Introduction to Cell Division:
List the 4 basic functions of cell division.
Repair, replace, reproduce, and grow cells
Why can cells not grow in size indefinitely?
Cells are limited in size because of limitations in their surface area to volume ratio, nutrient intake, and internal transport
As cells grow larger, the essential materials travel within the cell less effectively
Why is accurate cell division required for biological continuity?
Accurate cell division ensures:
New cells receive the correct number of chromosomes
Preserving genetic information across generations.
What is chromatin?
Fibres of SNA in its uncondensed form
How are chromatin and chromosomes related to one another?
Chromatins condense to form chromosomes during cell division
Chromosomes are made of tightly coiled chromatin
What is the importance of chromatin replication to successful cell division?
Ensures new cell receives a complete set of DNA
List and describe the stages of chromatin replication.
Initiation: Enzymes unwind the DNA at specific origins.
Elongation: New strands of DNA are synthesized using each original strand as a template.
Termination: DNA replication stops and the strands are checked for errors.
Mitosis:
What is mitotic cell division?
Occurs in all cells except gametes
1 cell division
2 final daughter cells produced
Same number of chromosomes in daughter cell compared to parent cell (diploid 2n = (n = 23))
No tetrads (synapsis chromosomes)
No crossing over
Identical genetics to parent cell
Repair, growth, reproduction
How much of a cell's life is spent in interphase and mitosis:
Interphase: 95% of the cell’s life
Mitosis: 5% of their cell-cycle time (less than 1 hour)
How can each of the following stages of mitosis be recognized?
Interphase
Cell prepares to divide: growth, DNA replication, cell functions
Early prophase
Chromatin begins to condense into visible chromosomes, nucleus present
Late prophase
Nuclear membrane breaks down; spindle fibers being to attach to chromosomes
Metaphase
Chromosomes line up in the middle (equator) of the cell
Anaphase
Sister chromatids are pulled apart to opposite sides of the cell
Telophase
Two new nuclei start to form; chromosomes begin to uncoil; spindle fibers disappear.
Cytokinesis:
Two new daughter cells are produced
What are chromatids and centromeres?
Chromatids:
Fibres of SNA in its uncondensed form
Exists during S phase of interphase to allow DNA to replicate
Centromeres:
The region where sister chromatids are joined and where spindle fibers attach during mitosis.
Describe cytokinesis in a plant cell
A cell plate forms in the center of the cell
Develops into a new cell wall, dividing the cell into two
How does this differ from animal cell cytokinesis?
The cell membrane pinches inwards to divide the cell into two
Called the cleavage furrow
State another difference between plant and animal cell mitosis.
No cell wall and cell plate in animal cells
Animal cells have cleavage furrow in telophase rather than a cell plate
Meiosis:
What is meiotic cell division?
Occurs in gamete cells
Double (2) the cell division (PMAT occurs twice)
IPMAT I and PMAT II
4 final daughter cells produces
Half amount of chromosomes as parent cell (haploid n)
Tetrads form (synapsis chromosomes)
Crossing over in prophase I
Genetically different from parent cell
Genetic diversity (genetic variation)
What is meant by the terms haploid (n) and diploid (2n):
Haploid
Contains half the number of chromosomes (n) as the parent cell (2n)
Ex. sperm and egg cells in humans, meiosis
Diploid
Containing pairs of chromosomes
All somatic cells are diploid
In humans 2n = 46
Zygote has 2n (n from female + n from male gametes)
What are homologous chromosomes?
Pair of chromosomes with the same genes at same location
NOT identical
May carry different versions of the gene/trait (alleles)
Same: Length, centromere location, banding pattern when stained
How does cytokinesis of meiotic cell division differ in males and females in humans?
Males = four equal sperm cells
Female = unequal, haploid one large egg cell (ovum) and 3 smaller polar bodies cells (which degenerate)
Errors in Meiosis
Two types of errors: Structure and Number
Structure
Deletion: a piece of chromosome is deleted
Duplication: Chromosome section appears twice or more times
Inversion: Section of chromosome is inverted
Translocation: segment of chromosome is attached to a different non-homologous chromosome (it should pair with homologous (same chromosome))
Number
Nondisjunction: when homologous chromosome pairs or sister chromatids do nope separate during meiosis
Mendelian Genetics:
Why are pea plants an ideal organism for studying inheritance? (give 2 reasons)
Easy and observable traits (ex. color and seed shape)
Reproduce quickly (cross pollination or self pollination)
State Mendel's Principle of Dominance.
