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This material is made freely available at www.njctl.org and is intended for the non-commercial use of students and teachers. These materials may not be used for any commercial purpose without the written permission of the owners. NJCTL maintains its website for the convenience of teachers who wish to make their work available to other teachers, participate in a virtual professional learning community, and/or provide access to course materials to parents, students and others.
Click to go to website:www.njctl.org
New Jersey Center for Teaching and Learning
Progressive Science Initiative
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AP BIOLOGY
Big Idea 3Part A
www.njctl.org
November 2012
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Big Idea 3:
Living systems store, retrieve, transmit and respond to
information essential to life processes.
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Slide 4 / 157 Big Idea 3
The following is the AP's explanation of the second Big Idea:
"Genetic information provides for continuity of life and, in most cases, this information is passed from parent to offspring via DNA. The double-stranded structure of DNA provides a simple and elegant solution for the transmission of heritable information to the next generation; by using each strand as a template, existing information can be preserved and duplicated with high fidelity within the replication process. However, the process of replication is imperfect, and errors occur through chemical instability and environmental impacts...
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"Random changes in DNA nucleotide sequences lead to heritable mutations if they are not repaired. To protect against changes in the original sequence, cells have multiple mechanisms to correct errors. Despite the action of repair enzymes, some mutations are not corrected and are passed to subsequent generations. Changes in a nucleotide sequence, if present in a protein-coding region, can change the amino acid sequence of the polypeptide. In other cases, mutations can alter levels of gene expression or simply be silent. In order for information in DNA to direct cellular processes, information must be transcribed (DNA→RNA) and translated(RNA→protein). The products of transcription and translation play an important role in determining metabolism, i.e., cellular activities and phenotypes. Biotechnology makes it possible to directly engineer heritable changes in cells to yield novel protein products."
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Big Idea 3: Part A
· The Discovery of Genes
· Chemistry of Nucleic Acids
· Chromosomes
Click on the topic to go to that section
· The Cell Cycle
· S-phase
· Mitosis
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The precipitate at the bottom of this flask is Deoxyribose Nucleic Acid. This chemical is the informational basis for all life.
Its properties allow for the storage of instructions to build living things.
Nucleic Acid
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Every molecule, organelle, cell, organ, organ system, organism and population is built by this molecule.
It is the building block of the genes that control how bodies are shaped and how organisms react to environmental factors.
This molecule is evolution.
Nucleic Acid
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"Individuals are not stable things, they are fleeting. Chromosomes too are shuffled into oblivion, like hands of cards soon after they are dealt. But the cards themselves survive the shuffling. The cards are the genes. They merely change partners and march on.
They are the replicators and we are their survival machines. When we have served our purpose we are cast aside. But genes are denizens of geological time: genes are forever."
The Selfish Gene
Richard Dawkins, Evolutionary Biologist and Oxford University professor.
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As an example, blue eyes are a phenotype; a physical trait, controlled by a single gene.
Genes Live Beyond Individuals
A recent study showed that a mutation in one individual's OCA2 gene, which produces the pigment that gives color to eyes, created a gene for blue eyes. This occurred 8,000 years ago and the new gene was passed generation to generation.
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Genes live beyond individuals
Today approximately 560,000,000 people have blue eyes. Each individual carries 2 copies of the original mutation. The gene has long outlived the human that it originated in.
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"Standing on the Shoulders of Giants"
The proof that DNA is the carrier of genetic information involved a number of important historical experiments. These include:
Griffith Transformation Experiment
Avery-Macleod-McCarty Experiment
Hershy-Chase Experiment
Contributions of Watson, Crick, Wilkins, and Franklin
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Primary Discovery
Nucleic acids were first isolated by the Swiss physician Friedrich Miescher who, in 1869, discovered a microscopic substance in the pus of discarded surgical bandages.
At the time it was an unknown cellular substance and was not considered important until many years later.
Miescher's Lab where he discovered nucleic acid
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Griffith and Transformation
In 1928 British Scientist Frederick Griffith was conducting experiments with mice to determine how bacteria made people sick.
Griffith isolated two different strains of pneumonia bacteria from mice and grew the bacteria on petri dishes in the lab.
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Griffith's Colonies
One strain grew in rough colonies and did not cause disease. The other strain grew in smooth colonies and caused disease.
