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WorksheetsBio Exam 2
Total questions: 177
Worksheet time: 2hrs 50mins
Caused by a genetic mutation in the beta-globin gene
Change 1 nucleotide in DNA, changes 1
_____ ____ Disease
(a)
Effects of Sickle Cell disease
Changes shape of RBC- doesn’t flow through capillaries
Blood clots, pain
Doesn’t bind oxygen well
RBCs don’t live as long-
anemia
All of these are correct
Round with a dent
No organelles
Full of hemoglobin protein that binds oxygen
Red Blood Cells
White Blood Cells
Proteins
DNA
Hemoglobin has 2 alpha-globins and 2 beta-globins
True
False
1 drop of blood=about 5 million RBCs
True
False
The main job of red blood cells is to move (a)
The more hemoglobin=the more oxygen you can move
True
False
You make proteins through ____ and ____
Transcription and Translation
Meiosis and Mitosis
Chromosomes and DNA
Nucleotides and Ribosomes
Modifying genes to reduce or eliminate the effects of a genetic disorder
Where does the genetic error come from?
Gene Therapy
Mutations
Gene Expression
Gene Synthesis
A change in DNA sequence
(a)
in coding sequence of a gene can change amino acid sequence
Can change the protein function
(a)
substitute one nucleotide for another
Point Mutations
Frameshift Mutations
Rearranged DNA Mutations
sections of DNA move
Point Mutations
Frameshift Mutations
Rearranged DNA Mutations
change codon reading
Point Mutations
Frameshift Mutations
Rearranged DNA Mutations
Silent mutation-Change one nucleotide to another, no change in amino acid sequence
Missense mutation-Change one nucleotide to another, different amino acid sequence in this location
Nonsense mutation-Change one nucleotide, introduces early stop codon
Point Mutations
Frameshift Mutations
Rearranged DNA Mutations
Insertion mutation-Insert one or more nucleotides, shifts reading frame of every codon after the insertion
Deletion mutation-Deleate one or more nucleotides, shifts reading frame of every codon after the deletion
Point Mutations
Frameshift Mutations
Rearranged DNA Mutations
Inversion mutation- a group of DNA nucleotides are flipped to read in reverse order, different amino acid sequence in this location
Translocation mutation-Move segments of DNA from one chromosome to another, fusing portions of different genes together
Point Mutations
Frameshift Mutations
Rearranged DNA Mutations
(reproductive cells ex) sperm or egg)
Passed on to the next generation
Mutation in Germ Cells
Mutation in Other Cells
Pass on to some cells in that individual
Mutation in Germ Cells
Mutation in Other Cells
Mutations can result from errors in (a) replication
Enzymes for DNA repair usually DON'T correct the mistakes
True
False
DNA mistakes occur but they ARE very common
True
False
Any physical agent that can damage DNA by changing the nucleotide sequence
(a)
Many things in the environments are mutagens
True
False
Different forms of genes are called (a)
1 copy of gene produces protection from _____
Malaria
Sickle Cell
2 copies of gene cause _____
Malaria
Sickle Cell
Positive effects are GREATER than negative
True
False
Something that introduces a gene
(a)
Viruses are CELLS
True
False
Not cells, but little chunks of DNA or RNA covered in proteins
(a)
____ bone marrow makes ____ blood cells
Red
White
While a fetus, people produce _____-____ rather than ____-_____
Gamma-globin, Beta-globin
Beta-globin, Gamma-globin
Hemoglobin: (_) beta parts and (_) alpha parts
1
2
3
4
Around the time of birth, RBCs produce
Less Gamma-globin
More Beta-globin
More Beta-globin
Less Gamma-globin
Sickle cell mutation only affects
Beta-globin
Gamma-globin
Bacteria gets infected with viruses,
(a) cuts DNA and inserts new DNA to provide bacteria with immunity to infection
Cells divide for____
Growth
Life
Healthy Life
Myosis
Makes sperm and egg with one set of chromosomes
Meiosis
Mitosis
2 sets of chromosomes, division of nucleus
Meiosis
Mitosis
Phase where DNA is replicated
S
G1
G2
G0
Grow and make new organelles
S
G1
G2
G0
Duplicate DNA (make identical copy of each chromosome)
S
G1
G2
G0
Getting ready for mitosis
S
G1
G2
G0
Doing normal job ,Not getting ready for mitosis
S
G1
G2
G0
Divides the cell in two
(a)
Growth and preperation
(a)
3 Parts of the Cell Cycle
