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Drosophila suppressor of sable protein [Su(s)] promotes degradation of aberrant and transposon-derived RNAs.
- Source :
-
Molecular and cellular biology [Mol Cell Biol] 2009 Oct; Vol. 29 (20), pp. 5590-603. Date of Electronic Publication: 2009 Aug 17. - Publication Year :
- 2009
-
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 alphabeta/alphagamma elements within an Hsp70 locus, and aberrant transcripts induced by Hsp70 promoter transgenes inserted at ectopic sites. We used the alphabeta 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 alphabeta element. Taken together, these results suggest that Su(s) binds to certain nascent transcripts and stimulates their degradation by the nuclear exosome.
- Subjects :
- Animals
Base Sequence
Chromosomes metabolism
Chromosomes ultrastructure
Drosophila Proteins genetics
Drosophila melanogaster genetics
Glue Proteins, Drosophila genetics
HSP70 Heat-Shock Proteins genetics
Hot Temperature
Molecular Sequence Data
RNA genetics
RNA-Binding Proteins genetics
Salivary Proteins and Peptides genetics
Drosophila Proteins metabolism
Drosophila melanogaster metabolism
Glue Proteins, Drosophila metabolism
HSP70 Heat-Shock Proteins metabolism
RNA metabolism
RNA Polymerase II metabolism
RNA-Binding Proteins metabolism
Salivary Proteins and Peptides metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1098-5549
- Volume :
- 29
- Issue :
- 20
- Database :
- MEDLINE
- Journal :
- Molecular and cellular biology
- Publication Type :
- Academic Journal
- Accession number :
- 19687295
- Full Text :
- https://doi.org/10.1128/MCB.00039-09