Meiosis Flashcards
Meiosis I
- “reductive division” (diploid -> haploid)
* separates homologous chromosomes
crossover/recombination
mixing of genes between homologous chromosomes during meiosis
meiosis II
chromatids separate -> 4 daughter cells (haploid)
spermatogenesis
- begins at puberty
- spermatogonium (2n) -> mitosis -> 1° spermatocyte (2n) -> meiosis I -> 2° spermatocyte (1n) -> meiosis II -> spermatid (1n) -> spermiogenesis -> spermatozoa
oogenesis
- 1° oocytes formed in utero -> arrested in prophase I
- at puberty 1° oocytes begin completing meiosis I each cycle -> 2° oocytes (1n) and polar bodies
- 2° oocytes arrested in metaphase II until fertilization
aneuploidy
- abnormal chromosome number (not multiple of 23), ie monosomy and trisomy
- disomy=normal
meiotic nondisjunction (NDJ)
- failure of chromosome pairs to separate
* most common mechanism of aneuploidy
Meiosis I NDJ
- homologous chromosomes fail to separate
* gametes have chromosomes from both parents
meiosis II NDJ
- sister chromatids fail to separate
* Ex: XYY males
crossover/recombination in occurances of NDJ
RARE
monosomy occurs with
- fertilization of 1n and 0n gametes
- usually not viable
- turner syndrome (45,X) is an example of a viable monosomy
trisomy occurs with
•fertilization of 1n and 2n gametes •not viable with most chromosomes •exceptions: trisomy 21 = down syndrome (95% due to NDJ) trisomy 18 = edward syndrome trisomy 13 = patau syndrome
maternal meiosis I NDJ
•common cause of trisomy
*higher risk because meiosis I is so drawn out in females
robertsonian translocation
- fusion of long arms of 2 acrocentric chromosomes; the short arms are lost
- no important consequence for individual with the translocation, but likely to have many offspring with chromosomal anomalies and many spontaneous abortions
acrocentric chromosome
chromosomes with centromeres near the end (13, 14, 21, 22)