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Transcript
Page 1
CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
EDUCACIÓN BILINGÜE
Biology Academy
Portfolio 4 Index
Session
Name: ____________________________________________________ Group:____________
1
2
Bk pgs
394-395
396-397
3
398-399
4
2
3
4
Points
What to do
Points
Make the following crosses according to their genotypes (3 pts each)
Inheritance of traits by pedigree charts interpretation (3 pts. Each)
9
Make a concept map on disorders caused by individual genes (cause
1 point, what it causes 1 point, description of disease 1 point)
9
8
403-404
405-409
Describe the Human Genome Project and its goals (3.5 each)
7
412-414
Assessment Chapter 14 (.5 per question unanswered)
10
LAB
SESSION 5
Laboratory 5 Using DNA to identify bodies
Integrated Activity 4 Biosong
obtained
6
Describe the causes of human genetic disorders (2 each)
Describe the processes involved in DNA Manipulation (cutting DNA 2
pts, separating DNA 2 pts. and reading DNA 2 pts.)
400-401
1
4
6
5
40
I ____________________________ understand that my portfolio is a collection of my school work
and my achievements. The contents exhibit my effort and progress as these elements relate to the
goals represented in my instructional program.
I agree to accept the responsibility for creating and managing my portfolio as I complete each
requirement. I will submit its content for periodic review to my instructor. In doing so, I understand
that the contents on my portfolio, as well as the way in which I have presented the contents, will be
evaluated for the purpose of judging my performance in school.
STUDENT SIGNATURE: ___________________________________
DATE:_____________
PARENT SIGNATURE: ________________________________________________________
I have read and understand the above portfolio agreement and have reviewed my child’s portfolio
requirements.
Page 2
CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
EDUCACIÓN BILINGÜE
Chapter 14 Human Heredity
14.1 Human Chromosomes
MAY WK 14-18
Session 1 BK 394-395
Objective: Describe the patterns of inheritance
Instructions: Make the following crosses according to their genotypes
1.
Make a cross a male blood type A homozygous marries a woman heterozygous blood type
B then report the possible blood types of the offspring and percentages.
2.
Make a cross a male blood type O homozygous marries a woman heterozygous blood type
A then report the possible blood types of the offspring and percentages.
Page 3
CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
EDUCACIÓN BILINGÜE
3.
Construct a Punnett square to show a cross between a father with normal vision and a
mother who is carrier of the colorblindness trait
Session 2 BK 396-397
Objective: Infer how traits are inherited over generations by interpreting pedigree charts
Instruction: Answer the following questions
1. Explain why some cats have different colors; consider the sex of the cat.
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2. Define pedigree and say why it is important
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CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
EDUCACIÓN BILINGÜE
14.2 Human Genetic Disorders
Session 3 BK Pg. 398-399
Objective: Describe the most common human genetic disorders
Instruction: Make a concept map on disorders caused by individual genes
Make a concept map on disorders caused by individual genes, include cause, what it causes,
description of the disease.
Page 5
CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
EDUCACIÓN BILINGÜE
Session 4 BK Pg. 400-401
Objective: Describe the causes of human genetic disorders
Instructions: Answer the following questions
1. Define non-disjunction.
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2. What is the result of non-disjunction?
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3. Express how different is nondisjunction in autosomal chromosomes and sex
chromosomes.
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4. Name two disorders caused by non-disjunction in the x chromosome.
