2009
DOI: 10.1007/s12192-009-0108-y
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Protein synthesis rates in Drosophila associate with levels of the hsr-omega nuclear transcript

Abstract: Transcripts of the Drosophila hsr-omega gene are known to interact with RNA processing factors and ribosomes and are postulated to aid in co-ordinating nuclear and cytoplasmic activities particularly in stressed cells. However, the significance of these interactions for physiological processes and in turn for whole-organism fitness remains an open question. Because hsr-omega's cellular expression characteristics suggest it may influence protein synthesis, and because both genotypic and expression variation of … Show more

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Cited by 10 publications
(14 citation statements)
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References 43 publications
(51 reference statements)
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“…In this context, it is interesting to note that under conditions of global inhibition of cellular protein synthesis, the level of the small cytoplasmic hsrv-c transcript is enhanced (Bendena et al 1989). It has also been reported more recently that the quantity and quality of hsrv transcripts affect levels of protein synthesis in flies ( Johnson et al 2009). Such possible effects of hsrv transcripts on the cellular translation apparatus may be yet another mechanism that may modulate cellular levels of DIAP1 in Rpr-or Grim-expressing cells.…”
Section: Discussionmentioning
confidence: 90%
“…In this context, it is interesting to note that under conditions of global inhibition of cellular protein synthesis, the level of the small cytoplasmic hsrv-c transcript is enhanced (Bendena et al 1989). It has also been reported more recently that the quantity and quality of hsrv transcripts affect levels of protein synthesis in flies ( Johnson et al 2009). Such possible effects of hsrv transcripts on the cellular translation apparatus may be yet another mechanism that may modulate cellular levels of DIAP1 in Rpr-or Grim-expressing cells.…”
Section: Discussionmentioning
confidence: 90%
“…Quantification of hsr-omega transcript levels Levels of omega-n and omega-c were estimated by real time RT-PCR as previously described (Collinge et al 2008;Johnson et al 2009a). Transcript specificity was assured by primer placement; for omega-n both primers were downstream of the full omega-c template (and upstream of the repeat region), and for omega-c the forward primer spanned the intron splice junction while the reverse primer was close-by (near the 5 0 end of the omega-c template, as depicted in Johnson et al 2009a).…”
Section: Derivation Of Mutant Linesmentioning
confidence: 99%
“…Transcript specificity was assured by primer placement; for omega-n both primers were downstream of the full omega-c template (and upstream of the repeat region), and for omega-c the forward primer spanned the intron splice junction while the reverse primer was close-by (near the 5 0 end of the omega-c template, as depicted in Johnson et al 2009a). Three replicate RNA extractions were made for each line for both basal and heatshocked treatments.…”
Section: Derivation Of Mutant Linesmentioning
confidence: 99%
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