Interphase
Mitosis
Cytokinesis
Meiosis
Correct Order
1, 2, 3
Interphase
Mitosis
Cytokinesis
Mitosis
Cytokinesis
Interphase
Cytokinesis
Interphase
Mitosis
Interphase
Cytokinesis
Mitosis
Chromosomes condense
Protein fibers attach to centromeres
1 Sister chromatid from each chromosome goes to each side of the cell
Mitosis
Meiosis
Mitosis has (_) stages
1
2
3
4
Chromosomes Condense
Prophase
Metaphase
Anaphase
Telophase
Chromosomes line up in the middle
Prophase
Metaphase
Anaphase
Telophase
Microtubules pull identical sister chromatids apart
Prophase
Metaphase
Anaphase
Telophase
Daughter cell nuclei are formed
Prophase
Metaphase
Anaphase
Telophase
1st stage of Mitosis
Prophase
Metaphase
Anaphase
Telophase
2nd stage of Mitosis
Prophase
Metaphase
Anaphase
Telophase
3rd stage of Mitosis
Prophase
Metaphase
Anaphase
Telophase
4th stage of Mitosis
Prophase
Metaphase
Anaphase
Telophase
Original parent cell splits into two daughter cells
Each has a full component of DNA
(a)
Cytokinesis
Before Mitosis
After Mitosis
Checkpoints, detect errors at various points in cell cycle
Repair Errors
Cell Division Quality Control
Apoptosis
Cytokinesis
Mitosis
Programmed cell death
(a)
Unregulated cell division
(a)
Mutations are common cause of cancer and they can be
Inherited:
In sperm and egg
(germ cells)
Acquired:
During mitosis in body
(somatic cells)
Both of these are correct
Mutations that disrupt ____ can cause cancer
Cell Cycle
Mitosis
Gene Expression
Phenotype
Change in the nucleotide sequence
(a)
How can you reduce the risk of cancer
All of these are correct
Don't Smoke,
Eat healthy
Get vaccinated
Avoid harmful environments
Get screened regularly, and get tested for hereditary cancers
Tissues that divide a lot can screw up ____ and cause cancer
Mitosis
Meiosis
Cytokinesis
Interphase
Muscle cells can divide
True
False
Neurons don't divide after your born
True
False
People get cancer when enough mutations accumulate to disrupt the _____ _____
(a)
Proto-onogens
Normally promote cell division and differentiation
Activated by growth factors
Can be mutated to become permanently activated
All of these are correct
Proto-oncogenes that when mutated they become oncogenes;
Genes that cause
(a)
Tumor Suppressor Genes
Normally pause cell division
Repair DNA
Initiate Cell Death
(Apoptosis)
Can be mutated to become inactivated
Genetic testing is performed by extracting DNA from the nucleus of white blood cells and looking for mutations in change of interest
Breast Cancer
BRCA1
Chromosome 17
Chromosome 13
Breast Cancer
BRCA2
Chromosome 17
Chromosome 13
Cancer usually takes a SINGLE mutation in development
True
False
Spread of cancer cells
Metastasis
Benign Tumor
Malignant Tumor
Non-cancerous tumor
(doesn't metastasize)
Metastasis
Benign Tumor
Malignant Tumor
Cancerous tumor
(metastasize)
Metastasis
Benign Tumor
Malignant Tumor
TREATING CANCER
Removes cancerous tissue
Most effective for solid tumors that are detected early
Ineffective for metastasized cancers
Surgery
Chemotherapy
Radiation
Targeted Therapy
Immunotherapy
TREATING CANCER
Inject toxic chemicals that kill rapidly dividing cells
Can kill metastatic cells throughout the body
Side effects are severe, especially rapidly dividing cells
ex) hair, digestive track, bone marrow
Surgery
Chemotherapy
Radiation
Targeted Therapy
Immunotherapy
TREATING CANCER
High-energy ionizing radiation directed at tumor cells
Kills cells by damaging their DNA
Can be very localized
Can also kill healthy cells near tumor
Surgery
Chemotherapy
Radiation
Targeted Therapy
Immunotherapy
TREATING CANCER
PARP inhibitors prevent DNA repair, but only in mutated cells
Normal cells are unaffected
Surgery
Chemotherapy
Radiation
Targeted Therapy
Immunotherapy
TREATING CANCER
ex) monoclonal antibodies
Bind to proteins in cancer cell membranes
Attract immune cells that kill cancer cells
Can carry toxic chemicals to cancer cells
Surgery
Chemotherapy
Radiation
Targeted Therapy
Immunotherapy
Cancer was more common years ago because there were_____
No environmental regulations
No way to diagnose it
No treatments available
No technology to determine what kind of cancer
Cancer is more common in _____ because _______ effects the immune system
