Back to Search
Start Over
The coding/non-coding overlapping architecture of the gene encoding the Drosophila pseudouridine synthase
- Source :
- BMC Molecular Biology, BMC Molecular Biology, Vol 8, Iss 1, p 15 (2007)
- Publication Year :
- 2007
- Publisher :
- Springer Science and Business Media LLC, 2007.
-
Abstract
- Background In eukaryotic cells, each molecule of H/ACA small nucleolar RNA (snoRNA) assembles with four evolutionarily conserved core proteins to compose a specific ribonucleoprotein particle. One of the four core components has pseudouridine synthase activity and catalyzes the conversion of a selected uridine to pseudouridine. Members of the pseudouridine synthase family are highly conserved. In addition to catalyzing pseudouridylation of target RNAs, they carry out a variety of essential functions related to ribosome biogenesis and, in mammals, to telomere maintenance. To investigate further the molecular mechanisms underlying the expression of pseudouridine synthase genes, we analyzed the transcriptional activity of the Drosophila member of this family in great detail. Results The Drosophila gene for pseudouridine synthase, minifly/Nop60b (mfl), encodes two novel mRNAs ending at a downstream poly(A) site. One species is characterized only by an extended 3'-untranslated region (3'UTR), while a minor mRNA encodes a variant protein that represents the first example of an alternative subform described for any member of the family to date. The rare spliced variant is detected mainly in females and is predicted to have distinct functional properties. We also report that a cluster comprising four isoforms of a C/D box snoRNA and two highly related copies of a small ncRNA gene of unknown function is intron-encoded at the gene-variable 3'UTRs. Because this arrangement, the alternative 3' ends allow mfl not only to produce two distinct protein subforms, but also to release different ncRNAs. Intriguingly, accumulation of all these intron-encoded RNAs was found to be sex-biased and quantitatively modulated throughout development and, within the ovaries, the ncRNAs of unknown function were found not ubiquitously expressed. Conclusion Our results expand the repertoire of coding/non-coding transcripts derived from the gene encoding Drosophila pseudouridine synthase. This gene exhibits a complex and interlaced organization, and its genetic information may be expressed as different protein subforms and/or ncRNAs that may potentially contribute to its biological functions.
- Subjects :
- Male
Gene isoform
Untranslated region
lcsh:QH426-470
Molecular Sequence Data
Genes, Insect
Biology
snoRNA
Pseudouridine
genomic
Open Reading Frames
chemistry.chemical_compound
Animals
Drosophila Proteins
RNA, Small Nucleolar
Amino Acid Sequence
RNA, Messenger
lcsh:QH573-671
Small nucleolar RNA
3' Untranslated Regions
Molecular Biology
Gene
Hydro-Lyases
Pseudouridine synthase activity
Genetics
lcsh:Cytology
Alternative splicing
Nuclear Proteins
RNA-Binding Proteins
pseudouridine synthase
ncRNA
Introns
lcsh:Genetics
Alternative Splicing
Drosophila melanogaster
chemistry
Female
Sequence Alignment
Drosophila Protein
Research Article
Subjects
Details
- ISSN :
- 14712199
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- BMC Molecular Biology
- Accession number :
- edsair.doi.dedup.....a9e93b4c0128b671931fd07d0530182a
- Full Text :
- https://doi.org/10.1186/1471-2199-8-15