When two different alleles are present, the dominant will show/mask to effect the recessive trait
State Mendel's Principle of Segregation.
Alleles of genes separate during meiosis and each offspring receives one allele from each parent.
What is meant by the term incomplete dominance?
No allele is completely dominant
Blending phenotype
New combination created
What is meant by the term codominance?
Both traits/alleles are shown/expressed
Heterozygous organism
Ex. black cow x white cow = cow with black and white spots
What is the purpose of a test cross?
Determines genotypes of an organism showing a dominant trait
Shows homozygous dominant or heterozygous
What disadvantage can you foresee in performing test crosses?
Time consuming
Many offspring to get clear results
Many results to consider
Distinguish between autosomes and sex chromosomes. How many pairs of each type do humans have?
46 total chromosomes in humans
Autosomes: non sex chromosomes, control most traits, 22 pairs (44 chromosomes)
Sex chromosomes: determine sex (XX female or XY male), 1 pair (2 chromosomes)
Sex-linked traits examples
Color Blindness
Hemophilia (body’s ability to make blood clots)
What is a pedigree? How can a pedigree help to trace genetically inherited traits?
A diagram of individual’s ancestors
Used in human genetics to analyze Mendelian inheritance of a certain trait
Used to track the inheritance of a gene
About Blood / Blood Types
Types: A, B, AB, O
IAIA / IAi, IBIB / IBi, IAIB, ii
Antigens
Substances (usually proteins)
Tiny markers on the surface of cells
Help determine blood type
Immune system uses antigens to recognize which cells belong in the body and which doesn’t
Antibodies
Tiny proteins made by the body to fight off foreign antigens (blood types)
Look and attack cells that don’t belong
Such as wrong blood types
Rh blood group (+) or (-)
Another kind of antigen on red blood cells
Have it = Rh (+)
Don’t have it = Rh (-)
Agglutination
When blood cells clump together
Blocks blood flow and is dangerous
Hemolysis
When red blood cells break open and release its contents
Happens due to bad reactions such as blood clotting
Can lead to serious damage like kidney damage
Definitions
Genetics
The study of heredity and variation of living organisms
How genetic information is passed from one generation to the next
Allele
A trait/gene inherited from generations / parents
Dominant allele
Form of a trait that always appears when an individual has alleles for it
Expressed in capital letters
Recessive allele
Form of a trait that always appears when an individual has 2 alleles for it (ex. aa)
Phenotype
Physical appearance/traits of an organism
ex . GOP: red x white
Genotype
Combination of alleles for any given trait / genetic makeup
Ex. GOP: XBXb x XbY
Gene
A designated segment of DNA on a chromosome
Position of a gene on a chromosome is called locus / loci
Genome
The complete DNA sequence of an organism
DNA
The chemical name for the molecule
Carries genetic instructions in all living things
Packaging of DNA with histone proteins for storage to result in a condensed chromosome
Structure: Have 3 components of nucleotides: Phosphate group, Pentose group, Nitrogenous bases
A, G, C, T/U,
Adenine (A), Guanine (G), Cytosine (C), Thymine (T) (DNA), Uracil (U) (RNA)
Base Pairing: A pairs with T/U (2 hydrogen bonds)
Base Pairing: G pairs with C (3 hydrogen bonds)
Somatic cell
A plant or animal cell that forms the body of the organism (not reproductive cells)
Karyotype
A photograph of sorted and paired homologous chromosomes in a cell
Can show missing or additional chromosomes in a person
Helps determine chromosome errors and disabilities
Zygote
Result of a cell from two gametes fusing
Synapsis
The alignment of homologous chromosomes
During prophase I and meiosis I
AKA crossing over (segments of DNA exchange with each other)
Chiasma
Point of contact or physical link between two non-sister chromatids
Trisomy
Gain an extra chromosome
Ex. down syndrome
Monosomy
Loss of one chromosome (nondisjunction)
Most are lethal (dangerous/deadly)
Can cause miscarriage
Genetic Reduction (outcome of meiosis)
Produces haploid daughter cells
Genetic Recombination (outcome of meiosis)
Different combinations of alleles
Genetic variation