Oogenesis
Also known as: oogonia, meiotic arrest
The production of female gametes, which begins before birth, pauses in prophase I for years to decades, resumes at each ovulation and completes only at fertilisation, yielding one oocyte and polar bodies from each primary oocyte.
Overview
Fetal life: primordial germ cells reach the gonadal ridges by week 6 and become oogonia, which multiply by mitosis to a peak of ≈6–7 million at about 20 weeks. From ≈11–12 weeks they enter meiosis to become primary oocytes, each surrounded by pregranulosa cells (primordial follicles), and arrest in diplotene of prophase I. Massive apoptosis (atresia) leaves ≈1–2 million at birth; no oogonia remain, so the pool is finite.
Childhood to menopause: atresia continues (≈300 000–400 000 at menarche). From puberty, in each cycle the oocyte of the dominant follicle completes meiosis I in response to the LH surge, producing a secondary oocyte (n, 2C) and the first polar body; the secondary oocyte is ovulated arrested in metaphase II. Meiosis II completes only at fertilisation, producing the second polar body. Over a lifetime only ≈400–500 oocytes are ovulated; menopause occurs when ≈1000 follicles remain.
Comparison with spermatogenesis: oogenesis is discontinuous, begins prenatally, draws on a non-renewing pool, produces one gamete per meiosis (unequal cytokinesis concentrating cytoplasm in the oocyte) and takes up to five decades; spermatogenesis is continuous from puberty, renews from stem cells, produces four gametes per meiosis and takes ≈64–74 days.
- Location
Ovarian cortex (fetal to menopause); completion of meiosis II in the uterine tube at fertilisation.
Parts & subdivisions
- OogoniaMitotically active germ cells present only before birth.
- Primary oocyteArrested in prophase I from fetal life until ovulation.
- Formed at ovulation; arrested in metaphase II until fertilisation.
- Polar bodiesFirst (after meiosis I) and second (after meiosis II).
Function
- Produces haploid female gametes with large cytoplasmic reserves.
- Generates genetic diversity by recombination and independent assortment.
Clinical significance
Premature ovarian insufficiency
Loss of ovarian function before 40 (≈1 % of women): Turner syndrome (45,X — accelerated atresia, streak ovaries), fragile X premutation, autoimmune oophoritis, chemotherapy/radiotherapy, surgery. High FSH, low estradiol and AMH; hormone replacement protects bone and heart.
Compiled from standard anatomy and physiology references — see the Reproductive System sources. For education only; not medical advice.