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Page 6
CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
EDUCACIÓN BILINGÜE
14.3 Studying the Human Genome
MAY WK 21-25
Session 1 BK 403-404
Objective: Describe the process of DNA Manipulation
Instruction: Write the steps for each of the following procedures involved in DNA Manipulation
Write the steps for each of the following procedures: cutting DNA, separating DNA and
reading DNA
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Page 7
CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
EDUCACIÓN BILINGÜE
Session 2 BK 405-406
Objective: Describe the Human Genome Project and its goals
Instructions- Describe the goals of the Human Genome Project
1. What were the goals of the human genome project?
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2. Explain briefly the technique of “shotgun sequencing”
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Page 8
CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
EDUCACIÓN BILINGÜE
Session 3 BK 412-414
Objective: Assessment Chapter 14
Instructions- Answer the following questions
1- A normal human diploid zygote contains
a. 23 chromosomes
b. 46 chromosomes
c. 44 chromosones
d. XXY chromosomes
2- A chart that traces the inheritance of a trait in a family is called a(n)
a- Pedigree
b- Karyotype
c- Genome
d- Autosome
3- An example of a trait that is determined by multiple alleles is
a- cystic fibrosis
b- ABO blood groups
c- Down syndrome
d- Colorblindness
4- What is the difference between autosomes and sex chromosomes?
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5- Is it possible for a person with blood type alleles IA an IB to have blood type A? Explain
your answer. (Refer to Figure 14-5 in your book page 394).
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6- Predict What are the possible genotypes of the parents of a male child who is colorblind?
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Page 9
CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
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7- Design an Experiment Fruit fly sex is determines by X and Y chromosomes, just as it is in
humans. Researchers suspect that a certain disease is caused by a recessive allele in a
gene located on the X chromosome in fruit flies. Design an experiment to test this
hypothesis.
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8- A mutation involving a change in a single DNA base pair
a- Will definitely result in a genetic disease.
b- Will have no effect on the organism’s phenotype
c- Will produce a positive change.
d- May have an effect on the organism’s phenotype.
9- Cystic fibrosis is caused by
a- Nondisjunction of an autosome
b- A change of three base pairs in DNA
c- Nondisjunction of a sex chromosome
d- Deletion of an entire gene from a chromosome.
10- Malaria is a disease caused by a
a- Gene mutation.
b- Defect in red blood cells
c- Bacterium found in water
d- Parasite carried by mosquitoes.
11- Analyze the human karyotype below. Identify the chromosomal disorder that it shows in
your book pg. 412. _________________________________________
12- What is a chromosomal disorder?
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13- Describe two sex- chromosome disorders.
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14- Infer Can a genetic counselor use a karyotype to identify a carrier of cystic fibrosis?
Explain
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Page 10
CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
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15- Interpret Graphs What can you infer about the relationship between the age of the
mother and the incidence of Down syndrome? (see Book pg. 413)
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16- The human genome consists of approximately how many DNA base pairs?
a- 30,000
b- 3,000,000
c- 300,000,000
d- 3,000,000,000
17- The fraction of the human genome that actually codes for proteins is about
a- 2%
b- 20%
c- 98%
d- 100%
18- Cutting DNA into small pieces that can be sequenced is accomplished by
a- Restriction enzymes
b- DNA polymerase
c- Gel electrophoresis
d- RNA polymerase
19- If you sequence short pieces of DNA and then use a computer to find overlapping
sequences that map to a much longer DNA fragment, you are using
a- Genomics
b- Hapmaps
c- Shotgun sequencing
d- Open reading frame analysis.
20- Describe the tools and processes that scientists use to manipulate human DNA.
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21- Explain why restriction enzymes are useful tools in sequencing DNA.
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Page 11
CENTRO DE INVESTIGACIÓN Y DESARROLLO DE
EDUCACIÓN BILINGÜE
22- What is an SNP (single nucleotide polymorphism)?
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23- What is bioinformatics?
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24- Draw Conclusions Scientists have searched the human genome database to find possible
promoter sequences. What is likely to be found near a promoter sequence?
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25- Infer Why does DNA move toward the positive end of the gel during gel electrophoresis?
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26- Observe The table on pg. 414 in your book, shows the DNA sequences that are
recognized by five different restriction enzymes and the location where those enzymes
cut. Which enzymes produce DNA fragments with “sticky ends”? What is the common
feature of the sequences cut by these enzymes?
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