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Differential expression of a protease gene family in African trypanosomes.
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- Author(s): Helm JR;Helm JR; Wilson ME; Donelson JE
- Source:
Molecular and biochemical parasitology [Mol Biochem Parasitol] 2009 Jan; Vol. 163 (1), pp. 8-18. Date of Electronic Publication: 2008 Sep 19.
- Publication Type:
Journal Article; Research Support, N.I.H., Extramural
- Language:
English
- Additional Information
- Source:
Publisher: Elsevier/North-Holland Biomedical Press Country of Publication: Netherlands NLM ID: 8006324 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0166-6851 (Print) Linking ISSN: 01666851 NLM ISO Abbreviation: Mol Biochem Parasitol Subsets: MEDLINE
- Publication Information:
Original Publication: Amsterdam, Elsevier/North-Holland Biomedical Press.
- Subject Terms:
- Abstract:
During their life cycle African trypanosomes must quickly adapt to the different environments of the tsetse fly midgut and the mammalian bloodstream by modulating expression of many of their genes. One group of these differentially expressed genes encodes different forms of a major surface protease. Using a luciferase reporter gene transiently or permanently transfected into trypanosomes, we show here that the 3'-UTRs of these protease genes are responsible for their differential expression. Deletion analysis of the 389-bp 3'-UTR of one of the protease genes, MSP-B, demonstrated that it contains a U-rich regulatory region of about 23bp (UCGUCUGUUAUUUCUUAGUCCAG), which suppresses expression of the reporter protein in bloodstream trypanosomes by as much as 25-fold, but has little effect on the reporter expression in procyclic (tsetse fly) trypanosomes. Replacing the entire 3'-UTR with just this 23-bp element mimicked most of the suppression effect of the complete 3'-UTR. Northern blots showed that the 23-bp element influences the steady state RNA level, but not enough to account for the 25-fold suppression effect. Polysome analyses showed that in procyclic trypanosomes more of the total protease mRNA is associated with intermediate-sized and large polysomes than in bloodstream trypanosomes. Thus, the 23-bp element of this protease gene affects both the level of RNA and its translation.
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- Grant Information:
T32 007511 United States PHS HHS; R01 AI059451-03 United States AI NIAID NIH HHS; T32 AI007511 United States AI NIAID NIH HHS; R01 AI059451 United States AI NIAID NIH HHS; T32 AI007511-12 United States AI NIAID NIH HHS
- Accession Number:
0 (3' Untranslated Regions)
0 (Protozoan Proteins)
0 (RNA, Protozoan)
EC 3.4.- (Peptide Hydrolases)
- Publication Date:
Date Created: 20081014 Date Completed: 20090205 Latest Revision: 20190508
- Publication Date:
20250114
- Accession Number:
PMC2633602
- Accession Number:
10.1016/j.molbiopara.2008.09.004
- Accession Number:
18848586
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