THEME 5 MOD 2 Flashcards
what cells aren’t derived from mitosis
gametes - from specialized germ cells in ovaries / testes
sexual reproducing organisms
- genes passed on to offspring through gametes
- offspring have genetic variation and inherit a unique combination of genes from both parents
production of gametes
- replication of parental sex cell precursors
- two rounds of meiotic cell division to make diploid number of chromosomes haploid
human male production of gamete
4 haploid sperm cells from one precursor sex cell
human female production of gametes
one sex cell precursor will produce one large egg cell and 3 non-gamete polar bodies which store extra chromosomal content
why arent human gametes produced by mitosis
- gametes would be diploid and give rise to offspring with double the chromosomes, leading to fatal effects in the offspring
How are gametes unique and variable within a parent
- recombination of parental homologous chromosomes
meiosis
- duplication of chromosomes
- 2 consecutive cell divisions resulting in 4 haploid daughter cells
Steps of meiosis I
interphase: duplication of chromosomes
meiosis I:
prophase I:
- condensation and synapsis (pairing and physical connection) of homologous chromosomes along their length
- all homologous chromosomes pair with each other and form a bivalent unit (pair of synapsed chromosomes, four stranded structure)
- synaptonemal complex facilitates connection between two homologous chromosomes
- cross over or recombination between homologous chromosomes (specifically between non-sister chromatids), evident at the chiasma or chiasmata(plural) between paired chromosomes
- cross over of homologous chromosomes results in breaking and rejoining between non-sister chromatids
- recombinant chromatids result in a combination of paternal and maternal segments of dna
- centromere duplication, movement, spindle formation and nuclear envelope breakdown occur
metaphase I: spindle apparatus randomly reorders pairs of homologous chromosome bivalents relative to each other, further adding to genetic diversity between gametes
anaphase I: proteins holding homologous pairs together break down (synaptonemal complex) and homologues of bivalents pulled to opposite polls
telophase I marks end of meiosis I: each half of the cell has a haploid set of duplicated chromosomes: each chromosome has a recombinant pair of sister chromatids
chromosomes slightly uncoil, nuclear envelope reforms
after meiosis I cell begins cytokinesis into two separate cells
sister chromatids vs homologous chromosomes
sister chromatids: pair from duplicated chromosome
non-sister chromatids: two pairs of sister chromatids, one of each parental origin, non sister chromatids have similar genetic material, but aren’t identical
Homologous chromosomes: individual chromosomes that have been inherited from each parent with different alleles of genes on the loci of each chromosome
steps of meiosis II
Meiosis II: equational division (each daughter cell has equal number of chromosomes
prophase II: 23 different and duplicated sister chromatids
- nuclear envelope breaks down, spindle apparatus forms, chromosomes condense
metaphase II: chromosomes positioned at the metaphase plate
anaphase II: proteins at centromere break down, allows sister chromatids to sperate to opposite pollsas individual chromosomes
Telophase II: end of meiosis II. separate duplicated sister chromatids. nuclear envelope reforms, chromosomes condense
cytokinesis follows
nondisjunction
IN MEIOSIS
failure of chromosomes to separate during meiosis I or sister chromatids to separate a meiosis II
- can result in gamete with one less or one extra chromosome, can lead to detrimental or lethal effects
IN MITOSIS: same principle, cause cancerous cells
mitosis vs meiosis
meiosis: very similar
differences:
- one interphase
- anaphase I: sister chromatids dont seperate, homologous chromosomes do
- meiosis II only has 23 chromosomes
gregor mendel
- studied pea plants and inheritance of traits, declaring two laws of inheritance
- discovered basis of inheritance before the structures of chromosomes were discovered
- studied 7 traits: seed colour, seed shape, seed pod shape and colour, flower colour, flower position, plant height
basis of mendel experiments
- started with two true breeding plants (over generations, offspring were always the same variety of parent). homozygous plants carried two identical allele
- crossed true breeding plants then cross bred offspring to determine any mathematical patterns to inheritance
how was an allele deemed recessive or dominant
when two true-breeding/homozygous plants were crossed, which phenotype showed
- cross between true-breeding yellow and green plants resulted in all yellow F1 generation, meaning yellow allele was dominant
- disproved blended model of inheritance
P generation, F1, F2
P: parental
F1: filial (son) 1
F2: filial 2
P: yellow and green true breeding plants
F1: all yellow
F2: …
dominant to recessive seed colour (and all traits) : 3:1
3/4 F2 phenotype: dominant for all traits
1/4 F2 phenotype:
recessive for all traits
Therefor, heritable factor of green plant masked in F1
mendels first law
- law of segregation
- alleles of a gene segregate into different gamete formation
- based upon: alternate forms of genes accountting for variation in inherited traits
- offspring will inherit two versions of the gene (one from both parents) and the dominant one will appear as a phenotype
- if organism is true breeding, allele found in all four gametes
punnet square
- consider all possible gametes of each parent
- predict offspring genotype and phenotype
how gametes get one specific allele
- homologous chromosomes equally segregated into gametes, each containing one allele of a gene
- if an organism has identical alleles at that gene locus across both chromosomes, each gamete will have the same allele
heterozygous plant probabilities in offspring
50% chance passing off Big A or little a
F2: 50% chance of getting big A allele from one parent and 50% chance of getting big A from other. Probability of inheriting AA: 50% times 50%= 25% (same for aa)
F2: probability of heterozygous genotype is twice that of the homozygous genotype as it can occur in two combinations. heterozygous genotype probability: 50%
underlying genotypic ratio of 1:2:1
how to determine underlying genotype?
- cross individual with recessive individual to determine if individual is hetero or homozygous
- if heterozygous: when crossed with homozygous recessive: half of the offspring will be heterozygous for the yellow allele, and half will be green (recessive homozygous)
- if homozygous: all offspring will be heterozygous for the yellow allele
- heterozygous genotype occurred 2:1 with homozygous genotype when crossing individuals, supporting 1:2:1 genotype ratio
monohybrids and monohybrid crosses definition
MONOHYBRIDS:
cross breed of two true breeding plants
F1: all heterozygous for the one trait followed in the cross
MONOHYBRID CROSSES:
cross between two heterozygous plants in F1