2. Chapter 17.1
The are two periods in the cell cycle
Interphase which is longer and iswhere the cell grows and
duplicates DNA which contains three phases of its own
G1 Phase where the cell starts at its smallest size and begins
active cell growth
Synthesis phase chromosones are duplicated and the cell
continues to grow
G2 Phase cell still growing and now preparing for cell division
Mitotic Phase is shorter and is where the nucleus and
cytoplasm divide it goes through two phases here
Mitosis is where the DNA that was duplicated is now divided
Cytokinesis where the cytoplasm is divided and two
daughter cells are formed
3. Chapter 17.2
DNA is packed with chromosomes
A gene is responsible for constructing one or more
proteins and is the smallest functioning part of a
chromosome
Before cell reproduction can happen the DNA
must be replicated
After the DNA is replicated is checked for errors
and damage that then get repaired
When DNA is transcribed it is only in one strand
then the DNA strand entwine with each other
again this process is making a protein
4. Chapter 17.3
Mitosis is when the nucleous divides
Prophase, begins when duplicated chromosones
are visable
Cytokinesis is when the cytoplasm is divided
Meiosis produces haploid daughter cells by
reducing chromosome number in half
There are two stages of meiosis
Meiosis I creates the hapliod daughter cells, but
they still has chromosomes in the duplicated state
Meiosis II separates the duplicated chromosomes
and there are four haploid daughter cells
5. Chapter 17.4
Cell reproduction must be regulated so it
does not go out of control, how is this done?
Most cells in the body dived but not all, and
the ones that do divided do so at different
paces
The cell division process is based off of
regulatory signals
Other influencing factors one how long a cell
takes to divide can be the environment
outside the cell
6. Chapter 17.5
The cells in you body beside your sperm or egg
cells have the same DNA at first
Differentiation takes place then the cell become
different from each other, and have different
forms and functions
Differentiation starts in the first stages of life when a
zygote becomes a blastocyst the inner cells
become different than the outer cells
Later in development differentiation continues to
occur when creating which cells are
skeletal, muscle, skin, nerves, etc.
7. Chapter 17.6
Reproductive cloning must be
undifferentiated cells
Embryo splittind is when a fertilized egg can
be divided into eight identical cells
They can be place in eight different
segregate mothers and create eight identical
offspring
Somatic cell nuclear transfer is the cloning of
an adult
A true clone of an adult can not be created
due to germ cells only have half a set of DNA
8. Chapter 17.7
Therapeutic cloning is when human cells are
cloned to help treat patients
The main purpose is to create duplicate
cells, tissue, organs for patients that need
then to save their lives
With todays medical technology the believe
this may be medical treatment in the future
They must however be careful because as they
get closer they may also be finding a way to
clone adults which could get out of control if it
got out
9. Chapter 18.1
Hyperplasia is when the rate of cell division is
increased
Hyperplasia can happen in normal cells but
not in the same way as it does in cancer cells
Hyperplasia will eventually cause a tumor
because of these rapid dividing cells some
cancerous and some not
Benign tumors remain in one place as a single
developed mass
The Benign tumors only affect a person health if
they get too big
10. Chapter 18.2
When cells divide uncontrollably and go
through physical changes this is when cancer
develops
When the cells no longer adhere to
eachother is when the cancer will begin to
spread to other tissues which means they are
malignant tumors
Cancer is the second most comon cause of
death in the U.S.
