|  |  |  |  | 
| EVOLUTION | MATTER & ENERGY | INFORMATION | INTERACTIONS | 
| 
 | 
 | ||||||||||||||||||||||||||||||||||||||||||
Changes/alignment with new 2019-2020 CED
| MONDAY 1/8 | TUESDAY 1/9 | WEDNESDAY 1/10 | THURSDAY 1/11 | FRIDAY 1/12 | |||||||
| SEMESTER TEST-4th Hr See test results HW: Start reading Chapter 13; WATCH these 3 videos to refresh your "Bio Brain" and take notes in your BILL by THURSDAY 1/18 Bozeman DNA & RNA part 1 Bozeman DNA & RNA part 2 Bozeman DNA Replication | SEMESTER TEST-5th Hr See test results HW: Start reading Chapter 13; WATCH these 3 videos to refresh your "Bio Brain" and take notes in your BILL by THURSDAY 1/18 Bozeman DNA & RNA part 1 Bozeman DNA & RNA part 2 Bozeman DNA Replication | ||||||||||
| MONDAY 1/15 | TUESDAY 2/16 | WEDNESDAY 2/17 | THURSDAY 2/18 | FRIDAY 1/19 | |||||||
| MLK DAY NO SCHOOL | TEST 
		STRATEGIES/FRQ's HW: Start reading Chapter 13; WATCH these 3 videos to refresh your "Bio Brain" and take notes in your BILL by THURSDAY 1/18 Bozeman DNA & RNA part 1 Bozeman DNA & RNA part 2 Bozeman DNA Replication | Cut out prep HW: Start reading Chapter 13; WATCH these 3 videos to refresh your "Bio Brain" and take notes in your BILL by THURSDAY 1/18 Bozeman DNA & RNA part 1 Bozeman DNA & RNA part 2 Bozeman DNA Replication | DNA 
		Cut & paste BILL-replication ?'s Build a DNA activity by Kim Foglia-Leading strand 3.A.1.b. Ligase Topoisomerase Replication ST. OLAF animations DNA replication HW: Start reading Chapter 13; WATCH these 3 videos to refresh your "Bio Brain" and take notes in your BILL by TODAY Bozeman DNA & RNA part 1 Bozeman DNA & RNA part 2 Bozeman DNA Replication | DNA 
		Cut & paste BILL-replication ?'s Build a DNA activity by Kim Foglia-lagging strand LO. 3.3; 3A.1.a.5; 3.A.1.b.1; Ligase Topoisomerase Replication ST. OLAF animations DNA replication HW: BILL DNA replication ?'s due TUES 1/23 | |||||||
| MONDAY 1/22 | TUESDAY 1/23 | WEDNESDAY 1/24 | THURSDAY 1/25 | FRIDAY 1/26 | |||||||
| DNA THEATER TRANSCRIPTION & mRNA PROCESSING 3.A.1.b.4; 3.A.1.c; LO 3.4 Genes to protein slide show Eukaryotic transcription Lactose persistance Translation modeling HW: 1. BILL- DNA replication ?'s due TOMORROW 2. BILL-Alternative gene splicing due WED 3.Take Google docs quiz 1 by THURS 4.Download DNA people slide show, watch video then take the Google docs quiz 2 by TUES 3.A.1.a.4. & LO 3.2 | BILL
		DNA replication ?'s 
		due TRANSLATION THEATER ST. OLAF animations -transcription -translation 3.A.1.b.4; 3.A.1.c; LO 3.4 What's a pirate's favorite Amino acid? HW: 1. BILL-Alternative gene splicing due TOMORROW 2.Take Google docs quiz 1 by TUES DNA to RNA to protein Puzzle Modified from Tom Mueller due FRI 
		3. Download 
				 
				
				DNA 
				people slide show, watch 
		video  then take the 
		 
		
		Google docs quiz 2 by TUES | BILL-Alternative gene splicing due 3.A.1.c.2 KNOW YOUR MOLECULES Desktop activity ORGANIZER 3.A.1.5. HW: 1.Take DNA Google docs quiz 1 by TOMORROW 2. DNA to RNA to protein Puzzle due FRI Modified from Tom Mueller 3. Download DNA people slide show, watch video then take the Google docs quiz 2 by TUES 3.A.1.a.4. & LO 3.2 | LUNCH HELP- TEST CORRECTIONS TAKE DNA GOOGLE DOCS QUIZ 1 by TODAY TATA boxes STRUCTURE/FUNCTION HW: 1. DNA to RNA to protein Puzzle due TOMORROW Modified from Tom Mueller 3. Download DNA people slide show, watch video then take the Google docs quiz 2 by TUES 3.A.1.a.4. & LO 3.2. | DNA to RNA to protein Puzzle
		due TODAY From Tom Mueller STRUCTURE/FUNCTION White boards HW: 1. Download DNA people slide show, watch video then take the Google docs quiz2 by TUES 3.A.1.a.4. & LO 3.2. | |||||||
| MONDAY 1/29 | TUESDAY 1/30 | WEDNESDAY 1/31 | THURSDAY 2/1 | FRIDAY 2/2 | |||||||
| 
 OPERONS Operon ?'s Pool Noodle Operons From Kristin Dotti CATALYST LEARNING CURRICULUM LO 3.21 & 3.23 McGraw Hill Tryptophan Repressor Lac Operon Lac operon induction Lactose persistance Virtual Lac Operon White board operons From Jennifer Forsyth 3.B.1 a; 3.B.1.b.; LO 3.23 [SP1.4] HW: See TO DO LIST 1. Download Viruses, bacteria, prions & DNA technology slide show and Watch Part 1 video AND TAKE Google Docs Quiz by WEDNESDAY 3. OPERON ?'s due TUE 4. Watch the DNA Technology videos Part 2 and Part 3 then take the Google docs quiz by FRIDAY | Download  
		DNA people slide show,
		Watch the 
		video  then take the 
		 
		
		Google docs quiz 2 
		by TODAY3.A.1.a.4. OPERONS OPERONS OPERONS OPERON ?'s due TUES 2/6 PBS RNAi video 3.A.1.c. & LO 3.4 HW: TO DO LIST 1. Download Viruses, bacteria, prions & DNA technology slide show and WATCH Part 1 AND take Google docs quiz by THURS 2.Watch the DNA Technology videos Part 2 and Part 3 then take the Google docs quiz by FRIDAY | NOVA
		
