Euchromatin

Euchromatin is composed of repeating subunits known as nucleosomes, reminiscent of an unfolded set of beads on a string, that are approximately 11 nm in diameter.[2] At the core of these nucleosomes are a set of four histone protein pairs: H3, H4, H2A, and H2B.[2] Each core histone protein possesses a 'tail' structure, which can vary in several ways; it is thought that these variations act as "master control switches" through different methylation and acetylation states, which determine the overall arrangement of the chromatin.[2] Approximately 147 base pairs of DNA are wound around the histone octamers, or a little less than 2 turns of the helix.[3] Nucleosomes along the strand are linked together via the histone, H1,[4] and a short space of open linker DNA, ranging from around 0-80 base pairs. The key distinction between the structure of euchromatin and heterochromatin is that the nucleosomes in euchromatin are much more widely spaced, which allows for easier access of different protein complexes to the DNA strand and thus increased gene transcription.[2]

Microscopy of heterochromatic versus euchromatic nuclei (H&E stain).

Euchromatin resembles a set of beads on a string at large magnifications.[2] From farther away, it can resemble a ball of tangled thread, such as in some electron microscope visualizations.[5] In both optical and electron microscopic visualizations, euchromatin appears lighter in color than heterochromatin - which is also present in the nucleus and appears darkly[6] - due to its less compact structure.[5] When visualizing chromosomes, such as in a karyogram, cytogenetic banding is used to stain the chromosomes. Cytogenetic banding allows us to see which parts of the chromosome are made up of euchromatin or heterochromatin in order to differentiate chromosomal subsections, irregularities or rearrangements.[7] One such example is G banding, otherwise known as Giemsa staining where euchromatin appears lighter than heterochromatin.[8]

Euchromatin is primarily regulated by post-translational modifications to its nucleosomes' histones, conducted by many histone-modifying enzymes. These modifications occur on the histones' N-terminal tails that protrude from the nucleosome structure, and are thought of to recruit enzymes to either keep the chromatin in its open form, as euchromatin, or in its closed form, as heterochromatin.[21] Histone acetylation, for instance, is typically associated with euchromatin structure, whereas histone methylation promotes heterochromatin remodeling.[22] Acetylation makes the histone group more negatively charged, which in turn disrupts its interactions with the DNA strand, essentially "opening" the strand for easier access.[21] Acetylation can occur on multiple lysine residues of a histone's N-terminal tail and in different histones of the same nucleosome, which is thought to further increase DNA accessibility for transcription factors.[21]

Phosphorylation of histones is another method by which euchromatin is regulated.[21] This tends to occur on the N-terminal tails of the histones, however some sites are present in the core.[21] Phosphorylation is controlled by kinases and phosphatases, which add and remove the phosphate groups respectively. This can occur at serine, threonine, or tyrosine residues present in euchromatin.[21][22] Since the phosphate groups added to the structure will incorporate a negative charge, it will promote the more relaxed "open" form, similar to acetylation.[22] In regards to functionality, histone phosphorylation is involved with gene expression, DNA damage repair, and chromatin remodeling.[22]

Another method of regulation that incorporates a negative charge, thereby favoring the "open" form, is ADP ribosylation.[22] This process adds one or more ADP-ribose units to the histone, and is involved in the DNA damage response pathway.[22]

• Histone Modifying Enzymes
• Constitutive Heterochromatin