Meiosis

For the article on the figure of speech, see meiosis (figure of speech). In biology, meiosis is the process that transforms one diploid cell into four haploid cells in eukaryotes in order to redistribute the diploid's cell's genome.

Meiosis forms the basis of sexual reproduction and can only occur in eukaryotes. In meiosis, the diploid cell's genome, which is composed of ordered structures of coiled DNA called chromosomes, is replicated once and separated twice, producing four sets of haploid cells each containing half of the original cell's chromosomes. These resultant haploid cells will fertilize with other haploid cells of the opposite gender to form a diploid cell again. The cyclical process of separation by meiosis and genetic recombination through fertilization is called the life cycle. The result is that the offspring produced during germination after meiosis will have a slightly different blueprint which has instructions for the cells to work, contained in the DNA. This allows sexual reproduction to occur.

Biochemically, meiosis uses many similar processes mitosis uses in order to manipulate the redistribution of chromosomes, but with a vastly different outcome.

History

Meiosis was discovered and described for the first time in sea urchin eggs in 1876, by noted German biologist Oscar Hertwig (1849-1922). It was described again in 1883, at the level of chromosomes, by Belgian zoologist Edouard Van Beneden (1846-1910), in Ascaris worms' eggs. The significance of meiosis for reproduction and inheritance, however, was described only in 1890 by German biologist August Weismann (1834-1914), who noted that two cell divisions were necessary to transform one diploid cell into four haploid cells if the number of chromosomes had to be maintained. In 1911 the American geneticist Thomas Hunt Morgan (1866-1945) observed cross-over in Drosophila melanogaster meiosis and provided the first true genetic interpretation of meiosis.

Occurrence of meiosis in eukaryotic life cycles

Meiosis occurs in all eukaryotic life cycles involving sexual reproduction, comprising of the constant cyclical process of meiosis and fertilization. This takes place alongside normal mitotic cell division. In multicellular organisms, there is an intermediary step between the diploid and haploid transition where the organism grows. The organism will then produce the germ cells that continue in the life cycle. The rest of the cells, called somatic cells, function within the organism and will die with it.

The organism phase of the life cycle can occur between the haploid to diploid transition or the diploid to haploid transition. Some species are diploid, grown from a diploid cell called the zygote. Others are haploid instead, spawned by the proliferation and differentiation of a single haploid cell called the gamete. Humans, for example, are diploid creatures. Human stem cells undergo meiosis to create haploid gametes, which are sperm cells for males or ova for females. These gametes then fertilize in the uterus of the female, producing a diploid zygote. The zygote undergoes progressive stages of mitosis and differentiation to create an embryo, the early stage of human life.

There are three types of life cycles that utilise sexual reproduction, differentiated by the location of the organisms stage.

In the gametic life cycle, of which humans are a part, the living organism is diploid in nature. Here, we will generalize the example of human reproduction stated previously. The organism's diploid germ-line stem cells undergo meiosis to create haploid gametes, which fertilize to form the zygote. The diploid zygote undergoes repeated cellular division by mitosis to grow into the organism. Mitosis is a related process to meiosis that creates two cells that are genetically identical to the parent cell. The general principle is that mitosis creates somatic cells and meiosis creates germ cells.

In the zygotic life cycle, the living organism is haploid. Two organisms of opposing gender contribute their haploid germ cells to form a diploid zygote. The zygote undergoes meiosis immediately, creating four haploid cells. These cells undergo mitosis to create the organism. Many fungi and many protozoa are members of the zygotic life cycle.

Finally, in the sporic life cycle, the living organism alternates between haploid and diploid states. Consequently, this cycle is also known as the alternation of generations. The diploid organism's germ-line cells undergo meiosis to produce gametes. The gametes proliferate by mitosis, growing into a haploid organism. The haploid organism's germ cells then combine with another haploid organism's cells, creating the zygote. The zygote undergoes repeated mitosis and differentiation to become the diploid organism again. The sporic life cycle can be considered a fusion of the gametic and zygotic life cycles, and indeed its diagram supports this conclusion.

