Abstract

Human, mouse, and Xenopus mRNAs encoding the U1 snRNP-specific U1 A protein contain a conserved 47 nt region in their 3′ untranslated regions (UTRs). In vitro studies show that human U1A protein binds to two sites within the conserved region that resemble, in part, the previously characterized UlA-binding site on U1 snRNA. Overexpression of human U1A protein in mouse cells results in down-regulation of endogenous mouse UlA mRNA accumulation. In vitro and in vivo experiments demonstrate that excess UIA protein specifically inhibits polyadenylation of pre-mRNAs that contain the conserved 3′ UTR from human UlA mRNA. Thus, U1 A protein regulates the production of its own mRNA via a mechanism that involves pre-mRNA binding and inhibition of polyadenylation.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call