Johnson L, Greenbaum D, Cichowski K, Mercer K, Murphy E, Schmitt E, Bronson R T, Umanoff H, Edelmann W, Kucherlapati R, Jacks T
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.
Genes Dev. 1997 Oct 1;11(19):2468-81. doi: 10.1101/gad.11.19.2468.
Mammalian ras genes are thought to be critical in the regulation of cellular proliferation and differentiation and are mutated in approximately 30% of all human tumors. However, N-ras and H-ras are nonessential for mouse development. To characterize the normal role of K-ras in growth and development, we have mutated it by gene targeting in the mouse. On an inbred genetic background, embryos homozygous for this mutation die between 12 and 14 days of gestation, with fetal liver defects and evidence of anemia. Thus, K-ras is the only member of the ras gene family essential for mouse embryogenesis. We have also investigated the effect of multiple mutations within the ras gene family. Most animals lacking N-ras function and heterozygous for the K-ras mutation exhibit abnormal hematopoietic development and die between days 10 and 12 of embryogenesis. Thus, partial functional overlap appears to occur within the ras gene family, but K-ras provides a unique and essential function.
哺乳动物的ras基因被认为在细胞增殖和分化的调节中起关键作用,并且在大约30%的人类肿瘤中发生突变。然而,N-ras和H-ras对小鼠发育并非必需。为了阐明K-ras在生长和发育中的正常作用,我们通过基因打靶在小鼠中使其发生突变。在近交遗传背景下,这种突变的纯合子胚胎在妊娠12至14天之间死亡,伴有胎儿肝脏缺陷和贫血迹象。因此,K-ras是ras基因家族中对小鼠胚胎发生必不可少的唯一成员。我们还研究了ras基因家族内多个突变的影响。大多数缺乏N-ras功能且为K-ras突变杂合子的动物表现出异常的造血发育,并在胚胎发生的第10至12天之间死亡。因此,ras基因家族内似乎存在部分功能重叠,但K-ras提供了独特且必不可少的功能。