Males, Testosterone
Females, Estrogen
Cancer survival rates have been going down
False
True
We get (_) of our mothers genes and (_) of our fathers genes
1/2
2/3
3/4
1/16
The half of the genes you get from your parents is not random, and predetermined
True
False
Each sperm and egg are unique
True
False
Humans are (a) organisms
Diploid
2 sets of Chromosomes
1 set of Chromosomes
3 sets of chromosomes
4 sets of chromosomes
Diploid organisms have (_) copies of every chromosome
1
2
3
4
(a) chromosomes that are a pair of chromosomes that contain the same gene
In a diploid cell, one is inherited from mom, and one from dad
True
False
Alternative versions of the same gene that have different nucleotide sequences
(a)
Caused by a single gene mutation
Creates a mutant allele of CFTR gene
One normal allele is sufficient to remain healthy-next express (a)
Which allele expresses Cystic Fibrosis, if any
NN
NC
CC
None of these are correct
Only NC and CC show Cystic Fibrosis
The particular set of genes in an individual
(a)
The physical expression resulting from these genes and environmental effects
(a)
Haploid: (_) set of chromosomes
1
2
3
4
Egg and Sperm are (Haploid OR Diploid) cells=________
Haploid
Diploid
Gametes
Alleles
Haploid + Haploid = _______
Haploid
Diploid
Mitosis
Meiosis
Diploid + Diploid = _______
Haploid
Diploid
Mitosis
Meiosis
Diploid + Haploid = _______
Haploid
Diploid
Mitosis
Meiosis
There are 2 cell divisions in ______
Mitosis
Meiosis
Separates homologous chromosomes
Each daughter cell is haploid
Each chromosome still has 2 sister chromatids
Meiosis 1
Meiosis 2
Separate sister chromatids (just like mitosis)
Meiosis produces 4 haploid daughter cells, which develop into sperm and egg
End up with four haploid cells
Sister chromatids separate-> Cytokinesis-> End up with 4 haploid cells
Meiosis 1
Meiosis 2
Meiosis 1
Step 1
Chromosomes replicate
Coil
Microtubules form meiotic spindle
Homologous chromosomes separate
Cytokinesis
Meiosis 1
Step 2
Chromosomes replicate
Coil
Microtubules form meiotic spindle
Homologous chromosomes separate
Cytokinesis
Meiosis 1
Step 3
Chromosomes replicate
Coil
Microtubules form meiotic spindle
Homologous chromosomes separate
Cytokinesis
Meiosis 1
Step 4
Chromosomes replicate
Coil
Microtubules form meiotic spindle
Homologous chromosomes separate
Cytokinesis
Meiosis 1
Step 5
Chromosomes replicate
Coil
Microtubules form meiotic spindle
Homologous chromosomes separate
Cytokinesis
Meiosis 2
Step 1
Sister chromatids seperate
Cytokinesis
4 haploid cells
Meiosis 2
Step 2
Sister chromatids seperate
Cytokinesis
4 haploid cells
Meiosis 2
Step 3
Sister chromatids seperate
Cytokinesis
4 haploid cells
Alleles of different genes are distributed independently of one another
Independent Assortment
Recombination
Heterozygote
Dominant Allele
Homozygote
Maternal and paternal chromosomes exchange DNA segment
Independent Assortment
Recombination
Heterozygote
Dominant Allele
Homozygote
Two different alleles (Ff)
Phenotype is normal
Individual is a carrier
Heterozygote
Dominant Allele
Homozygote
Two identical alleles (FF)
Phenotype is normal
________ recessive (ff)
(Cystic Fibrosis) phenotype is (CF) mutation
Heterozygote
Dominant Allele
Homozygote
Always expressed
Masks the other one
Heterozygote
Dominant Allele
Homozygote
Recessive Allele
Cystic Fibrosis is caused by a ______ allele
Dominant
Recessive
Affects phenotype only if the organism has 2 copies of that allele
Hidden by normal or dominant allele
3 genotypes (FF) (Ff) (ff)
2 phenotypes (Normal) (___ ____)
Cystic Fibrosis
Huntington's Disease
Cancer
Sickle Cell
In Cystic Fibrosis:
FF genotype will always pass the normal allele to offspring
ff genotype will always pass the CF allele
True
False
Huntington's Disease is a ______ genetic disorder
Dominant
Recessive
Most genes have just 2 versions (alleles) in a population
True
False
Most alleles do not occur at a 50% frequency in the population, although each allele is always 50% of an individual’s genome
True
False
Our entire genome is almost the same between males and females
True
False
What you get from your ancestors
(a)
Sex hormones are produced by
(a)
Humans have 23 pairs of chromosomes, 1 pair are sex chromosomes. What are the other 22?
