EVOLUTION | MATTER & ENERGY | INFORMATION | INTERACTIONS |
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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 |
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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 |
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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
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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. |
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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 |
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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 |
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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
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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 |
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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 |
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MONDAY 2/24 | TUESDAY 2/25 | WEDNESDAY 2/26 | THURSDAY 2/27 | FRIDAY 2/28 | |||||||
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ALL lab packets from Lab Day due |
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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 |
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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. |
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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 |
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