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114 Cards in this Set
- Front
- Back
Powerhouses for the cell. Produce the cell’s ATP.
______malfunctions can have serious consequences for an individual’s health. More than 100 genetic _______disorders have been identified, and all lead to energy shortage, muscle weakness and chronic fatigue. |
Mitochondria
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Three metabolic stages of cellular respiration:
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Glycolysis
Krebs cycle (a.k.a Citric Acid Cycle) Electron transport chain and oxidative phosphorylation |
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Glycolysis harvests chemical energy by ?
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breaking down glucose to pyruvate
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______is a catabolic pathway during which a six-carbon glucose is split into two three-carbon sugars, which are then rearranged by a stepwise process that produces two pyruvic acid molecules.
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glycolosis
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glycolosis Occurs in the ______
-Partially oxidizes glucose (C6) in two pyruvic acid (C3) molecules |
cytoplasm
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glycolosis:A multi-step pathway that takes place in the ______
Splits glucose to ______ Occurs________ O2 |
cytoplasm
with or without pyruvate |
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The reactions of glycolysis occur in two phases
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1. Glucose activation phase2. Energy harvest phase
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-uses cellular ATP to phosphorylate (adds a phosphate group to) the glycolysis intermediates
-costs two ATP molecules per glucose |
glucose activation
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-produces ATP
-yields 4 ATP molecules per glucose -2 molecules of NADH per glucose |
energy harvest
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Glycolysis is distinct from cellular respiration because
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Glycolysis does not occur in the mitochondria.
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If there is no oxygen present then the pyruvic acid molecules from glycolysis go through _______- anaerobic (takes place without O2)-No ATP production-results in the partial degradation of sugars-regenerates NAD+
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fermentation
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Two types of fermentation The two most common products of pyruvate reduction are either
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1. Alcohol fermentation2. Lactic acid fermentation
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How can glycolysis continue producing energy when oxygen is not present?
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Fermentation regenerates the NAD+ needed for glycolysis by allowing pyruvate to accept electrons and H+ from NADH
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How is champagne different from wine?
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Both are the result of alcohol fermentation. Yeast is allowed to consume the sugars in grapes. Alcohol is produced in the process.
With wine, this process is completed BEFORE being bottled up. With champagne, the fermentation process occurs INSIDE the champagne bottle. This produces CO2 bubbles, which pressurize inside the bottle. This is why the cork flies off when you open it. |
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You help a friend move, and the next day, your arms and legs are sore. What caused the soreness?
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Your overworked muscles did not get enough O2 and switched to fermentation, which builds up lactate.
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If there is NO oxygen around then _______ occurs following glycolysis. If there IS oxygen around, the pyruvic acid molecules from glycolysis go to the _________, followed by the ______ in cellular respiration- (ATP production
-results in the complete breakdown of sugars) |
fermentation
bridge reaction Kreb’s cycle |
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The reaction that connects glycolysis to the Krebs cycle is the _________
which converts pyruvic acid to acetyl CoA. |
bridge reaction
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Occurs in the mitochondrial matrix, the innermost part of the mitochondria.
-Completes the breakdown of glucose that glycolysis started. |
kreb's cycle
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The products of glycolysis and the Kreb’s cycle:
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-NADH and FADH2-a small amount of ATP generated
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Remember that for every molecule of glucose entering glycolysis there are _ pyruvate molecules that can enter the Krebs Cycle
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2
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two turns of the Krebs Cycle are needed to complete the
breakdown of__ glucose molecule. |
1
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So where’s all the energy??
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Stored in NADH and FADH2.
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-Located in the inner mitochondrial membrane
-Accepts energy in the form of electrons from NADH and FADH2 -Use the energy from electron transfers to make ATP via oxidative phosphorylation -Produces most (90%) of the ATP of cellular respiration. |
---The electron transport system
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Electrons from NADH and FADH2 pass through a series of enzymes and other proteins called the ___________.
Their energy is used to pump H+ from the matrix into the intermembrane compartment. Creates a gradient. |
electron transport chain
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People who suffer from chronic fatigue are often recommended to take over-the-counter _____ pills.
