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The precise structure of the chromatin fiber in the cell is not known in detail. [10] This level of chromatin structure is thought to be the form of heterochromatin, which contains mostly transcriptionally silent genes. Electron microscopy studies have demonstrated that the 30 nm fiber is highly dynamic such that it unfolds into a 10 nm fiber ...
Each subunit in the MCM structure contains two large N- and C-terminal domains. The N-terminal domain consists of three small sub-domains and appears to be used mainly for structural organization. [28] [1] The N-domain can coordinate with a neighboring subunit's C-terminal AAA+ helicase domain through a long and conserved loop.
The concentration and specific composition of histones used can determine local chromatin structure. For example, euchromatin is a form of chromatin with low nucleosome concentration - here, the DNA is exposed, promoting interactions with gene expression, replication, and organizational machinery.
The solenoid structure can increase this to be 40 times smaller. [2] When DNA is compacted into the solenoid structure can still be transcriptionally active in certain areas. [7] It is the secondary chromatin structure that is important for this transcriptional repression as in vivo active genes are assembled in large tertiary chromatin ...
Basic units of chromatin structure. Histone H2B is a structural protein that helps organize eukaryotic DNA. [5] It plays an important role in the biology of the nucleus where it is involved in the packaging and maintaining of chromosomes, [5] regulation of transcription, and replication and repair of DNA. [2]
The four H3 and H4 subunits form a tightly packed tetramer that associates with two H2A/H2B dimers to form each octamer. About 147 bp of DNA is wrapped around the octamer to form a nucleosome. Nucleosomes can be arrayed in the loosely packed beads-on-a-string form of chromatin, but are generally more tightly packaged into the 30-nm fiber.
Suggested by the idea that the structure of chromatin can be modified to allow or deny access of transcription activators, regulatory functions of histone acetylation and deacetylation can have implications with genes that cause other diseases. Studies on histone modifications may reveal many novel therapeutic targets.
S/MAR-functions: constitutive and facultative. A chromatin domain with constitutive S/MARs at its termini (I). When functional demands require the specific translocation of the constituent gene to the matrix, facultative S/MARs responds to topological changes which are initiated by the association of transcription factors (TF) and supported by histone acetylation.