A structural and transcription pattern for variant surface glycoprotein gene expression sites used in metacyclic stage Trypanosoma brucei

• Published in: Molecular and biochemical parasitology 1999-10, Vol.103 (2), p.141-154
• Main Authors: Graham, Sheila V., Terry, Sandra, Barry, J.David
• Format: Article
• Language: English
• Subjects: Animals; Antigenic Variation - genetics; Base Sequence; ESAG; Gene Expression Regulation; Metacyclic stage; Molecular Sequence Data; MVSG gene; Promoter Regions, Genetic; Promoters; Telomere - genetics; Transcription, Genetic; Trypanosoma brucei; Trypanosoma brucei brucei - genetics; Trypanosoma brucei brucei - growth & development; Variant Surface Glycoproteins, Trypanosoma - biosynthesis; Variant Surface Glycoproteins, Trypanosoma - genetics; VSG
• ISSN: 0166-6851; 1872-9428
• DOI: 10.1016/S0166-6851(99)00128-0

African trypanosomes first express the variant surface glycoprotein (VSG) at the metacyclic stage in the tsetse fly vector, in preparation for transfer into the mammal. Metacyclic (M)VSGs comprise a specific VSG repertoire subset and their expression is regulated differently from that of bloodstream VSGs, involving exclusively transcriptional regulation during the life cycle. To identify basic structural and functional features that may be common to MVSG telomeric transcription units, we have characterized the anatomy and transcription of the telomere containing the ILTat 1.61 MVSG gene. This telomere contains pseudogenes of the ESAG1 and ESAG9 families found in bloodstream VSG transcription units. The 1.61 MVSG occupies a monocistronic transcription unit and is transcriptionally controlled through the life cycle. The 1.61, and also the 1.22, MVSG transcription initiation site sequences resemble eukaryotic initiator elements. Sequence comparison reveals that four out of five characterized MVSG expression sites have a conserved region 2.0–4.7 kb long upstream of the MVSG. In some cases, this region contains not only the transcription initiation site that we have observed to be active in fly-transmitted trypanosomes but also, upstream, another sequence, described elsewhere as a ‘putative promoter’ for the MVAT set of MVSGs (Nagoshi YL, Alarcon CM, Donelson JE. A monocistronic transcript for a trypanosome variant surface glycoprotein, Mol Biochem Parasitol 1995;72:33–45). In fly-transmitted trypanosomes, the latter element is transcriptionally silent. Our analysis of the structure of MVSG telomeres suggests that metacyclic expression sites arose from bloodstream expression sites.