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In vitro assembly of the mouse U14
snoRNP core complex and identification of a 65-kDa box C/D-binding protein
Watkins NJ, Newman DR, Kuhn JF, Maxwell ES
RNA 4 (5): 582-593 MAY 1998
Abstract:
The eukaryotic nucleolus contains a diverse population of small nucleolar
RNAs (snoRNAs) that have been categorized into two major families based
on evolutionarily conserved sequence elements. U14 snoRNA is a member
of the larger, box C/D snoRNA family and possesses nucleotide box C and
D consensus sequences. In previous studies, we have defined a U14 box
C/D core motif that is essential for intronic U14 snoRNA processing. These
studies also revealed that nuclear proteins that recognize boxes C/D are
required, We have now established an in vitro U14 snoRNP assembly system
to characterize protein binding. Electrophoretic mobility-shift analysis
demonstrated that all the sequences and structures of the box C/D cove
motif required for U14 processing are also necessary for protein binding
and snoRNP assembly. These required elements include a base paired 5',3'
terminal stem and the phylogenetically conserved nucleotides of boxes
C and D, The ability of other box C/D snoRNAs to compete for protein binding
demonstrated that the box C/D core motif-binding proteins are common to
this family of snoRNAs. UV crosslinking of nuclear proteins bound to the
U14 core motif identified a 65-kDa mouse snoRNP protein that requires
boxes C and D for binding. Two additional core motif proteins of 55 and
50 kDa were also identified by biochemical fractionation of the in vitro-assembled
U14 snoRNP complex. Thus, the U14 snoRNP core complex is a multiprotein
particle whose assembly requires nucleotide boxes C and D.
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