2018
Dishevelled enables casein kinase 1-mediated phosphorylation of Frizzled 6 required for cell membrane localization
STRAKOVÁ, Kateřina, M. KOWALSKI-JAHN, Tomáš GYBEĽ, Jana VALNOHOVÁ, V.M. DHOPLE et. al.Základní údaje
Originální název
Dishevelled enables casein kinase 1-mediated phosphorylation of Frizzled 6 required for cell membrane localization
Autoři
STRAKOVÁ, Kateřina (203 Česká republika, domácí), M. KOWALSKI-JAHN (752 Švédsko), Tomáš GYBEĽ (703 Slovensko, domácí), Jana VALNOHOVÁ (203 Česká republika), V.M. DHOPLE (276 Německo), Jakub HARNOŠ (203 Česká republika, domácí), Ondřej BERNATÍK (203 Česká republika, domácí), Sri Ranjani GANJI (356 Indie, domácí), Zbyněk ZDRÁHAL (203 Česká republika, domácí), J. MULDER (752 Švédsko), C. LINDSKOG (752 Švédsko), Vítězslav BRYJA (203 Česká republika, garant, domácí) a G. SCHULTE (276 Německo)
Vydání
Journal of Biological Chemistry, Bethesda, USA, Amer. Soc. Biochem. Mol. Biol. 2018, 0021-9258
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10601 Cell biology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 4.106
Kód RIV
RIV/00216224:14310/18:00101768
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000458467300006
Klíčová slova anglicky
DEP DOMAIN; FUNCTIONAL-ANALYSIS; PLANAR POLARITY; BETA-ARRESTINS; DIX DOMAIN; I-EPSILON; RECEPTOR; RECRUITMENT; COMPLEX; GROWTH
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 18. 3. 2019 12:48, Mgr. Pavla Foltynová, Ph.D.
Anotace
V originále
Frizzleds (FZDs) are receptors for secreted lipoglycoproteins of the Wingless/Int-1(WNT) family, initiating an important signal transduction network in multicellular organisms. FZDs are G protein-coupled receptors (GPCRs), which are well known to be regulated by phosphorylation, leading to specific downstream signaling or receptor desensitization. The role and underlying mechanisms of FZD phosphorylation remain largely unexplored. Here, we investigated the phosphorylation of human FZD(6). Using MS analysis and a phospho-state- and -site-specific antibody, we found that Ser-648, located in the FZD(6) C terminus, is efficiently phosphorylated by casein kinase 1 is an element of (CK1 is an element of) and that this phosphorylation requires the scaffolding protein Dishevelled (DVL). In an overexpression system, DVL1, -2, and -3 promoted CK1-mediated FZD(6) phosphorylation on Ser-648. This DVL activity required an intact DEP domain and FZD-mediated recruitment of this domain to the cell membrane. Substitution of the CK1 is an element of-targeted phosphomo-tif reduced FZD(6) surface expression, suggesting that Ser-648 phosphorylation controls membrane trafficking of FZD(6). Phos-pho-Ser-648 FZD(6) immunoreactivity in human fallopian tube epithelium was predominantly apical, associated with cilia in a subset of epithelial cells, compared with the total FZD(6) protein expression, suggesting that FZD(6) phosphorylation contributes to asymmetric localization of receptor function within the cell and to epithelial polarity. Given the key role of FZD(6) in planar cell polarity, our results raise the possibility that asymmetric phosphorylation of FZD(6) rather than asymmetric protein distribution accounts for polarized receptor signaling.
Návaznosti
EE2.3.20.0180, projekt VaV |
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GA13-32990S, projekt VaV |
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GA17-16680S, projekt VaV |
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608180, interní kód MU |
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