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o·o·gen·e·sis (ō'ə-jĕn'ĭ-sĭs) ![]() |
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| Sci-Tech Encyclopedia: Oogenesis |
The generation of ova or eggs, the female gametes. Primordial germ cells, once they have populated the gonads, proliferate and differentiate into sperm (in the testis) or ova (in the ovary). The decision to produce either spermatocytes or oocytes is based primarily on the genotype of the embryo. In rare cases, this decision can be reversed by the hormonal environment of the embryo, so that the sexual phenotype may differ from the genotype. Formation of the ovum most often involves substantial increases in cell volume as well as the acquisition of organellar structures that adapt the egg for reception of the sperm nucleus, and support of the early embryo. In histological sections, the structure of the oocyte often appears random but as the understanding of its chemical and structural organization increases, an order begins to emerge. See also Ovum; Spermatogenesis.
Among lower vertebrates and invertebrates, mitotic divisions of the precursor cells, the oogonia, continue throughout the reproductive life of the adult; thus extremely large numbers of ova are produced. In the fetal ovary of mammals, the oogonia undergo mitotic divisions until the birth of the fetus, but a process involving the destruction of the majority of the developing ova by the seventh month of gestation reduces the number of oocytes from millions to a few hundred. Around the time of birth, the mitotic divisions cease altogether, and the infant female ovary contains its full complement of potential ova. At puberty, the pituitary hormones, follicle stimulating hormone (FSH), and luteinizing hormone (LH) stimulate the growth and differentiation of the ova and surrounding cells (see illustration). See also Mitosis.

Three-dimensional view of the cyclic changes in the mammalian ovary.
One important feature of oocyte differentiation is the reduction of the chromosome complement from the diploid state of the somatic cells to the haploid state of gametes. Fusion with the haploid genome of the sperm will restore the normal diploid number of chromosomes to the zygote. The meiotic divisions which reduce the chromosome content of the oocyte occur after the structural differentiation of the oocyte is complete, often only after fertilization. Unlike the formation of sperm, in which the two divisions of meiosis produce four equivalent daughter cells, the cytoplasm of the oocyte is divided unequally, so that three polar bodies with reduced cytoplasm and one oocyte are the final products. Generally, each fertilized oocyte produces a single embryo, but there are exceptions. Identical twins, for example, arise from the same fertilized egg. See also Meiosis.
The provision of nutrients for the embryo is a major function of the egg, and this is accomplished by the storage of yolk in the cytoplasm. Yolk consists of complex mixtures of proteins (vitellins), lipids, and carbohydrates in platelets, which are membrane-surrounded packets dispersed throughout the egg cytoplasm (ooplasm). The amount of yolk in an egg correlates with the nutritional needs of the embryo. Although the eggs of mammals are extremely small as compared to the fetus, the bulk of the nutrition is supplied by the placenta; yolk is required only until implantation in the uterine wall.
Egg cytoplasm also contains large stores of ribonucleic acid (RNA) in the form of ribosomal, messenger, and transfer RNA. These RNAs direct the synthesis of proteins in the early embryo, and may have a decisive influence on the course of development. The mechanism by which the RNA is supplied to the egg is the basis for a major classification of ovary types. Panoistic ovaries, in which the egg nucleus is responsible for the production of all the stored RNA in the ooplasm, are typical of vertebrates, primitive insects, and a number of invertebrates. The amounts of RNA produced during the meiotic prophase in such ovaries are much larger than those produced by a somatic cell, and thus special mechanisms seem to be involved in the synthetic process. See also Deoxyribonucleic acid (DNA); Ribonucleic acid (RNA).
| Veterinary Dictionary: oogenesis |
The development of mature ova from oogonia. See also avian oogenesis.
| Wikipedia: Oogenesis |
| Oogenesis |
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Oogenesis or oögenesis (pronounced /ˌoʊ.əˈdʒɛnɨsɪs/[1])is the creation of an ovum (egg cell). It is the female process of gametogenesis. It involves the various stages of immature ova.
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In mammals, the first part of oogenesis starts in the germinal epithelium which give rise to ovarian follicles(the functional unit of the ovary.)
Note that such an important process in animal life cycles is done completely without the aid of oo spindle-coordinating centrosomes.
