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General Biology Laboratory BIO 112
General Biology Laboratory BIO 112
Laboratory Study 4
Animal Development
Objectives
Introduction
Fertilization cannot be completed until the egg undergoes the divisions of meiosis
which reduce the chromosomes in the nucleus to one set (1N). Meiosis results in one
copy of each gene, on one chromosome from each homologous pair, in the mature egg.
The mature egg is a haploid cell. The meiosis that yields a mature egg involves unequal
divisions of cytoplasm, in both divisions, so the cell that becomes the egg gets the
majority of the cytoplasm. The other three cells that get only enough cytoplasm to
surround their nucleus are called polar bodies. The polar bodies soon die and the one
large remaining cell, the mature egg, is called an ovum.
The more motile gamete is the sperm (spermatozoan) and the male is defined by
the production of these gametes. Sperms also arise from mitotically multiplying dipoid
primordial germ cells. However, these cells do not grow and proceed directly to meiosis.
Meiosis reduces the chromosomes to one set in each of the four product cells, and the
cytoplasmic divisions are equal between all four cells. The haploid products of meiosis
in the male differentiate by producing structures needed to move them to and into an
ovum. These differentiated motile cells are called spermatozoa. In some species,
including humans, the differentiated spermatozoa has a head region containing the
nucleus and structures for penetrating the ovum, a mid-piece region that carries the
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General Biology Laboratory BIO 112 Morehouse College
machinery to transform chemical energy to kinetic energy, and a tail region that has a
flagellar structure for propulsion. In many species, this differentiation of spermatozoa
does not occur and even amoeboid sperms are possible.
Fertilization is the process in which the egg and sperm unite to form a zygote and
the haploid nuclei of each gamete contributes one set of chromosomes to make a dipoid
nucleus. The zygote undergoes mitotic divisions, cleavages, and the resulting
multicellular embryo undergoes a series of developmental events. Development consists
of three processes: differentiation, growth and translocation.
Growth is an increase in mass or volume resulting from cell division and cell
expansion. If molecules simply increase in number, the cell volume must increase and
the cell grows (expands). If molecules accumulate in a defined part of the cell, this
accumulation may change the characteristics of the cell. Thus, growth at one level of
organization (molecular) can result in differentiation at another level of organization
(cellular). Can you think of an example of growth at the cellular level that results in
differentiation at the tissue or organ level?
The fertilized egg, the zygote, and its daughter cells (blastomeres) undergo
repeated mitotic divisions and pass on to each generation of blastomeres an exact copy of
their entire genetic material. However, these blastomeres also receive different portions
of the cytoplasmic constituents which were compartmentalized during the growth of the
unfertilized ovum. Carrying identical genetic information, but differing in the
composition of their cytoplasm and being in different locations in an embryo results in
the blastomeres undergoing developmental changes. Different location in an embryo
results in different levels of access to nutrients and gas exchange which can influence
developmental processes. Cells become specialized to ultimately become, for example,
liver cells, nerve cells or muscle cell. Each specialized cell has a specific function and a
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General Biology Laboratory BIO 112 Morehouse College
complement of proteins and other molecules necessary for that specialized role. This
dynamic and complicated process is ultimately described in the “blueprint” information
in the DNA of the zygote. However, the expression of the DNA “blueprint” is regulated
by the environment, which includes the macromolecules received from the female parent
when the ovum was produced. The macromolecules present in the ovum are determined
by the genotype of the female parent and the environment in which the ovum was
produced. Developmental events occur in a predetermined sequence that build and are
influenced by those that preceed them. The control of developmental processes, and
ultimately the control of gene expression, is a subject of continuing intense research.
Understanding the control of gene expression is not only the key to understanding
development but also applies to the studies of cancer and molecular genetic technology.
Development can be divided into stages whose major events are described below.
These stages apply to all animals.
Fertilization: This is the fusion (uniting = syngamy) between an ovum and one
spermatozoan which occurs in two steps, egg activation and nuclear fusion (karyogamy).
Activation begins when the sperm penetrates the plasma membrane of the ovum.
