Show Menu
Cheatography

Unit 5 AP Bio Cheat Sheet (DRAFT) by

Review for the ap bio exam

This is a draft cheat sheet. It is a work in progress and is not finished yet.

Meiosi­s(5.1)

Meiosis
The process that all organisms go through in order to produce gamete­s(sex cells). The purpose it to create variation within the popula­tion. The daughter cells look similar to the parent cells but no exactly identical. It involves one round of DNA replic­ation and two round of cellular division. The resulting cells are haploid, meaning they have half of the genetic content of a typical cell.
Meiosis 1
The same as mitosis
Meiosis 2
Same as meiosis 1 except for the last phase where the cells divide into haploids.

Meiosis and Genetic Divers­ity­(5.2)

Crossing Over
Takes place during the first round of cellular division in meiosis. It is where homologous chromo­somes share genetic material. Homologous chromo­somes are two different versions of the same gene, one from mom and one from dad. Homologous chromo­somes exchange parts of their chromo­somes at the same location, therefore, no adding or subtra­cting genes, just exchanging the version of the gene.
Indepe­ndent Assortment
The way that chromo­somes line up for both the first and second rounds of meiosis. Depending on the original orient­ation of these chromo­somes, different daughter cells will form.
Random Fertil­ization
Means that there is a random chance that each egg and sperm will join one another. There are around a thousand sperm cells that can fertilize the one mature egg and the genetics found in each of them is distinct. The specific sperm that joins the specific egg for each fertil­ization is random, meaning that the same two parents are not going to produce the same child twice.
Nondis­jun­ction
Where meiotic errors occur. Creates cells with too many or too little chromo­somes which happens if the chromo­somes failed to separate properly during anaphase I or II. The result of nondis­jun­ction is miscar­riages or genetic defects.
 

Mendelian Geneti­cs(5.3)

Gregor Mandel
Came up with laws about genetics and inheri­tance including the law of indepe­ndent assortment which allows scientists to determine how genes are inherited from generation to generation
DNA
DNA and RNA are the genetic material of life. RNA is used to create proteins, so ribosomes are also found in all life
Law of Segreg­ation
States that two alleles from each parent are segregated during gamete format­ion(AKA meiosis). Basically, each gamete gets only one of the two copies of a specific gene.
Law of Indepe­ndent Assortment
States that two alleles get split up without regard to how the other alleles get split up. Basically, someone can get their father’s copy of genes for eye color but that doesn’t mean they would also get their father’s genes for hair color
Punnett Squares
Due to the rules that Gregor Mandel made, the frequency of inheri­tance can be determined when two indivi­duals are crossed through a Punnett square When a hetero­zygous and homozygous recessive is crossed, there is a 50% chance that the offspring will show up as dominant and a 50% chance that the offspring will show up as recessive.
Laws of Probab­ility
The laws of probab­ility can calculate the probab­ility of having a child with a certain trait. If A and B are mutually exclusive then: P(A or B) = P(A) + P(B) If A and B are indepe­ndent then: P(A and B) = P(A)*P(B) Pattern of Inheri­tance
Dihybrid
This inheri­tance is just like a monohybrid but instead of one gene being looked at and crossed, two genes are being crossed and looked at. Depending on the genotypes, different ratios can be made such as the 9:3:3:1 ratio
Sexlinked
Sexlinked genes involve genes that are linked to our X and Y chromo­somes instead of other autosomal chromo­somes. With these kinds of traits people will be affected if all of the X chromo­somes have the sex linked gene. Since males only have one X chromosome they are more likely to be affected. Women would need both of their X chromo­somes to have the sex linked gene depending if the disease or trait is dominant or hetero­zygous.
Evidence for Recessive
Two unaffected parents produce an affected child
Evidence for Dominant
Two affected parents produce an affected child. The only way for it to be recessive is if the family happens to mate with a lot of carriers. This is certainly possible, but if you see this, there is a strong likelihood that it may just be a single dominant trait traveling through the family tree is high
Evidence for sexlinked recessive
If a mother is affected, all of her sons will be affected. Carrier females will produce a dispro­por­tionate number of affected males. If you see signif­icantly more males shaded than females, there is a strong likelihood that the disorder is sex-linked recessive
Evidence for sexlinked dominant
If a father is affected, all of his daughters will be affected. If the mother is affected, her offspring will have a 50% chance of inheriting the condition, which isn’t any different than if it were autosomal dominant. In other words, mothers are NOT helpful in diagnosing the mechanism of inheri­tance as sex-linked dominant
Evidence for mitoch­ondrial
Yes, the chloro­plasts are inherited exclus­ively from the mother, just like the mitoch­ondria are (this applies to questions about plants). If a mother is affected, all of her offspring will be affected. If a father is affected, none of his offspring will be affected. These conditions involved disorder of ATP production (mitoc­hon­dria) or G3P production (chlor­opl­asts)
 

Non-Me­ndelian Genetics

Overall
Many traits do not follow Mendel's laws of dominant or recessive inheri­tance.
Multiple Alleles
Opposed to just having a dominant and recessive version of an allele, there many be more than two versions of a gene that contribute to the overall phenotype. Blood type is a strong example of this.
Sex-Linked Traits
Traits that exist on the sex chromo­somes wither X or Y.
Incomplete Dominance
Traits where neither allele is dominant over the other. Example is flower colors where some species have both red and white coloration but neither is dominant
Co-dom­inance
Traits in which both alleles are equally dominant, example is spots on cows.
Non-Nu­clear Inheri­tance
Inheri­tance from organe­lles. Chloro­plast and mitoch­ondria are randomly assorted so the traits are determined by chloro­plasts and mitoch­ondrion do not follow Mendelian rules.

Enviro­nmental Effects on Phenot­ype­(5.5)

Natural Selection
Some indivi­duals inherited traits or adapta­tions that raise their fitness, allowing them to survive and reproduce.
Enviro­nmental Changes
Coloration of mice. In an enviro­nment that has been covered in permafrost for the past thousand years will have a majority of mice in a light color. This allows the mice to easily blend in with their surrou­ndings.
Phenotypic Plasticity
Enviro­nmental factors can also influence the physical expression of genes(­Phe­notypic plasti­city). This occurs when indivi­duals with the same genotype exhibit different phenotypes in different enviro­nments. Organisms with phenotypic plasticity can change its physical traits in response to changes in the enviro­nment. An example of this is foxes as their coat turns white in the winter and back to orange once the snow is gone. This of course increases the organisms fitness.