Significance of Chromosomal Behaviour during Cell Division

Running head: GENETICS AND GENETIC ENGINEERING
GENETICS AND GENETIC ENGINEERING
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1GENETICS AND GENETIC ENGINEERING
Significance of chromosomal behaviour during cell division
Chromosomes can be defined as the DNA containing molecule which is responsible
for transmitting the heredity information over generations. It should be noted in this context
in eukaryotic organisms, the DNA is packaged with proteins within the nucleus. The structure
of the chromosome varies in appearance at different phases of the cell cycle. The
chromosomes condense and become significantly visible by light microscopy on entering the
cell division phase of mitosis or meiosis. During the interphase which is marked by the
combination of the G1, S and G2 phase, the chromosomes are de-condensed either partially
or fully and form chromatin which essentially constitutes a DNA wrapped around the histone
proteins (Okhura 2015). The chromosome is a single chromatid in the G1 phase. The S phase
marks DNA replication and in the G2 phase the cell enters into the early prophase stage. This
phase is marked by the presence of two sister chromatids containing the DNA joined at the
centromere. In the next stage the chromosomes line up at the centre of the cell and are held in
position by the spindle fibres. The anaphase marks the separation of the chromatids from the
sister chromatids. The separated chromatids are pulled at the opposite poles by the spindle
apparatus. The telophase marks the formation of the chromatid cluster at the opposite poles of
the cell. The chromatids gradually begin to condense and the final stage of cytokinesis
divides the cell into two daughter cells. Meiosis on the other hand comprises of the pairing up
of the homologous chromosomes side by side, which is referred to as synapsis in the
Prophase I step. The next step includes the separation of the homologous chromosomes
leading to the creation of haploid (n) cell. It is here that the law of segregation comes into
picture. This means that the separation of the pair of homologous chromosomes occur
independent of one another. This further explains the law of independent assortment which
states that the homologous chromosomes can acquire any possible combination from the

2GENETICS AND GENETIC ENGINEERING
maternal and paternal chromosomes. It should be acknowledged here that the Law of
segregation as well as the Law of Independent Assortment form the basis of the Mendelian
Genetics. Also, the first division only occurs after the daughter becomes genetically haploid.
This can be explained with the help of an example. Considering the cell division of the X and
Y chromosome, it can be said that two chromosomes pair up during the Prophase I and
separate after the first cell division. So after the first meiotic division, the cells wither contain
the X or the Y chromosome, it does not contain both and hence it is equivalent to a haploid
cell. After the meiosis I, the homologous chromosome segregate into different cells and each
of the homologues has a single copy of a gene. Also, each gene contains two different alleles
which would at this time be present in two separate cells. The cells comprise of duplicated
chromosomes but a single allele. The second meiotic division marks the separation of the
duplicated chromatids into 4 new haploid gametes. The division is similar to mitosis but it
should be understood that the end result comprises of the formation of cells with a single set
of homologous chromosome.