TY - JOUR
T1 - Wnt lipidation
T2 - Roles in trafficking, modulation, and function
AU - Hosseini, Vahid
AU - Dani, Christian
AU - Geranmayeh, Mohammad Hossein
AU - Mohammadzadeh, Fatemeh
AU - Nazari Soltan Ahmad, Saeed
AU - Darabi, Masoud
N1 - Funding Information:
This work was supported by grants from the Stem Cell Research Center at Tabriz University of Medical Sciences and the National Council for Development of Stem Cell Sciences and Technologies. We would like to thank Dr. Abby Cuttriss at the Office of International Scientific Visibility at the Université Côte d’Azur for her critical review and constructive comments on this manuscript.
Publisher Copyright:
© 2018 Wiley Periodicals, Inc.
PY - 2019/6
Y1 - 2019/6
N2 - The Wnt signaling pathway consists of various downstream target proteins that have substantial roles in mammalian cell proliferation, differentiation, and development. Its aberrant activity can lead to uncontrolled proliferation and tumorigenesis. The posttranslational connection of fatty acyl chains to Wnt proteins provides the unique capacity for regulation of Wnt activity. In spite of the past belief that Wnt molecules are subject to dual acylation, it has been shown that these proteins have only one acylation site and undergo monounsaturated fatty acylation. The Wnt monounsaturated fatty acyl chain is more than just a hydrophobic coating and appears to be critical for Wnt signaling, transport, and receptor activation. Here, we provide an overview of recent findings in Wnt monounsaturated fatty acylation and the mechanism by which this lipid moiety regulates Wnt activity from the site of production to its receptor interactions.
AB - The Wnt signaling pathway consists of various downstream target proteins that have substantial roles in mammalian cell proliferation, differentiation, and development. Its aberrant activity can lead to uncontrolled proliferation and tumorigenesis. The posttranslational connection of fatty acyl chains to Wnt proteins provides the unique capacity for regulation of Wnt activity. In spite of the past belief that Wnt molecules are subject to dual acylation, it has been shown that these proteins have only one acylation site and undergo monounsaturated fatty acylation. The Wnt monounsaturated fatty acyl chain is more than just a hydrophobic coating and appears to be critical for Wnt signaling, transport, and receptor activation. Here, we provide an overview of recent findings in Wnt monounsaturated fatty acylation and the mechanism by which this lipid moiety regulates Wnt activity from the site of production to its receptor interactions.
UR - http://www.scopus.com/inward/record.url?scp=85055246326&partnerID=8YFLogxK
U2 - 10.1002/jcp.27570
DO - 10.1002/jcp.27570
M3 - Scientific review articles
C2 - 30341908
AN - SCOPUS:85055246326
SN - 0021-9541
VL - 234
SP - 8040
EP - 8054
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 6
ER -