Appendix 4 • MHR 555
The cells in a multicellular organism fit into one
of two categories: somatic cells and germ cells.
Somatic cellsdivide by mitosis to make up the
specialized cells of the body that the organism
relies on for life processes. Somatic cells also
include stem cells that retain the ability to
develop into required specialized forms. The
mature body has several different kinds of stem
cells, each kind capable of forming a limited
number of specialized cells. In addition to these
cells, most multicellular organisms also have
germ cells— those cells that are set aside to
produce the next generation of organisms. Germ
cells include the specialized gametes (eggs and
sperm) formed by meiosis and the unspecialized
cells that produce them.
Part A: Somatic Cells
Cells follow a cell cycle of growth and division.
Unspecialized cells, like those found in the
early embryo, can divide rapidly. As cells begin
to specialize, some will specialize to the point
that they are terminally differentiated, and
are no longer able to divide. Terminally
differentiated cells are fully specialized and
unable to undergo further change. All of these
cells follow the cell cycle as outlined in Figure
A4.1. The cell cycle can be divided into the
two main phases of mitosis (division) and
interphase (growth and metabolism).
Interphase can be further divided into three
discrete phases: G 1 (Gap 1), S (Synthesis) and
G 2 (Gap 2). Cell activity varies through these
different phases. Cells rely on a system of timed
interactions among cell structures, and proteins
that control these interactions control the
sequence of events that lead towards cell
division. Some cells leave the cell cycle for G 0
(Gap 0) as quiescent postmitotic cells that are
metabolically active but do not grow or
continue along the cell cycle towards mitosis.
During the G 1 phase, the cell grows and there
is an increased level of protein synthesis and
DNA repair. Certain protein molecules act as
inhibitory factors that stop further progress and
keep a cell in G 1. Mutationsassociated with
some of these inhibitory factors can lead to
cancerous growth. Growth factors can induce
postmitotic or quiescent cells to move into G 1
to continue in the cell cycle. This is important
to stimulate tissue cells required to repair a
wound or activate immune system cells that are
required for an immune response. During the S
phase, DNA replicates to double the genome of
the cell. The centrosome, where microtubules
are created and co-ordinated, also duplicates in
preparation for mitosis. During the G 2 phase,
DNA replication stops and various protein
factors prepare the cell for mitosis, the M phase.
Figure A4.1The cell cycle. Cells in the cell cycle go
through G 1 (Gap 1), S (Synthesis), G 2 (Gap 2), and
M (Mitosis). A specialized cell may leave the cell cycle
for G 0 (Gap 0).
During the M phase, the cell goes through
visibly dramatic activity, as illustrated in
Figure A4.2 on page 556. During prophase,
the replicated DNA in the nucleus coils and
condenses to form distinct chromosomes.
Initially the chromosomes appear as single
threads, but later they appear as double threads
showing two chromatids. The centrosomes
separate to move away from each other and
form poles that will define the daughter cells.
In
te
rp
ah
es
G 1
G 0
G 2
S
growth and
repair
cell leaves the cell cycle
as a quiescent cell
replication
of DNA
synthesis of
proteins
time
M
ito
si
s
cytokinesis
telophase
anaphase
metaphase
prophase
4
APPENDIX
Cell Division