Heredity
What process occurs after DNA replication in meiosis but not typically in mitosis, contributing to genetic variation?
DNA methylation
Crossing over
Polymerase chain reaction
Translation initiation
Considering polygenic inheritance of skin pigmentation in humans, what pattern of inheritance might be observed in a family where both parents have intermediate shades, given the continuous variation displayed by the trait?
All children inheriting a mix of light and dark traits, producing a uniform tan hue disregarding any other variable factors, including environmental exposure.
No discernible relationship between parental and child’s skin tones, with random assortment of alleles unrelated to the progenitor’s phenotype.
Complete dominance, whereby children inherit darker or lighter skin tone based on whichever parent possesses stronger pigmented alleles, showing clear segregation patterns.
Intermediate shading among children with a bell curve distribution reflecting the additive effect of numerous genes controlling pigment production.
In a plant species where red flower color (R) is dominant over white (r), what unique phenotypic ratio would you expect in the F2 generation from a dihybrid cross RrYy x RrYy if there's linkage between R and Y genes and no crossing over occurs?
An equal distribution across all four possible phenotypes due to independent assortment rules being applied.
Traditional Mendelian dihybrid cross ratio of 9 red-yellow : 3 red-green : 3 white-yellow : 1 white-green.
A monohybrid cross phenotypic ratio of approximately three dominant phenotype to one recessive phenotype regardless of color combination.
A modified phenotypic ratio favoring parental types such as 12 red-yellow : 1 red-green : 1 white-yellow : 4 white-green.
In a dihybrid cross between two heterozygous individuals (AaBb x AaBb), what is the probability of producing an offspring with the genotype Aabb?
9/16
1/16
3/16
1/4
If humans have 46 chromosomes in their somatic cells, how many chromosomes will be found in their gametes (sex cells)?
92
23
46
11.5
Given that gene S is located very close to gene T on a chromosome, what prediction can you make about their recombination frequency?
The distance between genes S and T has no effect on recombination frequency since it is random for all gene pairs.
The recombination frequency will be low as they are less likely to be separated by crossing over events due to their proximity.
Genes S and T will have an intermediate recombination frequency since they're neither too close nor too far apart on the chromosome.
Recombination frequency will be high because genes closer together are more likely to undergo crossing over.
What structural adaptation allows histones to play their role in chromatin organization?
Their positive charge allows them to interact with negatively charged DNA.
Their carbohydrate components help stabilize DNA-histone interactions through glycosidic bonds.
Their enzyme activity provides energy for chromatin remodeling complexes.
Their hydrophobic exterior repels water, allowing tighter packing of DNA strands.

How are we doing?
Give us your feedback and let us know how we can improve
What is a main use of Punnett squares in genetics?
To identify mutated alleles causing disorders
To illustrate structure of DNA molecules
To trace evolutionary relationships between species
To determine probabilities of certain phenotypes in offspring
Why might calico coat coloration in cats serve as an example of X-linked inheritance?
It's caused by X-linked alleles that are inactivated randomly in females, producing patches of different colors.
Females can exhibit calico coat coloration because they inherit two identical alleles from both parents.
Male calicos are rare and usually sterile due to having abnormal sex chromosome complements.
Calico cats are typically male, indicating that color traits are carried on the Y chromosome along with sex determination.
Sex cells, or gametes, are created through which process?
DNA replication
Meiosis
Mitosis
Interphase