Deletions of retinoblastoma 1 (Rb1) and its repressing target S phase kinase-associated protein 2 (Skp2) are synthetic lethal in mouse embryogenesis

Hongling Zhao, Hongbo Wang, Frederick Bauzon, Zhonglei Lu, Hao Fu, Jinhua Cui, Liang Zhu

Research output: Contribution to journalArticle

3 Scopus citations

Abstract

Tumor suppressor pRb represses Skp2, a substrate-recruiting subunit of the SCFSkp2 ubiquitin ligase. Rb1+/- mice incur "twohit" 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;Rb1lox/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.

Original languageEnglish (US)
Pages (from-to)10201-10209
Number of pages9
JournalJournal of Biological Chemistry
Volume291
Issue number19
DOIs
Publication statusPublished - May 6 2016

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ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology

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