1 in every 3 get it
1 in every 4 die from it
11. Chapter 18.3
If the photo-oncogenes are mutated this may
contribute to a cause of cancer
Cancer can be passed down from generation to
generation through family genetics
Some causes of cancer can be from things we do
to our own body such as smoking and tanning
There are also internal factors that may contribute
such as internal chemical production or faulty
DNA reproduction
There are all of these factors that contribute yet
some cells may have multiple mutations before
they become cancerous
12. Chapter 18.4
Thebiggest sign for cancer detection and
the most common cancer diagnoses is
done when a tumor is detected
Usually done by X-ray, MRI, or PET Scan
Genetic testing can be done to detect
the presence of a mutated gene
however this does not always mean that
it’s cancerous
Cancer can by detected also by enzyme
tests
13. Chapter 18.5
Early diagnoses is the key to be able to treat
cancer
The main ways to get rid of the cancer are to take
secions of chemotherapy, radiation, or to
surgically remove it
There are many newer treatments that are now
being used also
Magnetism
Immunotherapy, to help boost the patients
immune system
Photodynamic therapy to target malignant cells
Molecular treatments that target specific genes
Drugs that cut off blood supply to the tumor
14. Chapter 18.6
The 10 most common cancers are:
Skin cancer
Three types and needs to be detected early
Lung cancer
Most commonly caused by smoking, and causes the most dealths
Breast cancer
Mostly in women and the soon found the better
Prostate cancer
Usually occurs after age 50, more common in men
Colon and rectum cancer
Most common sign is blood in stool
Lymphoma
Radiation and chemotherapy are most common treatments
Urinary Bladder cancer
Most common sign is blood in urine
Kidney cancer
Usually detected during rectal exam
Uterine cancer
Uterine bleeding is the most common sign
Leukemia
Usually treated with chemotherapy
15. Chapter 18.7
While most cancers can be preventedf there are
some that can not, we should do everything we can
to prevent the ones we can
The biggest prevention technique is do not smoke
Having a healthy diet also plays a big role in the
prevention of cancer
Other preventative mechanisms are
Knowing your family history
Know your body
Keep up on your medical screenings
Avoid direct sunlight and wear sunscreen
Drink in moderation
Stay infomed on new health information
16. Chapter 19.1
The DNA that is inherited from our parents is
what makes us who we are
We get two copies of each gene, one from
each parent, and some may be different due
to mutations and these different versions
genes are referred to as alleles
Genotype is a complete set of alleles that we
inherit
Phenotype is the physical and functional
expression of the alleles
17. Chapter 19.2
Patterns of inheritance for one or two
pairs of alleles can be shown by a Punnett
square
When one allele shows complete
dominance over the other this is a comon
pattern of phenotypic inheritance
Genes that are from different traits are
assorted independently of one another
18. Chapter 19.3
Some alleles don’t follow the previously
mentioned dominant pattern there are
two other dominance pattern they may
use
Incomplete dominance, which is when
heterozygotes exhibit an intermediate
phenotype
Codominance, which is when
heterozygotes express both phenotypes
equally
19. Chapter 19.4
Multiple genes influence one single trait in
polygenic inheritance
Our genotype and the environment we
are in both determine what our
phenotype will be
Linked alleles are alleles that are located
on the same chomosome and may be
inherited together
20. Chapter 19.5
Knowing whether a child is a male or female is
determined early by genes of the Y chromosome
If the Y chromosome is present it’s a male if there is
and absence of the Y chromosome it’s a female
Most sex-linked inheritance genes have nothing to
do with determining the sex of the fetus but they
are referred to as the inheritance of the genes
located on the sex chromosomes
Sex-linked inheritance has diseases associated
with it including hemophilia, colorblindness, and
muscular dystrophy
21. Chapter 19.6
Failure of homologous chromosome to
separate properly during mitosis or meiosis
which causes altered chromosome numbers
in the daughter cells is called nondisjunction
Down syndrome is usually cased when three
copies of chromosome 21 are inherited an
the biggest risk factor is parents age
especially the mother
If part of a chromosome is deleted it my be
fatal and if translocation occurs it could alter
the ability for the gene to function properly
22. Chapter 19.7
Recessive
alleles are to blame for most
autosomal heritable genetic diseases
Diseases such as Phenylketonuria, Tay-
Sachs dises and cystic fibrosis are all caused
from recessive alleles
Huntington
disease however is caused by
a dominant-lethal allele
These alleles are uncommon and usually
eliminat them selfes from population
23. Chapter 19.8
Genes can only influence generally
patterns of behavior or mood
Genes can not determine specific
behaviors