Lam Michael H, Liu Qinghua, Elledge Stephen J, Rosen Jeffrey M
Baylor College of Medicine, Department of Molecular and Cellular Biology, Interdepartmental Program in Cellular and Molecular Biology, Houston, Texas 77030, USA.
Cancer Cell. 2004 Jul;6(1):45-59. doi: 10.1016/j.ccr.2004.06.015.
The haploinsufficient tumor suppressor Chk1 is essential for embryonic cells, but the consequences of Chk1 loss in adult tissues are unknown. Using conditional Chk1 mice, we find that proliferating mammary cells lacking Chk1 undergo apoptosis leading to developmental defects. Conditional Chk1 heterozygosity increased the number of S phase cells and caused spontaneous DNA damage. Chk1+/- epithelia also exhibit a miscoordinated cell cycle in which S phase cells display an early mitotic phenotype. These cells maintain high levels of Cdc25A, which can promote inappropriate cell cycle transitions. Thus, Chk1 heterozygosity results in three distinct haploinsufficient phenotypes that can contribute to tumorigenesis: inappropriate S phase entry, accumulation of DNA damage during replication, and failure to restrain mitotic entry.
单倍剂量不足的肿瘤抑制因子Chk1对胚胎细胞至关重要,但Chk1在成年组织中缺失的后果尚不清楚。利用条件性Chk1小鼠,我们发现缺乏Chk1的增殖乳腺细胞会发生凋亡,导致发育缺陷。条件性Chk1杂合性增加了S期细胞的数量,并导致自发性DNA损伤。Chk1+/-上皮细胞也表现出细胞周期失调,其中S期细胞表现出早期有丝分裂表型。这些细胞维持高水平的Cdc25A,其可促进不适当的细胞周期过渡。因此,Chk1杂合性导致三种不同的单倍剂量不足表型,这些表型可促成肿瘤发生:不适当的S期进入、复制过程中DNA损伤的积累以及无法抑制有丝分裂进入。