Activation initiates many changes in the ovum such as an increase in metabolic rate, an
alteration in the permeability of the plasma membrane, and the lifting of the fertilization
membranes. Activation is followed by karyogamy to form the diploid zygote nucleus.
Depending on the species, sperm penetration of the egg plasma membrane and the
initiation of activation, precedes (and triggers) the first (in Ascaris round worms) or the
second (in frogs and humans) meiotic divisions. Karyogamy cannot occur until meiosis
is completed so there is always some delay between activation and karyogamy.
Cleavage: This is the stage during which mitotic divisions of the zygote produce a clone
of cells (blastomeres) which package the heterogeneous cytoplasm of the ovum in
separate cells each containing the same DNA information. Cleavage begins shortly after
fertilization and no increase in mass (or volume) occurs although the cell number
increases. The pattern of cleavage is influenced by the amount and distribution of yolk in
the ovum. Yolk is protein and lipid rich material in a mature ovum that is stored food for
the developing embryo. When large quantities of yolk are present in a zygote,
cytokinesis may not involve the entire zygote cytoplasm (incomplete cleavage).
Alternatively, if little yolk is present, cytokinesis involves the entire cytoplasm of the
zygote (complete cleavage).
Egg Types
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General Biology Laboratory BIO 112 Morehouse College
Telolecithal: Yolk is concentrated at one end of the ovum, near the vegetal
hemisphere (the region that becomes the ventral side of the animal). The nucleus
of the zygote is located in the animal hemisphere. The vegetal hemisphere region
is incorporated into the gut of the embryo while the embryo proper develops from
cells in the animal hemisphere. Depending on the amount of yolk, cleavage is
complete (frogs) or incomplete (birds). Incomplete cleavage results in the yolk
filled portion of the egg not being divided in cleavage cells (blastomeres).
Types of Cleavage
The precise form of early cleavage divisions is not the same in all animals.
Systematic variation occurs in the first division of the zygote, whether the first two cells
of the embryo are equal or unequal in size, and the relative positions of blastomeres
produced in successive cell divisions. There are two major patterns in the relative
positions of blastomeres, spiral cleavage (in protosomes) and radial cleavage (in
deuterostomes).
Spiral cleavage results in new blastomeres produced in the third cell division
(going from a 4-cell to an 8-cell embryo) positioned in the cleavage furrows of the
previously existing four cells located beneath them. If cleavage is complete, the first
division in spiral cleavage is unequal, producing one larger and one smaller cell. In
radial cleavage, new blastomeres are from the third mitotic division are positioned
directly above the previously existing four cells located beneath them. If cleavage is
complete, the first division in radial cleavage produces two cells of equal volume.
Blastulation: This is the process in which a ball of cells produced by the early cleavage
divisions is transformed to a sphere (sea urchin, human, frog) or sheet (birds) called a
blastula with a central (sphere) or underlying (sheet) cavity called a blastocoel.
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General Biology Laboratory BIO 112 Morehouse College
mesoderm, and the inner endoderm. All future organs develop from these three germ
layers. The ectoderm is the source of structures that have the most direct contact the with
external environment (skin, nervous system). Muscles, bone, and blood are all derived of
mesoderm, and digestive structures are all derived of the endoderm. The site of the
blastopore is the location of the mouth in organisms with spiral cleavage. Animals with
spiral cleavage are protostomes (first mouth). The site of the blastopore is the location of
the anus in animals with radial cleavage and the mouth forms at the opposite end of the
embryo. Animals with radial cleavage are deuterostomes (second mouth).
You will be performing sea urchin fertilizations under the microscope so you can
observed the fertilization process first-hand and see the first few cleavages occur.
Prepared slides and preserved embryos of will be available to observe and compare the
developmental stages in mollusks (protostomes), as well as sea urchins, frogs, and birds
(deuterostomes). Bring your lecture textbook to your laboratory class.
Acknowledgements
This study was reprinted with revision from H. Ikuma, P. Harley and C. Yocum (1985) Animal
Development, in Biology 105 Course Pack, Division of Biological Sciences, University of Michigan, Ann
Arbor. Revisions made 2/2005 by L. Blumer