Did notcause disease
Causeddisease
R straincolonies
S straincolonies
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Mice and the 2 strains
When he injected the mice with the rough (R) strain, they lived. When he injected the mice with the smooth (S) strain, they died.
However, when he heated the S strain of bacteria, killing them, and then injected the heat-killed S strain bacteria into the mice, they did not die.
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Mouse Mortality
Heating the S strain killed the bacteria and prevented them from passing disease to the mice.
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Griffith Experiment Part 2
Griffith then mixed heat-killed disease-causing S strain bacteria with live, harmless R strain bacteria and injected this mixture into mice.
Before neither heat-killed S strain or live R strain bacteria made the mice sick, but the mixture of the two caused the mice to develop pneumonia and die.
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Griffith: Part 2
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The Search for Genes
In Griffith's experiment why does the dead mouse contain living S strain when only dead S strain was injected? Theorize what may be happening.
Griffith's conclusion: Living R strain absorbs a chemical left from the dead S strain. This chemical transforms the living bacteria into the deadly S strain.
What we know now: Bacteria is capable of transformation. This is when DNA is taken in from the environment and incorporated into the bacteria's DNA. In this case the gene that produces the deadly toxin is absorbed.
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What was the chemical factor?
He also noted this factor was passed on as the bacteria reproduced.
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1 What is bacterial transformation?
A The inheritance of genetic material
B The exchange of genetic material between strains of bacteria
C The interaction between strains of bacteria
D The passage of genetic material from parent to offpsring
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2 Why was Griffith's experiment significant?
A It showed that a chemical factor transformed R strain bacteria into S strain bacteria
BIt proved dead bacteria could still transmit disease directly to mice
C It indicated proteins were the source of genetic material
D None of the above
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Closing in on the Genetic Material
After Griffith's experiment most scientists believed that the molecule transforming bacteria was a protein, not a nucleic acid.
In the early 1940s experiments performed by Oswald T. Avery and his colleagues at the Rockefeller Institute for Medical Research challenged that assumption.
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Closing in on the Genetic Material
Avery used a test tube assay. This is when a scientist compares differences in test tubes after treating each differently. The benefit is that you can discover more specific reactions.
This approach will lead to more information than dead or living mice can provide.
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Closing in on the Genetic Material
First he heat-killed the S strain bacteria and mixed it with detergent. This caused the bacterial cells to break apart. Their membranes lysed and spilled out the cell's contents.
The upper portion of the test tube, the lysate, contains less dense materials like proteins, enzymes, and nucleic acids. precipitate
lysate
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Closing in on the Genetic Material
The precipitate contained the large organelles and proteins of the cell. Avery isolated the lysate to use because it contained smaller molecules that were more likely to be the genetic material.
precipitate
lysate
lysate
DNA
RNA
Proteins
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Closing in on the Genetic Material
To be sure he took the S strain lysate and mixed it with R strain to see if it would transform the bacteria to S strain and it worked.
lysateR strain
S strain
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Closing in on the Genetic Material
It is easy to tell the difference from R and S because they look different when grown on a petri dish. (R for rough edge; S for smooth edge).
R strainS strain
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Closing in on the Genetic Material
Next Avery put in an enzyme that digests proteins into the lysate and did the same experiment. What do you suspect is the result and why?
R strainlysate mixed with an enzyme that digests protein
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Closing in on the Genetic Material
Next Avery put in an enzyme that digests proteins into the lysate and did the same experiment. What do you suspect is the result and why?
S strain
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Closing in on the Genetic Material
What could you do to confirm this result? In other words what would be another way to treat the lysate that would give usable data?
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Closing in on the Genetic Material
Avery and his team devised a technique that used alcohol to isolate and purify nucleic acids from solution.
In a later experiment they mixed the purified nucleic acid from S strain with R strain bacteria. What is the expected result?
S strain
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3 Avery's experiments provide proof that the molecule responsible for transforming bacteria was
A proteinB nucleic acid
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The Definitive Proof
The Hershey–Chase experiments were a series of experiments conducted in 1952 by Alfred Hershey and Martha Chase that confirmed DNA was the genetic material.
By this time many new discoveries allowed these scientists to go beyond what others had been able to discover about nucleic acids.
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The Definitive Proof
Most importantly, intense research on viruses at the time expanded the knowledge of these tiny particles.
