Our
genes are made of deoxyribonucleic acid (DNA). This remarkable molecule
contains all the information necessary to make a cell and DNA is able to pass
on this information when a cell divides.
In 1953 Watson and Crick proposed a
structure for DNA.
Watson and Crick’s conclusions :
1. The DNA structure is a
right-handed double helix.
2. The diameter of the helix of
DNA is 20A.
3. The length of each nucleotide
is 3.4A ; the helix contais ten nucleotides on a loop.
4. DNA consists of two strands,
which are antiparallel. Strands have a 5’ head and a 3’ tail.
5. The hereditary information is
encoded in DNA in a specific sequence of bases along the polynucleotide chain.
6. The base pairs are held
together by hydrogen bonds. These are two H-bonds between A and T and three
H-bonds between G and C.
7. The base pairs are located
inside the double helix, and sugar-phosphate backbone is located outside.
8. The polynucleotide chains have
the same hereditary information.
Each nucleotide consists of three major parts :
- a five-carbon sugar (pentose) ;
- a
flat,heterocyclic,nitrogen-containing organic base ;
- a negatively charged phosphate
group,which gives the polymer acidic property
The organic bases are two general types
: single-ringed pyrimidines and double-ringed purines. The purines are adenine
(A) and guanine (G). The pyrimidines are cytosine (C), thymine (T), and uracil
(U).
Since A always pairs with T, G always
pairs with C.
Chargaff”s rule
The purine : pyrimidine in double
stranded DNA is always 1.
Levels of DNA package are :
- Nucleosome
structure (Nucleosomes are the fundamental units of chromatin. The histones
form a disk-shaped complex called a nucleosome, which contains two complete
turns of double-stranded DNA wrapped around its surface, histones core has 8
proteins – two copies each of the H2A/H2B and H/H4 complexes)
- The
30 nm fibre (It is higher order chromatin organization. Histone H1 binds
between nucleosomes to give even more structure to chromatin. At higher ionic
strength or in the presence of Mg2+ nucleosome structure becomes more compact
and produces a fibre of about 30 nm in diameter. “The string” is called the 30
nm fibre.)
- Chromatin
loops : the 30 nm fibre is attached at various points to the nuclear matrix
to form a series of loops, containing 30-100 kbp of DNA (the folded fibre
model). By adding twists to make these nucleosome and solenoid structure, the
DNA is supercoiled. This structure with loops is called “lampbrush chromosome”.
-
Interphase chromatin (Chromatin loops are more coiled and form interphase
chromatin). During interphase (the period of the cell cycle where the cell is
not dividing), two types of chromatin can be distinguished :
a) Euchomatin, which consists of DNA
that is active,e.g., being expressed as protein.
b) Heterochromatin, which consists of
mostly inactive DNA. Heterochromatin can be
further distinguished into two
types :
1) Constitutive heterochromatin, which
is never expressed. It is located around
the centromere and usually contains
repetitive sequences.
2) Facultative heterochromatin, which is
sometimes expressed.
Individual chromosomes cannot be distinguished at this
stage – they appear
in the nucleus as a homogeneous tangled mix ofg DNA and
protein.
- Metaphase
chromosomes are higly condensed, duplicated chromosome of dividing cell. In
the early stages of mitosis or meiosis (cell division), the chromatin strands
become more and more condensed. They cease to function as accessible genetic
material (transcription stops) and become a compact transportable form. This
compact forms makes the individual chromosomes visible, and they form the
classic four arm structure, a pair of sister chromatids attached to each other
at the centromere. The shorter arms are called p arms (from the Fench
petit,small) and the longer arms are called q arms (q follows p in the Latin
alphabet; q-g “grande”). This is the only natural context in which individual
chromosomes are visible with an optical microscope.
Rujukan1. E.S. Klinstova,General Biology Part 1 Cell cycle and Molecular genetics, Publishing House of NNSMA, 2012
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