From DNA to Chromosome:
In a non-dividing eukaryotic cell, hereditary genetic material exists as an uncoiled, diffuse, entangled fibrous network called chromatin. During prophase of cell division, chromatin fibers undergo progressive dehydration, supercoiling, and condensation to form discrete, microscopically visible rod-like structures called chromosomes.
Chemical Composition of Chromatin:
- DNA (Deoxyribonucleic Acid): Approximately $40\%$. The macromolecular repository of genetic instructions consisting of two antiparallel polynucleotide strands twisted into a right-handed double helix (Watson-Crick model, 1953). Each nucleotide consists of: (i) a phosphate group, (ii) a deoxyribose sugar, and (iii) one of four nitrogenous bases: Adenine ($A$), Thymine ($T$), Guanine ($G$), or Cytosine ($C$). Base pairing rule: $A = T$ (two hydrogen bonds) and $G \equiv C$ (three hydrogen bonds).
- Histone Proteins: Approximately $60\%$. Basic, positively charged proteins rich in lysine and arginine residues. Eight histone molecules ($2\text{ each of } H_2A, H_2B, H_3, H_4$) aggregate to form a core histone octamer.
- The Nucleosome Unit: A core of 8 histone proteins wrapped around by approximately $146$ base pairs of double-stranded DNA in $1.65$ superhelical turns is called a nucleosome ('beads-on-a-string' structure). Nucleosomes coil further to form a $30\text{ nm}$ solenoid fiber, which loops around non-histone scaffold proteins to form the condensed metaphase chromosome!
Chromosome Morphology:
A duplicated metaphase chromosome consists of two identical longitudinal halves called sister chromatids, joined at a primary constriction point called the centromere (kinetochore). The centromere serves as the attachment site for mitotic spindle fibers during cell division.