Abstract

Heterochromatin has historically been considered the dark side of the genome. In part, this reputation derives from its concentration near centromeres and telomeres, regions of the genome repressive to nuclear functions such as DNA replication and transcription. The repetitive nature of heterochromatic DNA has only added to its “darkness”, as sequencing of these DNA regions has been only recently achieved. Despite such obstacles, research on heterochromatin blossomed over the past decades. Success in this area benefitted from efforts of Sergio Pimpinelli and colleagues who made landmark discoveries and promoted the growth of an international community of researchers. They discovered complexities of heterochromatin, demonstrating that a key component, Heterochromatin Protein 1a (HP1a), uses multiple mechanisms to associate with chromosomes and has positive and negative effects on gene expression, depending on the chromosome context. In addition, they updated the work of Carl Waddington using molecular tools that revealed how environmental stress promotes genome change due to transposable element movement. Collectively, their research and that of many others in the field have shined a bright light on the dark side of the genome and helped reveal many mysteries of heterochromatin.

Highlights

  • Heterochromatin has historically been considered the dark side of the genome

  • Protein 1a (HP1a) [24–27], a key component of heterochromatin, and mechanisms by which transposon movement has been linked to environmental stress

  • Heterochromatin Protein 1a (HP1a) is a member of a conserved family of chromatin proteins that share a domain structure consisting of an N-terminal chromodomain (CD)

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Summary

Heterochromatin

In the early 1900s, geneticists, such as Muller, Painter, and Schulze, described two types of chromosomal regions in the eukaryotic nucleus [1,2]. One type was electron dense, remained condensed during interphase, and possessed relatively few genes. In Drosophila, TEs represent nearly 20% of the genome, with at least 30% corresponding to full length, active elements [16]. Transposons deploy self-encoded integrases, endonucleases, and transposases to move around genomes As they move, they carry with them promoters, transcription factor binding sites, and polyadenylation signals [12,15–18]. Pimpinelli and his colleagues, as first described at these conferences. Protein 1a (HP1a) [24–27], a key component of heterochromatin, and mechanisms by which transposon movement has been linked to environmental stress. Together, these studies have provided a more complete picture of genome organization, transcriptional regulation, and evolutionary change

Expanding Functions of Heterochromatin Protein 1a
Connecting Transposon Regulation to Environmental Stress
Findings
Coalescence of a Heterochromatin Community
Full Text
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