“Comparing Hominid Skulls” Lab
PREDICT THE SPECIES OF YOUR FOSSIL SKULL:
I PREDICT IT IS A EARLY HOMINID.
Sunday, April 26, 2015
Monday, April 13, 2015
Name: Jennifer Cicchini
LAB
SOLVING GENETICS
PROBLEMS
Introduction:
One of the
facts of life involves the different types of offspring that can be produced as
a result of sexual reproduction. Offspring may have traits of one parent, both
parents, or neither parent. This depends upon the genes the offspring receive
from the parents. In order to determine
the probable appearance of an offspring, we must first know something about the
parents. What genes do they possess? We must know what possible genes can be
found in the gametes of each parent and the possible ways these genes may
combine during fertilization.
In today's
lab, your goal will be to learn how to solve genetics problems. First, here are
some terms for easy reference:
Phenotype - The physical
appearance of an organism.
Genotype - The genes of an
organism.
Allele - One of two or more
forms of the same gene.
Locus - A specific location on a
chromosome where a gene is found.
Heterozygote - An organism
having two different alleles for a trait.
Homozygote - An organism having
two of the same alleles for a trait.
Homologous Chromosomes -
Chromosomes having genes for the same kinds of characteristics that pair during
meiosis.
Genetics
Problem Solving:
In this activity, the class will be divided into groups.
Each group will be assigned a problem to
solve and write on the whiteboard. Everyone should follow along with their
explanation and write the results down for themselves on a separate sheet of
paper. It may help to solve the problems using the following guidelines:
a.
Assign letters (alleles) to the various
characteristics.
b.
Determine the phenotype and genotype of each
parent and indicate a mating.
c.
Determine all the possible kinds of gametes each
parent can produce.
d.
Determine all the possible allele combinations
that can result when these gametes combine to form the offspring, using a Punnett
square.
e.
Answer the question asked in the question.
Genetics
Problems:
1.
For each of the diploid genotypes presented
below, determine the genetic make up for all of the possible gametes that would
result through the process of meiosis. Remember, each egg or sperm must have
one of each letter. That letter can be upper or lower case.
a.
Rr , The genetic gametes would be R.r.
b.
RrYy The genetic gametes would be RY, ry, Ry,rY
c.
rrYy The genetic gametes would be rY, ry.
d.
RrYY The genetic gametes would be RY, rY
2.
For each of the following, state whether the genotype
of a diploid or haploid cell is represented.
a.
D , A haploid cell is represented.
b.
GG, A diploid cell is represented.
c.
P, A haploid cell is represented.
d.
Ee, A diploid cell is represented.
3.
Yellow guinea pigs crossed with white ones
always produce cream colored offspring. Two cream colored guinea pigs when
crossed produced yellow, cream and white offspring in the ratio of l yellow: 2
cream: l white. Explain how are these colors inherited? No calculations needed! Name the type of
inheritance this represents.
Both guinea pigs have two different alleles. It is a polygenic
inheritance.
4.
In sheep white is due to a dominant gene (B), black
to its recessive allele (b). A white ewe mated to a white ram produces a black
lamb. What are the genotypes of the parents? You might need to construct Punnet
squares experimenting with different crosses to come up with this answer. Name
the type of inheritance this represents.
The only way for the offspring to be black is if each parent has the
recessive allele (b), the parents are heterozygous. It is a incomplete
dominance inheritance
.
5.
In peas, yellow color (G) is dominant to green
color (g). A heterozygous yellow is crossed with a green. What is the expected
phenotype ratio of the offspring? Name the type of inheritance this represents.
The
phenotype of the offspring would be 3:1, ¾ would be yellow and ¼ would be
green. This type of inheritance is dominant.
6.
White color (Y) is dominant to yellow color (y)
in squash. A heterozygous white fruit plant is crossed with a yellow fruit
plant. What is the expected phenotype ratio of the offspring? What is this type
of inheritance called?
This is also
a dominate inheritance and the offspring phenotype would be 3:1, 3 white and 1
yellow.
7.
In certain flowers, a cross between homozygous
red and a homozygous white will always result in a pink flower. A cross is made
between two pink flowers. What is the predicted phenotype ratio of the colors
red, pink and white appearing in the offspring? What is this type of
inheritance called.
This is a codominace inheritance and the phenotype ratio would be 25%
red, 25 white and 50% pink.
8.
In humans, the condition for normal blood
clotting dominates the condition for non-clotting or hemophilia. Both alleles
are linked to the X chromosome. A male hemophiliac marries a woman who is a
carrier for this condition. In this respect, a carrier is a woman who has an
allele for normal blood clotting and an allele for hemophilia. What are the
chances that if they have a male child he will be normal for blood clotting? What
is this type of inheritance called?
The
inheritance type is called sex linked , there is a 50% chance that the male
child will be normal for blood clotting.
9.
A person with an allele for type A blood and
type O blood marries someone with an allele for type B blood and type O blood.
List the types of offspring they could have and the probability for each blood
type in the offspring. (A allele = IA, B allele = IB, O
allele = i) What is the expected phenotype ratio of the offspring? What is this
type of inheritance called?
The expected
phenotype ratio of the offspring would be 1/4 AB, 1/4 would be AO or type A, 1/4
BO or B, ¼ would be OO or O blood type. This type of inheritance is codominance.
10.
Skin color in humans becomes darker by the
number of dominant alleles; AABBCC have the darkest skin and aabbcc have the
lightest skin. Place these genotypes in sequence according to the color of skin
expected for each. Place the darkest skin first. What is this type of
inheritance called?
Genotypes:
AaBbCc, AAbbcc, aabbCc, AaBBCc, AaBBCC.
