Models and Principles in Animal Development (2 lectures) Flashcards

(33 cards)

1
Q

7 eukaryotic model organisms

A

Mouse, chicken, xenopus, zebrafish, drosophila, c. elegans, yeast

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2
Q

5 stages of vertebrate development

A

cleavage
blastula
gastrulation
neurulation
pharangula

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3
Q

cleavage stage

A

early cell division, but no increase in cytoplasmic mass

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4
Q

holoblastic cleavage

A

complete cleavage

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5
Q

meroblastic cleavage

A

incomplete cleavage, e.g. cells dividing only on one side

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6
Q

empty space in a cleaving embryo

A

blastocoel

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7
Q

blastula stage

A

hollow stage

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8
Q

gastrulation

A

germ layer formation, envagination of the mesoderm

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9
Q

neurulation

A

formation of the neural plate, folding of the neural tube

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10
Q

pharangula stage

A

post-anal tail, dorsal neural tube, segmentation- point at which vertebrate embryos tend to look very similar

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11
Q

hourglass model of development

A

period of morphological constraint- basic body structure being laid out w hox genes

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12
Q

xenopus pros and cons

A

pros
-easy to keep the adults
-external fertilisation, can get synchronised development of a bunch of embryos
-large embryos, easy to manipulate
cons
-slow to reach sexual maturity, annoying for genetics
-transgenics are difficult

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13
Q

zebrafish pros and cons

A

pros
-easy to keep, they’re fairly chill
external fertilisation for synchronised development
transparent, so good for microscopy
-short generation times- good for genetics
cons
-duplicated genome makes things hard sometimes

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14
Q

chicken pros and cons

A

pros
-eggs laid so easy to get to and manipulate
-windowing for easy access to the embryo
-good for grafting experiments
cons
-internal fertilisation, hard to access early stages
-embryos are dense
-long generation times, expensive to keep

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15
Q

unusual aspects of mouse development

A

inside of the gastrula ends up on the outside of the embryo- ‘flipped’ stage
embryo needs to ‘turn’ itself at 8ish days old

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16
Q

mice pros and cons

A

pros
-adults easy to keep in large numbers
-we know a lot about their genetics, so easy to do those kinds of experiments
-mammals, so more medically relevant
cons
-internal fertilisation and growth
-microscopy is a bit hard

17
Q

summary- considerations when picking a model organism

A

can adults be kept in the lab easily?
embryonic size and accessibility
what techniques can be applied- e.g. injection, grafting, culture
genetics?
phylogenetic position
does it have the right character

18
Q

cell fate

A

what a cell will, or has, become

19
Q

cell lineage

A

where a cell came from

19
Q

methods of tracking cell fate and lineage

A

photoconversion- activating a cell, and then following it
3D imaging- method of exactly tracing a lineage

19
Q

commitment

A

when cells are on a developmental path

20
Q

specification

A

reversible commitment

21
Q

determination

A

irreversible commitment

22
Q

differentiation

A

when specific functional cell types are formed (as inferred by morphology or transcriptional profiles)

23
how would we test if cells are committed?
looking at if the cells behave the same in culture as they do in vivo- e.g. do they make limb cells in culture
24
how can we tell if cells are specified or determined?
tranplantation- do cells fo what they do in the donor? this would make them determined
25
what did Mangold do
transplantation experiments on newts, showing that you can determine the functionality of specific regions early on in the embryo
26
what is an organiser region
region or group of cells which can both induce different fates of, and pattern, adjacent cells
27
what is pattern formation
the step generally preceding morphological change- distinct spatial territories are specified by different molecular or transcriptional identities
28
important model for determining positional identity
french flag model
29
what is a GRN
gene regulatory network- often quite complex set of gene interactions which help set up regions of a developing organism
30
key principles of the Turing reaction-differentiation model
-no external intervention -patterns emerge at the global level from local interactions among smaller components -idea of repression and activation systems- inhibitor which diffuses faster than the activator -often get oscillatory patterns just from this inhibitor/activator pattern
31
turing vs french flag models
french flag model focuses on how positional information can be determined by local morphogen gradient- turing model says this info doesn't directly correlate w morphogen conc turing model is a bit less about direct determination of positional information based exclusively on morphogen concentrations