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Diploid
two sets of chromosomes
zygotic chromosome # = 2n
Haploid
one set of chromosomes
zygotic chromosome # = n
Homologous chromosomes
duplicate versions of each chromosome
similar in size & shape, contain same genes in same locations (although maybe diff. versions)
What are haploid cells in the human body?
sex cells or gametes
each parent contributes a gamete to produce a zygote/diploid in offspring
Locus
position of a gene on a chromosome
Alleles
alternate versions of the same gene
Phenotype
physical traits
genotype
genetic makeup
Each generation in the cross
1) 1st generation = P generation (parent)
2) 2nd generation = F1 generation (filial)
3) 3rd generation = F2 generation
Law of Dominance
dominant allele masks the presence of the recessive allele
Law of Segregation
during gamete formation, the two alleles for each gene separate
each sex cell only receives one allele → genetic variation
Law of Independent Assortment
during meiosis I, each pair of homologous chromosomes is split, and which one aligns left or right during metaphase is diff. for each pair
two alleles for each trait are sorted independently of the two alleles for the other trait
Product Rule
if A and B are INDEPENDENT - events will occur simultaneously
P(A + B) = P(A) x P(B)
Sum Rule
if A and B are MUTUALLY EXCLUSIVE - either event will occur
P(A or B) = P(A) + P(B)
Linked genes
genes on the same chromosome that stay together during assortment and move as a group
tends to be inherited together
instead of 4 possible gamete combinations, there are only 2
Recombinants
offspring w/ new combinations of alleles that differ from their parents, created by genetic recombination during meiosis (crossing-over)
causes linked genes to not be linked
percentage of recombination: recombinants/total offspring, can also determine how far apart genes are in centimorgans
Frequency of crossing over
farther apart two linked alleles are, the more often the chromosome will cross over between them
Sex-linked traits
pair of chromosomes that determine sex, some traits are carried on sex chromosomes
female = XX
male = XY
Barr bodies
X chromosome that is condensed and visible
in females, one X is activated and the other is deactivated during embryonic development
Incomplete dominance
in some cases, traits will blend - either is dominant over the other
WW cross w/ RR = RW
Codominance
equal expression of both alleles - expression of one allele doesn’t prevent the expression of the other
AB blood type
Polygenic inheritance
trait that results from the interaction of many genes, each gene will have a small effect on a particular trait
Non-nuclear inheritance
mitochondrial inheritance - maternal line
mitochondria are always provided by the egg during sexual reproduction
in plants, mitochondria are provided by the ovule & are maternally inherited
Phenotypic plasticity
two individuals w/ the same genotype that have diff. phenotypes because they are in different environments
Meiosis
production of gametes
limited to sex cells in special sex organs called gonads
male gonads = testes
female gonads = ovaries
female gamete + male gamete = zygote
Meiosis phases
Meiosis I
prophase I, metaphase I, anaphase I, telophase I, cytokinesis I - ensures each gamete receives a haploid
Meiosis II
prophase II, metaphase II, anaphase II, telophase II, cytokinesis II - results in four unique haploid daughter cells
Prophase I
nuclear membrane disappears, chromosomes become visible, centrioles move to opposite poles of nucleus
chromosomes line up side-by-side w/ homologs (synapsis)
synapsis is followed by crossing-over - mixes alleles from dad & mom
Metaphase I
chromosome pairs (tetrads) line up at the metaphase plate, in random order
Anaphase I
each pair of chromatids within a tetrad moves to opposite poles
homologs separate w/ their centromeres intact
Telophase I
nuclear membrane forms around each set of chromosomes
Cytokinesis I
two daughter cells are formed (haploid)
Prophase II
chromosomes condense and become visible
Metaphase II
chromosomes move toward metaphase plate, in single file not as pairs
Anaphase II
chromatids of each chromosome split at the centromere, and each chromatid is pulled to opposite ends of each cell
Telophase II
nuclear membrane forms around each set of chromosomes
Cytokinesis II
four haploid cells are produced
spermatogenesis
4 sperm cells are produced for each diploid cell
oogenesis
egg cell or ovum is produced (only 1), 3 polar bodies are produced
Nondisjunction
chromosomes that fail to separate during meiosis
produces wrong # of chromosomes in a cell
occurs during anaphase I or II
Down syndrome
3 copies of 21st chromosomes
intellectual disability, developmental delays
low muscle tone, small hands/feet
Turners syndrome
in females where one X chromosome is missing/altered, affecting growth, development, and fertility
infertile
short stature
webbed necks/widely spaced nipples
autosomal vs sex-linked
autosomal: genes on non-sex chromosomes (autosomes), affecting males and females equally
sex-linked: genes on sex chromosomes, causing different patterns, often affecting males more for X-linked traits
chi-square test - when to reject/accept null hypothesis
reject: chi-square value > critical value - statistically significant difference in relationship, unlikely due to chance
accept: chi-square value < critical value - no significant difference, randomness
sexual vs asexual reproduction
sexual: involves two parents, creates genetically unique offspring through fusion of gametes, more variation but requires more energy (animals)
asexual: one parent, produces genetically identical clones via binary fission/budding, lacks variation but less energy (bacteria, plants)