These pills provide electrons that are needed to enter the electron transport chain and produce ATP for the cell. |
NADH
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KCN (potassium cyanide) capsules are dropped into a tank containing concentrated Sulfuric acid (H2SO4). This reaction produces deadly cyanide gas.
Cyanide binds to one of the proteins in the electron transport chain, preventing the passage of electrons and the production of ATP. Cells stop producing ATP, killing them within minutes. |
the gas chamber
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The energy-coupling mechanism.
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Chemiosmosis
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The electron transport chain ______ make ATP directly.
it generates a proton gradient across the inner mitochondrial membrane. |
does not
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is the coupling of exergonic electron flow down an electron transport chain to endergonic ATP production by the creation of a proton gradient across a membrane.
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chemiosmosis
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is the site of chemiosmotic ATP synthesis.
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The inner mitochondrial membrane
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For every NADH that feeds into the electron transport chain__ protons are moved from the mitochondrial matrix to the intermembrane compartment.
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3
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For every FADH2 that feeds into the electron transport chain _ protons are moved from the mitochondrial matrix to the intermembrane compartment.
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2
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For every proton that crosses back into the mitochondrial matrix one ATP is synthesized by
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ATP synthase.
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Cells can switch off the pathways they don’t need by
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feedback inhibition
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The ratio of ATP/ADP reflects the energy state of a cell.
Energy high => ATP/ADP ___ Energy low => ATP/ADP ____ |
high
low |
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---______is the process in which the genetic information of a cell is passed along to the next generation of cells.
Involves the division of a parent cell into 2 daughter cells. |
cell division
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Characteristics of cell division
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Replication of DNA
Equal distribution of DNA to opposite ends of the dividing cell Separation into two daughter cells |
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During the cell cycle ____ alternates with mitosis (a.k.a. M phase)
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interphase
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the period of the cell cycle when the cell is not dividing)
makes up about 90% of the cell cycle -high metabolic activity -chromosomes and organelles are duplicated |
interphase
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Cell division consists of
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nuclear division and cytoplasmic division.
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______ is the division of the nucleus.
-During this process the DNA is equally distributed into 2 daughter nuclei. |
Mitosis
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Mitosis is the division of the nucleus.
-During this process the DNA is equally distributed into 2 daughter nuclei. |
cytokinesis
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During the cell cycle the ______ replicate.---______ are threadlike structures composed of chromatin, which is DNAand proteins bound to it.
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chromosomes
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The genome of a eukaryotic cell is organized into multiple chromosomes
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Genome
Chromosomes Chromatin DNA + proteins |
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The eukaryotic chromosome has two “arms” which extend from a structure called the
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centromere
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After the DNA has replicated, there are now 2 chromosomes that are attached at the centromere.
These 2 chromosomes are called _________. So, DNA replication produces a replicated chromosome with 2 identical _________. |
sister chromatids
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During ____ (cell division), the 2 sister chromatids separate, and each chromatid forms an individual chromosome.
These 2 chromosomes get split between the 2 daughter cells resulting from a ______. |
mitosis
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If the chromosomes are photographed, the pairs can be arranged by size, shape and staining pattern to produce a
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karyotype
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are a pair of chromosomes that contain the same genes. They have the same size, centromere position and staining pattern. These are not the same as replicated chromosomes. For each pair of homologous chromosomes, you received one chromosome from your mother and one from your father.
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Homologous chromosomes
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is the condition where cells have pairs of homologous chromosomes
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diploid
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Each species has a characteristic number of chromosomes and the individual chromosomes are distinguished by __,__,___. Human cells contain __ chromosomes, __ pairs of homologous chromosomes.
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size, shape, and staining pattern-
46 23 |
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Humans: _____ (22 pairs) + 1 pair of sex chromosomes------_____ are the non-sex chromosomes
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autosomes
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Some cells have only half of the set of chromosomes and are called ____.---_____ is the condition in which cells contain one set of chromosomes.No pairs. -the ____ condition is found only in the gametes.
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haploid
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are haploid egg or sperm cells and contain half the number of chromosomes of ordinary cells.
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gametes
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Two haploid gametes unite during fertilization to form a _____ (a fertilized egg).
