Publication Date:
2002
abstract:
The Survival of Motor Neurons (SMN) protein, the product of the spinal muscular atrophy-determining gene, is part of a
large macromolecular complex (SMN complex) that functions in the assembly of spliceosomal small nuclear
ribonucleoproteins (snRNPs). Using cell extracts and purified components, we demonstrated that the SMN complex is
necessary and sufficient to mediate the ATP-dependent assembly of the core of seven Sm proteins on uridine-rich, small
nuclear ribonucleic acids (U snRNAs). In vitro experiments revealed strict requirements for ordered binding of the Sm
proteins and the U snRNAs to the SMN complex. Importantly, the SMN complex is necessary to ensure that Sm cores
assemble only on correct RNA targets and prevent their otherwise promiscuous association with other RNAs. Thus, the
SMN complex functions as a specificity factor essential for the efficient assembly of Sm proteins on U snRNAs and
likely protects cells from illicit, and potentially deleterious, nonspecific binding of Sm proteins to RNAs.
Iris type:
01.01 Articolo in rivista