growth and reproduction · 2019. 11. 1. · 1 g 1 checkpoint g 1 g 0 if a cell receives a go-ahead...
TRANSCRIPT
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Growth and Reproduction
Introduction to Biology
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The Key Roles of Cell Division
• The ability to reproduce is one of the key features that separates life from non-life.
• All cells have the ability to reproduce, by making exact copies of themselves.
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• In unicellular organisms, division of one cell reproduces the entire organism
• In multicellular organisms, cell division is needed for: o Development of an embryo from a
sperm/egg o Growth o Repair
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LE 12-2
Reproduction
100 µm
Tissue renewal Growth and development
20 µm 200 µm
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Asexual Reproduction • Asexual reproduction is reproduction
that involves a single parent producing an offspring. o The offspring produced are, in most cases,
genetically identical to the single cell that produced them.
o Asexual reproduction is a simple, efficient, and effective way for an organism to produce a large number of offspring.
o Prokaryotic organisms (like bacteria) reproduce asexually, as do some eukaryotes (like sponges)
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Sexual Reproduction • In sexual reproduction, offspring are
produced by the fusion of two sex cells – one from each of two parents. These fuse into a single cell before the offspring can grow. o The offspring produced inherit some
genetic information from both parents.
o Most animals and plants, and many single-celled organisms, reproduce sexually.
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Contrasting Reproduction Types
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Cell Division• Cells duplicate their genetic
material before they divide, ensuring that each daughter cell receives an exact copy of the genetic material, DNA.
• A dividing cell duplicates its DNA, allocates the two copies to opposite ends of the cell, and only then splits into daughter cells.
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Cellular Organization of the Genetic Material
• A cell’s endowment of DNA (its genetic information) is called its genome.
• DNA molecules in a cell are packaged into chromosomes.
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• The genetic information that is passed on from one generation of cells to the next is carried by chromosomes.
• Every cell must copy its genetic information before cell division begins.
• Each daughter cell gets its own copy of that genetic information.
• Cells of every organism have a specific number of chromosomes.
Chromosomes
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Prokaryotic Chromosomes
• Prokaryotic cells lack nuclei. Instead, their DNA molecules are found in the cytoplasm.
• Most prokaryotes contain a single, circular DNA molecule, or chromosome, that contains most of the cell’s genetic information.
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Eukaryotic Chromosomes • In eukaryotic cells, chromosomes
are located in the nucleus, and are made up of chromatin.
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• Chromatin is composed of DNA and histone proteins.
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• DNA coils around histone proteins to form nucleosomes.
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• The nucleosomes interact with one another to form coils and supercoils that make up chromosomes.
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Chromosomes During Cell Division
• In preparation for cell division, DNA is replicated and the chromosomes condense
• Each duplicated chromosome has two sister chromatids, which separate during cell division
• The centromere is the narrow “waist” of the duplicated chromosome, where the two chromatids are most closely attached
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LE 12-4
Chromosome duplication (including DNA synthesis)
0.5 µm
Centromere
Sister chromatids
Separation of sister
chromatids
Centromeres Sister chromatids
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Phases of the Cell Cycle• The cell cycle consists of
o Mitotic (M) phase (mitosis and cytokinesis) o Interphase (cell growth and copying of
chromosomes in preparation for cell division)
• Interphase (about 90% of the cell cycle) can be divided into subphases: o G1 phase (“first gap”) o S phase (“synthesis”) o G2 phase (“second gap”)
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LE 12-5
G1
G2
S (DNA synthesis)
INTERPHASE
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G1 Phase: Cell Growth• In the G1
phase, cells increase in size and synthesize new proteins and organelles.
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S Phase: DNA Replication• In the S (or
synthesis) phase, new DNA is synthesized when the chromosomes are replicated.
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G2 Phase: Preparing for Cell Division
• In the G2 phase, many of the organelles and molecules required for cell division are produced.
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M Phase: Cell Division• In eukaryotes, cell
division occurs in two stages: mitosis and cytokinesis. o Mitosis is the
division of the cell nucleus.
o Cytokinesis is the division of the cytoplasm.
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Important Cell Structures Involved in Mitosis
• Chromatid – each strand of a duplicated chromosome
• Centromere – the area where each pair of chromatids is joined
• Centrioles – tiny structures located in the cytoplasm of animal cells that help organize the spindle
• Spindle – long proteins (part of the cytoskeleton) that the centrioles produce o Helps move the chromosomes into place.
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Prophase• During
prophase, the first phase of mitosis, the duplicated chromosome condenses and becomes visible.
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Prophase • The centrioles
move to opposite sides of nucleus and help organize the spindle.
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Prophase • The spindle
forms and DNA strands attach at a point called their centromere.