---____ is a diploid cell that results from the union of two haploid gametes. |
zygote
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The mitotic phase (M-phase) of the cell cycle is divided into five phases
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EARLY PROPHASE, LATE PROPHASE, METAPHASE, ANAPHASE AND TELOPHASE
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This is part of the cytoskeleton in eukaryotic cells.
It separates the chromosomes into the daughter cells during cell division. Remember, during S-phase, prior to cell division, the chromosomes duplicate. So each duplicated chromosome consists of a pair of sister chromatids. |
spindle apparatus
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-chromatin condenses-spindle apparatus forms
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Mitosis – Early Prophase
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These are protein structures on chromosomes where spindle fibers attach during mitosis.
Think of these as handles on the chromosomes that the spindle fibers hold onto. |
Kinetochores
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-nuclear envelope disappears
-Microtubules from spindle attach to the kinetochore of chromosomes -polar microtubules radiate toward the cell’s equator. Each microtubule attaches to a separate sister chromatid. |
late prophase
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-chromosomes move to and align on the equator of the cell.
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metaphase
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-sister chromatids divide into separate daughter chromosomes and move toward opposite poles.
-movement of the chromosome is accomplished by depolymerization of the microtubules at the kinetochore. (they break apart). -cell begins to elongate because the polar microtubules slide past each other and push the poles apart. |
anaphase
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-daughter chromosomes arrive at poles
-kinetochore microtubules disappear -polar microtubules elongate (pushing out on the ends of the cells) helps causes the formation of the cleavage furrow.daughter nuclear envelopes form -chromatin begins de-condensing. |
telophase
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By the end of telophase replication of the nucleus is complete and two______are present.
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genetically identical daughter nuclei
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Only one parent
Single parent passes on all its genes Rare genetic differences in offspring are the result of DNA changes, or mutations |
asexual reproduction
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Two parents give rise to offspring
Each parent passes on half its genes Greater genetic variation with offspring being genetically different from their parents and siblings |
sexual reproduction
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is a pre-requisite for sexual reproduction.
Occurs in the ovaries and the testes in mammals. A meiotic division followed by 2 rounds of cytokinesis to produce 4 daughter cells that become gametes (sperm or egg). Gametes carry HALF the genetic material of the parent. So the cells produced by ______are not identical to the parent cell. |
meiosis
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Meiosis reduces chromosome number from diploid to _____.
-_____ replication precedes meiosis (just like mitosis). In meiosis, each daughter cell receives one member of each pair of homologous chromosomes |
haploid
chromosomes |
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A second division, called ____separates the sister chromatids and puts one chromatid into each daughter nuclei.
So, at the end of meiosis, there are __ haploid daughter nuclei, each with one copy of each homologous chromosome. |
meiosis II
4 |
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Homologous chromosomes undergo pairing up
Sister chromatids are linked at centromeres, non-sister chromatids are linked at chiasmata Genetic crossing over occurs, exchange of genetic info between un-identical chromosomes. |
Unique events occur during meiosis I
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-Chromosomes condense
-Homologous chromosomes undergo pairing up |
MEIOSIS I
Prophase I |
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-Sister chromatids are linked at centromeres, non-sister chromatids are linked at chiasmata
-Genetic crossing over occurs |
MEIOSIS I
Prophase I |
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are the regions of paired homologous chromosomes where
chromatids have exchanged genetic material because of crossing over |
chiasmata
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nuclear envelope disappears
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MEIOSIS I
Prophase I |
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-chromosome pairs align at the equator, called the metaphase plate
-kinetochores of sister chromatids face same pole -centromeres of homologues face opposite poles. |
MEIOSIS I
Metaphase I |
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-spindle microtubules interact with kinetochore fibers
-homologous chromosomes move toward opposite poles -sister chromatids remain attached (this is different than mitosis) |
MEIOSIS I
Anaphase I |
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-chromosomes arrive at poles
-cell divides |
MEIOSIS I
Telophase I and cytokinesis |
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nuclear membrane that was reformed at telophase I breaks down
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MEIOSIS II
Prophase II |
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-Chromosomes align at metaphase plate as in mitosis
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MEIOSIS II
Metaphase II |
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-Sister chromatids separate and move toward opposite poles
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MEIOSIS II
Anaphase II |
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-nuclei form at opposite poles
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MEIOSIS II
Telophase II and cytokinesis |
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-cell division occurs
-four haploid daughter cells are the final result |
MEIOSIS II
Telophase II and cytokinesis |
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_____ is a unit of DNA that encodes information needed to produce proteins, cells, and entire organisms
Can be a few hundred to many thousands of nucleotides in length The location of a gene on a chromosome is called its _____ |
gene
locus (or loci) |
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-Each species has a characteristic number of chromosomes -Human cells contain __chromosomes,__ pairs.
