Microtubules Flashcards

1
Q

unstable microtubule structure

A

singlet made of 13 protofilaments arranged in a cylinder

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2
Q

examples of unstable/dynamic MT

A

spindle or centrosome

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3
Q

exception to unstable singlet

A

axon MTs are stabilized by acetylation

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4
Q

stable microtubules

A

doublets (13+10) and triplets (13+10+10)

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5
Q

examples of MT doublets

A

cilia and flagella

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6
Q

examples of MT triplets

A

centrioles and basal bodies

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7
Q

gamma-tubulin ring complex

A

facilitates rapid nucleation of MTs; on plus end

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8
Q

MTOC

A

microtubule organizing center on minus ends of microtubules

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9
Q

interphase cell MTOC

A

centrosome

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10
Q

dividing cell MTOC

A

spindle pole

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11
Q

MTOC for ciliated cell

A

basal body

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12
Q

MTOC’s provide _

A

directionality for movement

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13
Q

GTP cap

A

provides stabilization at end of MTs

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14
Q

GDP on microtubules

A

causes rapid disassembly and shrinkage

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15
Q

acetylation

A

stabilizes microtubules

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16
Q

drugs that destabilize MTs

A

colchicine, vinblastine, nocodozole

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17
Q

drugs that stabilize MTs

A

taxol

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18
Q

treadmilling

A

GTP adds to one end while GDP breaks off at another end –> results in what looks like forward motion of same sized strand

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19
Q

example of MT treadmilling

A

when chromosomes move from metaphase plate towards spindle poles

20
Q

example of treadmilling in actin filaments

A

cilia in ears carrying sensations in

21
Q

basal body

A

9 triplet MTs

22
Q

primary cilia

A

sensory role in almost all non-dividing cells; intraflagellar transport

23
Q

primary cilia structure

A

axoneme (9 doublet MT) + 1 basal body

24
Q

motile cilia structure

A

axoneme (9+2 doublet MTs) and no basal body

25
motile cilia
found on multi-ciliated epithelial cells in respiratory and reproductive tracts and brain
26
motile cilia are required for _
EC fluid flow
27
examples of ciliopathies
Bardet-Biedl Syndrome and polycystic kidney disease
28
Bardet-Biedl Syndrome
mutation in genes encoding cilia intraflagellar transport
29
symptoms of Bardet-Biedl Syndrome
retinal degeneration, loss of smell, kidney dysfunction, polydactyly, obesity, diabetes
30
polycystic kidney disease
mutation in PKD1 and PKD2 that are found in primary cilia of kidneys
31
polycystic kidney disease symptoms
renal cysts, hypertension, pain, and/or UTIs
32
PKD hypothesis
primary cilia monitor fluid flow and regulate cell proliferation through calcium signaling through renal tubules --> loss of function blocks signaling pathway which leads to cell proliferation and cyst formation
33
dynein
inner and outer arm on motile cilia to facilitate movement
34
respiratory problems
immotile respiratory cilia
35
sterility
immotile flagella in sperm and cilia in oviduct
36
dynein provides _
retrograde movement (back to cell body); minus end motors
37
cause of sinus inversus
bilateral symmetry is broken by fluid flow across nodal cells in base of embryo (because of dynein mess up
38
kinesins
anterograde movement, plus end motors
39
kinesins play a role in
spindle assembly, chromosome segregation, vesicle and organelle transport
40
dyneins play a role in
cilia movement, vesicle transport
41
myosin and kinesin _
evolved from same protein
42
dynein evolved from _
AAA ATPase
43
mechanochemical cycle of kinesin
ADP/ATP exchange in leading head causes lagging head to swivel forward; highly processive
44
dynein microtubule motor
tail bound to cargo or MT --> goes to first ATP domain --> goes through domains 1-4 --> at stalk, goes up to bind MT --> then goes through 5 and 6 domain
45
axonemical/ciliary dynein
dimer or trimer, defective genes in kartagener syndrome
46
cytoplasmic dynein
dimer; vesicle movement, spindle and chromosome segregation
47
communication between actin and microtubules
cell migration, spindle orientation, vesicle trafficking, immunological synapse