Meiosis Flashcards
What is a diploid cell?
A nucleus with two full sets of chromasomes (2n)
Found in most cells
What is a haploid cell?
A nucleus with one full set of chromasomes (n)
Found in gametes
Are gametes diploid or haploid?
Haploid
What is a zygote?
A cell formed when two haploid gametes fuse at fertalisation
What is meosis?
Cell division leading to 4 haploid cells
What are the stages of meiosis?
Prophase 1 Metaphase 1 Anaphase 1 Telophase 1 Prophase 2 Metaphase 2 Anaphase 2 Telophase 2 Cytokenesis
What happens at prophase 1?
Each chromasome appears in a condensed form with two chromatids
Homolougous chromasomes associate with each other
Crossing over occurs
What is crossing over?
Enzymes cut out parts of chromasomes and join parts of the maternal and paternal chromasomes together.
What happens during metaphase 1?
Spindle fibres form and the chromasoems line up along the equator in two lines
What happens during anaphase 1?
The centromeres do not break and one pair of chromatids (one chromasome) is pulled to each side of the cell
Each new cell has half the number of chromasomes as the original as it doesn’t have any copies
What happens during telophase 1?
The nuclear membrane reforms and the cells may divide
What happens in prophase 2?
New spindles are formed
What happens in metaphase 2?
The chromasomes line up along the equator
What happens in anaphase 2?
The centromeres break and chromatids are pulled to opposite sides of the cell
What happens in telophase 2?
The nuclear envelop reforms and the cell divides which gives rise to 4 haploid daughter cells
How is variation introduced in meiosis?
Independent assortment
Crossing over
How does independent assortment lead to genetic variation?
Chromasomes from the person’s parents are distributed randomally so that when they line up along the cell centre, chromasomes from any parent could be pull to either side of the cell
How does crossing over lead to genetic variation?
Enzymes cut and join different parts of enzymes together so the chromasomes each contain a mix of both maternal and paternal DNA
What is a translocation mutation?
When one part of the chromasome breaks off and joins to a competely different part of another chomasome that codes for something different
Like a bit of chromasome 4 joining to chromasome 13