		
		
		Epigenetics TED-Epigenetics Lick your rat Dutch Hunger Winter Epigenetics & Father's diet Sheep help scientists study Huntington's Epigenetic tags on sperm & obesity Epigenetic changes & autism Epigenetics, Autism, & Twins HW: TO DO LIST 1. BILL-Methyl groups due WED 3. Download Viruses, bacteria, prions & DNA technology slide show and watch the DNA Technology videos Part 2 and Part 3 then take the Google docs quiz by FRIDAY | Download Viruses, bacteria, prions & DNA technology slide show and WATCH Part 1 AND TAKE the Google docs quiz by TODAY Kuru Prions PREE-ONS ? or PRY-ONS ? "Catch up" day Work on Operon ?Transcription/Translation Venn, BILL-Methyl groups HW: TO DO LIST 1 Download Viruses, bacteria, prions & DNA technology slide show and watch the DNA Technology videos Part 2 and Part 3 then take the Google docs Google Docs quiz by TOMORROW 2. Transcription/Translation Venn due MON Operon ? due TUES BILL-Methyl groups due WED | Watch the DNA Technology videos Part 2 and Part 3 then take the Google Docs Quiz by TODAY PLASMID ACTIVITY Plasmid ?'s 3.A.1.e & f Recombinant plasmid cut & paste from Biologycorner.com Plasmid DNA Insulin DNA Sumanas plasmid video Plasmid tutorial: HW:TO DO LIST 1. Recombinant plasmid ?'s due MONDAY 2. Online Textbook-Complete INVESTIGATION: How can gel electrophoresis be used to analyze DNA? by TUES 3. RFLP ?'s DUE WED | |||||||
| MONDAY 2/5 | TUESDAY 2/6 | WEDNESDAY 2/7 | THURSDAY 2/8 | FRIDAY 2/9 | |||||||
| Transcription/translation VENN due DESKTOP RFLP ANALYSIS DESKTOP RFLP ANALYSIS ?'s 3.A.1.e; SP 6.1 & 6.2 HW:TO DO LIST 1.Preview Labs at LabBench DNA analysis/Bacterial transformation and complete the Prelab ?'s before THURS | OPERON packet DUE SUB HERE CHANGE OF PLANS! You really need to understand the 2 labs you will do on LAB DAY so we are going to concentrate on doing the preview today and skip doing GEL #2 since you already saw how Gel #1 worked. 1. Make this correction for Gel #1 in your packet 2. Use LAB BENCH site to preview labs for LAB DAY next week DNA analysis/Bacterial transformation TAKE NOTES IN YOUR BILLand complete the Prelab ?'s before THURS | BILL-Methyl 
		groups due Know your molecules #2 organizer #2 HW: See To DO LIST Preview Labs at LabBench DNA analysis/Bacterial transformation and complete the Prelab ?'s before TOMORROW | Preview 2 Labs at LabBench DNA analysis/Bacterial transformation and complete the Prelab ?'s due TODAY Small interfering RNA's (siRNA) 2.E.1.b.5 Bozeman-DNA experiments Griffith experiment Avery, et.al video Avery experiment opener 3.A.1.a.4 Paternity Problems due tomorrow Modified from Access Excellence Draw a Plasmid/DNA HW: RECOMBINANT PLASMID ?'s DUE TOMORROW | RECOMBINANT PLASMID ?'s DUE Practice with micropipetters Mutations BILL notes BILL-mutation compare 3.C.1.a.1; 3.C.1.c.1; 3.A.1.c.2 McGraw Hill videos Deletion & insertion frameshifts Substitutions Bozeman-Mutations 
		Pearson: 
 
 HW: Desktop RFLPAnalysis ? due MON | |||||||
| MONDAY 2/12 | TUESDAY 2/13 | WEDNESDAY 2/14 | THURSDAY 2/15 | FRIDAY 2/16 | |||||||
| DESKTOP RFLP ?'s due AP BIO LAB DAY 
 
 Bozeman video LAB 6: Bacterial Transformation & DNA FINGERPRINTING LAB We are the World (watch this before the PCR song) BIORAD Scientists for Better PCR PCR 
 | LAB DAY PART DEUX 
 
 Check answers Kahoot Review over DNA, RNA, proteins, viruses, bacteria, DNA technology DNA clickers HW: Finish pGLO packet ?'s up to DAY 2 before TOMORROW | LAB Wrap up Check transformation plates Class time to work on finishing labs HW: Finish data analysis, graphing, and lab ?'s for Niemann-Pick GLO transformation lab ?'s due TOMORROW | pGLO LAB PACKET DUE Niemann Pick LAB PACKET DUE GMO's GMO Pros/Cons Scishow GMOs StarTalk/Neil Degrasse Tyson-GMO's GMO's- Good or Bad PROS: Nebraska Corn Board Eye on Nye-GMO GMO's CONS: Are GMO's Bad for our Health? Viral replication HW: Study for TEST TUES | NO SCHOOL HW: Study for TEST TUES | |||||||
| MONDAY 2/19 | TUESDAY 2/20 | WEDNESDAY 2/21 | THURSDAY 2/22 | FRIDAY 2/23 | |||||||
| NO SCHOOL | 
 MC TEST Chapter 13-17 DNA structure, Replication, Transcription, Translation, Bacteria, Viruses, DNA Technology HW: 1. Watch "Draw Photosynthesis" video and fill in your DIAGRAM showing the steps by FRIDAY | Finish MC test today HW: 1. Watch "Draw Photosynthesis" video and fill in your DIAGRAM showing the steps by FRIDAY 2 Start "Reading for understanding" Chapters 8, 9, 10 3. REVIEW your "BIO" brain for Chap 8 & 9 | WRITE FRQs in class from LIST I CHOOSE 1. Watch "Draw Photosynthesis" video and fill in your DIAGRAM showing the steps by FRIDAY 2 Start "Reading for understanding" Chapters 8, 9, 10 3. REVIEW your "BIO" brain for Chap 8 & 9 4. BILL Draw Chloroplast DUE MON | Watch "Draw Photosynthesis" video and fill in your DIAGRAM showing the steps by TODAY HW: BILL Draw Chloroplast DUE MON | |||||||
| MONDAY 2/24 | TUESDAY 2/25 | WEDNESDAY 2/26 | THURSDAY 2/27 | FRIDAY 2/28 | |||||||
|  | ALL lab packets from Lab Day due |  | |||||||||
| MONDAY 4/3 | TUESDAY 4/4 | WEDNESDAY 3/5 | THURSDAY 3/6 | FRIDAY 3/7 | |||||||
| IN CLASS ESSAYS I pick from | EVOLUTION TO DO LIST | Make DNA Test corrections by 
		3:30 TODAY HW: | 
		
