Insertion of the promoter for a variant surface glycoprotein gene expression site in an RNA polymerase II transcription unit of procyclic Trypanosoma brucei.

Abstract:

:The variant-specific surface glycoprotein (VSG) genes of Trypanosoma brucei are invariably expressed near the ends of chromosomes (telomeres). We have targeted a VSG gene expression site (ES) promoter driving a selectable marker gene (neomycin phosphotransferase) into a chromosome-internal transcription unit, the tubulin gene array of procyclic trypanosomes. To avoid read through transcription of the marker gene from the tubulin promoter, we targeted the ES promoter in inverse orientation relative to tubulin gene transcription. The only correctly targeted transformant obtained contained the marker gene close to the border of the tubulin gene array, and expression of this gene was relatively low. Possible reasons for the low targeting efficiency and expression level are discussed.

journal_name

Mol Biochem Parasitol

authors

Zomerdijk JC,Kieft R,Borst P

doi

10.1016/0166-6851(93)90205-c

subject

Has Abstract

pub_date

1993-02-01 00:00:00

pages

295-304

issue

2

eissn

0166-6851

issn

1872-9428

pii

0166-6851(93)90205-C

journal_volume

57

pub_type

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