Li Q, Lu Q, Hwang J Y, Büscher D, Lee K F, Izpisua-Belmonte J C, Verma I M
The Salk Institute, La Jolla, California 92037, USA.
Genes Dev. 1999 May 15;13(10):1322-8. doi: 10.1101/gad.13.10.1322.
IkappaB kinases (IKKs) IKK1 and IKK2 are two putative IkappaBalpha kinases involved in NF-kappaB activation. To examine the in vivo functions of IKK1, we generated IKK1-deficient mice. The mutant mice are perinatally lethal and exhibit a wide range of developmental defects. Newborn mutant mice have shiny, taut, and sticky skin without whiskers. Histological analysis shows thicker epidermis, which is unable to differentiate. Limbs and tail are wrapped inside the skin and do not extend properly out of the body trunk. Skeleton staining reveals a cleft secondary palate, split sternebra 6, and deformed incisors. NF-kappaB activation mediated by TNFalpha and IL-1 is diminished in IKK1-deficient mouse embryonic fibroblast (MEF) cells. The IKK complex in the absence of IKK1 is capable of phosphorylating IkappaBalpha and IkappaBbeta in vitro. Our results support a role for IKK1 in NF-kappaB activation and uncover its involvement in skin and skeleton development. We conclude further that the two related kinases IKK1 and IKK2 have distinct functions and can not be substituted for each other's functions.
IκB激酶(IKKs)中的IKK1和IKK2是两种推测参与NF-κB激活的IκBα激酶。为了研究IKK1的体内功能,我们培育出了IKK1基因缺陷型小鼠。这些突变小鼠在围产期致死,并表现出广泛的发育缺陷。新生突变小鼠皮肤发亮、紧绷且发黏,没有胡须。组织学分析显示表皮增厚,无法分化。四肢和尾巴包裹在皮肤内,不能正常伸出躯干。骨骼染色显示有腭裂、第6块胸骨分裂以及门齿畸形。在IKK1缺陷的小鼠胚胎成纤维细胞(MEF)中,由肿瘤坏死因子α(TNFα)和白细胞介素-1(IL-1)介导的NF-κB激活减弱。在体外,缺乏IKK1时的IKK复合物能够磷酸化IκBα和IκBβ。我们的结果支持IKK1在NF-κB激活中的作用,并揭示了其参与皮肤和骨骼发育。我们进一步得出结论,两种相关激酶IKK1和IKK2具有不同的功能,不能相互替代。