		
		
		
		
		
		
		
		Bacteria, 
		viruses, prions
		
		
		
		Kuru
		
		
		
		Prions in the news 
		
		
		
		
		
		Prions video
		
		
		
		NOVA-Brain eaters/Prions
		
		
		
		CJDt
		type with me trial link
| Slide shows POWERPOINT version 
		DOWNLOAD POWERPOINT | DNA people Watch the DNA people video then take the Google docs quiz 
		
		Chapter 13-DNA 
		Notes 
		Chapter 14-Genes 
		to polypeptides 
		Notes 
		Chapter 17 Gene Regulation
		Notes 
		
		Chap 17 Viruses, bacteria, prions & DNA technology
		
		Notes | 
|  Handouts 
		
		
		TEACHER LINKS: 
		DNA Replication VIDEOS 
 
		
		Snurp splicing MCGraw Hill videos -Transduction -
		
		Griffith experiment Sumanas 
		
		Transcription/translation Plasmid essay | VOCAB 
		Learning 
		objectives KNOW YOUR MOLECULES #2 WITH BARCODES ORGANIZER 
		
		
		
		
		
		
		
		
		
		
		Beta-Globin gene
		
		
		Activity 
		
		 
		
		Genetic code decoder 
		
		DNA fingerprinting 
		modified from Jim Buckley 
		
		 
		Mr. Knight 
 
		Who Ate the Cheese? 
		Activity BILL Trade and Grade 
		
		FUNNIES | 
HOW DO YOU SAY IT?
prion
endonuclease
bacteriophage    
bacteriophage
ligase
synthetase
| Bozeman Biology Videos | RNA Kill switches for cancer | ||||||
| DNA & RNA Video Essentials | DNA Part 2 | Transcription Translation 4/7/12 | What is DNA? | DNA Fingerprinting 5/11/12 | Viral Replication | Secret of Life | |
| Central Dogma Transcription Translation | Gene Regulation | Replication 4/7/12 | Molecular Biology 4/30/12 | Topoisomerase | Topoisomerase | Meselson-Stahl Experiment 5/11/12 | |
| Mutations 5/9/12 | New Labs 8 & 9 (Old Lab 6) | Lab 6 Cellular Respiration | |||||
| YOU TUBE VIDEOS | |||||||
| We are the World Watch 1st Scientists for Better PCR BioRad-PCR (with subtitles) | Bio Rad- GTCA (with subtitles) Biology Despacito | CRASH COURSE DNA | Astonishing Molecular Machines | Central Dogma Song | Mr. Hsu DNA Replication Song | ABC News-Age reversal in mice Colbert Report-Ronald DePinho Blame it on the DNA | I'll make a Protein Out of You | 
|  Translation
		
		GIF | DNAtube DNA Replication Telomerase Replication Translation Chromosome #2 | Nova: Cracking the code of life PHYLO NPR story | NOVA RNAi | Catalase Floating Disc Lab | TED TALKS RNAi | HHMI-Telomeres | What is a GM food? | 
| Crash Course- Extreme Genetic Engineering | CRISPR-TED talks National Geographic-CRISPR | It's OK to be SMART DNA | |||||
Davud Knuffke's Prezis
| Molecular Genetics 1 - DNA Introduction | Molecular Genetics 2 - Central Dogma | Molecular Genetcis 3- Regulation of Gene Expression | Molecular Genetics 4 - Viruses | Molecular Genetics 5- Biotechnology | 
| Review games & Tutorials | |
| Review What you should already know? (Old BIO I & II slideshows/review games) ONLINE QUIZZES/ACTIVITIES Chapters 13-17 Review over DNA, RNA, proteins, viruses, bacteria, DNA technology KAHOOT DNA Interactive Crosswords Chapter 16-DNA Chapter 17-From Gene to Protein Central Dogma tutorial DNA Replication Wiley Protein synthesis race DNA structure and replication quiz DNA replication game Virtual gel electrophoresis BIOLOGY CORNER DNA Quiz 1 DNA Quiz 2 DNA Quiz 3 DNA Quiz 4 DNA Quiz 5 DNA Quiz 6 Mrs. Muskopf-DNA Technology Viruses Chromosomes & Karyotypes QUIA GAMES Protein synthesis-Rags to riches Biotechnology DNA DNA DNA DNA structure and function Gene regulation and translation DNA RNA battleship Nucleic acid games Learn genetics- Transcribe & Translate a gene Genetic code game Build a DNA Science Geek DNA: Structure and Function RNA: Structure and Transcription Translation: Protein Synthesis Unit 5 Storyboard: From DNA to Protein Unit 5 Test Review Transcription/Translation game Sequencing DNA for yourself QUIA Replication of DNA-Battleship game Protein synthesis interactive DNA Interactive Transcription Game Sequence for yourself | 
		
