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Extremely divergent histone H4 sequence from Trypanosoma cruzi: evolutionary implications.
G C Toro1, C Wernstedt, C Medina
1Department of Cell Biology and Genetics, School of Medicine, University of Chile, Santiago.
Journal of Cellular Biochemistry
|July 1, 1992
Summary
Trypanosoma cruzi histone H4 shows significant divergence from other species, with a unique unblocked amino terminus and two variants. This suggests varying evolutionary rates for histone H4 across different lineages.
Area of Science:
- Molecular Biology
- Evolutionary Biology
- Parasitology
Background:
- Histones are core components of chromatin, crucial for DNA packaging and gene regulation.
- Core histones (H2A, H2B, H3, H4) are generally highly conserved across eukaryotes.
- Trypanosoma cruzi, the causative agent of Chagas disease, possesses unique biological characteristics.
Purpose of the Study:
- To identify and characterize histone H4 from Trypanosoma cruzi.
- To investigate the evolutionary conservation of histone H4 by comparing its sequence to homologous proteins from other species.
- To analyze the amino acid sequence of T. cruzi histone H4 for unique features and evolutionary implications.
Main Methods:
- Electrophoretic separation of Trypanosoma cruzi histones.
- Amino-terminal sequencing of a specific histone (histone e).
- Comparative sequence analysis of histone H4 from T. cruzi, human, yeast, and Tetrahymena.
Main Results:
- Histone e from T. cruzi was confirmed to be histone H4.
- T. cruzi histone H4 exhibits an unblocked amino terminus, unlike other known H4 proteins.
- Two variants of T. cruzi histone H4 were identified.
- The amino acid sequence of T. cruzi histone H4 is highly divergent compared to human, yeast, and Tetrahymena H4.
Conclusions:
- Trypanosoma cruzi histone H4 is the most divergent reported to date.
- Evolutionary rates of histone H4 amino-terminal sequences vary significantly among different lineages.
- A potential slowdown in the evolutionary rate of the histone H4 amino-terminal domain in metazoa may be linked to new functional roles.