Investigation of the methylation of Numb by the SET8 protein lysine methyltransferase

被引:7
|
作者
Weirich, Sara [1 ]
Kusevic, Denis [1 ]
Kudithipudi, Srikanth [1 ]
Jeltsch, Albert [1 ]
机构
[1] Univ Stuttgart, Inst Biochem, D-70569 Stuttgart, Germany
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
关键词
PRODUCT SPECIFICITY; GENOME INTEGRITY; AUTOMETHYLATION; CHROMATIN; STABILITY; MECHANISM; P53; G9A;
D O I
10.1038/srep13813
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It has been reported that the Numb protein is methylated at lysine 158 and 163 and that this methylation is introduced by the SET8 protein lysine methyltransferase [Dhami et al., (2013) Molecular Cell 50, 565-576]. We studied this methylation in vitro using peptide arrays and recombinant Numb protein as substrates. Numb peptides and protein were incubated with recombinant SET8 purified after expression in E. coli or human HEK293 cells. However, no methylation of Numb by SET8 was detectable. SET8 methylation of Histone H4 and p53 peptides and proteins, which were used as positive controls, was readily observed. While SET8 methylation of Numb in cells cannot be ruled out, based on our findings, more evidence is needed to support this claim. It appears likely that another not yet identified PKMT is responsible for the reported methylation of Numb in cells.
引用
收藏
页数:7
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