Genetics and Evolution Flashcards
Are gene products always proteins?
no, tRNA and rRNA genes and other small nuclear RNA genes do not encode polypeptides
Locus?
specific location where a gene is located on a specific chromosome
Can all physical traits be mapped on a single locus?
no, some complex traits can be controlled by many different genes and can map on many loci
Is it possible for there to be more than two different alleles of a specific gene?
yes
What is true of an individual that has two different alleles at a given locus?
there is a different allele on each of the two members of a homologous pair
Can a haploid organism like an adult fungus have recessive alleles?
no because there is only one copy of the gene
Classical Dominance?
there are three genotypes (CC, Cc, cc) but only two phenotypes are expressed because whenever the dominant is present it will be expressed
Incomplete Dominance?
phenotype is a blended mix of the alleles (red and white make pink flowers)
How many phenotypes are possible if red and white flowers display incomplete dominance?
3 (red, white, pink)
Codominance?
two alleles are both expressed but not blended (ABO blood)
What is the phenotype of an individual heterozygous for blood type A and B alleles?
AB
What is the phenotype of an individual heterozygous for blood type B and i alleles?
B
If a woman heterozygous for type A blood marries a man who is heterozygous for type B blood, what are the possible genotypes of their children?
A (A,i)
B (B,i)
AB (A,B)
O (i,i)
The Rhesus factor (Rh) follows a _____ _____ pattern.
classically dominant
Rh positive = RR, Rr
Rh negative = rr
Pleiotropism?
altering of many different, seemingly unrelated aspects of the organism’s phenotype
Polygenism?
complex traits that are influenced by many different genes (ex. height)
Penetrance?
likelihood that a person with a given genotype will express the expected phenotype
Epistasis?
expression of alleles for one gene is dependent on a different gene
100 people are homozygous for an allele that is implicated in cancer, but only 20 develop cancer. What are potential explanations for why only some people express a gene if they have the same genotype?
- the trait for cancer is probably polygenic
- cancer development is also influenced by the environment, such as exposure to carcinogens, which complicates the penetrance of the gene
What pattern of expression will a recessive allele on the X chromosome display in males?
it will always be expressed because men only have one X chromosome
Sex linked traits?
traits determined by genes on the X or Y chromosome
What type of cell division produces haploid cells from diploid cells by reducing the number of copies of each chromosome for two to one?
meiosis
Where does meiosis occur in males? females?
What is the end result for both?
males- testes, haploid spermatozoa
females- ovaries, ova
What are the specialized cells in males that undergo meiosis? females?
males- spermatogonia
females- oogonia
What makes meiosis different than mitosis?
meiosis has two rounds of cell division
recombination occurs between homologous chromosomes
What happens in prophase 1 of meiosis? (longest phase)
- chromosomes condense
- nuclear envelope breaks down
- synapsis- homologous chromosomes pair with each other, bring two copies of each gene on two different chromosomes close together (paired chromosomes are called bivalent or tetrad)
- Crossing over or recombination- genes are cut and then re ligated with genes swapped (genetic variation)
Does crossing over change the number of genes on a chromosome?
no if done error free, it is a one for one swap
Does recombination create combinations of alleles on a chromosome that are not found in the parent?
yes, it contains the same genes, but the alleles could be different and mixed up
What happens in Metaphase 1?
- alignment along the metaphase plate occurs
- tetrads are aligned at the center (mitosis- sister chromatids are aligned at the center)
What happens in Anaphase 1?
homologous chromosomes separate and sister chromatids remain together
What happens in Telophase 1?
- divides into two cells
- at this point, the cells are haploid (pair of sister chromatids)
What is the purpose of the second set of meiosis?
to separate the sister chromatids so that each cell has a single set of unreplicated chromosomes
What is the difference between meiosis 2 and mitosis?
in meiosis 2 there is a haploid number of chromosomes
mitosis there is a diploid number
What is the result after Telophase 2?
4 haploid cells have been produced from a single diploid parent cell
When homologous chromosomes separate, do all paternal and maternal chromosomes stay together in the daughter cells?
no, they separate randomly to increase genetic variation
Are the sister chromatids that separate during meiotic anaphase 2 identical in their DNA sequence?
no, they would be though if recombination had not occurred during prophase 1
Which of the following occur in meiosis, but not mitosis?
- separation of sister chromatids on microtubules
- pairing of homologous chromosomes
- recombination between sister chromatids
just 2
- happens in both
- recombination occurs between homologous chromosomes, not sister chromatids
If cells are blocked in meiotic metaphase 2 and prevented from moving on in meiosis, which one of the following will be prevented?
A. crossing over
B. separation of homologous chromosomes
C. separation of sister chromatids
D. breakdown of nuclear envelope
C
A. happens during prophase 1
B. occurs during anaphase 1
C. occurs in anaphase 2
D. occurs in prophase 1 or 2
Nondisjunction?
failure of homologous chromosomes to separate during meiosis 1 and sister chromatids during meiosis 2
A gamete normally has how many copies of each chromosome?
one (haploid)
Gametes resulting from nondisjunction will have how many copies of a given chromosome?
either 2 or none
How many copies of the chromosome will the zygote have if a nondisjunction gamete fuses with a normal gamete?
either 3 (trisomy) or 1 (monosomy)
Turner Syndrome?
only one X chromosome and no Y, female features but underdeveloped ovaries
In an individual with down syndrome, are the defects in development caused by an absence of genetic info?
no, there is too much
Mendel’s Law of Segregation?
- the two alleles of an individual are separated and passed on to the next generation singly
- ex. if a pea is heterozygous, Gg, its gametes will contain either G or g but never both
At what stage of meiosis are different alleles of a gene separated?
meiosis 1 when homologous chromosomes separate
Mendel’s Law of independent assortment?
- alleles of one gene will separate into gametes independently of alleles for another gene
- ex. shape gene and color genes do not influence each other
F1 generation?
progeny of a testcross
If the color gene and the shape gene are right next to each other on a chromosome, will they display independent assortment?
no, linkage
Rule of multiplication?
the probability of both of two independent events happening can be found by multiplying the odds of either event alone
Rule of addition?
the chance of either of two events happening (either A or B happens, not both)
A man is homozygous for eye color, bb, is married to a woman who is heterozygous at the same gene: Bb. What re the chances that a child will have Bb genotype and be a boy?
50% chance of Bb
50% chance of boy
.5 * .5 = 25%