Before discussing the
steps a cell must undertake to replicate, a deeper understanding of the
structure and function of a cell’s
genetic information is necessary. A
cell’s DNA, packaged as a
double-stranded DNA molecule, is called its genome. In prokaryotes, the genome is composed of a single,
double-stranded DNA molecule in the form of a loop or circle (Figure 1.). The region in the cell containing this genetic
material is called a nucleoid. Some prokaryotes also have smaller loops of DNA called plasmids
that are not essential for normal growth.
Bacteria can exchange
these plasmids with other bacteria, sometimes receiving beneficial
new genes that the recipient can add to their chromosomal DNA. Antibiotic
resistance is one trait that often
spreads through a bacterial colony
through plasmid exchange.
Figure
1. Prokaryotes, including bacteria and
archaea, have
a single, circular chromosome located in
a central region called the nucleoid.
In eukaryotes, the genome
consists of several double-stranded linear DNA molecules (Figure 2.). Each species of eukaryotes has a
characteristic number of chromosomes in the nuclei of its cells. Human body
cells have 46 chromosomes, while human gametes
(sperm or eggs) have 23 chromosomes each. A typical body cell, or somatic
cell, contains two matched sets of chromosomes, a configuration known as diploid. The letter n is used to represent a single set of
chromosomes; therefore, a diploid organism
is designated 2n. Human cells that
contain one set of chromosomes are called gametes, or sex cells; these are eggs and sperm, and are designated 1n,
or haploid.
Figure
2. There are 23 pairs
of homologous chromosomes in a female human
somatic cell. The condensed chromosomes are viewed within the nucleus (top), removed from a cell in mitosis and spread out
on a slide (right),
and artificially arranged according
to length (left); an arrangement like this is called a karyotype. In this image,
the chromosomes were exposed to fluorescent
stains for differentiation
of the different
chromosomes. A method of staining called “chromosome painting” employs fluorescent dyes
that highlight
chromosomes in different colors.
(credit: National Human Genome Project/NIH)
Matched pairs of
chromosomes in a diploid organism
are called homologous (“same
knowledge”) chromosomes. Homologous chromosomes are the same length and
have specific nucleotide segments called genes
in exactly the same location, or locus.
Genes, the functional units of chromosomes, determine specific characteristics
by coding for specific proteins. Traits
are the variations of those characteristics. For example, hair color is a
characteristic with traits that are blonde, brown, or black.
Each copy of a homologous pair of chromosomes originates from a different
parent; therefore, the genes themselves are not identical. The variation of individuals within a species
is due to the specific combination of the genes inherited from both parents.
Even a slightly altered sequence of nucleotides within a gene can result in an
alternative trait. For example, there are three possible gene sequences on the
human chromosome that code for blood type: sequence A, sequence B, and sequence O. Because all diploid human cells have two copies of the chromosome that determines blood type, the blood type (the trait) is determined by which
two versions of the marker gene are inherited. It is possible to have two
copies of the same gene sequence on both homologous chromosomes, with one on
each (for example, AA, BB, or OO), or two different
sequences, such as AB.
Minor variations of traits, such as blood type, eye color, and handedness, contribute to the natural variation
found within a species. However, if the entire DNA sequence from any pair
of human homologous chromosomes is compared, the difference is less than one percent. The sex chromosomes, X and Y, are the single exception to the rule of
homologous chromosome uniformity: Other than a small amount of homology
that is necessary to accurately produce gametes, the genes
found on the X and Y chromosomes are
different.
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