AP Biology (2015) - Unit 3.A - Inheritance PowerPoints

AP Biology (2015) - Unit 3.A - Inheritance PowerPoints
AP Biology (2015) - Unit 3.A - Inheritance PowerPoints
AP Biology (2015) - Unit 3.A - Inheritance PowerPoints
AP Biology (2015) - Unit 3.A - Inheritance PowerPoints
AP Biology (2015) - Unit 3.A - Inheritance PowerPoints
AP Biology (2015) - Unit 3.A - Inheritance PowerPoints
AP Biology (2015) - Unit 3.A - Inheritance PowerPoints
AP Biology (2015) - Unit 3.A - Inheritance PowerPoints
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This 238-slide package of teaching PowerPoint presentations covers all of 3.A (Inheritance) in the AP Biology (2015) curriculum. Each slide includes the 'Essential Knowledge' being covered as well as key terms that students should make note of (editable).

Section 3.A includes four sections (slide counts):

     • 3.A.1 - DNA & RNA (122)
     • 3.A.2 - Cell Division (48)
     • 3.A.3 - Mendelian Patterns (50)
     • 3.A.4 - Non-Mendelian Patterns (18)

The presentations themselves contains minimal information as they are intended to be used with teacher guidance. There are 'Video' slides throughout which link to relevant and informative YouTube content. The slides are formatted to be visually pleasing and to also print well for handouts or revision. Please see the preview file (first 8 slides) for an idea of the aesthetic and level of detail in the presentation. The relevant 'Essential Knowledge' can be found below.

Suggested Use:

I have had success using these presentations to review topics after students have been exposed to the material at home. I typically have the class read relevant material (book, site, etc.) and then watch the videos the day before introducing a topic. During the class period, I use the slides to structure the discussion around the AP Bio Essential Knowledge objectives. The remaining class time is spent reinforcing the knowledge or working on activities geared toward the 'Learning Objectives'.

**These presentations are based on the AP Biology Course Guide and does not follow any textbook

As always, please let me know if you have any suggestions for improvements. These are always a work in progress!

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Dokimi AP Biology PPTs:

Big Idea 1 - Evolution (BUNDLE)

     • 1.A - Evolution (all)n
          1.A.1 - Natural Selection
          1.A.2/3 - Phenotypic Variation & Genetic Drift
          1.A.4 - Evidence for Evolution
     • 1.B - Phylogeny
     • 1.C - Speciation
     • 1.D - Origin of Life

Big Idea 2 - Matter

     • 2.A - Energy & Matter (all)
          2.A.1 - Energy Input (free)
          2.A.2 - Energy Capture & Storage
          2.A.3 - Environmental Exchanges/Interaction
     • 2.B - Cell Membrane

Big Idea 3 - Information

     • 3.A - Inheritance (all)
          3.A.1 - DNA & RNA
          3.A.2 - Cell Division
          3.A.3 - Mendelian Patterns
          3.A.4 - Non-Mendelian Patterns (free)

Big Idea 4 - Interactions & Complexity (BUNDLE)

     • 4.A - Interactions (all)
          4.A.1 - Biomolecules
          4.A.2/3/4 - Differentiation, Organelles & Organ System Interactions
          4.A.5/6 - Community & Ecosystem Interactions
     • 4.B - Competition & Cooperation
     • 4.C - Diversity

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The Essential Knowledge covered includes:

Unit 3.A - INHERITANCE

Heritable information provides for continuity of life.

3.A.1 - DNA & RNA

DNA, and in some cases RNA, is the primary source of heritable information.

a. Genetic information is transmitted from one generation to the next through DNA or RNA.

     - 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.

b. DNA and RNA molecules have structural similarities and differences that define function.

     - 1. Both have three components — sugar, phosphate and a nitrogenous base — which form nucleotide units that
       are connected by covalent bonds to form a linear molecule with and 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.

     - 1. The enzyme RNA-polymerase reads the DNA molecule in the to 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.
          -- 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 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.
          -- 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.

e. Genetic engineering techniques can manipulate the heritable information of DNA and, in special cases, RNA.

     - 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


3.A.2 - Cell Division

In eukaryotes, heritable information is passed to the next generation via processes that include the cell cycle and mitosis or meiosis plus fertilization.

a. The cell cycle is a complex set of stages that is highly regulated with checkpoints, which determine the ultimate fate of the cell.