		DNA Sequencing Wiley RNA WORLD TELOMERES | 
| What to Know DNA | What to Know Gene to Protein | What to Know Gene Regulation | What to Know DNA Technology | 
| UNIT 1 Chemistry of Life | |
| ENDURING 
		UNDERSTANDING SYI-1 Living systems are organized in a hierarchy of structural levels that interact | |
| ESSENTIAL KNOWLEDGE SYI-1.A.1 The subcomponents of biological molecules and their sequence determine the properties of that molecule. | |
| TOPIC 1.2 Elements of Life | |
| ENDURING UNDERSTANDING ENE-1 The highly complex organization of living systems requires constant input of energy and the exchange of macromolecules | |
| LEARNING OBJECTIVE ENE-1.A Describe the composition of macromolecules required by living organisms. | ESSENTIAL KNOWLEDGE ENE-1.A.1 Organisms must exchange matter with the environment to grow, reproduce, and maintain organization. ENE-1.A.2 Atoms and molecules from the environment are necessary to build new molecules— a. Carbon is used to build biological molecules such as carbohydrates, proteins, lipids, and nucleic acids. Carbon is used in storage compounds and cell formation in all organisms. b. Nitrogen is used to build proteins and nucleic acids. Phosphorus is used to build nucleic acids and certain lipids. | 
| TOPIC 1.3 Introduction to Biological Macromolecules | |
| ENDURING 
		UNDERSTANDING SYI-1 Living systems are organized in a hierarchy of structural levels that interact | |
| LEARNING OBJECTIVE SYI-1.B Describe the properties of the monomers and the type of bonds that connect the monomers in biological macromolecules. | ESSENTIAL KNOWLEDGE SYI-1.B.1 Hydrolysis and dehydration synthesis are used to cleave and form covalent bonds between monomers. X EXCLUSION STATEMENT—The molecular structure of specific nucleotides and amino acids is beyond the scope of the AP Exam. X EXCLUSION STATEMENT—The molecular structure of specific carbohydrate polymers is beyond the scope of the AP Exam. | 
| TOPIC 1.4 Properties of Biological Macromolecules | |
| LEARNING OBJECTIVE SYI-1.B Describe the properties of the monomers and the type of bonds that connect the monomers in biological macromolecules. | ESSENTIAL KNOWLEDGE SYI-1.B.2 Structure and function of polymers are derived from the way their monomers are assembled— a. In nucleic acids, biological information is encoded in sequences of nucleotide monomers. Each nucleotide has structural components: a five-carbon sugar (deoxyribose or ribose), a phosphate, and a nitrogen base (adenine, thymine, guanine, cytosine, or uracil). DNA and RNA differ in structure and function | 
| TOPIC 1.5 Structure and Function of Biological Macromolecules | |
| ENDURING 
		UNDERSTANDING SYI-1 Living systems are organized in a hierarchy of structural levels that interact. | |
| LEARNING OBJECTIVE SYI-1.C Explain how a change in the subunits of a polymer may lead to changes in structure or function of the macromolecule | ESSENTIAL KNOWLEDGE SYI-1.C.1 Directionality of the subcomponents influences structure and function of the polymer— a. Nucleic acids have a linear sequence of nucleotides that have ends, defined by the 3’ hydroxyl and 5’ phosphates of the sugar in the nucleotide. During DNA and RNA synthesis, nucleotides are added to the 3’ end of the growing strand, resulting in the formation of a covalent bond between nucleotides. b. DNA is structured as an antiparallel double helix, with each strand running in opposite 5’ to 3’ orientation. Adenine nucleotides pair with thymine nucleotides via two hydrogen bonds. Cytosine nucleotides pair with guanine nucleotides by three hydrogen bonds. | 
| TOPIC 1.6 Nucleic Acids | |
| ENDURING UNDERSTANDING IST-1 Heritable information provides for continuity of life. | |
| LEARNING OBJECTIVE IST-1.A Describe the structural similarities and differences between DNA and RNA. | ESSENTIAL KNOWLEDGE IST-1.A.1 DNA and RNA molecules have structural similarities and differences related to their function— a. Both DNA and RNA have three components—sugar, a phosphate group, and a nitrogenous base—that form nucleotide units that are connected by covalent bonds to form a linear molecule with 5’ and 3’ ends, with the nitrogenous bases perpendicular to the sugar-phosphate backbone. b. The basic structural differences between DNA and RNA include the following: i. DNA contains deoxyribose and RNA contains ribose. ii. RNA contains uracil and DNA contains thymine. iii. DNA is usually double stranded; RNA is usually single stranded. iv. The two DNA strands in double-stranded DNA are antiparallel in directionality. | 
| UNIT 6 Gene Expression and Regulation | |
| TOPIC 6.1 DNA and RNA Structure | |
| ENDURING UNDERSTANDING IST-1 Heritable information provides for continuity of life. | |
| LEARNING OBJECTIVE IST-1.K Describe the structures involved in passing hereditary information from one generation to the next. | IST-1.K.1 DNA, and in some cases RNA, is the primary source of heritable 
		information. IST-1.K.2 Genetic information is transmitted from one generation to the next through DNA or RNA— a. Genetic information is stored in and passed to subsequent generations through DNA molecules and, in some cases, RNA molecules. b. Prokaryotic organisms typically have circular chromosomes, while eukaryotic organisms typically have multiple linear chromosomes. IST-1.K.3 Prokaryotes and eukaryotes can contain plasmids, which are small extra-chromosomal, double-stranded, circular DNA molecules. | 
| LEARNING OBJECTIVE IST-1.L Describe the characteristics of DNA that allow it to be used as the hereditary material. | IST-1.L.1 DNA, and sometimes RNA, exhibits specific nucleotide base 
		pairing that is conserved through evolution: adenine pairs with thymine 
		or uracil (A-T or A-U) and cytosine pairs with guanine (C-G)— a. Purines (G and A) have a double ring structure. b. Pyrimidines (C, T, and U) have a single ring structure | 
| TOPIC 6.2 Replication | |
| ENDURING UNDERSTANDING IST-1 Heritable information provides for continuity of life | |
| 
		 | IST 1.M.1 DNA replication ensures continuity of 
		hereditary information— 
		 | 
| IST 1.N Describe the mechanisms by which genetic information flows from DNA to RNA to protein 
 
 
 
