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Review
. 2021 Jul 5:9:699639.
doi: 10.3389/fcell.2021.699639. eCollection 2021.

Keeping Balance Between Genetic Stability and Plasticity at the Telomere and Subtelomere of Trypanosoma brucei

Affiliations
Review

Keeping Balance Between Genetic Stability and Plasticity at the Telomere and Subtelomere of Trypanosoma brucei

Bibo Li. Front Cell Dev Biol. .

Abstract

Telomeres, the nucleoprotein complexes at chromosome ends, are well-known for their essential roles in genome integrity and chromosome stability. Yet, telomeres and subtelomeres are frequently less stable than chromosome internal regions. Many subtelomeric genes are important for responding to environmental cues, and subtelomeric instability can facilitate organismal adaptation to extracellular changes, which is a common theme in a number of microbial pathogens. In this review, I will focus on the delicate and important balance between stability and plasticity at telomeres and subtelomeres of a kinetoplastid parasite, Trypanosoma brucei, which causes human African trypanosomiasis and undergoes antigenic variation to evade the host immune response. I will summarize the current understanding about T. brucei telomere protein complex, the telomeric transcript, and telomeric R-loops, focusing on their roles in maintaining telomere and subtelomere stability and integrity. The similarities and differences in functions and underlying mechanisms of T. brucei telomere factors will be compared with those in human and yeast cells.

Keywords: RAP1; TRF; Trypanosoma brucei; genome stability; telomere.

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Conflict of interest statement

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Trypanosoma brucei has a large VSG gene pool. (A) A representative subtelomeric VSG gene array. (B) A typical minichromosome with a subtelomeric VSG gene. (C) A representative bloodstream form VSG expression site, which is a polycistronic transcription unit and can be expressed while T. brucei proliferates in its mammalian host. (D) A representative metacyclic VSG expression site, which is a monocistronic transcription unit and can be expressed while T. brucei resides in the salivary gland of its insect vector. (E) Major VSG switching pathways. VSGac stands for the originally active VSG. VSGsil stands for an originally silent VSG.
FIGURE 2
FIGURE 2
TRF homologs from various organisms. The DNA binding Myb domain, the homodimerization TRFH domain, the N-terminal acidic domain of human TRF1 and basic GAR domain of human TRF2 are marked whenever identified. In addition, Leishmania amazonensis TRF has been identified and shown to associate with the telomere (da Silva et al., 2010). T. brucei, Trypanosoma brucei; T. vivax, Trypanosoma vivax; T. evansi, Trypanosoma evansi; T. cruzi, Trypanosoma cruzi; L. major, Leishmania major; L. amazonensis, Leishmania amazonensis; A. thaliana, Arabidopsis thaliana; C. griseus, Cricetulus griseus; H. sapiens, Homo sapiens; M. musculus, Mus musculus; O. sativa, Oryza sativa; G. gallus, Gallus gallus; S. pombe, Schizosaccharomyces pombe.
FIGURE 3
FIGURE 3
Repressor activator protein 1 (RAP1) homologous. Tb, Trypanosoma brucei; Hs, Homo sapiens; Sc, Saccharomyces cerevisiae; Sp, Schizosaccharomyces pombe.

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