Exposure of mammalian cells to radiation triggers the ultraviolet (UV)
response, which includes activation of activator protein-1 (AP-1) and
nuclear factor kappa B (NF-kappaB). This was postulated to occur by i
nduction of a nuclear signaling cascade by damaged DNA. Recently, indu
ction of AP-1 by UV was shown to be mediated by a pathway involving Sr
c tyrosine kinases and the Ha-Ras small guanosine triphosphate-binding
protein, proteins located at the plasma membrane. It is demonstrated
here that the same pathway mediates induction of NF-kappaB by UV. Beca
use inactive NF-kappaB is stored in the cytosol, analysis of its activ
ation directly tests the involvement of a nuclear-initiated signaling
cascade. Enucleated cells are fully responsive to UV both in NF-kappaB
induction and in activation of another key signaling event. Therefore
, the UV response does not require a signal generated in the nucleus a
nd is likely to be initiated at or near the plasma membrane.