Dysregulation of protein modification by ISG15 results in brain cell injury

被引:132
作者
Ritchie, KJ
Malakhov, MP
Hetherington, CJ
Zhou, LM
Little, MT
Malakhova, OA
Sipe, JC
Orkin, SH
Zhang, DE
机构
[1] Scripps Res Inst, Dept Mol & Expt Med, MEM L51, La Jolla, CA 92037 USA
[2] Harvard Univ, Sch Med, Div Hematol Oncol, Childrens Hosp, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Howard Hughes Med Inst, Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
interferon; ubiquitin; knockout;
D O I
10.1101/gad.1010202
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
UBP43 (USP18) is a protease that removes the ubiquitin-like modifier ISG15 from conjugated proteins. Here we present the first report of dysregulation of protein ISG15 modification by the generation of UBP43 knockout mice. In the absence of UBP43, brain tissue showed an elevated level of ISG15 conjugates, and cellular necrosis was evident in the ependyma. Such disruption of the blood-brain barrier resulted in severe neurologic disorders. These results demonstrate that UBP43 plays a critical role in maintaining the homeostatic balance of ISG15-conjugated protein, and that regulation of cellular levels of ISG15 protein modification is essential for brain cell function.
引用
收藏
页码:2207 / 2212
页数:6
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