Genetics and Evolution Flashcards
when does crossing over occur in meiosis?
during prophase I
In meiosis I, prophase I, the nonhomolgous chromosomes (not the sister chromatids) align very precisely in synpasis. The paired chromosomes are called a ____ or _____
bivalent or tetrad
distinguish between meiosis metaphase I and metaphase II
in metaphase I, the nonhomologus chromosomes are paired up at the metaphase plate, and it’s the nonhomolous pairs that are separated
in metaphase II, the sister chromatids (attached via a centromere) align at the metaphase plate and are separated from each other
are the sister chromatids that separate during meiosis II identical?
No, not if the nonhomologous chromosomes underwent recombination during prophase I
what is the synaptonemal complex (SC)?
this is a protein complex that attaches to the nonhomologous chromosomes in prophase I and align & attach them in a central region with another SC protein. This whole SC protein complex is required for crossing over
movements in meiosis II are identical to those in mitosis, except that in meiosis II, the cells are ____, whereas the cells in mitosis are _____
haploid, diploid
*also note that the nonsister chromatids in metaphase II are nonidentical, whereas the sister chromatids in mitosis are identical
when are the cells considered haploid in meiosis?
when the cells reach telophase I, they are considered haploid
what is nondisjunction?
occurs when there is failure of chromosomes to separate during meiosis; gametes will either have 2 copies or no copies of a given chromosome. when they form a zygote, the zygote will therefore have either 3 copies (trisomy) or no copies (monosomy).
nondisjunction is not generally lethal, but typically results in sterility and organisms suffer intellectual disability
distinguish between the law of segregation and law of independent assortment
law of segregation: refers to the 2 alleles of 1 gene (one allele on one chromosome and the other allele located on the other chromosome); each allele is separated and passed onto the next generation independently.
law of independent assortment: refers to 2 genes on different chromosomes, the alleles of one gene will separate independently from the alleles of the other genes
What is the rule of multiplication in probability?
P(A & B) = P(A) x P(B)
this is the probability of both of 2 independent events happening concurrently, and can be found by multiplying the odds of either event alone
what is the rule of addition in probability?
P(A or B) = P(A) + P(B) - (P(A) x P(B))
this calculates the chances of either of the 2 events happening: you add the chances of either event happening and subtract the probability of the 2 events occurring together
Man genotype = bb & woman’s phenotype = Bb. What are the chances of an offspring being Bb genotype & be a boy?
P(Bb genotype) = 50%, or 1/2
P(boy) = 50%, or 1/2
Thus, P(A and B) = 1/2 x 1/2 = 1/4 = 25%
distinguish between incomplete dominance and codominance
incomplete: a heterozygote is a blended mix of both alleles i.e. red and white alleles produces the color pink
codominance: 2 alleles are both expressed but are not blended i.e. blood types A and B
explain the following terms:
1) pleiotropism
2) polygenism
3) penetrance
4) epistasis
5) recessive lethal alleles
1) pleiotropism: one gene effects many aspects of an organism’s phenotype that appear to be unrelated i.e. mutation in one gene may cause altered development of heart, bone, and inner ears
2) polygenism: one phenotypic trait is influenced by multiple genes i.e. height is influenced by growth factors, receptors, hormones, bone deposition, muscle development, and etc.
3) penetrance: describes the likelihood that a person w/ a given genotype will express the expected phenotype (a gene can have high, incomplete, or low penetrance) i.e. women who carry a breast CA gene will display variable rates of breast CA depending on their diet, and there also may genes at other loci that can affect the penetrance of the breast CA gene
4) epistasis: expression of alleles for one gene is dependent on a different gene i.e. curly hair gene cannot be expressed if a different gene causes baldness
5) recessive allele genes: mutant alleles can cause death of an organism when present in a homozygous manner. these genes typically code for essential gene products
what is linkage?
refers to genes that are located on the same chromosome and therefore may not display independent assortment
If alleles T & G and t & g are linked, and you cross TtGg and ttgg, what will be the phenotypic ratio of the offspring?
1:1 phenotypic and genotypic ratio in this scenario
2 genes that express independent assortment & no linkage: what is the phenotypic ratio of crossing 2 heterozygous individuals TtGg x TtGg?
9:3:3:1
9 will be phenotypically dominant in both traits
3 will be phenotypically dominant in T, but phenotypically recessive in g
3 will be phenotypically recessive in t, but be phenotypically dominant in G
1 will be phenotypically recessive in both traits