Lecture 5 - Tissue Patterning Flashcards

(50 cards)

1
Q

define cell differentiation

A

the acquisition of specialised cell functions (cell fates) via differential genome expression

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2
Q

ectoderm

A

epidermis and nervous system

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3
Q

mesoderm

A

muscles, connective tissue, bones, blood, kidneys, etc

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4
Q

endoderm

A

gut, lungs, pancreas, liver, etc

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5
Q

what is a lineage tree and what does it show?

A

it is a diagram that shows you the cells that you get after a zygote is formed as a function of time

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6
Q

what is required for different cell fates?

A

differential genome expression

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7
Q

how is differential genome expression achieved?

A

through cis regulatory elements - this is what transcription factors bind to, controlling transcription

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8
Q

state two ways in which cell fate can be acquired

A
  1. asymmetric division
  2. symmetric division, then perception of a signal
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9
Q

asymmetric vs symmetric division

A

asymmetric - child cells are born with different fates
symmetric - child cells are born the same, but acquire different fates as a result of influences acting on them

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10
Q

asymmetric division —– partitions cell fate determinants

A

unevenly

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11
Q

describe asymmetric division

A
  • some specific cell fate markers are unevenly distributed before division
  • after division, one child cell will inherit more of this cell fate marker than the other
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12
Q

what does asymmetric division require?

A

correct spindle alignment and cytokinesis

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13
Q

are most proteins and cellular components distributed evenly or unevenly?

A

evenly

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14
Q

what can symmetric and asymmetric divisions create?

A

tissue patterns

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15
Q

describe how asymmetric and symmetric divisions can work together to create functional organisms

A
  • some cells divide symmetrically to create a field of similar cells
  • other cells continue divide asymmetrically to create several different cell types
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16
Q

in a cell division graph, what do different colours and black lines mean?

A

different colours = different types of cells
black lines = sister cells

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17
Q

after symmetric division, what are three ways in which cell fate may be acquired?

A
  1. lateral inhibition
  2. induction by diffusible signals
  3. other mechanisms
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18
Q

define stochastic

A

temporary

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19
Q

describe lateral inhibition

A
  1. both cells might start the same
  2. some tiny or short-lived difference between the two cells tips the balance
  3. molecular mechanisms will amplify these differences
  4. the cells will acquire different fates
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20
Q

what results from lateral inhibition?

A

creates a pattern of isolated differentiated cells in a field of relatively undifferentiated cells

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21
Q

give an example of lateral inhibition

A

some fly epidermal cells will develop into sensory bristles

22
Q

describe Delta and Notch as an example of lateral inhibition

A

Delta activates Notch signals; Notch signals inhibit Delta expression:
1. at the start, both the top and bottom cells have Delta, activating Notch in each other.
2. Notch inhibits cell specialisation and Delta expression.
3. Eventually, one cell will win out - it will have active Delta and will specialise, whilst activating Notch on the neighbouring cells and causing them to remain unspecialised.

23
Q

describe how induction by diffusible signals happens

A
  • one or more cells in the organiser tissue secrete a morphogen
  • morphogens are diffusible signals that can affect cell differentiation; they diffuse and act on nearby cells
  • cells respond to the morphogenetic by taking on a new cell fate
  • this creates a pattern of bands or rings of different cell fates around the source
24
Q

why is it that morphogens have such diverse impacts?

A

cells can respond differently to the same morphogenetic given at different concentrations

25
what does the diffusion range of the morphogen depend on?
- how much morphogenetic is made and for how long - diffusion rate of the signal - stability of the signal
26
are morphogens always active?
no; morphogens cannot be indefinitely active
27
how were morphogens discovered?
through transplant experiments
28
describe the transplant experiments that were conducted on amphibian embryos to identify morphogens
- two copies of organiser tissue created two dorsal sides and a shared ventral side - the organiser tissue induced structures that the host would not normally make (eg an amphibian with two backs) - however, if the opposite (ventral) piece was transplanted, nothing was observed
29
why is it that we did not observe anything unusual when repeating the transplant experiment with a different tissue?
the ventral cells are not organiser cells, so they don't make a difference on the development of the tissue
30
totipotent cells
can become any cell type (usually only cells very early after fertilisation)
31
pluripotent cells
can become any adult cell type
32
give an example of pluripotent cells and explain why they are not totipotent
blastomeres; they lose the ability to form ALL extra-embryonic tissues.
33
multipoint cells
can become multiple cell types
34
give two examples of multipotent cells
mesoderm, ectoderm
35
what are two ways in which multiple signals can be combined during cell fate determination?
- cell memory/sequential signaling - combinatorial signaling
36
distinguish between cell memory/sequential signaling and combinatorial signaling
cell memory/sequential signaling: a cell’s past exposures to signals change how it responds to later signals. combinatorial signaling: a cell’s response depends on multiple signals received at the same time.
37
what is a possible effect of sequential induction and how does this work?
sequential induction can generated regulatory hierarchies: - the same morphogenetic produced by cell type C can have different effects on cell types A and B - this can divide the body into segments
38
what do regulatory hierarchies consist of?
gene regulation affecting other gene regulation affecting other gene regulation
39
give an example of how multiple signals can overlap to create complex patterns
different transcription factor gradients can produce really complex patterns and combinations
40
what is the impact of segmentation on the animal body?
it creates repeats with variation in the animal body
41
describe how transcription factors act in a regulatory hierarchy in drosophila
1. anterior-posterior 2. define head, thorax, abdomen 3. segments within the heat, thorax, and abdomen 4. polarity within each segment 5. body parts develop from segments due to Hox proteins
42
what is the function of Hox genes?
they determine which body parts will develop from a segment
43
how is Hox gene expression organised?
- Hox genes are expressed in different segments and specify different body parts - Hox genes are organised on chromosomes in order of expression
44
Hox genes are organised into a ---- ------ on chromosomes
Hox complex
45
define a gene complex
genes located in a nearby segment of DNA
46
how many copies of the Hox complex do humans have? how are these similar to each other?
4; the order of Hox genes on the chromosome remains the same
47
what do Hox genes encode?
transcription factors
48
how do Hox genes partly explain different segmentation in different organisms?
the downstream targets that Hox proteins activate differ between organisms
49
what is the impact of Hox gene mutations?
they alter which body parts develop in a segment
50
loss or gain of function Hox gene mutants cause
body parts to develop in a segment where they should not normally be