Humans: _______ (22 pairs) + 1 pair of sex chromosomes---______ are the non-sex chromosomes. |
46
23 autosomes |
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____ are sequences of nucleotides at specific locations on chromosomes
__________ carry the same kinds of genes for the same characteristics Genes for the same characteristic are found at the same_____ on both homologous chromosomes |
genes
Homologous chromosomes loci |
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Genes for a characteristic found on homologous chromosomes may not be identical
Alternative versions of genes found at the same gene locus are called _____. _____ are formed by mutations. |
alleles
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An organism’s two alleles may be the same or different
Each cell carries two alleles per characteristic, one on each of the two homologous chromosomes If both homologous chromosomes carry the same allele (gene form) at a given gene locus, the organism is _____at that locus-- If two homologous chromosomes carry different alleles at a given locus, the organism is ______ at that locus, also called _____. |
homozygous
heterozygous hybrid |
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_____________predicts offspring genotypes and phenotypes from combinations of parental gametes
Assign letters to the different alleles of the characteristic under consideration (uppercase for dominant, lowercase for recessive) 2. Determine the possible gametes from both parentsWrite the gametes from each parent, along each side of a 2 x 2 grid (Punnett square) 4. Fill in the genotypes of each pair of combined gametes in the grid. 5. Determine the genotypic ratio based on the outcome of the Punnett Square. 6. Based on the which traits are dominant, and which are recessive, calculate the predicted phenotypic ratio. |
The Punnett square method
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How Were the Principles of Inheritance Discovered?
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Gregor Mendel - Austrian monk in a monastery in the late 1800s
--Discovered patterns of inheritance and many essential facts about genes, alleles, and the distribution of alleles in gametes during sexual reproduction He chose edible pea plant for his experiments Allowed him to see patterns in the way plant characteristics were inherited |
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Why Pea plants?
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Pea flowers have stamens, the male structures that produce pollen. Pollen contains the sperm (male gametes); sperm are gametes and pollen is the vehicle
Pea flowers have carpels, female structures housing the ovaries, which produce the eggs (female gametes) Pea flower petals enclose both male and female flower parts and prevent entry of pollen from another pea plant |
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Because of their structure, pea flowers naturally _______
Pollen from the stamen of a plant transfers to the carpel of the same plant, where the sperm then fertilizes the plant’s eggs |
self-fertilize
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Mendel was able to mate two different plants by _________
Female parts (carpels) were dusted with pollen from other selected plants |
(cross-fertilization)
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The key to Mendel’s success:
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He chose a simple experimental design
He chose to study individual characteristics (called traits) that had unmistakably different forms, such as white versus purple flowers He started out by studying only one trait at a timeHe followed the inheritance of these traits for several generations, counting the numbers of offspring with each type of trait By analyzing these numbers, he saw the basic patterns of inheritance emerge |
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How Are Single Traits Inherited?
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Pea plants that are homozygous for a particular characteristic always produce the same phenotype
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A ______is the mating of pollen and eggs (from same or different parents)
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genetic cross
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Mendel’s flower color experiments:
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Crossed a true-breeding (homozygous) purple flower plant with a true-breeding (homozygous) white-flower plant (the P generation)
The F1 generation consisted of all purple-flowered plants |
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The inheritance of dominant and recessive alleles on homologous chromosomes can explain the results of Mendel’s crosses
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Each trait is determined by pairs of genes; each organism has two alleles for each gene, one on each homologous chromosome.
