* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download 2017 Reg of Mitosis Genetics Protein Synth Regulation Review
Gene therapy of the human retina wikipedia , lookup
Site-specific recombinase technology wikipedia , lookup
Frameshift mutation wikipedia , lookup
Polycomb Group Proteins and Cancer wikipedia , lookup
Microevolution wikipedia , lookup
No-SCAR (Scarless Cas9 Assisted Recombineering) Genome Editing wikipedia , lookup
X-inactivation wikipedia , lookup
Long non-coding RNA wikipedia , lookup
Nucleic acid analogue wikipedia , lookup
Short interspersed nuclear elements (SINEs) wikipedia , lookup
Artificial gene synthesis wikipedia , lookup
Designer baby wikipedia , lookup
Deoxyribozyme wikipedia , lookup
Therapeutic gene modulation wikipedia , lookup
Vectors in gene therapy wikipedia , lookup
Point mutation wikipedia , lookup
Messenger RNA wikipedia , lookup
Epigenetics of human development wikipedia , lookup
Polyadenylation wikipedia , lookup
RNA interference wikipedia , lookup
Nucleic acid tertiary structure wikipedia , lookup
History of RNA biology wikipedia , lookup
RNA silencing wikipedia , lookup
Mir-92 microRNA precursor family wikipedia , lookup
RNA-binding protein wikipedia , lookup
Epitranscriptome wikipedia , lookup
Regulation of the Cell Cycle, Non-Mendelian Genetics , Protein Synthesis, & Eukaryotic Control of Gene Expression Big Daddy!! Regulation of the Cell Cycle (Chapter 12 pgs. 242-248) Be able to explain what is being checked at the G1 , G2, and M checkpoint. Be able to explain how different types of cyclin and CDK’s help to regulate and initiate the next phase at each checkpoint. Know what each cyclin / CDK combination phosphorylates in order to initiate the next phase of the cell cycle. Be able to compare and contrast all of the differences between normal and cancerous cells (colorful sheet!) Know the signal transduction pathway that controls moving past the point of no return (G1 checkpoint) Be able to explain the significance of p53 , Ras, p21, in the production of a cancerous cell. You should be able to explain why you need at least 3 mutations in order to have a cancerous situation Genetics (portions of chapters 14 and 15) Compare and contrast different Non-Mendelian modes of inheritance to classical Mendelian inheritance and to each other including . . . Incomplete Dominance, Multiple allelic, Codominance, Sex-Linked, Autosomal Linked (same chromosome) , Polygenic, Pleiotropic, Environmental, mitochondrial and Y-linked. (pink sheet) Complete genetics problems including all of the above inheritance. Use chi-square analysis (goodness of fit) to reject or not reject null hypothesis of a certain type of inheritance. Analyze pedigrees and use process of elimination to figure out the type of inheritance Be able to explain why X-linked recessive disorders are more prevalent in male offspring Protein Synthesis (Chapter 17) Explain the central dogma of informational flow Be able to analyze and explain data from Beadle and Tatum’s classical experiment with mold that helped support the one gene – one enzyme hypothesis Be able to explain that one gene does not always code for one polypeptide, but it always codes for one RNA transcript Provide what the small letters mean and the purpose of each of the following types of RNA . . . o mRNA o rRNA o tRNA o snRNA o ncRNA o siRNA o miRNA o piRNA Be able to explain how the function of each type of RNA is dictates by its unique sequence of nucleotides which sometime dictates the unique shape of each type of RNA Be able to flawlessly use the mRNA codon chart as shown on page 339 Be able to explain in detail transcription including (initiation, elongation and termination) Be able to explain why processing can occur in eukaryotes but not in prokaryotes Be able to explain specifics regarding RNA splicing , and cap and tail placement and purposes. Know the structure of a spliceosome and explain how it recognizes introns and catalyzes the reaction of splicing. Know the function of each type of RNA polymerase in eukaryotes (I, II and III) Be able to explain how RNA polymerase II reads and builds Explain how RNA polymerase gets the energy to build new RNA strands and explain the complementary base pairing strategy. Know what UTR stands for and where it is in the RNA transcript Be able to compare and contrast the primary transcript and final transcript Be able to explain alternative RNA splicing and its evolutionary significance Know that each exon codes for a specific domain in the final polypeptide/protein Be able to explain in detail translation including (initiation, elongation, and termination) Be able to explain how tRNA gets a specific amino acid loaded onto the 3’ end Be able to explain what wobble means Know the purpose of the E, P, and A site on the large ribosomal subunit Be able to explain how certain polypeptides are targeted to stay in the cytoplasm, be transported to a membrane (organelle or cell), or exit the cell Be able to explain what each of the following is and the significance of each o Point mutation o Substitution o Silent mutation o Missense mutation o Nonsense mutation o Insertions o Deletions o Frameshift mutations o Mutagens Regulation of Eukaryotic Gene Expression (Chapter 18) Be able to explain pre-transcriptional control mechanisms, RNA processing, and post translational control mechanisms that are utilized by eukaryotic cells Be able to explain our regulation activity and use specific genes that are turned on or off in red blood cells, intestinal lining cells, smooth muscle cells in the intestine, and beta cells in the pancreas Be able to explain the mechanisms that can turn off certain sections of chromosomes for long period of time and compare and contrast euchromatin and heterochromatin Be able to compare general transcription factors and specific transcription factors including purpose and place of DNA attachment. Be able to explain the purpose of enhancers, silencers, activators, repressors, DNA bending proteins and your close personal friend RNA polymerase II. Make sure you know how to say TATA correctly or else it will freak out even your bestest of friends! Be able to compare how multiple genes that are involved in a pathway can all be turned on at the same time even though they are found on different chromosomes Be able to model how micoRNA’s target and affect mRNA Be able explain the significance of RNAi Be able to compare different cancer treatment strategies including radiation, chemotherapy, surgery, and immunotherapy. Be able to model a mechanism where a virus can cause a type of cancer