     - 1. Interphase consists of three phases: growth, synthesis of DNA, preparation for mitosis.
     - 2. The cell cycle is directed by internal controls or checkpoints. Internal and external signals provide stop-and
          go signs at the checkpoints.
          -- Mitosis-promoting factor (MPF)
          -- Cancer results from disruptions in cell cycle control
     - 3. Cyclins and cyclin-dependent kinases control the cell cycle.
     - 4. Mitosis alternates with interphase in the cell cycle.
     - 5. When a cell specializes, it often enters into a stage where it no longer divides, but it can reenter the cell
          cycle when given appropriate cues. Nondividing cells may exit the cell cycle; or hold at a particular stage
          in the cell cycle.

b. Mitosis passes a complete genome from the parent cell to daughter cells.

     - 1. Mitosis occurs after DNA replication.
     - 2. Mitosis followed by cytokinesis produces two genetically identical daughter cells.
     - 3. Mitosis plays a role in growth, repair, and asexual reproduction
     - 4. Mitosis is a continuous process with observable structural features along the mitotic process. Evidence of
          student learning is demonstrated by knowing the order of the processes (replication, alignment, separation).

c. Meiosis, a reduction division, followed by fertilization ensures genetic diversity in sexually reproducing organisms.

     - 1. Meiosis ensures that each gamete receives one complete haploid (1n) set of chromosomes.
     - 2. During meiosis, homologous chromosomes are paired, with one homologue originating from the maternal
          parent and the other from the paternal parent. Orientation of the chromosome pairs is random with respect to
          the cell poles.
     - 3. Separation of the homologous chromosomes ensures that each gamete receives a haploid set of chromosomes composed of both maternal and paternal chromosomes.
     - 4. During meiosis, homologous chromatids exchange genetic material via a process called “crossing over,” which
          increases genetic variation in the resultant gametes.
     - 5. Fertilization involves the fusion of two gametes, increases genetic variation in populations by providing for
          new combinations of genetic information in the zygote, and restores the diploid number of chromosomes.


3.A.3 - Mendelian Patterns

The chromosomal basis of inheritance provides an understanding of the pattern of passage (transmission) of genes from parent to offspring.

a. Rules of probability can be applied to analyze passage of single gene traits from parent to offspring.

b. Segregation and independent assortment of chromosomes result in genetic variation.

     - 1. Segregation and independent assortment can be applied to genes that are on different chromosomes.
     - 2. Genes that are adjacent and close to each other on the same chromosome tend to move as a unit; the
          probability that they will segregate as a unit is a function of the distance between them.
     - 3. The pattern of inheritance (monohybrid, dihybrid, sex-linked, and genes linked on the same homologous
          chromosome) can often be predicted from data that gives the parent genotype/phenotype and/or
          the offspring phenotypes/genotypes.

c. Certain human genetic disorders can be attributed to the inheritance of single gene traits or specific chromosomal changes, such as nondisjunction.

     - Sickle cell anemia
     - Huntington’s disease
     - X-linked color blindness
     - Trisomy 21/Down syndrome

d. Many ethical, social and medical issues surround human genetic disorders.

     - Reproduction issues
     - Civic issues such as ownership of genetic information, privacy, historical contexts, etc.


3.A.4 - Non-Mendelian Patterns

The inheritance pattern of many traits cannot be explained by simple Mendelian genetics.

a. Many traits are the product of multiple genes and/or physiological processes.

     - 1. Patterns of inheritance of many traits do not follow ratios predicted by Mendel’s laws and can be identified by quantitative analysis, where observed phenotypic ratios statistically differ from the predicted ratios.

b. Some traits are determined by genes on sex chromosomes.

     - Sex-linked genes reside on sex chromosomes (X in humans).
     - In mammals and flies, the Y chromosome is very small and carries few genes.
     - In mammals and flies, females are XX and males are XY; as such, X-linked recessive traits are always expressed
          in males.
     - Some traits are sex limited, and expression depends on the sex of the individual, such as milk production in
          female mammals and pattern baldness in males.

c. Some traits result from nonnuclear inheritance.

     - 1. Chloroplasts and mitochondria are randomly assorted to gametes and daughter cells; thus, traits determined
          by chloroplast and mitochondrial DNA do not follow simple Mendelian rules.
     - 2. In animals, mitochondrial DNA is transmitted by the egg and not by sperm; as such, mitochondrial-determined
          traits are maternally inherited.
Total Pages
238 pages
Answer Key
N/A
Teaching Duration
2 months
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