 
 | 1.N.1 | 
| IST 1.N.2 Genetic information flows from a sequence of 
		nucleotides in DNA to a sequence of bases in an mRNA molecule to a 
		sequence of amino acids in a protein. | |
| 1.N.3 RNA polymerases use a single template strand 
		of DNA to direct the inclusion of bases in the newly formed RNA 
		molecule. This process is known as transcription. | |
| IST 1.N.4 The DNA strand acting as the template strand 
		is also referred to as the noncoding strand, minus strand, or antisense 
		strand. Selection of which DNA strand serves as the template strand 
		depends on the gene being transcribed. | |
| IST 1.N.5 The enzyme RNA polymerase synthesizes mRNA 
		molecules in the 5’ to 3’ direction by reading the template DNA strand 
		in the 3’ to 5’ direction. | |
| IST 1.N.6 In eukaryotic cells the mRNA transcript 
		undergoes a series of enzyme-regulated modifications— | |
| IST 1.O Describe how the phenotype of an organism is determined by its genotype | IST 1.O.1 Translation of the mRNA to generate a 
		polypeptide occurs on ribosomes that are present in the cytoplasm of 
		both prokaryotic and eukaryotic cells and on the rough endoplasmic 
		reticulum of eukaryotic cells. | 
| IST 1.O 1 In prokaryotic organisms, translation of the 
		mRNA molecule occurs while it is being transcribed. | |
| IST 1.O.3 Translation involves energy and many 
		sequential steps, including initiation, elongation,and termination.  | |
| IST 1.O. 4 The salient features of translation include— | |
| IST 1.O.5 Genetic information in retroviruses is a 
		special case and has an alternate flow of information: from RNA to DNA, 
		made possible by reverse transcriptase, an enzyme that copies the viral 
		RNA genome into DNA. This DNA integrates into the host genome and 
		becomes transcribed and translated for the assembly of new viral 
		progeny. | |
| IST 2.A | IST 2.A.1 Regulatory sequences are stretches of DNA that interact with regulatory proteins to control transcription | 
| IST 2.A.2 Epigenetic changes can affect gene expression 
		through reversible modifications of DNA or histones. | |
| IST 2.A.3 The phenotype of a cell or organism is 
		determined by the combination of genes that are expressed and the levels 
		at which they are expressed— | |
| IST 2.B Explain how the location of regulatory 
		sequences relates to their function. | IST 2.B.1 Both prokaryotes and eukaryotes have groups 
		of genes that are coordinately regulated— | 
| IST | IST 2.C.1 Promoters are DNA sequences upstream of the 
		transcription start site where RNA polymerase and transcription factors 
		bind to initiate transcription. | 
| IST 2.C.2 Negative regulatory molecules inhibit gene 
		expression by binding to DNA and blocking transcription. | |
| IST 2.D Explain the connection between the regulation 
		of gene expression and phenotypic differences in cells and organisms. | IST 2.D.1 Gene regulation results in differential gene expression and influences cell products and function | 
| IST 2.D.2 | |
| IST | IST 2.E.1 Changes in genotype can result in changes in 
		phenotype— | 
| IST 2.E.2 Alterations in a DNA sequence can lead to 
		changes in the type or amount of the protein produced and the consequent 
		phenotype. DNA mutations can be positive, negative, or neutral based on 
		the effect or the lack of effect they have on the resulting nucleic acid 
		or protein and the phenotypes that are conferred by the protein. | |
| IST | IST 4.A.1 Errors in DNA replication or DNA repair 
		mechanisms, and external factors, including radiation and reactive 
		chemicals, can cause random mutations in the DNA— | 
| IST 4.A.2 Errors in mitosis or meiosis can result in 
		changes in phenotype— | |
| IS | IST 4.B.1 Changes in genotype may affect phenotypes 
		that are subject to natural selection. Genetic changes that enhance 
		survival and reproduction can be selected for by environmental 
		conditions— | 
| IST 
 | IST 1.P.1 Genetic engineering techniques can be used to 
		analyze and manipulate DNA and RNA— | 

| Use of our material: We have worked very hard on 
		activities, Powerpoints/games/worksheets, etc to make this a resource 
		for our students. If you are using our materials, please give us credit 
		for our efforts by listing us as a source with links to our site. DO NOT 
		USE these materials for commercial purposes.  
		PLEASE DO NOT POST ANSWER KEYS FOR OUR MATERIALS TO OTHER WEBSITES! | 
2015 OLD CED
Big Idea 2: Biological systems utilize free energy and molecular building blocks 
to grow, to 
reproduce and to maintain dynamic homeostasis. 
Enduring understanding 2.C: Organisms use feedback mechanisms to regulate growth 
and reproduction, and to maintain dynamic homeostasis. 
Essential knowledge 2.C.1: Organisms use feedback mechanisms 
to maintain their internal environments and respond to external 
environmental changes. 
a. Negative feedback mechanisms maintain dynamic homeostasis for a particular 
condition (variable) by regulating physiological processes, 
returning the changing condition back to its target setpoint.
To foster student understanding of this concept, instructors can choose an 
illustrative example such as: 
•
Operons in gene regulation 
	
	Essential knowledge 2.E.1: Timing and coordination of specific events are
	
	
	necessary for the normal development of an organism, and 
	these events are regulated by a variety of mechanisms. 
	
	
	a. Observable cell differentiation results from the expression of genes
	
	
	for tissue-specific proteins. 
	
	
	b. Induction of transcription factors during development results in 
	
	sequential gene expression. 
	
	
	Evidence of student learning is a demonstrated understanding of each of the 
	following: 
	
	1. Homeotic genes are involved in developmental patterns and 
	
	sequences. 
	
	
	2. Embryonic induction in development results in the correct 
	
	timing of events. 
	
3. Temperature and the availability of water determine seed germination in most plants.
	
	4. Genetic mutations can result in abnormal development. 
	
	5. Genetic transplantation experiments support the link between gene 
	expression and normal development. 
	
	
	6. Genetic regulation by microRNAs plays an important role in the 
	development of organisms and the control of cellular
	functions. 
	
	
	c. Programmed cell death (apoptosis) plays a role in the normal 
	
	development and differentiation. 
	
	
	Students should be able to demonstrate understanding of the above concept by 
	using an illustrative example such as: 
	
	•
	Morphogenesis of fingers and toes 
	
	•
	Immune function 
	
	•
	C. elegans development 
	
	•
	Flower development 
	
	
	✘✘Names of the 
	specific stages of embryonic development are beyond the scope of the course 
	and the AP Exam.
Learning Objectives: 
LO 2.31 
The student can connect concepts in and across domains 
to show that timing and coordination of specific events are necessary for normal 
development in an organism and that these 
events are regulated by multiple mechanisms. [See SP 7.2] 
LO 2.32 
The student is able to use a graph or diagram to analyze 
situations or solve problems (quantitatively or qualitatively) that 
involve timing and coordination of events necessary for normal 
development in an organism. [See SP 1.4] 
LO 2.33 
The student is able to justify scientific claims with 
scientific evidence to show that timing and coordination of several events are 
necessary for normal development in an organism and that these events are 
regulated by multiple 
mechanisms. [See SP 6.1]
LO 2.34 
The student is able to describe the role of programmed 
cell death in development and differentiation, the reuse of 
molecules, and the maintenance of dynamic homeostasis. [See SP
7.1]
Big Idea 3: Living systems store, retrieve, transmit 
and respond to information essential to life processes.
Enduring understanding 3.A: Heritable information provides for continuity of life.
	
	
	a. Genetic information is transmitted from one generation to the next 
	
	through DNA or RNA. 
	
