Skip Navigation


MBE Advance Access originally published online on June 2, 2004
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Supplementary Material
Right arrow All Versions of this Article:
21/9/1712    most recent
msh179v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (14)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Cooper, J. L.
Right arrow Articles by Henikoff, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cooper, J. L.
Right arrow Articles by Henikoff, S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Mol. Biol. Evol. 21(9):1712-1718. 2004
DOI: 10.1093/molbev/msh179
© 2004 by the Society for Molecular Biology and Evolution. ISSN: 0737-4038

Adaptive Evolution of the Histone Fold Domain in Centromeric Histones

Jennifer L. Cooper and Steven Henikoff

Howard Hughes Medical Institute, Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Wash.

E-mail: steveh{at}fhcrc.org.

Centromeric DNA, being highly repetitive, has been refractory to molecular analysis. However, centromeric structural proteins are encoded by single-copy genes, and these can be analyzed by using standard phylogenetic tools. The centromere-specific histone, CenH3, replaces histone H3 in centromeric nucleosomes, and is required for the proper distribution of chromosomes during cell division. Whereas histone H3s are nearly identical between species, CenH3s are divergent, with an N-terminal tail that is highly variable in length and sequence. Both the N-terminal tail and histone fold domain (HFD) are subject to adaptive evolution in Drosophila. Similarly, comparisons between Arabidopsis thaliana and Arabidopsis arenosa detected adaptive evolution, but only in the N-terminal tail. We have extended our evolutionary analyses of CenH3s to other members of the Brassicaceae, which allowed the detection of positive selection in both the N-terminal tail and in the HFD. We find that adaptively evolving sites in the HFD can potentially interact with DNA, including sites in the loop 1 region of the HFD that are required for centromeric targeting in Drosophila. Other adaptively evolving sites in the HFD can be localized on the structure of the nucleosome core particle, revealing an extended surface in addition to loop 1 in which conformational changes might alter histone–DNA contacts or water bridges. The identification of adaptively evolving sites provides a structural basis for the interaction between centromeric DNA and the protein that is thought to underlie the evolution of centromeres and the accumulation of pericentric heterochromatin.

Key Words: centromere • histone • adaptive evolution • Arabidopsis • Brassicaceae


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
Y. Dalal, T. Furuyama, D. Vermaak, and S. Henikoff
Inaugural Article: Structure, dynamics, and evolution of centromeric nucleosomes
PNAS, October 9, 2007; 104(41): 15974 - 15981.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
A. Kawabe, S. Nasuda, and D. Charlesworth
Duplication of Centromeric Histone H3 (HTR12) Gene in Arabidopsis halleri and A. lyrata, Plant Species With Multiple Centromeric Satellite Sequences
Genetics, December 1, 2006; 174(4): 2021 - 2032.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
H.-R. Lee, P. Neumann, J. Macas, and J. Jiang
Transcription and Evolutionary Dynamics of the Centromeric Satellite Repeat CentO in Rice
Mol. Biol. Evol., December 1, 2006; 23(12): 2505 - 2520.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
R. E. Baker and K. Rogers
Phylogenetic Analysis of Fungal Centromere H3 Proteins
Genetics, November 1, 2006; 174(3): 1481 - 1492.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
I. Lermontova, V. Schubert, J. Fuchs, S. Klatte, J. Macas, and I. Schubert
Loading of Arabidopsis Centromeric Histone CENH3 Occurs Mainly during G2 and Requires the Presence of the Histone Fold Domain
PLANT CELL, October 1, 2006; 18(10): 2443 - 2451.
[Abstract] [Full Text] [PDF]


Home page
Brief Funct Genomic ProteomicHome page
J. Ausio
Histone variants--the structure behind the function
Brief Funct Genomic Proteomic, September 1, 2006; 5(3): 228 - 243.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
A. E. Hall, G. C. Kettler, and D. Preuss
Dynamic evolution at pericentromeres
Genome Res., March 1, 2006; 16(3): 355 - 364.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
H.-R. Lee, W. Zhang, T. Langdon, W. Jin, H. Yan, Z. Cheng, and J. Jiang
From The Cover: Chromatin immunoprecipitation cloning reveals rapid evolutionary patterns of centromeric DNA in Oryza species
PNAS, August 16, 2005; 102(33): 11793 - 11798.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
S. E. Hall, S. Luo, A. E. Hall, and D. Preuss
Differential Rates of Local and Global Homogenization in Centromere Satellites From Arabidopsis Relatives
Genetics, August 1, 2005; 170(4): 1913 - 1927.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.