Zhao Hongling, Wang Hongbo, Bauzon Frederick, Lu Zhonglei, Fu Hao, Cui Jinhua, Zhu Liang
From the Department of Developmental and Molecular Biology, and Ophthalmology & Visual Sciences, and Medicine, The Albert Einstein Comprehensive Cancer Center and Liver Research Center, Albert Einstein College of Medicine, Bronx, New York 10461.
From the Department of Developmental and Molecular Biology, and Ophthalmology & Visual Sciences, and Medicine, The Albert Einstein Comprehensive Cancer Center and Liver Research Center, Albert Einstein College of Medicine, Bronx, New York 10461
J Biol Chem. 2016 May 6;291(19):10201-9. doi: 10.1074/jbc.M116.718049. Epub 2016 Mar 10.
Tumor suppressor pRb represses Skp2, a substrate-recruiting subunit of the SCF(Skp2) ubiquitin ligase. Rb1(+/-) mice incur "two-hit" pituitary tumorigenesis; Skp2(-/-);Rb1(+/-) mice do not. Rb1(-/-) embryos die on embryonic day (E) 14.5-15.5. Here, we report that Skp2(-/-);Rb1(-/-) embryos died on E11.5, establishing an organismal level synthetic lethal relationship between Rb1 and Skp2 On E10.5, Rb1(-/-) placentas showed similarly active proliferation and similarly inactive apoptosis as WT placenta, whereas Rb1(-/-) embryos showed ectopic proliferation without increased apoptosis in the brain. Combining Skp2(-/-) did not reduce proliferation or increase apoptosis in the placentas but induced extensive apoptosis in the brain. We conditionally deleted Rb1 in neuronal lineage with Nes-Cre and reproduced the brain apoptosis in E13.5 Nes-Cre;Rb1(lox/lox);Skp2(-/-) embryos, demonstrating their synthetic lethal relationship at a cell autonomous level. Nes-Cre-mediated Rb1 deletion increased expression of proliferative E2F target genes in the brains of Skp2(+/+) embryos; the increases rose higher with activation of expression of apoptotic E2F target genes in Skp2(-/-) embryos. The brain apoptosis was independent of p53 but coincident with proliferation. The highly activated expression of proliferative and apoptotic E2F target genes subsided with gradually reduced roles of Skp2 in preventing p27 protein accumulation in the brain in late gestation, allowing the embryos to reach full term with normally sized brains. These findings establish that Rb1 and Skp2 deletions are synthetic lethal and suggest how this lethal relationship might be circumvented, which could help design better therapies for pRb-deficient cancer.
肿瘤抑制因子pRb可抑制Skp2,Skp2是SCF(Skp2)泛素连接酶的底物招募亚基。Rb1(+/-)小鼠会发生“两次打击”的垂体肿瘤发生;而Skp2(-/-);Rb1(+/-)小鼠则不会。Rb1(-/-)胚胎在胚胎期(E)14.5 - 15.5天死亡。在此,我们报告Skp2(-/-);Rb1(-/-)胚胎在E11.5天死亡,确立了Rb1和Skp2在机体水平上的合成致死关系。在E10.5天,Rb1(-/-)胎盘显示出与野生型胎盘相似的活跃增殖和相似的不活跃凋亡,而Rb1(-/-)胚胎在大脑中显示出异位增殖且凋亡未增加。联合缺失Skp2并未降低胎盘的增殖或增加凋亡,但在大脑中诱导了广泛的凋亡。我们用Nes-Cre在神经谱系中条件性删除Rb1,并在E13.5天的Nes-Cre;Rb1(lox/lox);Skp2(-/-)胚胎中重现了大脑凋亡,证明了它们在细胞自主水平上的合成致死关系。Nes-Cre介导的Rb1缺失增加了Skp2(+/ +)胚胎大脑中增殖性E2F靶基因的表达;在Skp2(-/-)胚胎中,随着凋亡性E2F靶基因表达的激活,这种增加更为显著。大脑凋亡独立于p53但与增殖同时发生。在妊娠后期,随着Skp2在阻止大脑中p27蛋白积累方面的作用逐渐减弱,增殖性和凋亡性E2F靶基因的高度激活表达减弱,使胚胎能够足月出生,大脑大小正常。这些发现确立了Rb1和Skp2缺失是合成致死的,并提示了这种致死关系可能如何被规避,这有助于为pRb缺陷型癌症设计更好的治疗方法。