	
	Evidence of student learning is a demonstrated understanding of each of the 
	following: 
	
	
	1. Genetic information is stored in and passed to subsequent generations 
	through DNA molecules and, in some cases, RNA
	molecules. 
	
	
	2. Noneukaryotic organisms have circular chromosomes, while eukaryotic 
	organisms have multiple linear chromosomes, although in 
	biology there are exceptions to this rule. 
	
	
	3. Prokaryotes, viruses and eukaryotes can contain plasmids, which are small 
	extra-chromosomal, double-stranded circular
	DNA 
	molecules. 
	
	
	4. The proof that DNA is the carrier of genetic information involved a 
	number of important historical experiments. These 
	
	include: 
	
	
	i. Contributions of Watson, Crick, Wilkins, and Franklin on 
	
	the structure of DNA 
	
	
	ii. Avery-MacLeod-McCarty experiments 
	iii. Hershey-Chase experiment 
	
	
	5. DNA replication ensures continuity of hereditary information. 
	i. Replication is a semiconservative process; that is, one strand serves as 
	the template for a new, complementary strand. 
	ii. Replication requires DNA polymerase plus many other essential cellular 
	enzymes, occurs bidirectionally, and differs in the 
	production of the leading and lagging strands. 
	
	
	6. Genetic information in retroviruses is a special case and has 
	
	an alternate flow of information: from RNA to DNA, made 
	
	possible by 
	reverse transcriptase, an enzyme that copies the
	viral RNA genome into DNA. This DNA 
	integrates into the host genome and 
	becomes transcribed and translated for the assembly of new viral progeny. 
	[See also 3.C.3] 
	
	
	topoisomerase, are outside the scope of the course for the purposes of the AP 
	Exam.
	
	b. DNA and RNA molecules have structural similarities and differences that 
	define function. [See also 4.A.1] 
	
	
	Evidence of student learning is a demonstrated understanding of each of the 
	following:	
	
	bonds to form a linear molecule with 3' and 5' ends, with the nitrogenous 
	bases perpendicular to the 
	sugar-phosphate backbone. 
	
	2. The basic structural differences include: 
	i. DNA contains deoxyribose (RNA contains ribose). 
	ii. RNA contains uracil in lieu of thymine in DNA. 
	iii. DNA is usually double stranded, RNA is usually single 
	
	stranded. 
	
	
	iv. The two DNA strands in double-stranded DNA are antiparallel in 
	directionality. 
	
	
	3. Both DNA and RNA exhibit specific nucleotide base pairing that is 
	conserved through evolution: adenine pairs with thymine or uracil (
	A-T or A-U) and cytosine pairs with guanine
	(C-G). 
	
	i. Purines (G and A) have a double ring structure. 
	ii. Pyrimidines (C, T and U) have a single ring structure. 
	
	4. The sequence of the RNA bases, together with the structure of the RNA 
	molecule, determines RNA function. 
	i. mRNA carries information from the DNA to the ribosome. 
	ii. tRNA molecules bind specific amino acids and allow information in the 
	mRNA to be translated to a linear 
	peptide sequence. 
	iii. rRNA molecules are functional building blocks of 
	
	ribosomes. 
	
	iv. The role of RNAi includes regulation of gene expression at the 
	level of mRNA transcription. 
	
	
	c. Genetic information flows from a sequence of nucleotides in a gene 
	
	to a sequence of amino acids in a protein. 
	
	
	
	Evidence of student learning is a demonstrated understanding of each of 
	the following: 
	
	
	1. The enzyme RNA-polymerase reads the DNA molecule in the 
	3' to 5' direction and synthesizes complementary mRNA molecules that 
	determine the order of amino acids in the
	polypeptide. 
	
	
	2. In eukaryotic cells the mRNA transcript undergoes a series of 
	enzyme-regulated modifications. 
	
	
	To foster student understanding of this concept, instructors can choose an 
	illustrative example such as: 
	
	
	•
	Addition of a poly-A tail 
	
	
	•
	Addition of a GTP cap 
	
	
	•
	Excision of introns 
	
	
	3. Translation of the mRNA occurs in the cytoplasm on the 
	
	ribosome. 
	
	
	4. In prokaryotic organisms, transcription is coupled to 
	
	translation of the message. Translation involves energy and many steps, 
	including 
	initiation, elongation and termination. 
	
	
	✘✘
	The details and 
	names of the enzymes and factors involved in each of these steps are beyond 
	the scope of the course andthe AP®Exam.
	
	
	The salient features include:
	i. The mRNA interacts with the rRNA of the ribosome to initiate translation 
	at the (start) codon. 
	ii. The sequence of nucleotides on the mRNA is read in triplets 
	
	called codons. 
	
	
	iii. Each codon encodes a specific amino acid, which can be deduced by using 
	a genetic code chart. Many amino acids 
	have more 
	than one codon. 
	
	
	✘✘ 
	Memorization of the genetic code is beyond the scope of the course 
	and the AP Exam. 
	
	
	iv. tRNA brings the correct amino acid to the correct place on 
	
	the mRNA. 
	
	
	v. The amino acid is transferred to the growing peptide chain. 
	
	
	
	vi. The process continues along the mRNA until a "stop" codon 
	
	is reached. 
	
	
	vii. The process terminates by release of the newly synthesized 
	
	peptide/protein. 
	
	
	d. Phenotypes are determined through protein activities. 
	
	
	To foster student understanding of this concept, instructors can choose an 
	illustrative example such as: 
	
	
	•
	Enzymatic reactions 
	
	
	•
	Transport by proteins 
	
	
	•
	Synthesis 
	
	
	•
	Degradation 
	
	
	e. Genetic engineering techniques can manipulate the heritable 
	
	information of DNA and, in special cases, RNA. 
	
