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Mol. Cell. Biol., Mar 1996, 1241-1246, Vol 16, No. 3
SH Mayrand, PA Fung and T Pederson
The C heterogeneous ribonucleoprotein particle (hnRNP) protein bind to
nascent pre-mRNA and may participate in assembly of the early
prespliceosome. Ser/Thr phosphorylation of the C1 hnRNP protein in HeLa
nuclear extracts regulates its binding to pre-mRNA (S. H. Mayrand, P. Dwen,
and T. Pederson, Proc. Natl. Acad. Sci. USA 90:7764-7768, 1993). We have
now further investigated the phosphorylation cycle of the C1 hnRNP protein,
with emphasis on its regulation. Pretreatment of nuclear extracts with
micrococcal nuclease eliminated the phosphorylation of C1 hnRNP protein,
but pretreatment with DNase did not, suggesting a dependence on RNA.
Oligodeoxynucleotide-targeted RNase H cleavage of U1, U2, and U4 small
nuclear RNAs did not affect the phosphorylation of C1 hnRNP protein.
However, cleavage of nucleotides 78 to 95, but not other regions, of U6
small nuclear RNA resulted in an inhibition of the dephosphorylation step
of the C1 hnRNP protein phosphorylation cycle. This inhibition was as
pronounced as that seen with the serine/threonine protein phosphatase
inhibitor okadaic acid. C1 hnRNP protein dephosphorylation could be
completely restored by the addition of intact U6 RNA. Add-back experiments
with mutant RNAs further delineated the minimal region essential for C1
protein dephosphorylation as residing in nucleotides 85 to 92 of U6 RNA.
These results illuminate a hitherto unanticipated function of U6 RNA: the
modulation of a phosphorylation-dephosphorylation cycle of C1 hnRNP protein
that influences the binding affinity of this protein for pre- mRNA. This
newly revealed function of U6 RNA is likely to play a very early role in
the prespliceosome assembly pathway, prior to U6 RNA's entry into the
mature spliceosome's active center.
Copyright © 1996, American Society for Microbiology
A discrete 3' region of U6 small nuclear RNA modulates the phosphorylation cycle of the C1 heterogeneous nuclear ribonucleoprotein particle protein
Cell Biology Group, Worcester Foundation for Biomedical Research, Shrewsbury, Massachusetts 01545, USA.
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