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Prophase • The
nucleolus disappears and nuclear envelope breaks down.
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Metaphase • During
metaphase, the second phase of mitosis, the centromeres of the duplicated chromosomes line up across the center of the cell.
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Metaphase • The spindle fibers
connect the centromere of each chromosome to the two poles of the spindle.
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Anaphase • During anaphase,
the third phase of mitosis, the centromeres are pulled apart and the chromatids separate to become individual chromosomes.
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Anaphase • The
chromosomes separate into two groups near the poles of the spindle.
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Telophase • During telophase,
the fourth and final phase of mitosis, the chromosomes spread out into a tangle of chromatin.
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Telophase • A nuclear
envelope re-forms around each cluster of chromosomes.
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Telophase • The spindle
breaks apart, and a nucleolus becomes visible in each daughter nucleus.
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• Cytokinesis is the division of the cytoplasm.
• The process of cytokinesis is different in animal and plant cells.
Cytokinesis
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Cytokinesis in Animal Cells
• The cell membrane is drawn in until the cytoplasm is pinched into two equal parts.
• Each part contains its own nucleus and organelles.
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LE 12-9a
Cleavage furrow 100 µm
Contractile ring of microfilaments
Daughter cells
Cleavage of an animal cell (SEM)
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Cytokinesis in Animal Cells
• In plants, the cell membrane is not flexible enough to draw inward because of the rigid cell wall.
• Instead, a cell plate forms between the divided nuclei that develops into cell membranes.
• A cell wall then forms in between the two new membranes.
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LE 12-9b
1 µm
Daughter cells Cell plate formation in a plant cell (TEM)
New cell wall Cell plate
Wall of parent cell
Vesicles forming cell plate
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LE 12-10
Nucleus Cell plate Chromosomes Nucleolus
Chromatin condensing 10 µm
Prophase. The chromatin is condensing. The nucleolus is beginning to disappear. Although not yet visible in the micrograph, the mitotic spindle is starting to form.
Prometaphase. We now see discrete chromosomes; each consists of two identical sister chromatids. Later in prometaphase, the nuclear envelope will fragment.
Metaphase. The spindle is complete, and the chromosomes, attached to microtubules at their kinetochores, are all at the metaphase plate.
Anaphase. The chromatids of each chromosome have separated, and the daughter chromosomes are moving to the ends of the cell as their kinetochore micro- tubules shorten.
Telophase. Daughter nuclei are forming. Meanwhile, cytokinesis has started: The cell plate, which will divide the cytoplasm in two, is growing toward the perimeter of the parent cell.
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LE 12-6ca
INTERPHASE PROPHASE PROMETAPHASE
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LE 12-6ca
INTERPHASE PROPHASE PROMETAPHASE
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LE 12-6ca
INTERPHASE PROPHASE PROMETAPHASE
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LE 12-6da
METAPHASE ANAPHASE TELOPHASE AND CYTOKINESIS
10 µ
m
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LE 12-6da
METAPHASE ANAPHASE TELOPHASE AND CYTOKINESIS
10 µ
m
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LE 12-6da
METAPHASE ANAPHASE TELOPHASE AND CYTOKINESIS
10 µ
m
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Virtual Onion Root Tip Mitosis Lab
Click here to start
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Binary Fission• Prokaryotes (bacteria and
archaea) reproduce by a type of cell division called binary fission
• In binary fission, the chromosome replicates (beginning at the origin of replication), and the two daughter chromosomes actively move apart
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LE 12-11_1
Origin of replication
Cell wall
Plasma membrane
Bacterial chromosome
E. coli cell
Two copies of origin
Chromosome replication begins. Soon thereafter, one copy of the origin moves rapidly toward the other end of the cell.
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LE 12-11_2
Origin of replication
Cell wall
Plasma membrane
Bacterial chromosome
E. coli cell
Two copies of origin
Chromosome replication begins. Soon thereafter, one copy of the origin moves rapidly toward the other end of the cell.
Replication continues. One copy of the origin is now at each end of the cell.
Origin Origin
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LE 12-11_3Origin of replication
Cell wall
Plasma membrane
Bacterial chromosome
E. coli cell
Two copies of origin
Chromosome replication begins. Soon thereafter, one copy of the origin moves rapidly toward the other end of the cell.
Replication continues. One copy of the origin is now at each end of the cell.
Origin Origin
Replication finishes. The plasma membrane grows inward, and new cell wall is deposited.
Two daughter cells result.