	
	
	To foster student understanding of this concept, instructors can 
	
	choose an illustrative example such as: 
	
	
	
	•
	Electrophoresis 
	
	
	•
	Plasmid-based transformation 
	
	
	•
	Restriction enzyme analysis of DNA 
	
	
	
	•
	Polymerase Chain Reaction (PCR) 
	
	
	f. Illustrative examples of products of genetic engineering include: 
	
	
	
	•
	Genetically modified foods 
	
	
	•
	Transgenic animals 
	
	
	•
	Cloned animals 
	
	
	•
	Pharmaceuticals, such as human insulin or factor X 
Learning Objectives: 
LO 3.1 
The student is able to construct scientific explanations that 
use the structures and mechanisms of DNA and RNA to support 
the claim that DNA and, in some cases, that RNA are the primary 
sources of heritable information. [See SP 6.5] 
LO 3.2 
The student is able to justify the selection of data from 
historical investigations that support the claim that DNA is the 
source of heritable information. [See SP 4.1] 
LO 3.3 
The student is able to describe representations and 
models that illustrate how genetic information is copied for transmission 
between generations. [See SP 1.2] 
LO 3.4 
The student is able to describe representations and 
models illustrating how genetic information is translated into 
polypeptides. [See SP 1.2]
LO 3.5 
The student can justify the claim that humans can 
manipulate heritable information by identifying at least two 
commonly used technologies. [See SP 6.4] 
LO 3.6 The student can predict how a change in a specific DNA or RNA sequence can result in changes in gene expression. [See SP 6.4]
Enduring understanding 3.B: Expression of genetic information involves cellular 
and molecular mechanisms. 
	
	Essential knowledge 3.B.1: Gene regulation results in differential gene
	
	
	expression, leading to cell specialization. 
	
	
	a. Both DNA regulatory sequences, regulatory genes, and small 
	
	regulatory RNAs are involved in gene expression. 
	
	Evidence of student learning is a demonstrated understanding of each 
	
	of the following: 
	
	1. Regulatory sequences are stretches of DNA that interact with regulatory 
	proteins to control transcription. 
	
	To foster student understanding of this concept, instructors can 
	
	choose an illustrative example such as: 
	
	•
	
	
	Promoters 
	
	•
	
	
	Terminators 
	
	•
	
	
	Enhancers 
	
	
	2. A regulatory gene is a sequence of DNA encoding a regulatory 
	
	protein or RNA. 
	
	
	b. Both positive and negative control mechanisms regulate gene expression in 
	bacteria and viruses. 
	
	Evidence of student learning is a demonstrated understanding of each 
	
	of the following: 
	
	1. The expression of specific genes can be turned on by the presence 
	
	of an inducer. 
	
	
	2. The expression of specific genes can be inhibited by the 
	
	presence of a repressor. 
	
	
	3. Inducers and repressors are small molecules that interact with regulatory 
	proteins and/or regulatory sequences. 
	
	
	4. Regulatory proteins inhibit gene expression by binding to DNA and 
	blocking transcription (negative control). 
	
	
	5. Regulatory proteins stimulate gene expression by binding to DNA and 
	stimulating transcription (positive control) or binding to repressors 
	to inactivate repressor function. 
	
	
	6. Certain genes are continuously expressed; that is, they are 
	
	always turned "on," e.g., the ribosomal genes. 
	
	c. In eukaryotes, gene expression is complex and control involves
	
	regulatory genes, regulatory elements and transcription factors that 
	
	
	act in concert. 
	
	
	Evidence of student learning is a demonstrated understanding of each 
	
	of the following: 
	
	1. Transcription factors bind to specific DNA sequences and/or other 
	regulatory proteins. 
	
	2. Some of these transcription factors are activators (increase expression), 
	while others are repressors (decrease expression). 
	
	
	3. The combination of transcription factors binding to the 
	
	regulatory regions at any one time determines how much, if any, 
	
	of the 
	gene product will be produced. 
	
	
	d. Gene regulation accounts for some of the phenotypic differences between 
	organisms with similar genes. 
	
Learning Objectives: 
LO 3.18 
The student is able to describe the connection between 
the regulation of gene expression and observed differences 
between different kinds of organisms. [See SP 7.1] 
LO 3.19 
The student is able to describe the connection between the 
regulation of gene expression and observed differences between 
individuals in a population. [See SP 7.1] 
LO 3.20 
The student is able to explain how the regulation of 
gene expression is essential for the processes and structures that 
support efficient cell function. [See SP 6.2] 
LO 3.21 
The student can use representations to describe how 
gene regulation influences cell products and function. 
See SP 1.4] 
	
	
	Essential knowledge 3.B.2: A variety of intercellular and intracellular
	
	
	signal transmissions mediate gene expression. 
	
	
	a. Signal transmission within and between cells mediates gene 
	
	expression. 
	
	
	To foster student understanding of this concept, instructors can choose an 
	illustrative example such as: 
	
	•
	Cytokines regulate gene expression to allow for cell replication
	
	
	and division. 
	
	•
	Mating pheromones in yeast trigger mating gene expression. 
	
	
	•
	Levels of cAMP regulate metabolic gene expression in bacteria. 
	
	
	•
	Expression of the SRY gene triggers the male sexual development 
	pathway in animals. 
	
	•
	Ethylene levels cause changes in the production of different enzymes, 
	allowing fruits to ripen. 
	
	•
	Seed germination and gibberellin. 
	
	
	b. Signal transmission within and between cells mediates cell 
	
	function. 
	
	
	To foster student understanding of this concept, instructors can
	
	
	choose an illustrative example such as: 
	
	
	•
	Mating pheromones in yeast trigger mating genes expression and sexual 
	reproduction. 
	
	•
	Morphogens stimulate cell differentiation and development. 
	
	
	•
	Changes in p53 activity can result in cancer.
	
	
	•
	HOX genes and their role in development. 
	
Learning Objectives: 
LO 3.22 
The student is able to explain how signal pathways 
mediate gene expression, including how this process can affect 
protein production. [See SP 6.2] 
LO 3.23 
The student can use representations to describe 
mechanisms of the regulation of gene expression. [See SP 1.4] 
Enduring understanding 3.C: The processing of genetic information is imperfect 
and is a source of genetic variation. 
	