Process

Because meiosis is a "one-way" process, it cannot be said to engage in a cell cycle that mitosis does. However, the preparatory steps that lead up to meiosis are identical in pattern and name to the interphase of the mitotic cell cycle.

Interphase is divided into three phases:

Growth 1 (G₁) phase: Characterized by increasing cell size from accelerated manufacture of organelles, proteins, and other cellular matter.
Synthesis (S) phase: The genetic material is replicated.
Growth 2 (G₂) phase: The cell continues to grow.

It is immediately followed by meiosis I, which divides one diploid cell into two haploid cells by the separation of homologous chromosomes, and meiosis II, which divides two haploid cells into four haploid cells by the separation of sister chromatids. Meiosis I and II are both divided into prophase, metaphase, anaphase, and telophase subphases, similar in purpose to their analogous subphases in the mitotic cell cycle. Therefore, meiosis encompasses the interphase (G₁, S, G₂), meiosis I (prophase I, metaphase I, anaphase I, telophase I), and meiosis II (prophase II, metaphase II, anaphase II, telophase II).

Meiosis I

Prophase I

In the prophase stage, the cell's genetic material, which is normally in a loosely arranged pile known as chromatin, condenses into visible threadlike structures. Along the thread, centromeres are visible as small beads of tightly coiled chromatin. Recall that centromeres are connection sites between sister chromatids, which are not yet distinguishable. As the chromatin becomes progressively ordered and visible, homologous chromosomes find each other and bind together. In this process, called synapsis, a protein structure called the synaptonemal complex attaches the homologous chromosomes tightly together all along their lengths.

The zygotene stage sees the completion of synapsis. The combined homologous chromosomes are said to be bivalent, a reference to the two homologous chromosomes. They may also be referred to as a tetrad, a reference to the four sister chromatids. During this stage, one percent of DNA that wasn't replicated during S phase is replicated. The significance of this cleanup act is unclear.

The pachytene stage heralds crossing over. Nonsister chromatids of homologous chromosomes exchange segments of genetic information. Because the chromosomes cannot be distinguished in the synaptonemal complex, the actual act of crossing over is not perceivable through the microscope. n.m .,m . .

During the diplotene stage, the synaptonemal complex degrades. Homologous chromosomes fall apart and begin to repel each other. The chromosomes themselves uncoil a bit, allowing some transcription of DNA. They are held together by virtue of recombination nodules, betraying the sites of previous crossing over, the chiasmata.

Chromosomes recondense during the diakinesis stage. Sites of crossing over entangle together, effectively overlapping, making chismata clearly visible. In general, every chromosome will have crossed over at least once. The nucleoli disappears and the nuclear membrane disintegrates into vesicles.

During these stages, centrioles are migrating to the two poles of the cell. These centrioles, which were duplicated during interphase, function as microtubule coordinating centers. Centrioles sprout microtubules, essentially cellular ropes and poles, during crossing over. They invade the nuclear membrane after it disintegrates, attaching to the chromosomes at the kinetochore. The kinetochore functions as a motor, pulling the chromosome along the attached microtubule toward the originating centriole, like a train on a track. There are two kinetochores on each tetrad, one for each centrosome. Prophase I is the longest phase in meiosis.

Microtubules that attach to the kinetochores are known as kinetochore microtubules. Other microtubules will interact with microtubules from the opposite centriole. These are called nonkinetochore microtubules.

Metaphase I

As kinetochore microtubules from both centrioles attach to their respective kinetochores, the homologous chromosomes align equidistant above and below an imaginary equatorial plane, due to continuous counterbalancing forces exerted by the two kinetochores of the bivalent. Because of independent assortment, the orientation of the bivalent along the plane is random. Maternal or paternal homologues may point to either pole.

