Myosin VI regulates endocytosis of the cystic fibrosis transmembrane conductance regulator (Q24298963)

GOA release 2020-03-11

Myosin VI

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Agnieszka Swiatecka-Urban

GOA release 2020-03-11

author

1

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George M. Langford

object named as

George M Langford

7

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author name string

Cary Boyd

2

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Bonita Coutermarsh

3

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Katherine H Karlson

4

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Roxanna Barnaby

5

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Laura Aschenbrenner

6

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Tama Hasson

8

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Bruce A Stanton

Journal of Biological Chemistry

9

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language of work or name

English

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publication date

3 September 2004

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published in

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volume

279

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issue

36

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page(s)

38025-31

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cites work

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Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

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Misfolding diverts CFTR from recycling to degradation: quality control at early endosomes

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Membrane traffic in polarized epithelial cells

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Clathrin-dependent endocytosis

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Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel

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Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylation

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Hyperacidification of cellubrevin endocytic compartments and defective endosomal recycling in cystic fibrosis respiratory epithelial cells

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Unconventional Myosins, Actin Dynamics and Endocytosis: A Ménage à Trois?

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Unconventional myosins in cell movement, membrane traffic, and signal transduction

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Myosin VI isoform localized to clathrin-coated vesicles with a role in clathrin-mediated endocytosis

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Class VI myosin moves processively along actin filaments backward with large steps

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Myosin VI is an actin-based motor that moves backwards

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Expression of myosin VI within the early endocytic pathway in adult and developing proximal tubules

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Myosin VI, an actin motor for membrane traffic and cell migration

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Myo6 facilitates the translocation of endocytic vesicles from cell peripheries

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Myosin VI: two distinct roles in endocytosis

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Porcine myosin-VI: characterization of a new mammalian unconventional myosin

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The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

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Novel myosin VI isoform is abundantly expressed in retina

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Uncoated endocytic vesicles require the unconventional myosin, Myo6, for rapid transport through actin barriers

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A mutation in the cystic fibrosis transmembrane conductance regulator generates a novel internalization sequence and enhances endocytic rates

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NF-kappaB-mediated IAP expression induces resistance of intestinal epithelial cells to apoptosis after polyamine depletion

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The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane

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PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator

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Inhibition of endocytosis causes phosphorylation (S256)-independent plasma membrane accumulation of AQP2

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Myosin VI binds to and localises with Dab2, potentially linking receptor-mediated endocytosis and the actin cytoskeleton

21 January 2018

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DOC-2/DAB2 is the binding partner of myosin VI.

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Disabled-2 colocalizes with the LDLR in clathrin-coated pits and interacts with AP-2

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Role of myosin VI in the differentiation of cochlear hair cells

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MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss

21 January 2018

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Saturation of the endocytic pathway for the transferrin receptor does not affect the endocytosis of the epidermal growth factor receptor.

21 January 2018

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Distinct saturable pathways for the endocytosis of different tyrosine motifs

21 January 2018

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Hypertonic media inhibit receptor-mediated endocytosis by blocking clathrin-coated pit formation

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Clathrin and HA2 adaptors: effects of potassium depletion, hypertonic medium, and cytosol acidification

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The beta 1 and beta 2 subunits of the AP complexes are the clathrin coat assembly components

21 January 2018

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7 January 2021

Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study Consortium

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https://api.crossref.org/works/10.1074%2FJBC.M403141200

7 January 2021

Efficient endocytosis of the cystic fibrosis transmembrane conductance regulator requires a tyrosine-based signal

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https://api.crossref.org/works/10.1074%2FJBC.M403141200

7 January 2021

Rme-1 regulates the recycling of the cystic fibrosis transmembrane conductance regulator

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https://api.crossref.org/works/10.1074%2FJBC.M403141200

7 January 2021

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7 January 2021

Heterotrimeric G proteins, vesicle trafficking, and CFTR Cl- channels

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https://api.crossref.org/works/10.1074%2FJBC.M403141200

7 January 2021

Subcellular localization of CFTR to endosomes in a ductal epithelium

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https://api.crossref.org/works/10.1074%2FJBC.M403141200

7 January 2021

Exocytosis is not involved in activation of Cl- secretion via CFTR in Calu-3 airway epithelial cells

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https://api.crossref.org/works/10.1074%2FJBC.M403141200

7 January 2021

A3 adenosine receptors regulate Cl- channels of nonpigmented ciliary epithelial cells

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https://api.crossref.org/works/10.1074%2FJBC.M403141200

7 January 2021

Functional and molecular characterization of an anion exchanger in airway serous epithelial cells

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https://api.crossref.org/works/10.1074%2FJBC.M403141200

7 January 2021