Hershey and Chase concentrated on bacteriophages. These viruses that infected and killed bacteria were known to only be composed of 2 things: proteins and DNA
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4 Viruses are considered non-living because
I. They cannot reproduce on their own
II. Their nucleic acid does not code for protein
III. They are not made of cells
A III onlyB II and IIIC I, II, and IIID I and III
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5 When a virus infects a bacteria cell, what part of the virus enters the bacteria?
A Only the nucleic acidB The nucleic acid and the virus head it is contained inC Only the tail fibersD Only the head
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The Definitive Proof
Secondly, a lot was being learned about radioactivity. Since they could not see the viruses, Hershey and Chase used a novel approach that took advantage of a new technique called radioactive labeling. This allowed them to track different parts of the virus by looking for radiation.
A geiger counter can find and measure radioactive particles
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The Definitive Proof
Hershey and Chase began by creating 2 kinds of radioactive viruses using a labeling technique. Below is how they made virus A.
bacteriophages
Viruses grow via lytic cycle. When they make proteins they must use the radioactive sulfur.
bacteriaradioactive SULFUR
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6 In the lytic cycle of phages
A Phage DNA is incorporated into the host cell's genome
B The viral capsid is assembled according to the genetic information of the capsid
C The entire phage is taken into the bacteriumD The cell typically dies, releasing many copies of the virus
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The Definitive Proof
The procedure is repeated to make virus B with a change in the radioactive material.
bacteriophages
Viruses grow via lytic cycle. When they make DNA they must use the radioactive phosphorus.
bacteriaradioactive PHOSPHORUS
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7 In Hershey's and Chase's experiment, the viruses' DNA will contain ________ and protein will contain ____________.
A sulfur, phosphorusB phosphorus, sulfur
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The Definitive Proof
Summary of Hershey Chase experiments:
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The Double Helix
With the data collected by Hershey and Chase the focus of the scientific community shifted to nucleic acids. DNA in particular became the focus of scientists looking to make the next big discovery.
Two pairs of scientists working in the same facility ultimately made the discoveries about DNA that led to the modern understanding of the genetic material.
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The Double Helix
Watson and Crick deciphered from the photo that DNA was a double helix. They began to build models of the structure so they could speculate on how DNA can:
1) Self replicate
2) Code for all the traits of living things
The discoverers of the DNA structure, James Watson,
left, and Francis Crick, with their model of a DNA
molecule. (A. Barrington Brown/Photo Researchers, Inc.)
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DNA and Modern Medicine
The discovery of the structure and function of DNA has led to astounding leaps in understanding of biology, heredity, and modern medicine.
"It's impossible to overstate the importance of knowing the structure of DNA." - Francis Collins, Director of the Human Genome Project
Click Here to see a DNA timeline
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8 The scientists associated with the discovery of the structure of DNA were:
A Hershey and Chase
B Watson, Crick, Wilkins, and Franklin
C Avery, MacLeod, and McCarty
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9 These scientists showed that DNA was at the root of bacterial transformation.
A Hershey and Chase
B Watson, Crick, Wilkins, and Franklin
C Avery, MacLeod, and McCarty
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10 Four of the following terms all involve the experiment of Hershey and Chase. Choose the one which does not belong.
A helix structure
B DNA
C virus
D host
E bacteriophage
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RNA and DNA
RNA and DNA are the 2 nucleic acids necessary for living organisms.
This diagram reviews the major differences in structure
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RNA and DNA
Uracil is a nitrogenous base in RNA but not DNA.
Thyamine is a nitrogenous base in DNA but not RNA.
RNA is single stranded and can fold into many shapes.
DNA is double stranded and can only be a double helix.
1 21
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DNA
DNA is an informational molecule encoding the genetic instructions used in the development and functioning of all known living organisms
This diagram highlights the major chemical features.
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DNA
The two strands run in opposite directions to each other and are therefore anti-parallel, one backbone being 3' (three prime) and the other 5' (five prime). This refers to the direction the 3rd and 5th carbon on the sugar molecule is facing.
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DNA
Nucleotides are the monomers that build the polymer strands
phosphateNitrogenous
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RNA
Nucleotides also build the single stranded polymer of RNA molecules. The single strandedness of the RNA allows it to fold on itself making many shapes.
The shape of the molecule is dictated by the sequence of nucleotides.
A hairpin loop form of RNA. Highlighted are the nucleobases (green) and the ribose-phosphate backbone (blue).
