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27 Cards in this Set

  • Front
  • Back

Cell lineage

follow the individual descendants of identified cells

Transplantation

progenitor cells from donor to genetically different host animal or into cell culture


unaltered phenotype = intrinsically determined


new fate = influenced by environmental factors


1.take cell at some stage of development


2.put it into genetically different environment or similar or different area


3.stays the same, internally determined


changes, environmentally determined


just adding and taking away factors in cell culture

Intrinsically determined

unaltered phenotype

Environmentally determined

new fate, phenotype

Transcriptional cascade/hierarchy

transcription factors direct the expression of other transcription factors by either activation or repression in the progenitor that progressively restrict fate choices in their descendents


daughter cell inherits that transcription factor could restrict its ability to respond to factors in the environment

Forward genetics

cause random mutogenesis and screen for what might have changed

Reverse genetics

knockouts, over expression


gene first

C. elegans

know the lineage of every cell


can now change progenitors at different stages and compare

plasticity

some progeny always die in programmed cell death

organizer region

dorsal lip of the blastopore


specialized regions of the animal alter the fate of some of the cells to generate organ specific specialization

Sydney Brenner

cell autonomous developmental program (European, depends on lineage)


highly reproducible cell-cell interactions


(American, where you are now matters)


used laser ablations of single cells at specific points in development

Proliferation of neighbors

not strict replacement


neighbor can adopt missing cell fate and original progeny for that cell are missing

Gene regulation

as cells become more differentiated they express a limited subset of their gene pool, rendering them responsive to fewer environmental influences


they can only change if they retain the ability to sense the loss (as of a neighbor cell) AND still have the ability to alter the expression of appropriate proteins

Mosaic Development

laser ablation of one progenitor usually results in loss of all the neurons that would have been generated by it

Q

divides into 2 daughter cells Q1.a and Q1.p

Q1.p

produces a touch cell and an interneuron

Unc-86

gene turned on and starts process to create a touch cell


KO results in no mechanosensory neuron, instead Q' (just another Q cell)


combines with mec-3 into a heterodimer to create a brand new transcription factor to activate the genes for a mechanosensory neuron



regulates neurotransmitter expression and axon outgrowth in the egg-laying neurons

mec-3

in mutants the cells that would be touch cells are born but they do not differentiate into mechanosensory neurons, they become interneurons


affects neural subtype


codes for transcription factor (LIM-homeodomain family)


directly regulated by Unc-86 transcription factor

mec-7/ mec-12/ mec-17

encode proteins that are used in the differentiation of the specialized touch cell cytoskeleton


KO produces defective touch cells and an interneuron

Bag of worm mutants

20 genes define a hierarchical transcription cascades affecting egg-laying neuron development


unable to lay eggs


eggs are still fertilized, hatch, feel on mom from inside until only epidermis is left

ASE neurons

gustatory neurons


mirror images of each other


one can taste sodium (ASELeft) and the other chloride (ASERight)


results from P2 signalling arise 8 generation later

P2 blastomere

sends signals to ABp blastomere byt not the ABa

ASEL

left, sodium


begins to preferentially express the transcription factor Die-1


targets MicroRNAs


promotes lys-6


targets and represses Cog-1 mRNA

ASER

right, chloride


begins to preferentially express the transcription factor Cog-1


targets MicroRNAs


promotes mir-273


targets and represses Die-1

Double negative feedback loop

a cell that can taste Cl can't taste Na

Dorsoventral genes

msh,ind,vnd


transcription factors that divide the embryo dorsoventrally

Temporally coordinated transcription factors

expressed at various times in neuroblasts as they divide to form ganglion mother cells


leads to expression of the next and inhibits the previous


KO skips that factor