaced radial cleavage


Meroblastic cleavage - Telolecithal


--> Bilateral, Discodial


Meroblastic - Centriolecithal


--> Superficial

How do cells and tissues know how to develop

Through mutual interactions- induction and competence


Context of their environment - position in body and neighbor cells

Cell fate determined by

1. Asymmetric cell divisions


2. Cell to cell interactions


3. Cell-cell communications


4. Position of the cell in an embryo

Asymmetric cell divisions

From cells that have different cytoplasm determinants, significant during early cleavage, unequal distribution of maternal mRNA and maternal proteins in cytoplasm

Asymetric Patterning Molecules

Bound to egg cytoskeleton on only one side - two different cell shapes


Transported along cytoskeleton - different metabolic activity or motility


Associated with centrosome - influence mitotic spindle formation

Symmetric division

Different daughter cells based on cell-cell interactions and cell-cell comunications

Cell-cell interactions

Tight junctions - sheets of cells


Anchoring junctions - cytoskeletons of adjacent cells


Communicating junctions - small molecules can pass between gap junctions (animal cells) or plasmodesmata (plant cells)

Cell-cell communications

Induction - usually close range between two or more cells and tissues


Inducer - produces/ sends signal morphogen


Responder - target cell must be capable of responding via receptor for morphogen


Competence - response ability at that time

Instructive or Permissive induction

Instructive - signal is necessary to initiate new gene expression


Permissive - responder has already been specified, environment that allows expression of traits

Morphogen

Signaling molecule


Ligand, ion, hormone, protein, polypeptide growth factor


Produced by inducer


Directs fates by varying in concentration


Positional information leads to pattern formation

Juxtacrine


Paracrine


Endocrine


Autocrine

Direct contact


Neighboring cells


Hormones


Paracrine factor

Morphogen gradients

conduct proliferation and differentiation through concentration gradient


control 2D cell polarity

Signal transduction systems

1. Receptor has enzymatic activity - tyrosine kinase


2. Receptor coupled to heterotrimeric G protein -GPCRs


3. Intracellular receptors - cytoplasm or nuc


4. Channel linked receptors - ionotropic

Receptor with enzymatic activity

Ligands - protein hormones or paracrine factors


Ligand binds, receptor activation through dimerization and autophosphorylation


Activated receptor adds phosphate to tyrosine


Cascade

Kinase cascade

Series of protein kinases that phosphorylate eachother in succession


Amplifies as they go


e.g.) Mitogen-activated protein kinases

G Protein Cell Signaling

Ligand binds to receptor, binds to inactie G protein, alpha sub switches GDP for GTP, G protein activated


Alpha detaches, binds and activates effector, cellular response

Intracellular receptors

Hydrophobic ligand easily passes through membrane


Binds to receptor in cytoplasm or nucleus and changes conformation


Receptor is transcription factor and changes gene expression