Affiliation:
1. Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3280
Abstract
ABSTRACT
RNA-binding proteins act at various stages of gene expression to regulate and fine-tune patterns of mRNA accumulation. One protein in this class is
Drosophila
Su(s), a nuclear protein that has been previously shown to inhibit the accumulation of mutant transcripts by an unknown mechanism. Here, we have identified several additional RNAs that are downregulated by Su(s). These Su(s) targets include cryptic wild-type transcripts from the developmentally regulated
Sgs4
and
ng1
genes, noncoding RNAs derived from tandemly repeated αβ/αγ elements within an
Hsp70
locus, and aberrant transcripts induced by
Hsp70
promoter transgenes inserted at ectopic sites. We used the αβ RNAs to investigate the mechanism of Su(s) function and obtained evidence that these transcripts are degraded by the nuclear exosome and that Su(s) promotes this process. Furthermore, we showed that the RNA binding domains of Su(s) are important for this effect and mapped the sequences involved to a 267-nucleotide region of an αβ element. Taken together, these results suggest that Su(s) binds to certain nascent transcripts and stimulates their degradation by the nuclear exosome.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
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