When two different alleles are present in an organism, the dominant allele may mask the recessive allele, even though the recessive allele is still present The pairs of alleles on homologous chromosomes separate, or segregate, from each other during meiosisChance determines which allele is included in a given gameteTrue-breeding organisms have two copies of the same allele for a given gene and are homozygous for that gene; hybrid organisms have two different alleles for a given gene and are heterozygous for that gene |
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The particular combination of the two alleles carried by an individual is called the ______
The physical expression of the genotype is known as the _____ (for example, purple or white flowers) |
genotype
phenotype |
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______ is used to deduce whether an organism with a dominant phenotype is homozygous or heterozygous
Cross the unknown dominant-phenotype organism (P_) with a homozygous recessive organism (pp) If the dominant-phenotype organism is homozygous dominant (PP), only dominant-phenotype offspring will be produced (Pp) If the dominant-phenotype organism is heterozygous (Pp), approximately half the offspring will be of recessive phenotype (pp) |
test cross
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How is sex determined in the offspring?
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Mammals have a set of sex chromosomes that dictate gender
Females have two X chromosomes Males have an X chromosome and a Y chromosome The rest of the (non-sex) chromosomes occur in identical pairs and are called autosomes |
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In the genes studied by Mendel, one allele was dominant over the other, which was recessive
Some alleles, however, are incompletely dominant over others When the heterozygous phenotype is intermediate between the two homozygous phenotypes, the pattern of inheritance is called |
incomplete dominance
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Human hair texture is influenced by a gene with two incompletely dominant alleles, _______ an ___
A person with two copies of the__ allele has curly hair Someone with two copies of the__ allele has straight hair Heterozygotes (with the ____ genotype) have wavy hair |
C1 and C2
C1 c2 C1C2 |
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An individual may have at most two different gene alleles
A species may have ________for a given characteristic However, each individual still carries two alleles for this characteristic |
multiple alleles
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Human blood group genes produce blood types A, B, AB, and O
There are____ in this system: A, B, and o |
three alleles
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__ and ___ code for enzymes that add different sugar molecules to the ends of glycoproteins that protrude from red blood cells
______ codes for a nonfunctional enzyme that doesn’t add any sugar molecules Blood types A, B, AB, and O arise as a result of the actions of these alleles |
Alleles A and B
allele o |
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People with AA or Ao genotypes have blood type _; people with BB or Bo genotypes have blood type _; people with oo genotypes have blood type _
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A
B O |
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AB individuals have both the A and the B allele, so they produce both types of enzymes
Consequently, the plasma membranes of their red blood cells have both A and B glycoproteins When heterozygotes express the phenotypes of both of the homozygotes (in this case, both A and B glycoproteins), the pattern of inheritance is called |
codominance
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People make antibodies to the type of glycoproteins they __
People with type A blood make B antibodies; people with type B blood make A antibodies People with type O blood make both type A and type B antibodies; type AB blood groups make no antibodies |
lack
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The antibodies cause red blood cells that bear foreign glycoproteins to
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clump together and rupture
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Type __ blood, lacking any sugars, is not attacked by antibodies in A, B, or AB blood, so it can be transfused safely to all
Universal donorBecause people with type__blood produce both A and B antibodies, they can receive blood only from other type __ donors Their antibodies would attack any donated blood cells bearing A or B glycoproteins |
o
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The environment influences the expression of genes
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The environment in which an organism lives profoundly affects its phenotype
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Some human genetic disorders are sex-linked
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The X chromosome contains many genes that have no counterpart on the Y chromosome
Because males have only one X chromosome, they have no other allele to exert dominance over a sex-linked (X-linked) allele causing disease |
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The incorrect separation of chromosomes in meiosis is known as
-______ causes gametes to have too many and too few chromosomes Most embryos that arise from fusion of gametes with abnormal chromosome numbers spontaneously abort, but some survive to birth and beyond |
nondisjunction
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Some genetic disorders are caused by abnormal numbers of autosomes
_________, afflicted individuals have three copies of chromosome 21 ______includes several distinctive physical characteristics, including weak muscle tone, a small mouth held partially open because it cannot accommodate the tongue, and distinctively shaped eyelids ______is also characterized by low resistance to infectious diseases, heart malformations, and varying degrees of mental retardation, often severe |
In trisomy 21 (Down syndrome)
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