Meiosis in Embryology

Comprehensive reference on gamete formation and clinical significance

Stage Phase Key Events & Mechanisms Chromosome Status Embryology Relevance & Clinical Significance
PRE-MEIOSIS Interphase (Pre-Meiotic)
Germ cell growth
DNA replication (S phase)
Centrosome duplication
Diploid (2n)
46 chromosomes
92 chromatids (4C DNA)
Foundation for embryonic development.
Errors cause catastrophic DNA damage.
Sets stage for proper chromosome segregation.
MEIOSIS I Prophase I
Chromosome condensation
Synapsis
CROSSING OVER (chiasmata)
Chiasmata visible
Max condensation
Tetrad formation (bivalents)
23 tetrads (46 chromosomes)
92 chromatids
MOST CRITICAL STAGE: Primary source of genetic diversity.
Diplotene arrest in females → maternal age effect.
Chiasma failure → nondisjunction.
MEIOSIS I Metaphase I
Tetrads align at equator
Independent assortment
Spindle attachment
23 tetrads aligned
Maternal/paternal orientation random
Second major diversity source: 8.4M+ chromosome combinations.
Random alignment errors → aneuploid gametes.
MEIOSIS I Anaphase I
Homologous chromosomes separate
Sister chromatids remain attached
Nondisjunction possible
Separating to haploid sets
Each pole: 23 chromosomes (46 chromatids)
PRIMARY SOURCE OF EMBRYONIC ANEUPLOIDY: ~90% of Trisomy 21.
Maternal nondisjunction risk ↑ with age.
MEIOSIS I Telophase I & Cytokinesis
Unequal division
Polar body formation
Two haploid (n) cells:
Secondary oocyte (23 chromosomes)
First polar body
Female-specific: Unequal cytokinesis conserves cytoplasm.
Secondary oocyte arrests at Metaphase II until fertilization.
MEIOSIS II Interkinesis
Brief interphase
NO DNA replication
Haploid (n)
23 chromosomes (46 chromatids)
Critical 'no replication' prevents polyploidy.
Short duration reduces error risk.
MEIOSIS II Metaphase II
Chromosomes align singly
Spindle attachment
23 chromosomes aligned
Each = 2 chromatids
Female clinical checkpoint: Oocytes arrested here until fertilization triggers completion.
MEIOSIS II Anaphase II
Sister chromatids separate
Nondisjunction possible
Separating to single chromatids
Each pole: 23 chromosomes (23 chromatids)
Causes ~10% of aneuploidies.
Paternal errors more common here than Meiosis I.
MEIOSIS II Telophase II & Cytokinesis
Nuclear envelopes reform
Cytoplasm divides
Four haploid (n) cells:
23 chromosomes each
23 chromatids each (1C DNA)
Sex-specific outcomes: Males - 4 functional sperm.
Females - 1 functional ovum + 2-3 polar bodies.
SUMMARY Core Functions
Chromosome number control (23+23=46)
Genetic diversity engine
Gamete quality control
Ensures proper diploid number in zygote
#1 cause of miscarriage: Aneuploidy (>50% first-trimester losses).
Leading congenital disorders: Down, Edwards, Patau syndromes.

Key Embryology Takeaways

Meiosis creates gametes before fertilization – mitosis builds the embryo
Prophase I and Anaphase I errors are primary sources of chromosomal disorders
Maternal age effect due to decades-long diplotene arrest in females
Genetic diversity ensures each embryo has a unique developmental blueprint
Polar body formation conserves resources for early embryonic development
Meiotic errors cause >50% of first-trimester miscarriages

Color Legend

Critical Stages
Female-Specific
Sex-Specific Outcomes
Selected Row