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RNA
RNA makes the molecular machinery necessary for the function of DNA. It plays a major role in the replication of DNA and the reading of the information stored in DNA.
Three- dimensional representat ion of the small ribosomal subunit . RNA is in brown, protein in blue. The act ive site is in the middle (red). This molecule reads the genet ic code.
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11 Four of the following are associated with DNA. Choose the one which is not.
A uracil
B thyamine
C adenine
D guanine
E cytosine
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12 If one strand of DNA is CGGTAC, the complementary strand would be:
A GCCTAG
B CGGTAC
C TAACGT
D GCCATG
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13 If one strand of DNA is AGCTGA, the complementary strand would be:
A TCGACU
B TCGACT
C AGCTGA
D AGTCGA
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Chromosomes Defined
A chromosome is an organized structure of DNA and protein found in cells. It is a single piece of coiled DNA containing many genes.
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Chromosomes Defined
Chromosomes vary widely between different organisms. The DNA molecule may be circular or linear, and can be composed of 100,000 to over 3,750,000,000 nucleotides in a long chain.
Typically, eukaryotic cells have large linear chromosomes and prokaryotic cells have smaller circular chromosomes.
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Prokaryotic Chromosomes
This is a chromosomal map of a bacteria, H. orenii.
Like all bacteria, this circular DNA molecule contains all the genes that are needed to make the entire organism.
This particular bacterial genome is made of ~2,500,000 nucleotides. Each different color in the outer circle represents another gene.
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Eukaryotic Chromosomes
In eukaryotes, nuclear chromosomes are packaged by proteins into a condensed structure called chromatin. This allows the very long DNA molecules to fit into the cell nucleus.
Chromosomes are the essential unit for cellular division and must be replicated, divided, and passed successfully to their daughter cells to ensure the genetic diversity and survival of offspring.
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Eukaryotic Chromosomes
Since eukaryotes are larger and more complex, eukaryotic chromosomes are much larger and require more complex methods for storage of their numerous genes.
Special proteins called histones fold and pack the DNA strand into tight coils.
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Eukaryotic Chromosomal Structure
see next slide
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see next slide
Eukaryotic Chromosomal Structure
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Eukaryotic Chromosomal Structure
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Eukaryotic Chromosomal Structure
This diagram represents a eukaryotic chromosome after replication has occurred. (1) Chromatid – one of the two identical copies of the chromosome.
(2) Centromere – the point where the two chromatids touch, and where the microtubules attach during cell division.
(3) Short arm.
(4) Long arm.
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Eukaryotic Chromosomal Structure
Chromosomes are often represented as genetic maps that show the loci of genes. This is a representation of human chromosome 7.
3
4
2
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Human Chromosomes
Each band represents a gene or a group of genes that code for a phenotype of the human. Humans have 23 pairs of chromosomes in each of their cells that contain multiple copies of ~40,000 genes.
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Eukaryotic Chromosomal Structure
Chromosomes can be diploid, 2 versions of each chromosome, or haploid, 1 version of each chromosome.
N= Number of chromatids
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Human Karyotype
A karyotype is a photograph of the actual chromosomes of an individual human. A nucleus is isolated and the chromosomes are removed and arranged. They can be used to learn about possible chromosomal abnormalities.
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Human Karyotype
What can you learn about this individual from their chromosomes?
Most likely a normal
female
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Human Karyotype
What can you learn about this individual from their chromosomes?
Abnormal number of sex chromosomes
Klinefelter syndrome
XXY
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The Life of a Cell
The life of a eukaryotic cell can be defined by the time between cell divisions. When a parent cell divides (mitosis) it produces 2 daughter cells. Over time each daughter cell will go through a series of events that will lead to the daughter cell becoming a parent cell.
Parent
Parent
Parent
Daughters
Daughters
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Human Karyotype
What can you learn about this individual from their chromosomes?
Male with extra chromosome 21
Down Syndrome
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The Life of a Cell
The cell cycle is the stages a cell goes through from division to division.
M = Miotic phase
I = Interphase
G1 = Gap Phase1
S = DNA synthesis Phase
G2 = Gap Phase 2
G0 = Gap Phase 0
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Most cells spend more than 90% of the total time of their life cycle in interphase.
There are 3 distinct sub-phases to interphase:
Interphase
· Gap 1 (G1)
· Synthesis (S Phase)
· Gap 2 (G2)
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Gap 1 (G1 phase)
The cell increases in size.