It consists of several processes: oocytogenesis, ootidogenesis and the final maturity to form an ovum. Folliculogenesis is a separate process during ootidogenesis.
| Cell type | ploidy | Process | Process completion |
| Oogonium | diploid | Oocytogenesis (mitosis) | third trimester (forming oocytes) |
| primary Oocyte | diploid | Ootidogenesis (meiosis 1) (Folliculogenesis) | Dictyate in prophase I for up to 50 years |
| secondary Oocyte | haploid | Ootidogenesis (meiosis 2) | Halted in metaphase II until fertilization |
| Ovum | haploid |
Oogonium --(Oocytogenesis)--> Primary Oocyte --(Meiosis I)-->First Polar Body (Discarded afterward) + Secondary oocyte --(Meiosis II)--> Secondary Polar Body(Discarded afterward) + Ovum
The creation of oogonia traditionally doesn't belong to oogenesis, but to the common path of gametogenesis together with spermatogenesis.
At the start of the menstrual cycle some 12-20 Primary follicles begin to develop under the influence of elevated FSH to form secondary follicles. The Primary follicles have formed from primordial follicles which developed in the ovary at around 10–30 weeks after conception. By around day 9 of the cycle only one healthy secondary follicle is remaining, with the rest having undergone atresia. The remaining follicle is called the dominant follicle and is responsible for producing large amounts of oestradiol during the late follicular phase. Oestradiol production depends on co-operation between the theca and granulosa cells. On day 14 of the cycle an LH surge occurs which is triggered by positive feedback of oestradiol. This causes the secondary follicle to turn into a tertiary follicle which ovulates some 24–36 hours later. An important event in the tertiary follicle is that the primary oocyte completes the first meiotic division with formation of a polar body and a secondary oocyte. The empty follicle then forms a corpus luteum.[citation needed]
Oogenesis starts with oogonial transformation into primary oocytes, called oocytogenesis[2]. Oocytogenesis is completed either before or shortly after birth.
It is commonly said that when oocytogenesis is completed, no additional primary oocytes are created, in contrast to the male spermatogenesis, where gametocytes are continuously created. In other words, oocytes reach their maximum at ~20[3] weeks of gestational age, when there are seven million of them; however at birth this has already been reduced to approximately 1-2 million.
Recently, however, two publications have challenged the belief that a finite number of oocytes are set around the time of birth.[4][5] Renewal of ovarian follicles from germline stem cells (originating from bone marrow and peripheral blood) was reported in the postnatal mouse ovary.
Due to the revolutionary nature of these claims, further experiments are required to examine the dynamics of small follicle formation.
The succeeding ootidogenesis is the step in which the primary oocyte turns into an ootid. It is achieved by meiosis. The primary oocyte is even defined from its role to undergo meiosis[6].
However, although this process begins at prenatal age, it stops at prophase I. In late fetal life, all oocytes, still primary oocytes, have taken this halt in development, called dictyate. First after menarche they continue to develop, although only a few do so every menstrual cycle.
Meiosis I of ootidogenesis starts at embryonic age, but halts in diplotene of prophase I until puberty. For those primary oocytes continuing to develop in each menstrual cycle, however, synapsis occurs and tetrads form, enabling and crossing over. As a result of meiosis I, the primary oocyte becomes the secondary oocyte and the first polar body.
Immediately after meiosis I, the haploid secondary oocyte initiates meiosis II. However, this, too is halted in metaphase II. However, this only lasts until fertilization, if such occurs. When meiosis II is completed, an ootid and another polar body are created.
Synchronously with ootidogenesis, the ovarian follicle surrounding it develops from a primordial follicle to a preovulatory one.
Both polar bodies disintegrate at the end of Meiosis II leaving only the ootid which undergoes maturation and eventually matures into an ovum.
The function of forming polar bodies is to discard the extra haploid set of chromosomes(n)
Many protists produce egg cells in structures termed archegonia. Some algae and the oomycetes produce eggs in oogonia. In the brown alga Fucus, all four egg cells survive oogenesis, which is an exception to the rule that generally only one product of female meiosis survives to maturity.
In plants, oogenesis occurs inside the female gametophyte via mitosis. In many plants such as bryophytes, ferns, and gymnosperms, egg cells are formed in archegonia. In flowering plants, the female gametophyte has been reduced to an eight-celled embryo sac within the ovule inside the ovary of the flower. Oogenesis occurs within the embryo sac and leads to the formation of a single egg cell per ovule.
In ascaris, the oocyte does not even begin meiosis until the sperm touches it, in contrast to mammals, where meiosis is completed in the estrus cycle.
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