Biology 102 - General Biology
Cell Division
Meiosis and Sexual Reproduction

There is a special kind of cell division that occurs exclusively in the
gonads (ovaries and testes) of eukaryotic organisms. This special cell
division is called meiosis. In the ovary it is referred to as oögenesis
and in the testes as spermatogenesis. Meiosis produces the gametes called
eggs (ovum, sing., ova, plural) and sperm. It involves two cell divisions
and therefore four cells result from each meiotic event. The primary oöcytes
and spermatocytes are originally produced by mitosis but then enter Meiosis
I followed by Meiosis II.
In human (and other mammalian) females, oögenesis begins during
fetal development and is arrested in the Metaphase I until the time of
ovulation. Fertilization triggers the completion of Meiosis II in the
oöcyte. Ovulation ends with menopause. In human (and other mammalian)
males, spermatogenesis begins with sexual maturity (puberty) and does
not stop. Chromosome errors are more common in the egg as the female gets
older and gene mutations are more common in the sperm as the male gets
older.
Chromosome errors increase with increasing maternal age
The purpose of meiosis is to produce haploid (1n) gametes. Another purpose
is to recombine genes from the parents of the individual in whom meiosis
is occurring. Both the reduction of the chromosome number from 2n to 1n
and the recombination of genes is accomplished in an amazingly simple
way. After the DNA is replicated in the S phase preceding meiosis, the
homologous chromosomes (each composed of two chromatids) pair up in Prophase
I and then crossing over, breakage and reunion occurs between the two
homologs thereby ensuring recombination of genes between the two homologs.
At Metaphase I of meiosis, the homologous chromosomes (each still composed
of two chromatids) line up on the metaphase plate. Therefore, in meiosis,
the chromosomes must "go to the (meiosis) dance" with a partner. You may
recall that in mitosis, the homologous chromosomes do not pair up with
their homolog and that they each "go to the (mitosis) dance" alone. The
pairing of homologous chromosomes in meiosis assures that the resulting
gametes have a wide variety of gene combinations and that they receive
only one member of each pair of chromosomes. The new combinations of genes
are due both to the crossing over, breakage and reunion between the homologs
and the random assortment of maternal and paternal homologs along the
metaphase plate. The pairing up of homologs is what also assures that
in meiosis there will be a reduction of the number of chromosomes from
2n to 1n, with one member of each homologous pair in the gamete.
The homologous chromosomes must pair up gene for gene. Each homolog has
already duplicated and is composed of two chromatids. The chromatids crossover,
break and rejoin. At least one crossing over event per chromosome arm
is obligatory for successful meiosis. Thus the resulting chromatids (soon
to be chromosomes) contain genes from both the parents (of the individual
who is making the gamete). Each chromosome in the gamete will then contain
a new arrangement of genes with some from each parent homolog. Another
source of variation is provided since we have two parents who contribute
different genes to the offspring. Sex is any mechanism which results in
the recombination of genes to provide variation in the offspring. The
new combinations of genes in the offspring may prove to be more successful.
At Metaphase I the pairing brings the centromeres of the paired homologs
to the metaphase plate in the center of the cell where the homologs separate
(still composed of two chromatids) during Anaphase I. Telophase I is short
and results in the formation of two cells each with one member of each
homologous pair and still composed of two chromatids. There is no DNA
replication after Telophase I prior to Prophase II.
Meiosis II resembles mitosis because it is here that the chromatids separate.
In Metaphase II the chromosomes, each composed of two chromatids, line
up in the center of the spindle and in Anaphase II, the two chromatids
separate. In Telophase II, cytokinesis gives rise to two cells from each
of the two cells resulting from Meiosis I for a total of four cells from
the original cell. In spermatogenesis, all four resulting cells form functional
spermatocytes. In the female, in oögenesis, only one of the four
becomes the functional oocyte. The other three cells are called polar
bodies and are discarded.
Sperm and eggs from the same species have the same number of chromosomes.
However, the sperm is specialized for motility and has a nucleus to hold
the chromosomes but has almost no cytoplasm. It is equipped with a flagellum
(cilia in some organisms) and mitochondria to provide energy for the motility.
The egg, on the other hand, accumulates an unusually large amount of cytoplasm
which is filled with ribosomes, mitochondria, and nutrients (yolk) to
provide sufficient nutrients during cleavage of the zygote to form the
embryo. The fertilized egg is called the zygote. The zygote undergoes
mitosis known as cleavage to form the embryo. There is no growth until
later.
To emphasize the importance of pairing of homologous chromosomes for
the success of meiosis, we will learn about two instances when meiosis
fails. Mules are interspecies hybrids from a horse mother and donkey father.
(A hinny is the result of the opposite cross.) The diploid number in the
horse is 64 (2n=64) and the diploid number in the donkey is 62 (2n=62)
The fertilization of the horse egg (n=32) by the donkey sperm (n=31) gives
rise to a zygote with 63 chromosomes which successfully undergoes mitosis
to form the mule. During mitosis, there is no need for homologous chromosomes,
however, when meiosis is attempted in the mule gonad, there is a need
for homologous chromosomes to pair up. The horse and donkey chromosomes
are not homologous, nor are there an even number of chromosomes so pairing
cannot occur. Therefore meiosis is unsuccessful and the mule is sterile.
Another example concerns the "seedless" watermelon. Since plants, unlike
animals, do not mind having extra sets of chromosomes tetraploid (4n)
watermelons can easily be created. There are diploid (2n=22); triploid
(3n=33), and tetraploid (4n=44) watermelons. When the tetraploid plant
(4n =44) undergoes meiosis, it makes gametes with a diploid number, of
chromosomes (2n=22). An ordinary watermelon is 2n=22 and makes gametes
which are n=11. If you cross a 4n, tetraploid watermelon with a 2n, diploid
watermelon, you will get a 3n, triploid watermelon. The 2n egg (or sperm)
combines with a 1n sperm (or egg) and a 3n zygote is formed which divides
by mitosis to form a 3n, triploid watermelon. All is well until the 3n,
triploid watermelon attempts meiosis. Since there is more than a pair
of homologous chromosomes the required pairing and recombination cannot
occur, and, therefore, meiosis fails. The 3n, triploid watermelon thus
fails to form viable seeds. Instead it produces small rudimentary, white,
infertile seeds and the watermelon is referred to as seedless.
Comparisons between mitosis and meiosis
Homologous chromosomes pair up in meiosis but not in mitosis
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