학술논문

ROCK‐dependent phosphorylation of NUP62 regulates p63 nuclear transport and squamous cell carcinoma proliferation
Document Type
article
Source
EMBO Reports. 19(1)
Subject
Biochemistry and Cell Biology
Biological Sciences
1.1 Normal biological development and functioning
Underpinning research
Generic health relevance
Active Transport
Cell Nucleus
Amino Acid Sequence
Atlases as Topic
Carcinoma
Squamous Cell
Cell Differentiation
Cell Line
Tumor
Cell Nucleus
Cell Proliferation
Computational Biology
Cytosol
Female
Gene Expression Regulation
Neoplastic
HEK293 Cells
Head and Neck Neoplasms
Humans
Membrane Glycoproteins
Membrane Proteins
Nuclear Pore Complex Proteins
Phosphorylation
Rho Guanine Nucleotide Exchange Factors
Signal Transduction
Skin Neoplasms
Uterine Cervical Neoplasms
rho-Associated Kinases
Developmental Biology
Biochemistry and cell biology
Language
Abstract
p63, more specifically its ΔNp63α isoform, plays essential roles in squamous cell carcinomas (SCCs), yet the mechanisms controlling its nuclear transport remain unknown. Nucleoporins (NUPs) are a family of proteins building nuclear pore complexes (NPC) and mediating nuclear transport across the nuclear envelope. Recent evidence suggests a cell type-specific function for certain NUPs; however, the significance of NUPs in SCC biology remains unknown. In this study, we show that nucleoporin 62 (NUP62) is highly expressed in stratified squamous epithelia and is further elevated in SCCs. Depletion of NUP62 inhibits proliferation and augments differentiation of SCC cells. The impaired ability to maintain the undifferentiated status is associated with defects in ΔNp63α nuclear transport. We further find that differentiation-inducible Rho kinase reduces the interaction between NUP62 and ΔNp63α by phosphorylation of phenylalanine-glycine regions of NUP62, attenuating ΔNp63α nuclear import. Our results characterize NUP62 as a gatekeeper for ΔNp63α and uncover its role in the control of cell fate through regulation of ΔNp63α nuclear transport in SCC.