نتایج جستجو برای: sumo1

تعداد نتایج: 347  

Journal: :Nucleic Acids Research 2006
Ju-Ming Wang Chiung-Yuan Ko Lei-Chin Chen Wen-Lin Wang Wen-Chang Chang

NF-IL6beta regulates gene expression and plays function roles in many tissues. The EGF-regulated cyclooxygenase-2 (cox-2) expression is mediated through p38(MAPK) signaling pathway and positively correlates with NF-IL6beta expression in A431 cells. NF-IL6beta coordinated with c-Jun on cox-2 transcriptional activation by reporter and small interfering RNA assays. NF-IL6beta could directly bind t...

Journal: :Journal of virology 2011
José González-Santamaría Michela Campagna María Angel García Laura Marcos-Villar Dolores González Pedro Gallego Fernando Lopitz-Otsoa Susana Guerra Manuel S Rodríguez Mariano Esteban Carmen Rivas

The vaccinia virus (VACV) E3 protein is essential for virulence and has antiapoptotic activity and the ability to impair the host innate immune response. Here we demonstrate that E3 interacts with SUMO1 through a small ubiquitin-like modifier (SUMO)-interacting motif (SIM). SIM integrity is required for maintaining the stability of the viral protein and for the covalent conjugation of E3 to SUM...

Journal: :The Journal of biological chemistry 2006
Christina-Maria Hecker Matthias Rabiller Kaisa Haglund Peter Bayer Ivan Dikic

SUMO proteins are ubiquitin-related modifiers implicated in the regulation of gene transcription, cell cycle, DNA repair, and protein localization. The molecular mechanisms by which the sumoylation of target proteins regulates diverse cellular functions remain poorly understood. Here we report isolation and characterization of SUMO1- and SUMO2-binding motifs. Using yeast two-hybrid system, bioi...

Journal: :Molecular cell 2012
Andreas Werner Annette Flotho Frauke Melchior

RanBP2/Nup358 is an essential protein with roles in nuclear transport and mitosis, and is one of the few known SUMO E3 ligases. However, why RanBP2 functions in vivo has been unclear: throughout the cell cycle it stably interacts with RanGAP1*SUMO1 and Ubc9, whose binding sites overlap with the E3 ligase region. Here we show that cellular RanBP2 is quantitatively associated with RanGAP1, indica...

2014
Takako Niikura Yoshiko Kita Yoichiro Abe

Mutations in superoxide dismutase 1 (SOD1) are a major cause of familial amyotrophic lateral sclerosis (ALS), whereby the mutant proteins misfold and aggregate to form intracellular inclusions. We report that both small ubiquitin-like modifier (SUMO) 1 and SUMO2/3 modify ALS-linked SOD1 mutant proteins at lysine 75 in a motoneuronal cell line, the cell type affected in ALS. In these cells, SUMO...

2014
Anita C. Bellail Jeffrey J. Olson Chunhai Hao

Ubiquitination governs oscillation of cyclin-dependent kinase (CDK) activity through a periodic degradation of cyclins for orderly cell cycle progression; however, the mechanism that maintains the constant CDK protein levels throughout the cell cycle remains unclear. Here we show that CDK6 is modified by small ubiquitin-like modifier-1 (SUMO1) in glioblastoma, and that CDK6 SUMOylation stabiliz...

Journal: :Nature communications 2016
Tobias Ritterhoff Hrishikesh Das Götz Hofhaus Rasmus R Schröder Annette Flotho Frauke Melchior

Continuous cycles of nucleocytoplasmic transport require disassembly of transport receptor/Ran-GTP complexes in the cytoplasm. A basic disassembly mechanism in all eukaryotes depends on soluble RanGAP and RanBP1. In vertebrates, a significant fraction of RanGAP1 stably interacts with the nucleoporin RanBP2 at a binding site that is flanked by FG-repeats and Ran-binding domains, and overlaps wit...

Journal: :Gland surgery 2023

Background: Estrogen plays a crucial role in the tumorigenesis of breast cancer (BC), and epigenetic modification by SUMOylation is essential for development. However, mechanism underlying estrogen’s actions on protein its effect BC development are still incompletely understood.

Journal: :The Journal of Cell Biology 2004
Sowmya Swaminathan Florian Kiendl Roman Körner Raffaella Lupetti Ludger Hengst Frauke Melchior

The RanGTPase activating protein RanGAP1 has essential functions in both nucleocytoplasmic transport and mitosis. In interphase, a significant fraction of vertebrate SUMO1-modified RanGAP1 forms a stable complex with the nucleoporin RanBP2/Nup358 at nuclear pore complexes. RanBP2 not only acts in the RanGTPase cycle but also is a SUMO1 E3 ligase. Here, we show that RanGAP1 is phosphorylated on ...

2017
Chengmin Wang Huimin Liu Jing Luo Lin Chen Meng Li Wen Su Na Zhao Shelan Liu Li Xie Yaxiong Jia Hua Ding Xiufeng Wan Hongxuan He

Several post-translational modifications in host cells are hijacked by pathogens to facilitate their propagation. A number of components of the influenza virus have been reported to be modified by small ubiquitin-like modifier (SUMO) proteins during infection. We hypothesized that the MAPK/ERK pathway could be modified by SUMO1 because the SUMOylation of MEK1 was quickly eliminated after influe...

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