SR proteins are essential for the splicing of messenger RNA precursors
in vitro, where they also alter splice site selection in a concentrat
ion-dependent manner. Although experiments involving overexpression or
dominant mutations have confirmed that these proteins can influence R
NA processing decisions in vivo, similar results with loss-of-function
mutations have been lacking. Now, a system for genetic depletion of t
he chicken B cell line DT40 has revealed that the SR protein ASF/SF2 (
alternative splicing factor/splicing factor 2) is essential for viabil
ity in these cells((1)). This study opens the way for a complete funct
ional dissection of this protein, and other SR proteins, in vivo.