The cell increases its supply of proteins, particularly those used in the duplication process.
Duplication of organelles occurs.
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Synthesis (S-phase)
DNA replication occurs.
At the end of this sub-phase, each chromosome in the cell has doubled. The two copies of a chromosome remain attached at a central point called a centromere. Each copy is then know as a sister chromatid.
centromere
sister chromatid
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Gap 2 (G2 phase)
The cell completes its growth in preparation for division.
Increases its supply with even more proteins.
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Mitotic Phase (M phase)
This phase is the mechanical division of the nucleus and cytoplasm of the cell which results in full cell division.
Both daughter cells will enter G1 phase after the mitotic phase is complete.
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14 At which stage does DNA replication occur?
A Gap 1 B S phase C Gap 2 D Mitotic phase
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15 At which stage does duplication of organelles occur?
A Gap 1 B S phase C Gap 2 D Mitotic phase
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Cell Cycle Checkpoint Control
Cell cycle checkpoints are control mechanisms that ensure the proper division of cells. These checkpoints verify whether the processes at each phase of the cell cycle have been accurately completed before progression into the next phase.
The cell cycle checkpoints are made up of protein kinases and adaptor proteins that all play roles in the maintenance of the cell division.
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Cell Cycle Checkpoint ControlG1 Checkpoint - The first checkpoint is located at the end of the cell cycle's G1 phase, before entry into S phase. This is a key point that dictates wether the cell should divide, delay division, or enter a resting stage.
The G1 checkpoint is where eukaryotes typically arrest the cell cycle if cell division is unnecessary or impossible. Then the cell passes into G0 for an extended period of no division or growth
Nerve and Muscle cells are non-dividing cells which get stuck at a "G0 phase" because the G1 checkpoint is never given the ok to proceed.
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Cell Cycle Checkpoint ControlG2 Checkpoint - The second checkpoint is located at the end of G2 phase, triggering the start of the M phase. In order for this checkpoint to be passed, the cell has to check a number of factors to ensure the cell is ready for mitosis. Most importantly is that the chromosomes have duplicated properly.
If this checkpoint is passed, the cell initiates the many molecular processes that signal the beginning of mitosis.
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Cell Cycle Checkpoint ControlMetaphase Checkpoint - The mitotic spindle checkpoint occurs at the point in metaphase where all the chromosomes have aligned at the mitotic plate. The tension created by spindle fibers, the mechanism for pulling chromosomes apart, is what is checked before division proceeds.
If this checkpoint is not passed the cell division will be halted and the cell will die. If the mechanism has failed then the resulting daughter cells may be dangerous to the rest of the organism.
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Kinases Control the CheckpointsCyclin-dependent kinases (CDKs) are a family of protein kinases first discovered for their role in regulating the cell cycle.
Kinases are enzymes that catalyze the transfer of a phosphate group from ATP to a specified molecule. When activated these proteins have a large impact on cell processes.
CDKs must be activated by a chemical known as a cyclin. The complex is known as maturation promotion factor (MPF).
MPF
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Cyclins
Cyclins are a family of proteins that control the progression of cells through the cell cycle by activating cyclin-dependent kinase (Cdk) enzymes.
Cyclins were originally named because their concentration varies in a cyclical fashion during the cell cycle. The oscillations of the cyclins, namely fluctuations in cyclin gene expression, induce oscillations in Cdk activity to drive the cell cycle.
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Cyclin Activity During the Cell Cycle
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Kinases Control the CheckpointsThe CDK, Cyclin, MPF control system is highly complex. Many factors are still unknown. The important points are:
-Cyclin is produced when the cell is completing S-phase as a signal that chromosomes have been successfully copied.
-When Cyclin and CDK combine and form a high concentration of MPF in the cell, the cell will begin to enter M phase
-When chromosome pairs are successfully separated there is a release of a chemical that breaks down cyclin, reducing MPF. This low MPF induces the start of G1 phase
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Replication
The functions of a cell are determined by its DNA.
Cells have to reproduce many times. In complex organisms, trillions of copies are made from one original cell.
But when cells reproduce, they must replicate (or copy) their DNA.
The structure of DNA reveals how trillions of copies of the DNA in one of your cells can be made, and be almost exactly the same each time.
