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Huang, Yan

https://orcid.org/0000-0002-7623-6613

Mayo Clinic

Mayo Clinic

Citations 2

[Corrigendum] Silencing of type Iγ phosphatidylinositol phosphate kinase suppresses ovarian cancer cell proliferation, migration and invasion
Cao, Siyu , Chen, Chunhua , Xue, Junli , Huang, Yan , Yang, Xiaofeng , Ling, Kun

Oncology Reports | February 18, 2021 | Volume: 45 | Issue: 4 | Pages: No page available

10.3892/or.2021.7982 Get It

An association between type Iγ PI4P 5-kinase and Exo70 directs E-cadherin clustering and epithelial polarization
Xiong, Xunhao, Xu, Qingwen , Huang, Yan , Singh, Raman Deep , Anderson, Richard A. , Leof, Edward B. , Hu, Jinghua , Ling, Kun

Molecular Biology of the Cell | November 2, 2011 | Volume: 23 | Issue: 1 | Pages: 87-98

10.1091/mbc.e11-05-0449 Get It

E-Cadherin–mediated formation of adherens junctions (AJs) is essential for the morphogenesis of epithelial cells. However, the mechanisms underlying E-cadherin clustering and AJ maturation are not fully understood. Here we report that type Iγ phosphatidylinositol-4-phosphate 5-kinase (PIPKIγ) associates with the exocyst via a direct interaction with Exo70, the exocyst subunit that guides the polarized targeting of exocyst to the plasma membrane. By means of this interaction, PIPKIγ mediates the association between E-cadherin and Exo70 and determines the targeting of Exo70 to AJs. Further investigation revealed that Exo70 is necessary for clustering of E-cadherin on the plasma membrane and extension of nascent E-cadherin adhesions, which are critical for the maturation of cohesive AJs. In addition, we observed phosphatidylinositol-4,5-bisphosphate (PI4,5P 2 ) accumulation at E-cadherin clusters during the assembly of E-cadherin adhesions. PIPKIγ-generated PI4,5P 2 is required for recruiting Exo70 to newly formed E-cadherin junctions and facilitates the assembly and maturation of AJs. These results support a model in which PIPKIγ and PIPKIγ-generated PI4,5P 2 pools at nascent E-cadherin contacts cue Exo70 targeting and orient the tethering of exocyst-associated E-cadherin. This could be an important mechanism that regulates E-cadherin clustering and AJ maturation, which is essential for the establishment of solid, polarized epithelial structures.