Journalartikel

Histone modifications in Trypanosoma brucei


AutorenlisteMandava, V; Fernandez, JP; Deng, H; Janzen, CJ; Hake, SB; Cross, GAM

Jahr der Veröffentlichung2007

Seiten41-50

ZeitschriftMolecular and Biochemical Parasitology

Bandnummer156

Heftnummer1

ISSN0166-6851

DOI Linkhttps://doi.org/10.1016/j.molbiopara.2007.07.005

VerlagElsevier


Abstract
Several biological processes in Trypanosoma brucei are affected by chromatin structure, including gene expression, cell cycle regulation, and life-cycle stage differentiation. In Saccharomyces cerevisiae and other organisms, chromatin structure is dependent upon posttranslational modifications of histones, which have been mapped in detail. The tails of the four core histones of T brucei are highly diverged from those of mammals and yeasts, so sites of potential modification cannot be reliably inferred, and no cross-species antibodies are available to map the modifications. We therefore undertook an extensive survey to identify posttranslational modifications by Edman degradation and mass spectrometry. Edman analysis showed that the N-terminal alanine of H2A, H2B, and H4 could be monomethylated. We found that the histone H4 N-terminus is heavily modified, while, in contrast to other organisms, the histone H2A and H2B N-termini have relatively few modifications. Histone H3 appears to have a number of modifications at the N-terminus, but we were unable to assign many of these to a specific amino acid. Therefore, we focused our efforts on uncovering modification states of H4. We discuss the potential relevance of these modifications.



Autoren/Herausgeber




Zitierstile

Harvard-ZitierstilMandava, V., Fernandez, J., Deng, H., Janzen, C., Hake, S. and Cross, G. (2007) Histone modifications in Trypanosoma brucei, Molecular and Biochemical Parasitology, 156(1), pp. 41-50. https://doi.org/10.1016/j.molbiopara.2007.07.005

APA-ZitierstilMandava, V., Fernandez, J., Deng, H., Janzen, C., Hake, S., & Cross, G. (2007). Histone modifications in Trypanosoma brucei. Molecular and Biochemical Parasitology. 156(1), 41-50. https://doi.org/10.1016/j.molbiopara.2007.07.005


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