(a)
The default condition is _____
Male
Female
Activation of _____ development is when the fetus gets a surge of _______ at about 6 weeks after conception
Female,
Estrogen
Male,
Testosterone
The SRY gene on the Y chromosome signals adrenal glands to produce testosterone
This causes gonads to develop into testes
Activates other genes
Suppresses other genes
All of these are correct
Only developing and activating are correct
Sex does not have only two genotypes
True
False
More or fewer chromosomes than normal
(a)
Genotype + Environment =
(a)
Determined by an allele on the X chromosome
X-linked trait
Y-linked trait
Females (XX) normal copy on the X chromosome masks the ______ disease allele on the other X chromosomes
(Males have no second X to mask)
Recessive
Dominant
Duchenne Muscular Dystrophy (DMD)
Make defective muscle protein called dystrophy
Muscles deteriorate
People usually die from respiratory or cardiac failure
There are many ways to mutate the gene
All of these are correct
How many forms of DMD are there?
10
20
30
40
If a father has a DMD allele
The father passes his X chromosome to his daughters and his Y chromosomes to his sons
The allele is only passed to the fathers daughters
The allele is only passed to the fathers sons
DMD is only an X linked gene, so no sons would inherit DMD
If a mother has a DMD allele
The mother passes one of her two X chromosomes to each of her children
1/2 of male children express DMD
Mostly affects the males but can skip a generation
DMD will only affect the daughters
Visual representation of the occurrence of phenotypes across generations use a (a) to follow inheritance pattern
Why do some traits appear to blend in offspring?
ex) Familial Hypertrialemia
Incomplete dominance
Heterozygote Phenotype
Codominace
Homozygote Phenotype
Phenotype is intermediate
Dominant allele does not completely mask the other
Incomplete dominance
Heterozygote Phenotype
Codominace
Homozygote Phenotype
Measurable effect on the phenotype of having one versus two
Incomplete dominance
Heterozygote Phenotype
Codominace
Homozygote Phenotype
Phenotypes of both alleles are expressed in heterozygotes
ex) Blood Types
Incomplete dominance
Heterozygote Phenotype
Codominace
Homozygote Phenotype
The 3 blood type alleles
A
B
O
Z
Possible genotypes for blood type are a combination of these three alleles
AA
AO
BB
BO
and
OO
AB
In blood types A and B are DOMINANT
O is RECESSIVE
True
False
Environment can influence how genes are expressed.
True
False
Type A has (blank) antigens; antibodies against (blank)
(a)
Type B has (blank) antigens; antibodies against (blank)
(a)
Type AB has (blank) antigens; antibodies against (blank)
(a)
Type O has (blank) antigens; antibodies against (blank)
(a)
Antibodies in receiver ______ the red blood cells from donor, which causes red blood cells to clump and clot
Attack
Protect
Cause no change
The universal donar
A
AB
B
O
The universal receiver
A
AB
B
O
Another gene affecting blood type
(a)
Height
Phenotype
Genotype
Polygenic
Dominant Trait
A single trait determined by the interaction between alleles of more than one gene
(a)
Most phenotypes are
multifactorial
Affected by genes and environment
Continuous variation
All of these are correct
The (a) of a trait is what percent of the pairs of twins have the same trait
The attachment of -CH3 groups to DNA.
-Tends to decrease gene expression
(a)
Something other than the normal number of chromosomes
(a)
Down syndrome (trisomy __ ) - extra copy of chromosome __
12
21
14
20
Due to nondisjunction(fail to come apart) of chromosomes during meiosis
-Chromosomes separate unequally
When nondisjunction happens during meiosis 1 or 2, gametes can end up with either extra or fewer chromosomes
Aneuploidy
Amniocentesis
Karyotype
Nondisjunction
removes amniotic fluid containing fetal cells
Aneuploidy
Amniocentesis
Karyotype
Nondisjunction
analysis of the fetal cells can identify missing or extra chromosomes
Aneuploidy
Amniocentesis
Karyotype
Nondisjunction
Risk of aneuploidy increases with mother’s age
True
False
Eggs begin forming in fetal ovaries, Stop in meiosis 1
True
False
As eggs age, chance that chromosomes will separate abnormally DECREASES
True
False
Older males also make more defective sperm (been through many rounds of meiosis)
True
False
The ways that genes interact with other genes and the environment are complicated
-Create huge phenotypic variation in populations
True
False