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The Evolution of Mitosis• Since prokaryotes evolved
before eukaryotes, mitosis probably evolved from binary fission
• Certain protists exhibit types of cell division that seem intermediate between binary fission and mitosis
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LE 12-12Bacterial chromosome
Chromosomes
Microtubules
Prokaryotes
Dinoflagellates (Type of plankton)
Intact nuclear envelope
Kinetochore microtubules
Kinetochore microtubules
Intact nuclear envelope
Diatoms (Type of Algae)
Centrosome
Most eukaryotes
Fragments of nuclear envelope
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The Cell Cycle Control System
• The sequential events of the cell cycle are directed by a distinct cell cycle control system, which is similar to a clock
• The clock has specific checkpoints where the cell cycle stops until a go-ahead signal is received
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LE 12-14G1 checkpoint
G1 S
M
M checkpoint G2 checkpoint
G2
Control system
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• For many cells, the G1 checkpoint seems to be the most important one
• If a cell receives a go-ahead signal at the G1 checkpoint, it will usually complete the S, G2, and M phases and divide
• If the cell does not receive the go-ahead signal, it will exit the cycle, switching into a non-dividing state called the G0 phase
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LE 12-15
G1
G1 checkpoint
G1
G0
If a cell receives a go-ahead signal at the G1 checkpoint, the cell continues on in the cell cycle.
If a cell does not receive a go-ahead signal at the G1 checkpoint, the cell exits the cell cycle and goes into G0, a nondividing state.
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• An example of external signals is density-dependent inhibition, in which crowded cells stop dividing
• Most animal cells also exhibit anchorage dependence, in which they must be attached to a substratum (connective tissue) in order to divide
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LE 12-18aCells anchor to dish surface and divide (anchorage dependence).
When cells have formed a complete single layer, they stop dividing (density-dependent inhibition).
If some cells are scraped away, the remaining cells divide to fill the gap and then stop (density-dependent inhibition).
25 µm Normal mammalian cells
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LE 12-18b
Cancer cells do not exhibit anchorage dependence or density-dependent inhibition.
Cancer cells 25 µm
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Loss of Cell Cycle Controls in Cancer Cells
• Cancer cells do not respond normally to the body’s control mechanisms
• Cancer cells form tumors, masses of abnormal cells within otherwise normal tissue
• If abnormal cells remain at the original site, the lump is called a benign tumor
• Malignant tumors invade surrounding tissues and can metastasize, exporting cancer cells to other parts of the body, where they may form secondary tumors
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LE 12-19
Cancer cell
Blood vessel
Lymph vessel Tumor
Glandular tissue
Metastatic tumor
A tumor grows from a single cancer cell.
Cancer cells invade neighboring tissue.
Cancer cells spread through lymph and blood vessels to other parts of the body.
A small percentage of cancer cells may survive and establish a new tumor in another part of the body.
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Question:Question:When and where does When and where does DNA Replication DNA Replication take take
place?place?
Synthesis Phase (S phase)Synthesis Phase (S phase)
• S phase in interphase of the cell cycle.• Nucleus of eukaryotes
Mitosis-prophase-metaphase-anaphase-telophase
G1 G2
Sphase
interphase
DNA replication takesDNA replication takesplace in the S phase.place in the S phase.
DNA Replication
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Macromolecules: Nucleic Acids
• Examples: o RNA (ribonucleic acid)
• single helix o DNA (deoxyribonucleic acid)
• double helix
• Structure: o monomers = nucleotides
RNA DNA
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Nucleotides • 3 parts
o nitrogen base (C-N ring) o pentose sugar (5C)
• ribose in RNA • deoxyribose in DNA
o phosphate (PO4) group
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Types of nucleotides • 2 types of nucleotides
o different nitrogen bases o purines
• double ring N base • adenine (A) • guanine (G)
o pyrimidines • single ring N base • cytosine (C) • thymine (T) • uracil (U)
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Pairing of nucleotides • Nucleotides bond between
DNA strands o H bonds o purine :: pyrimidine o A :: T
• 2 H bonds o G :: C
• 3 H bonds
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DNA molecule
• Double helix o H bonds between
bases join the 2 strands
• A :: T • C :: G
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But how is DNA copied? • Replication of DNA o base pairing suggests
that it will allow each side to serve as a template for a new strand
o Zipper Model
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Proteins carry out the process of replication.
• DNA serves only as a template. DNA just stores the information.
• Enzymes and other proteins do the actual work of replication. o Enzymes unzip the double helix. o Free-floating nucleotides form hydrogen bonds with the
template strand. nucleotide
The DNA molecule unzips in both directions.
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Polymerase enzymes form covalent bonds between nucleotides in the new strand.
DNA polymerase enzymes bond the nucleotides together to form the double helix.
DNA polymerase
new strand nucleotide
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• DNA replication is semiconservative. One strand is conserved and the complementary
strand is new. original strand new strand
Two molecules of DNA
• Two new molecules of DNA are formed, each with an original strand and a newly formed
strand.