Chromatin structure in African trypanosomes
Trypanosomiasis, also known as African sleeping sickness, is a fatal infection caused by the parasite Trypanosoma brucei. A European study investigated how Trypanosoma brucei evades immune attack.
Trypanosomes have developed a remarkable strategy for escaping host
immune responses by periodically changing the variant surface
glycoprotein (VSG) expressed on the surface of the parasite. Although
there are hundreds of VSG genes in the genome, the bloodstream form of
the parasite expresses only one gene at a time.
Gene expression is tightly linked with chromatin structure and the
accessibility of the transcribed regions by various transcription
factors. Chromatin remodelling is driven by specialised proteins that
modify associated histones. Accumulating evidence indicates that histone
H1 can negatively or positively regulate gene transcription.
The scope of the EU-funded 'Chromatin and antigenic variation: The
role of histone H1 in gene regulation in African trypanosomes'
(HISTONEH1TRYP) project was to elucidate the mechanism behind this VSG
monoallelic expression. The work focused on histone H1 and how it
controls antigenic variation in T.brucei.
Experimental data indicated that although histone H1 is dispensable
for parasite growth in culture, it determines parasite fitness in vivo.
Histone H1 works by compacting chromatin at various regions throughout
the parasite genome and thereby regulates transcription of various genes
including VSG.
Collectively, the findings of the HISTONEH1TRYP project unveil a
novel function of histone H1 in the antigenic variation and immune
evasion of T.brucei. This information could form the basis for the
design of novel therapeutics targeting histone H1 modifications.
published: 2015-03-12