haploid: a cell containing a single set of chromosomes (unpaired chromosomes) = n
diploid: a cell containing pairs of homologouschromosomes, one from each parent 2n
homologouschromatids: pairs of chromosomes in a diploid cell, one from each parent, of similar size and containing the same genes (which may have alternative alleles)
somatic cell: all cells in a multicelluler organism other than the gametes = 2n
gamete: a haploid cell required for sexual reproduction (sperm/pollen for males and egg/ovum for females) = n
fertilisation: fusion of male and female gametes to form a zygote n+n = 2n
zygote: a diploid cell formed as a result of the fusion of two haploidgamtes = 2n
number of chromosomes halved: important as diploid number is restored during fertilisation, there are 4 cell divisions in meiosis resulting in 4 cells with half the number of chromosomes of somatic cells - both meiotic nuclear divisions have the same phases as mitosis ie: meiosis I (1st division) - prophase phase I, metaphase phase I, anaphase phase I, telophase phase I, Meiosis II (2nd division) - pro phase II, meta phase II, ana phase II, telo phase II
there is no interphase II as there is no DNA replication before second meioticcell division
importance of meiosis (p2)
genetic variation: unlike mitosis, meiosis allows for genetic variation in resultant cells
process of meiosis I (p1):
interphase
a diploid cell starts the process
mitosis: DNA replicates in S phase
prophase I
nuclear envelope degrades
centrioles migrate to opp. poles
spindle forms
longest stage of mieosis
chromosomes appear
homologous chromosomes to form bivalents
corssing over occurs
process of meiosis I (p2):
metaphase I
line up at equator
homologous pairs seperate
bivalents line up at equator
bivalents have 3 possible orientations
each bivalent orients itself independently of the others
maternal and paternal chromsomes of each bivalent can form at either pole
independent assortment occurs there are 2(23) possible combinations of orientation
process of meiosis I (p3):
Anaphase I:
spindle fibres shorten
reduction division occurs:
homologous chromosomes are seperated (2n->n)
only one copy of each pair of homologous chromosomes will be retained by each cell, albeit doubled up
resultant cells will be haploid
process of meiosis II (p1): seperates sister chromatids
telophase I and cytokinesis:
nuclear envelope reforms
spindle fibres disassemble
there is no (or short) interphase II
chromosomes disperse
chromatin reforms
no DNA replication occurs as there is no interphase II
prophase II:
nuclear envelope degrades
centrioles migrate to opposite poles
spindle forms
chromosomes appear
meiosis II (p2):
metaphase II:
chromosomes line up at equator
sister chromatids are no longer identical
chromosomes orientate themselves independently of each other
chromatids can be in either orientation
independent assortment occurs
there are 2(23) possible combinations of orientation
anaphase II:
spindle fibres shorten
non-individual sister chromatids are pulled to opposite poles
telophase I and cytokinesis:
nuclear envelope reforms
spindle fibres disassemble
cytokinesis follows giving rise to 4 haploid cells
cells have 1/2 quantity of DNA of origincal - all cells are genetically different
chromsomes disperse
chromatin reforms
nucleolus reappears
Prophase I:
longest stage of meiosis:
chromosomes condense and appear
homologous chromosomes pair up to form bivalents
a bivalent or tetrad: homologs attached together by a thin network of protein
( no pairing of homologous chromosomes occurs in mitosis)
each pair of homologous chromosomes has:
similar length
same position of centrosomes
same loci of genes
adjoining non-sister chromatids of homologous pair are attached at points called chiasmata
at chiasmata, there is a breakage + rejoining of non-sister chromatids where genetic material is exchanged ie crossing over occurs
prophase I (p2)
crossing over/genetic recombination: alleles are exchanged between the maternal and paternal chromosomes
chiasmata and crossing over can occur on several places on the homologous pair of chromosomes
genetic recombination is different fro every set of homologous chromosomes in every cell, thus contributing to genetic variation