	Essential 
knowledge 3.C.1. Changes in genotype can result in changes in phenotype
a. Alterations in a DNA sequence can lead to changes in 
the type or amount of the protein produced and the consequent phenotype. [See 
also 3.A.1] 
Evidence of student learning is a demonstrated understanding of the following:
1. DNA mutations can be positive, negative or neutral 
based on the effect or the lack of effect they have on the resulting nucleic 
acid or protein and the phenotypes that are conferred by the protein. 
b. Errors in DNA replication or DNA repair 
mechanisms, and external factors, including radiation and reactive chemicals, 
can cause random changes, e.g., mutations in the DNA. 
Evidence of student learning is a demonstrated understanding of 
the following: 
1. Whether or not a mutation is detrimental, beneficial or neutral depends 
on the environmental context. Mutations are the primary source of genetic 
variation. 
c. Errors in mitosis or meiosis can result in changes 
in phenotype. Evidence of student learning is a demonstrated 
understanding of each of the following: 
1. Changes in chromosome number often result in new phenotypes, including 
sterility caused by triploidy and increased vigor of other polyploids. [See also 
3.A.2] 
2. Changes in chromosome number often result in human 
disorders with developmental limitations, including Trisomy 21 (Down syndrome) 
and XO (Turner syndrome). [See also 3.A.2, 3.A.3] 
d. Changes in genotype may affect phenotypes that are 
subject to natural selection. Genetic changes that enhance survival and 
reproduction can be selected by environmental conditions. [See also 1.A.2, 
1.C.3] 
To foster student understanding of this concept, instructors can 
choose an illustrative example such as: 
•    Antibiotic resistance mutations 
•    Pesticide resistance mutations 
•    Sickle cell disorder and heterozygote advantage 
Evidence of student learning is a demonstrated 
understanding of the following: 
1. Selection results in evolutionary change. 
 Learning Objectives: 
LO 3.24 The student is able to 
predict how a change in genotype, when expressed as a phenotype, provides a 
variation that can be subject to natural selection. [See SP 6.4, 7.2] 
LO 3.25 The student can create a 
visual representation to illustrate how changes in a DNA nucleotide sequence can 
result in a change in the polypeptide produced. [See SP 1.1] 
LO 3.26 The student is able to 
explain the connection between genetic variations in organisms and phenotypic 
variations in populations. [See SP 7.2] 
Essential knowledge 3.C.2: Biological systems have 
	multiple processes that increase genetic variation. 
	
a. The imperfect nature of DNA replication and 
	repair increases variation. 
b. The horizontal acquisitions of genetic 
	information primarily in prokaryotes via transformation (uptake of naked 
	DNA), transduction (viral transmission of genetic information), conjugation 
	(cell-to-cell transfer) and transposition (movement of DNA segments within 
	and between DNA molecules) increase variation. [See also 1.B.3] 
✘✘ Details and specifics about the various processes are beyond the scope of the course and the AP Exam.
c. Sexual reproduction in eukaryotes involving 
	gamete formation, including crossing-over during meiosis and the random 
	assortment of chromosomes during meiosis, and fertilization serve to 
	increase variation. Reproduction processes that increase genetic variation 
	are evolutionarily conserved and are shared by various organisms. [See also 
	1.B.1, 3.A.2, 4.C.2, 4. C3] 
✘✘ The details of sexual reproduction cycles in various plants and animals are beyond the scope of the course and the AP Exam. However, the similarities of the processes that provide for genetic variation are relevant and should be the focus of instruction.
Learning Objectives: 
LO 3.27 The student is able to 
compare and contrast processes by which genetic variation is produced and 
maintained in organisms from multiple domains. [See SP 7.2] 
LO 3.28 The student is able to 
construct an explanation of the multiple processes that increase variation 
within a population. [See SP 6.2] 
	
	
	Essential knowledge 3.C.3: Viral replication results in genetic variation, 
	and viral infection can introduce genetic variation into the hosts. 
	
	
	
	a. Viral replication differs from other reproductive strategies and 
	generates genetic variation via various mechanisms. [See also 1.B.3]
	
	
	
	Evidence of student learning is a demonstrated understanding of each 
	
	of the following: 
	
	1. Viruses have highly efficient replicative capabilities that allow for 
	rapid evolution and acquisition of new phenotypes. 
	
	2. Viruses replicate via a component assembly model allowing one virus to 
	produce many progeny simultaneously via the lytic
	cycle. 
	
	
	3. Virus replication allows for mutations to occur through usual 
	
	host pathways. 
	
	
	4. RNA viruses lack replication error-checking mechanisms, and 
	
	thus have higher rates of mutation. 
	
	
	5. Related viruses can combine/recombine information if they 
	
	infect the same host cell. 
	
	
	6. HIV is a well-studied system where the rapid evolution of a virus within 
	the host contributes to the pathogenicity of viral
	infection. 
	
	
	b. The reproductive cycles of viruses facilitate transfer of genetic 
	
	information. 
	
	
	Evidence of student learning is a demonstrated understanding of each 
	
	of the following: 
	
	
	1. Viruses transmit DNA or RNA when they infect a host cell. 
	
	[See also 1.B.3] 
	To 
	foster student understanding of this concept, instructors can choose an 
	illustrative example such as: 
	
	
	•
	Transduction in bacteria 
	
	
	•
	Transposons present in incoming DNA 
	
2. 
	Some viruses are able to integrate into the host DNA and establish a latent 
	(lysogenic) infection. These latent viral 
	
	genomes can result in new properties for the host such as 
	
	increased pathogenicity in bacteria. 
	
Learning Objectives: 
LO 3.29 
The student is able to construct an explanation of how 
viruses introduce genetic variation in host organisms. [See SP 6.2]
LO 3.30 
The student is able to use representations and appropriate 
models to describe how viral replication introduces genetic 
variation in the viral population. [See SP 1.4] 
| Chemistry of Life | Cells | Cell Division | Metabolism | 
| Genetics | DNA, RNA, Proteins | Evolution | Parade | 
| Plants | Body systems | Ecology | Exam Prep | 
| OTHER UNITS | Riedell Science Home | APBIO Teacher help | Riedell Bio Teacher help | 
SHOW WHAT YOU KNOW VIDEOS
Sarah
Holly F & Hannah
Holly H & Jenny
Sangah & Ally
Cole & Mia
Jesse
Jessica
Mackenzie & Blair?
Erica & Heidi
Jameson & Sydney
|  | If you find something useful, would like to suggest new links, or have corrections...please let me know. | 
SOURCES:
 http://www.zmescience.com/wp-content/uploads/2012/04/dna.jpg
http://www.zmescience.com/wp-content/uploads/2012/04/dna.jpg
| MONDAY 2/13 | TUESDAY 2/14 | WEDNESDAY 2/15 | THURSDAY 2/16 | FRIDAY 2/17 | 
| Bozeman
		
		DNA Replication Bozeman DNA & RNA part 1 Bozeman DNA & RNA part 2 | Metabolism TEST |