Asexual reproduction
Single cell passes genes to its offspring without the fusion of gametes (ex: binary fission)
Sexual reproduction
Two parent cells give rise to offspring that have unique combinations of genes inherited from both
Chromosomes in human cells
Human somatic cells have 23 pairs of chromosomes
each pair consists of 2 homologous chromosomes, or homologs (1 from each parent)
Karyotype
An ordered display of the pairs of chromosomes
Meiosis
Like mitosis, chromosomes are first duplicated… then meiosis happens in two sets of cell divisions, meiosis I and meiosis II
instead of 2 diploid daughter cells, the 2 sets of cell divisions result in 4 haploid daughter cells
Stages of Meiosis I - Prophase I
chromosomes condense
Homologous chromosomes pair up and form tetrads
Crossing over occurs = non sister chromatids exchange DNA
average of 1-3 crossing over events per pair in humans
Synapsis and crossing over
zipper-like structure called synaptonemal complex forms during this synapsis (attachment)
DNA breaks at matching points and a piece of paternal chromatid replaces piece of maternal chromatid, and vice versa, producing recombinant (recombined) chromosomes
Each homologous pair has 1 or more X-shaped regions called chiasmata
Metaphase I
homologous pairs line up randomly at the equator via independent assortment (randomly)
Microtubules from one pole attach to kinetochore of one chromosome of each tetrad
Independent assortment of chromosomes
Each pair of chromosomes sorts maternal and paternal homologs pair into daughter cells independently of the other cells
Number of combinations possible is 2n (humans: 2²3)
Anaphase I
pairs of homologous chromosomes separate
One chromosome move toward each pole
Sister chromatids remain attached at the centromere and move as one unit
Telophase I and Cytokinesis
At the beginning of telophase I, each half of the cell has haploid set of chromosomes!
each chromosome still consists of two sister chromatids
Cytokinesis usually occurs simultaneously, forming two haploid daughter cells
No new chromosome duplication before meiosis II
Prophase II
Spindle apparatus forms
Chromosomes still composed of two chromatids
Metaphase II
Chromosomes are arranged at the equator
Because of crossing over in meiosis I, sister chromatids are no longer genetically identical
Kinetochores attach to microtubules extending from opposite poles
Anaphase II
Sister chromatids separate and move as two newly individual chromosomes
Telophase II and Cytokinesis
Nuclear membranes form, and chromosomes start to loosen
Final result is four daughter cells, each with haploid set of unduplicated chromosomes
Each daughter cell is genetically distinct from others, and from the parent cell
Origins of Genetic Variation Among Offspring
*Mechanisms contribute to genetic variation:
1) crossing over
2) independent assortment
3) random fertilization
any sperm can fuse with any egg
Crossing over
Mutations are original source of genetic diversity
Independent assortment
Reshuffling of genes during meiosis produces more genetic variation
Random fertilization
Natural selection results in the accumulation of genetic variations favored by the environment