3.3 Flashcards
What is meiosis
process by which sex cells (gametes) are made in the reproductive organs
Meiosis 1
The 1st meiotic division is a reduction division*(diploid→haploid)in which homologous chromosomes are separated
meiosis I: the number of cells is doubled but the number of chromosomes is not. This results in 1/2 as many chromosomes per cell.
Meiosis 2
The 2nd division separates sister chromatids (these chromatids may not be identical due to crossing over in prophase I)
Prophase 1
- homologous chromosomes undergo a process called*synapsis→ synapsis: chromosomes pair up to form abivalent
(or tetrad)
homologous chromosomes are held together at points calledchiasmata(singular: chiasma)
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Crossing over of genetic material between non-sister chromatids occurs at chiasmata
- result of exchanging genetic material → new gene combinations are formed on chromatids (recombination)
- Once chiasmata are formed, the homologous chromosomes condense as bivalents and then are separated in meiosis
- If crossing overoccurs then all 4 haploid daughter cells will be geneticallydistinct (sister chromatids are no longer identical)
where does crossing over occur
at the chiasmata
What promotes genetic variation
- crossing over
- random orientation
- fusion of gametes from different parents
In what phase does crossing over occur?
prophase 1
When does random assortment of chromosomes occur
metaphase 1
The failure of chromosomes to separate may occur via:
- Failure of homologues to separate in Anaphase I (resulting in four affected daughter cells)
- Failure of sister chromatids to separate in Anaphase II (results in only 2 daughter cells being affected)
synapsis
when chromosomes pair up to form a bivalent
what does crossing over result in
new gene combinations are formed on chromatids (recombination)
monosomy
chromosomal abnormality - when there is 1 less chromosome
nuchal translucency
- non-invasive
- ultrasound looking at nuchal fluid behind the neck of the foetus - large about is strongly correlated w Down syndrome
chronic villus sampling
- invasive
- sample of chronion (villi - placenta tissue) via tube inserted through the cervix
- cells are cultured & then karyotypes
- 1% risk of miscarriage
amniocentesis
- invasive
- sample of amniotic fluid (contains foetal cells) with a needle guided by camera/ultrasound
- 0.5% of miscarriage