The
darkest to lightest genotypes in sequence are: AaBBCC, AaBBCc, AaBbCc, AAbbcc,
aabbCc
This
type of inheritance is polygenic.
THIS IS A PHOTO I DREW OF WHAT MY 16 YR OLD SON WOULD LOOK LIKE ACCORDING TO THE GENETICS I ENDED UP WITH FROM THE FLIP A COIN LAB.
Part
1. Flip-a-coin
2.
Ideally,
the lab is performed with two pretend parents. If you work alone, that is fine;
you will represent both parents! All sorts of things are possible today
with reproductive technology :-).
3.
It is
most important to understand that each "parent" will flip a coin, and
the heads or tails on that flip of the coin represents one allele from
the egg or sperm. See video here for help understanding how to complete the data sheet,
below. Apologies for any background “hum.”
4.
Record
your data in the Flip-a-coin
Genetics Data Sheet. When
it opens, it will might be "Read-only." Save with a new name to
another location and then type in your data. Then you will be able to save the
changes you make.
5.
When
all the coin tossing is finished you created a child!
6.
Sketch
your child at age 16, including the characteristics you have determined by
flipping the coin.
8.
Attach
both the data sheet and a photo or scan of the drawing of your son or daughter
to your blog site.
Eyebrows (II) | N | N | NN | not connected |
Eyebrow color | H | h | Hh | same as hair |
Eyes distance apart | e | E | eE | average distance |
Eyes size | E | e | Ee | medium |
Eyes shape | A | A | AA | almond |
Eyes slant | h | h | hh | upward slant |
Eyelashes | l | L | lL | long |
Eye color | abc | ABC | aAbBcC | Hazel |
Mouth size | m | m | mm | narrow |
Lips | l | l | ll | thin |
Protruding lower lip | h | h | hh | absent |
Dimples | d | D | dD | present |
Nose size | n | N | nN | average |
Nose shape | r | r | rr | pointed |
Nostril shape | r | R | rR | rounded |
Earlobe Attachment | F | F | FF | free |
Freckles on checks | f | f | ff | absent |
Hair color | abcd | AbCD | aAbbcCdD | dark blonde |
Sunday, April 5, 2015
PART TWO:
DNA TECHNOLOGIES:
The DNA technology I chose is Recombinant DNA Technology; It is a method in which the chosen DNA of
one organism (Donor) is introduced to combine with the DNA of another organism
termed as recipient organism. The result of it is that, the recipient organism
acquires the genetic abilities of the donor. Altering the genome of an organism
through introducing genes of interest is termed as gene manipulation or DNA
recombinant technology. According to this mechanism has the capability to
engineer new organisms, it is termed as genetic engineering. The reason I picked this
is because I am Diabetic and found it interesting how they make insulin using
recombinant DNA. When they first started making insulin they used animal DNA
such as pigs but now it made using human DNA.
As the illustration
below shows the process of recombinant DNA, The DNA of the donor organism and
the gene of interest is isolated and cut into fragments through using
restriction endoclease. The fragments of the vector DNA and the fragments of
the donor DNA are combined into DNA ligase which. Then it becomes the
Recombinant DNA (rDNA). The introduction of the rDNA into the E Coli causes a multiplication
of rDNA after this it creates multiplication of identical copies of rDNA.
"Recombinant DNA
Technology." Recombinant DNA Technology. Web. 5 Apr. 2015.
<http://www.tutorsglobe.com/homework-help/botany/recombinant-dna-technology-71762.aspx>.
DNA LAB (online)
Part 1. Your
Personal Chromosome
1.
My
chromosome was number 6.The eight genes
on my chromosome are:
1.
Hemochromatosis is a disorder of iron metabolism wherein
the body retains excess iron. Excess
iron is deposited in a variety of organs leading to their failure, and
resulting in serious illnesses including cirrhosis, hepatomas, diabetes,
cardiomyopathy, arthritis, and hypogonadotropic hypogonadism.
2. Opioid Receptor Gene encodes the opioid
receptor which is the primary site of action for the most commonly used opioids
including morphine, heroine and methadone. This receptor is a membrane of the
g-protein coupled protein receptor family.
3. Estrogen receptor is a ligand –activated
transcription factor composed of several domains important for hormone binding,
DNA binding. It is also responsible for alternate splicing results in several
ESRI, Mrna transcripts.
4. Connective tissue growth factor: The protein
encoded by this gene is a mitogen that is secreted by vascular endothelial
cells. The protein plays a role in cell adhesion in many cell types and is
related to platelet derived growth factor.
5. Tumor Necrosis Factor is a multifunctional pro
inflammatory cytokine secreted mostly by monocytes and macrophages. The primary
role of TNF is the regulation of immune cells.
6. Advanced glycosylation end product is an
important receptor for the amyloid beta peptide and it increases in Alzheimer’s
disease. This protein is increased in neurons close to deposits of amyloid beta
peptides and to neurofibrillary tangles.
7. Vascular endothelial growth factor is produced
by many cell types including tumor cells, macrophages, Platelets, keratinocytes
and renal mesangial cells. They also
play a role in normal physiological functions such as bone formation, wound
healing and development.
8.
Interlukin is a pro inflammatory cytokine that is secreted primarily by
activated T cells and that has been implicated in several inflammatory
diseases. It also stimulates a variety of cells to produce inflammatory
mediators.
Genes cite source: "DNA Interactive:
Discovering the DNA Structure and beyond." DNA Interactive: Discovering the
DNA Structure and beyond. Web. 4 Apr. 2015. <http://www.dnai.org/>.
Pick one favorite of these eight genes.
1.
I found all the genes that I researched were really
interesting. They all play an interesting role in our chromosomes. I did find
that the one I seemed to relate to is the estrogen receptor and the different
conditions that involve the gene like Breast cancer and artherosclerosis.
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