Nature genetics · 1999
Genomic instability in Gadd45a-deficient mice.
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Hollander M C, Sheikh M S, Bulavin D V, Lundgren K, Augeri-Henmueller L, Shehee R, Molinaro T A, Kim K E, Tolosa E, Ashwell J D, Rosenberg M P, Zhan Q, Fernández-Salguero P M, Morgan W F, Deng C X, Fornace A J
Аннотация
Gadd45a-null mice generated by gene targeting exhibited several of the phenotypes characteristic of p53-deficient mice, including genomic instability, increased radiation carcinogenesis and a low frequency of exencephaly. Genomic instability was exemplified by aneuploidy, chromosome aberrations, gene amplification and centrosome amplification, and was accompanied by abnormalities in mitosis, cytokinesis and growth control. Unequal segregation of chromosomes due to multiple spindle poles during mitosis occurred in several Gadd45a -/- cell lineages and may contribute to the aneuploidy. Our results indicate that Gadd45a is one component of the p53 pathway that contributes to the maintenance of genomic stability.
Предметные рубрики MeSH
AnimalsApoptosisCell CycleCell DivisionCell Transformation, NeoplasticCellular SenescenceCentrosomeEmbryo, MammalianFemaleFibroblastsG1 PhaseGamma RaysGene DeletionGenes, rasIntracellular Signaling Peptides and ProteinsMaleMiceMice, Inbred C57BLMice, KnockoutNeoplasmsPhenotypeProteinsThymus HyperplasiaGADD45 Proteins