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Discussion
In DNA packaging, there are three levels required to condense DNA into a eukaryotic chromosome.
1. The first level involves the packaging of DNA as a negative supercoil involving a positively charge
octamer of histone molecules, two each of histones H2a, H2b, H3, and H4 wrapping the DNA 1.65 times
which structurally forms into nucleosome and creating the appearance of “beads” on a string, to
produce the 11-nm-diameter interphase chromatin fiber.
2. The second level involves an additional supercoiling of the 11-nm nucleosome fiber in which Histone
H1 is involved, making its appearance even shorter, tighter, compact and thicker to produce the 30-nm
chromatin fiber. This packaging is usually in two forms: Solenoid 30 nm fiber and Zigzag 30 nm fiber.
3. Finally, the 30 nm fiber further coils and produces 300nm length loops. Nonhistone chromosomal
proteins form a scaffold that is involved in condensing the 30-nm chromatin fiber into the tightly packed
metaphase chromosomes. The 300-nm fibers are packed and folded to produce a 250-nm-wide fiber.
Tight helical coiling of the 250-nm fiber, in turn, produces the structure that appears in metaphase: a
pair of chromatids approximately 1400 nm in width.
In prokaryotic DNA packaging, supercoiling is one way to compress DNA into smaller spaces. The
overall process of DNA packaging is achieved through coiling, compacting, and supercoiling. The process
starts with the circular chromosomal DNA being compacted through the formation of loop structures
that are held in place by DNA binding protein. The formation of loop domains compacts the DNA about
tenfold. Further compaction is accomplished through a process known as super coiling. Furthermore,
DNA looping and supercoiling make the bacterial chromosome more compact so that it can fit within the
nucleoid of the bacterial cell.
1. Hippocrates: Brick and Mortar Theory