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Watson & CrickWhen Watson and Crick published the structure of DNA in a short article in 1953 they stated:
"It has not escaped our notice that the specific pairing we have postulated immediately suggests a possible copying mechanism for the genetic material."
The fact that there are two DNA strands that are mirror images of one another suggested how copies could be made of each DNA sequence.
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DNA Molecule as Template
Each molecule of DNA is made of a template strand and a new strand.
The template is used to make the new strand.
The template strand is also known as the parent strand since it came from the original DNA molecule.
The new strand is also known as the daughter strand.
templatestrand
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The 5' end has a phosphate group at the end.
The 3' end has an -OH group at the end.
DNA is Anti-ParallelEach strand has two ends: a 5' end and a 3' end. The two strands of DNA always run in opposite directions. They are said to be anti-parallel to each other.
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The template strands of the DNA molecule separate and the new strands are made on the inside.
Separation of Strands
Click here to see an animation of the mechanism of replication
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Nucleotides can only be added to the -OH end (3`), not the 5`so all new strands are made in the 5' - 3' direction.
Adding New Nucleotides
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DNA nucleotide monomers are made ahead of time and stored in the cell.
DNA polymerase is the enzyme responsible for adding each new nucleotide to the growing strand.
Enzyme Catalyzed Reaction
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Two parent strands
One parent and one daughter strand
One parent and one daughter strand
Semi-Conservative DNA ReplicationThe result of this process is 2 new DNA molecules each having an old template strand and new strand. This is called semi-conservative because it "conserves" some of the old DNA in each copy.
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16The 3' end of a DNA strand has a phosphate at the end.
True
False
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17Why does a DNA strand only "grow" in the 5' to 3' direction?
A because DNA can only add nucleotides to the 3' end of the molecule
B because DNA can only add nucleotides to the 5' end of the molecule
C because mRNA can only read a DNA molecule from 5' to 3'
D because mRNA can only read a DNA molecule from 3' to 5'
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3' ATCGGGTTAACGCGTAAA 5' template strand
5' ______________________ 3' new strand
Replication Practice
What is the sequence of the new strand?
3' GGTTACTAATCGAGCCCCT 5' template strand
5' ______________________ 3' new strand
What is the sequence of the new strand?
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18If the parent DNA strand is 5' ATCGATACTAC 3', what will the daughter stand be
A 5' TAGCTATGATG 3'
B 3' ATCGATACTAC 5'
C 5' UAGCUAUGAUG 3'
D 3' TAGCTATGATG 5'
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The Molecular Process of Replication
A strand of DNA is replicated in segments. At intervals down the DNA molecule portions of the 2 strands separate creating replication bubbles. Either side of the replication bubble is know as a replication fork.
Click Here forAnimation
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Replication Fork
DNA replication is a precise process that must minimize error. To do this cells use many enzymes in a complex process that uses template strands to create new DNA molecules
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Topoisomerase binds to the DNA strand and cuts the double helix, causing the molecule to untwist and relax.
DNA Replication In-Depth
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Helicase breaks hydrogen bonds between nucleotide base pairs causing the two strands to separate and form areplication fork.
Small proteins called single-stranded binding proteins stabilize each strand.
DNA Replication In-Depth
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Single stranded binding proteins ensure that the nucleotide pairs do not re-bind after helicase passes.
Replication Fork
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19 Which enzyme causes the double helix to unwind by breaking hydrogen bonds?
A Topoisomerase
B Helicase
C Polymerase
D RNAse
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Since the strands are anti-parallel they are arranged in opposite directions. In order to replicate both strands in the same direction there are 2 different strategies, one for each template ( leading and lagging).
Replication Fork
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The leading strand is simple since it runs 3' to 5'. DNA polymerase can follow behind helicase and simply copy the template as it is being exposed.
Replication Fork
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DNA polymerase can only read in the 3' to 5' direction. So on the lagging strand there has to be a way to make the new strand in reverse. It starts with an enzyme called primase that adds RNA nucleotides as a primer for DNA polymerase.
Replication Fork
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DNA polymerase can latch onto the RNA primers and begin to write fragments of the new strand. Since it is going away from the replication fork it only does a portion, then it jumps back in front of the portion it just did to start again.
Replication Fork
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The fragments formed by this process are called Okazaki fragments. When the RNA primers fall away from the strand, gaps are left between the fragments that must be repaired.
