scholarly journals DYRK1A binds to an evolutionarily conserved WD40-repeat protein WDR68 and induces its nuclear translocation

2011 ◽  
Vol 1813 (10) ◽  
pp. 1728-1739 ◽  
Author(s):  
Yoshihiko Miyata ◽  
Eisuke Nishida
2008 ◽  
Vol 17 (4) ◽  
pp. 163-170 ◽  
Author(s):  
Myung Whan Suh ◽  
Dong Hoon Shin ◽  
Ho Sun Lee ◽  
Ji Yeong Park ◽  
Chong Sun Kim ◽  
...  

Unlike mammals, avian cochlear hair cells can regenerate after acoustic overstimulation. The WDR1 gene is one of the genes suspected to play an important role in this difference. In an earlier study, we found that the WDR1 gene is over-expressed in the chick cochlea after acoustic overstimulation. The aim of this study was to compare the expression of WDR1 before and after acoustic overstimulation in the chick vestibule. Seven-day-old chicks were divided into three groups: normal group, damage group, and regeneration group. The damage and regeneration group was exposed to 120 dB SPL white noise for 5–6 hours. The damage group was euthanized shortly after the impulse, but the regeneration group was allowed to recover for 2 days. The utricle, saccule, and the three ampullae of each semicircular canal were dissected and immunohistochemically stained with anti-WD40 repeat protein 1 antibody. For quantitative analysis, immunoreactive densities were measured and quantitative real-time RT PCR was performed. WD40 repeat protein 1 expression was elevated in all the semicircular canals and utricle, two days after an acoustic overstimulation (P = 0.001). WDR1 mRNA expression was 1.34 times higher in the regeneration group compared to the normal group, but it was not statistically significant. Exceptionally, WD40 repeat protein 1 expression did not increase in the saccule of the regeneration group. Elevated WDR1 expression in the avian vestibule may have a role in the hair cell regenerating ability as in the avian cochlea. A similar mechanism of hair cell regeneration may exist in the avian cochlea and vestibule.


2019 ◽  
Vol 9 ◽  
Author(s):  
Felix M. Brehar ◽  
Mihnea P. Dragomir ◽  
George E. D. Petrescu ◽  
Radu M. Gorgan

Cell Cycle ◽  
2016 ◽  
Vol 15 (3) ◽  
pp. 413-424 ◽  
Author(s):  
Nicholas R. Lim ◽  
Yvonne Y. C. Yeap ◽  
Ching-Seng Ang ◽  
Nicholas A. Williamson ◽  
Marie A. Bogoyevitch ◽  
...  

2010 ◽  
Vol 10 (1) ◽  
pp. 169 ◽  
Author(s):  
Hong-Ju Li ◽  
Nai-You Liu ◽  
Dong-Qiao Shi ◽  
Jie Liu ◽  
Wei-Cai Yang
Keyword(s):  

Author(s):  
Kira Vanessa Blankenbach ◽  
Gennaro Bruno ◽  
Enrico Wondra ◽  
Anna Katharina Spohner ◽  
Natalie Judith Aster ◽  
...  

2012 ◽  
Vol 125 (21) ◽  
pp. 5096-5109 ◽  
Author(s):  
M. A. Bogoyevitch ◽  
Y. Y. C. Yeap ◽  
Z. Qu ◽  
K. R. Ngoei ◽  
Y. Y. Yip ◽  
...  

2015 ◽  
Vol 35 (18) ◽  
pp. 3255-3255
Author(s):  
Chi K. Leung ◽  
Koichi Hasegawa ◽  
Ying Wang ◽  
Andrew Deonarine ◽  
Lanlan Tang ◽  
...  

2011 ◽  
Vol 92 (7) ◽  
pp. 1561-1570 ◽  
Author(s):  
Chang-Jun Guo ◽  
Wei-Jian Chen ◽  
Li-Qun Yuan ◽  
Li-Shi Yang ◽  
Shao-Ping Weng ◽  
...  

The ankyrin (ANK) repeat is one of the most common protein–protein interaction motifs, found predominantly in eukaryotes and bacteria, but the functions of the ANK repeat are rarely researched in animal viruses, with the exception of poxviruses. Infectious spleen and kidney necrosis virus (ISKNV) is a typical member of the genus Megalocytivirus in the family Iridoviridae and is a causative agent of epizootics in fish. The genome of ISKNV contains four putative viral ANK (vANK) repeat proteins and their functions remain largely unknown. In the present study, it was found that ORF124L, a vANK repeat protein in ISKNV, encodes a protein of 274 aa with three ANK repeats. Transcription of ORF124L was detected at 12 h post-infection (p.i.) and reached a peak at 40 h p.i. ORF124L was found to localize to both the nucleus and the cytoplasm in mandarin fish fry cells. ISKNV ORF124L interacted with the mandarin fish IκB kinase β protein (scIKKβ), and attenuated tumour necrosis factor alpha (TNF-α)- or phorbol myristate acetate (PMA)-induced activity of a nuclear factor κB (NF-κB)–luciferase reporter but did not interfere with the activity of an activator protein 1 (AP-1)–luciferase reporter. Phosphorylation of IκBα and nuclear translocation of NF-κB were also impaired by ISKNV ORF124L. In summary, ORF124L was identified as a vANK repeat protein and its role in inhibition of TNF-α-induced NF-κB signalling was investigated through interaction with the mandarin fish IKKβ. This work may help to improve our understanding of the function of fish iridovirus ANK repeat proteins.


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