Cytoskeleton II Flashcards

1
Q

What binds to and stabilizes F-actin?

A

phalloidin

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1
Q

The formation and contraction of the actomyosin ring drives the ____ and _____.

A

cleavage furrow; separation of daughter cells

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2
Q

phalloidin

A

from death cap, binds to and stabilizes F-actin

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2
Q

Activation of forming leads to _____ formation.

A

parallel actin bundle

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2
Q

Myosin II, characteristic of _____, forms hetero-oligomers involving two heavy chains and two copies of each of two light chains.

A

striated muscle

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3
Q

Lissencephaly

A

defect of brain development- no gyri- loss of n-cofilin

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4
Q

_____ are filamentous polymers (~7 nm diameter) of actin monomers.

A

Microfilaments

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4
Q

WASp

A

Wiskott-Aldrich syndrome protein

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5
Q

_____ is observed in microvilli inclusion disease.

A

Loss of microvilli

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5
Q

Rho activation causes the formation of ____ and ____.

A

stress fibers and focal adhesions

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7
Q

In the presence of divalent cations and ATP, ____ assembles to form two stranded, helical filaments called ____.

A

G-actin; F-actin

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8
Q

Activation of _____ leads to parallel actin bundle formation.

A

forming

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9
Q

Myosin II, characteristic of striated muscle, forms hetero-oligomers involving ____ and two copies of each of ____.

A

two heavy chains; two light chains

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10
Q

_____ are held together by the cross-linking proteins villin and fimbrin.

A

Actin bundles

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11
Q

_____ are essential for amoeboid motility and muscle contraction.

A

Microfilaments

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12
Q

_____ are critical for cell shape, movement, and polarity.

A

Microfilaments (MFs)

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13
Q

N-cofilin is an ____.

A

actin filament depolymerizing factor

14
Q

____ stimulates Arp2/3 complexes.

A

WASp

14
Q

The formation and contraction of the ____ drives the cleavage furrow and separation of daughter cells.

A

actomyosin ring

16
Q

Microfilaments are essential for ______ and _____.

A

amoeboid motility; muscle contraction

16
Q

____ causes the formation of stress fibers and focal adhesions.

A

Rho activation

18
Q

Actin bundles are held together by the cross-linking proteins ____ and _____.

A

villin; fimbrin

18
Q

___ activates the formation of veils.

A

Rac

18
Q

____ activates the protrusion of fillopodia.

A

Cdc42

20
Q

_____, characteristic of striated muscle, forms hetero-oligomers involving two heavy chains and two copies of each of two light chains.

A

Myosin II

22
Q

Adherens junctions (AJs) proteins include ____ and _____.

A

cadherins and catenins

23
Q

Rac activates the formation of ____.

A

veils

24
Q

Wiskott-Aldrich syndrome (WAS)

A

x-linked immunodeficiency disease- WASp mutations

26
Q

Actin filament nucleation typically occurs at the ____.

A

plasma membrane

27
Q

Microfilaments (MFs) are critical for cell ____, _____, and _____.

A

shape; movement; polarity

28
Q

_____ is an actin filament depolymerizing factor.

A

N-cofilin

30
Q

Microfilaments are filamentous polymers (~7 nm diameter) of ____.

A

actin monomers

31
Q

The____ nucleates MF polymerization from the minus-end, allowing rapid elongation at the plus-end.

A

Arp2/3 complex

32
Q

Loss of microvilli is observed in _____.

A

microvilli inclusion disease

35
Q

_____ typically occurs at the plasma membrane.

A

Actin filament nucleation

36
Q

WASp stimulates _____.

A

Arp2/3 complexes

37
Q

What is epithelial-to-mesenchimal (EMT) transition?

A

internalization of cadherins and loss of cell-cell adhesions cancers

38
Q

The Arp2/3 complex nucleates MF polymerization from ____, allowing rapid elongation at _____.

A

the minus-end; the plus-end

39
Q

Cdc42 activates the protrusion of _____.

A

fillopodia

40
Q

In the presence of _____ and ____, G-actin assembles to form two stranded, helical filaments called F-actin.

A

divalent cations; ATP