Anaphase I

Kinetochore microtubules shorten, severing the recombination nodules and pulling homologous chromosomes apart. Since each chromosome only has one kinetochore, whole chromosomes are pulled toward opposing poles, forming two haploid sets. Each chromosome still contains a pair of sister chromatids. Nonkinetochore microtubules lengthen, pushing the centrioles further apart. The cell elongates in preparation for division down the middle.

Telophase I

The first meiotic division effectively ends when the centromeres arrive at the poles. Each daughter cell now has half the number of chromosomes but each chromosome consists of a pair of chromatids. The microtubules that make up the spindle network disappear, and a new nuclear membrane surrounds each haploid set. The chromosomes uncoil back into chromatin. Cytokinesis, the pinching of the cell membrane in animal cells or the formation of the cell wall in plant cells, occurs, completing the creation of two daughter cells.

Cells enter a period of rest known as interkinesis or interphase II. No DNA replication occurs during this stage. Note that many plants skip telophase I and interphase II, going immediately into prophase II.

Meiosis II

Prophase II takes an inversely proportional time compared to telophase I. In this prophase we see the disappearance of the nucleoli and the nuclear envelope again as well as the shortening and thickening of the chromatids. Centrioles move to the polar regions and are arranged by spindle fibres. The new equatorial plane is rotated by 90 degrees when compared to meiosis I, perpendicular to the previous plane.

In metaphase II, the centromeres contain two kinetochores, organizing fibers from the centrosomes on each side. This is followed by anaphase II, where the centromeres are cleaved, allowing the kinetochores to pull the sister chromatids apart. The sister chromatids by convention are now called sister chromosomes, and they are pulled toward opposing poles.

The process ends with telophase II, which is similar to telophase I, marked by uncoiling, lengthening, and disappearance of the chromosomes occur as the disappearance of the microtubules. Nuclear envelopes reform; cleavage or cell wall formation eventually produces a total of four daughter cells, each with an haploid set of chromosomes. Meiosis is complete.

Significance of meiosis

Meiosis facilitates stable sexual reproduction. Without the halving of ploidy, or chromosome count, fertilization would result in zygotes that have twice the number of chromosomes than the zygotes from the previous generation. Successive generations would have an exponential increase in chromosome count, resulting in an unwieldy genome that would cripple the reproductive fitness of the species. Polyploidy, the state of having three or more sets of chromosomes, also results in developmental abnormalities or lethality.

Most importantly, however, meiosis produces genetic variety in gametes that propagate to offspring. Recombination and independent assortment allow for a greater diversity of genotypes in the population. A system of creating diversity (meiosis) allows a species to maintain stability under environmental change.

Nondisjunction

The normal separation of chromosomes in Meiosis I or sister chromatids in meiosis II is termed disjunction. When the separation is not normal, it is called nondisjunction. This results in the production of gametes which have either more or less of the usual amount of genetic material, and is a common mechanism for trisomy or monosomy. Nondisjunction can occur in the meiosis I or meiosis II phases of cellular reproduction, or during mitosis.

This is a cause of several medical conditions in humans, including:

Down Syndrome - trisomy of chromosome 21
Patau Syndrome - trisomy of chromosome 13
Edward Syndrome - trisomy of chromosome 18
Klinefelter Syndrome - an extra X chromosome in males
Turner Syndrome - only one X chromosome present in females
XYY Syndrome - an extra Y chromosome in males
Triple X Syndrome - an extra X chromosome in females

Meiosis in humans

In females, meiosis occurs in precursor cells known as oogonia that divide twice into oocytes. These stem cells stop at the diplotene stage of meiosis I and lay dormant within a protective shell of somatic cells called the follicle. Follicles begin growth at a steady pace in a process known as folliculogenesis, and a small number enter the menstrual cycle. Menstruated oocytes continue meiosis I and arrest at meiosis II until fertilization. The process of meiosis in females is called oogenesis.

In males, meiosis occurs in precursor cells known as spermatogonia that divide twice to become sperm. These cells continuously divide without arrest in the seminiferous tubules of the testicles. Sperm is produced at a steady pace. The process of meiosis in males is called spermatogenesis.

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