Mendelian laws. There are four main types of inheritance, autosomal recessive, autosomal dominant, or sex- linked. Autosomal recessive and dominant traits mean that the traits are carried/ passed down on genes that are not found on sex chromosomes, X and Y. Sex- linked traits are traits that are found on only the X or Y chromosomes. Also, the class learned about traits that do not follow Mendelian laws. For example, pigmentation of the skin is related to many traits, not just one, this is called polygenic traits. There are many other types of non- Mendelian genetics like codominance, which is when an organism is heterozygous but does not display the dominant allele, but a mix of the dominant and recessive alleles. There is also epistasis, which is when a gene controls how another gene functions (one gene acts as a light switch for the other gene turning it on or off). To apply these new teachings, each person in class in a group of three or two researched a specific genetic disorder and created a voice thread about the disorder that they researched. Each voicethread included the type of inheritance of the disorder, where the mutated gene was located, symptoms of the disorder, how the disorder affects an individual, and lastly to interview a person who has or works with this specific disorder and include the interview into the voicethread in some way. The genetic disorders varied from eye cancers, to muscular dystrophy, to 22q11.2 deletion syndrome. Then, every student needed to individually comment on each voicethread discussing grows and glows. Another activity we did to better understand genetics was watch the documentary Cracking the Code of Life. This documentary followed how Celera and the Human Genome Project connected to solving many genetic mutations and the technologies that are being used to cure and find treatments for cystic fibrosis, Tay Sachs, cancers, and many other types of illnesses. Check out AP Bio Rockstars for posts about Cracking the Code of Life documentary as well as for links to look at thevoicethread projects!
Chapter 16 was all about the replication of DNA. In order to help better understand, we created our own DNA in class. Using paper, we drew out a DNA molecule on green paper. We then used helicase, scissors, to open and unwound our DNA. Then, a new nucleotides are matched up by DNA polymerase in the 3' to 5' direction of the original strand. Polymerase can only read DNA in the 3'- 5' direction, but since DNA is anti-parallel, DNA polymerase cannot read the other half of the original DNA strand, called the Lagging Strand. Thus, an enzyme called primase makes RNA primers on the lagging strand of DNA telling Polymerase when to start and stop, called Okazaki fragments. Ligase, tape in the representation done in class, then sticks these fragments together. The result is two identical DNA molecules.
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| DNA Replication activity that we did in class! Green represents the original strand of DNA while the pink represents the newly formed sections of DNA which results in two identical DNA molecules |


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