Replication Fork
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DNA ligase finishes the job by filling in the gaps between the Okazaki fragments and "proofreading" the strand to be sure there are no mismatches among nucleotide pairs.
Replication Fork
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DNA ligase finishes the job by filling in the gaps between the Okazaki fragments and "proofreading" the strand to be sure there are no mismatches among nucleotide pairs.
Replication Fork
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20 In this diagram, the highlighted arrows are pointing to
A The leading strand
B DNA Polymerase
C Okazaki Fragments
D DNA Ligase
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21 The green dot represents which enzyme?
A Helicase
B Ligase
C DNA Primase
D DNA Polymerase
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22 The highlighted arrow is pointing to the
A Parent strand
B Leading strand
C Lagging strand
D Okazaki fragment
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23 The highlighted arrow is pointing to the
A Lagging strand
B Leading strand
C Replication fork
D Replication bubble
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Mitotic Phase
After a cell completes its preparation for division, it enters the mitotic phase.
There are 2 sub-phases to this phase - Mitosis (the division of the nucleus) and Cytokinesis (the division of the cytoplasm).
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prophase
anaphase
Sub-phases of Mitosis
Mitosis is further broken down into 5 sub-phases.
metaphase
telophase
prometaphase
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· Arrays of microtubles called spindles start to form from 2 centrosomes(microtubule organizing centers in the cell)
· Centrosomes start to travel to the opposite ends (poles) of the cell
· Nuclear envelope starts to break apart
centrosomes
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· Nucleoli and nuclear membrane disappear
· Spindle is nearly completed and ready to provide a scaffold for chromosomes to travel
· Chromosomes attach to the spindle at their kinetochores - a protein structure at the centromere region of the sister chromatids
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Image of a human cell during division showing:
spindles from the centrosome in green
chromosomes in blue
kinetochores in pink
Centrosomes vs. Kinetochores
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· Spindle is completely formed
· Chromosomes align on the Metaphase plate (the equator of the cell)
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24The phase of mitosis during which the nuclear envelope breaks apart is called
A interphase
B prophase
C metaphase
D anaphase
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25Which of the following pairs is correct?
Akinetochore:makes spindle; centromere:holds chromatids together
Bkinetochore:attaches to spindle; centrosome:holds chromatids together
Ccentrosome:makes spindle; centromere:holds chromatids together
Dcentrosome:holds chromatids together; kinetochore:attaches to spindle
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26During which phase do chromosomes line up on a plane located along the equator of the cell?
A interphase
B prophase
C metaphase
D anaphase
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· Sister chromatids separate from each other at the centromere and are pulled to the 2 poles by the spindle fibers
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· Nuclear envelope reappears around the chromosomes
· Nucleoli reappear
· Cell elongation continues
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Cytokinesis
· Cytokinesis differs for plant and animal cells
· Following telophase, the cytoplasm divides.
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27During which phase does the nuclear envelope re-form?
A interphase
B metaphase
C anaphase
D telophase
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28The process by which the cytoplasm of a eukaryotic cell divides is called
A mitosis
B cytokinesis
C teloplase
D spindle formation
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29Which of these is not like the others?
A CytokinesisB TelophaseC AnaphaseD MetaphaseE PrometaphaseF Prophase
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Cytokinesis - Animal Cells
A ring of microfilaments forms a contractile ring around the outside of the cell.
The ring forms a cleavage furrow which splits the cytoplasm in two.
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Cytokinesis - Plant CellsVesicles containing cell wall material collect in the center of the cell and then fuse together.
The cell plate forms from the inside out and turns into a wall between the 2 new cells.
The membranes surrounding the vesicles fuse to form new parts of the plasma membrane.
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Comparison of Cytokinesis
animal cell
plant cell
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30Cytokinesis in a plant cell is a result of the cell:
A spontaneously dividing
B forming a cleavage furrow in the middle
C splitting from the inside out
D a cell wall being created
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Summary of Phases of the Cell CycleInterphase· Gap 1 (G1)· Synthesis (S Phase)· Gap 2 (G2)
Mitotic Phase (M phase)· Mitosis Prophase Prometaphase Metaphase Anaphase Telophase· Cytokinesis
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Review: Label The Sub-Phases of Mitosisand Cytokinesis
Telophase
CytokinesisMetaphaseProphase Prometaphase
Anaphase
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