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The Evolution of Epitype

Richard B. Meagher
Richard B. Meagher
Department of Genetics, University of Georgia, Athens, Georgia 30602
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  • For correspondence: meagher@uga.edu

Published June 2010. DOI: https://doi.org/10.1105/tpc.110.075481

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    Figure 1.

    Nucleotide Sequence Composition Directs the Positioning of H2AZ-Enriched Nucleosomes in Saccharomyces.

    The frequency distribution of the combined number of AA, TT, AT, and TA dinucleotides (dashed line) or GG, CC, GC, and CG dinucleotides (solid line) at each base pair along the 147 bp of nucleosomal DNA. Repeats of G+C-rich dinucleotides are more commonly in the major groove (gray shaded areas) facing inward against the nucleosome. A+T-rich dinucleotides are generally in the major grooves facing outward from the nucleosome. The bottom axis shows the distance in base pairs from zero at the center of dyad symmetry. (Adapted by permission from Macmillan Publishers Limited: Nature, Albert et al. [2007], copyright 2007.)

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    Figure 2.

    Cytosine Methylation Patterns Are Conserved among the Members of the Human Plasminogen Precursor Gene Family PGL, PGLA, and PGLB1/B2.

    In human liver, where all four genes are expressed, one of the two alleles for each gene are cytosine methylated 5MeC (black stars) at nearly all seven CpG sites. The other allele remains unmethylated (white stars). In skeletal and heart muscle, where the genes are not expressed, both alleles for each gene are nearly all cytosine methylated at all seven sites. (Adapted from Cortese et al. [2008], with permission from Elsevier.)

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    Figure 3.

    MADS Box Repressors of Flowering FLC, MAF4, and MAF5 Share an Uncommon Bimodal H2AZ Distribution Pattern in Arabidopsis.

    (A) and (C) All three MADS box transcription factor genes share in bimodal pattern of H2AZ deposition with peaks at their 5′ and 3′ ends in seedlings.

    (B) and (D) Maps of FLC, MAF4, and MAF5 genes and their exon structures (black boxes), and regions PCR amplified to quantify H2AZ-enriched sequences (1 to 10 for FLC and 1 to 11 for MAF4 and MAF5). (Redrawn from Deal et al. [2007].)

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The Evolution of Epitype
Richard B. Meagher
The Plant Cell Jun 2010, 22 (6) 1658-1666; DOI: 10.1105/tpc.110.075481

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The Evolution of Epitype
Richard B. Meagher
The Plant Cell Jun 2010, 22 (6) 1658-1666; DOI: 10.1105/tpc.110.075481
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  • Article
    • Abstract
    • INTRODUCTION
    • WHAT IS THE RELATIONSHIP BETWEEN EPIGENETIC CONTROL AND DEVELOPMENTAL PHENOTYPE?
    • WHAT IS THE RELATIONSHIP BETWEEN EPIGENETIC CONTROL AND THE EVOLUTION OF ORGANISMAL PHENOTYPE?
    • WHAT IS THE PHYLOGENETIC EVIDENCE THAT EPITYPE EVOLVES FROM ANCESTRAL GENES FOLLOWING GENE DUPLICATION?
    • WHAT ARE THE EVOLUTIONARY RATES OF CHANGE FOR DIFFERENT EPITYPES?
    • THE INFLUENCE OF ENVIRONMENT
    • GENETICS, EPIGENETICS, AND SEMANTICS
    • CONCLUSIONS AND FUTURE CONSIDERATIONS
    • Acknowledgments
    • Footnotes
    • References
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In this issue

The Plant Cell Online: 22 (6)
The Plant Cell
Vol. 22, Issue 6
Jun 2010
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More in this TOC Section

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  • Barbara McClintock’s Unsolved Chromosomal Mysteries: Parallels to Common Rearrangements and Karyotype Evolution
  • Periodic Lateral Root Priming: What Makes It Tick?
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