Monday, May 11, 2015

Ch 14
Human Heredity

14.1
Human Chromosomes

Karyotypes
A Human Karyotype
A typical human cell has 23 pairs of chromosomes. These chromosomes have been cut out of a photograph and arranged to form a karyotype.

A karyotype shows the complete diploid set of chromosomes grouped together in pairs, arranged in order of decreasing size. Scientists the but out the chromosomes from the photographs and arrange them in a picture.


Genome - The full set of genetic information that an organism carries in its DNA.

Sex Chromosomes - Two of the 46 chromosomes in the human genome are known as sex chromosomes, because they determine the sex of the individual. 

Males have one X chromosome and one Y chromosome (XY)

Females have two X chromosomes (XX)

Males and females are born in a roughly 50:50 ratio.

All human egg cells carry a single X chromosome.

Half of all sperm cells carry an X chromosome (23,X)
and half of all sperm cells carry a Y chromosome (23, Y)

This ensures that just about half the zygotes will be males and half will be females.




More than 1200 genes are found on the X chromosome. Not all of these are gender related.
The Y chromosome is much smaller  than the X chromosome and contains only about 140 genes, most of which are associated with male sex determination and sperm development.


Autosomes
The remaining 44 human chromosomes (pair 1-22) (not sex chromosomes) are called autosomes.

So, a human genome consists of 44 autosomes and 2 sex chromosomes.

Human Chromosomes
Human chromosomes follow several patterns of inheritance including:
Dominant and Recessive Alleles
Codominant Alleles
Incomplete Dominant Alleles
Multiple Alleles

Sex-Linked Inheritance
Genes that are located on the X and Y chromosomes are considered "sex-linked", even if they have nothing to do with the determination of sex.

Genes found on the Y chromosome are passed directly from father to son.

Because males only have one X chromosome, if there is a defect in a gene located on it, then the defective gene will be expressed. But, since females have two X chromosomes, a defective gene on only one of those chromosomes won't be expressed if it is recessive. Therefore, females can "carry" traits that may only show up in their sons if the son receives the defective chromosome. 

Colorblindness is one of those sex-linked chromosomes that usually only shows up in men who have received the defective X chromosome from their mother. If a female receives two defective alleles for a recessive disease, (one from each parent) then the female would express the disease. 
Because of this, colorblindness is much more prevalent in males (1 in 12) than in females (1 in 200).

X Chromosome Inactivation
Since females have two X chromosomes, female cells adjust by randomly switching off one of them. The "switched off" chromosome condenses and forms a "Barr Body" in the nucleus. Barr bodies are only found in females.
An example of how two different alleles (one on each X chromosome) show up in different locations on the body of the same organism is that of a calico cat. This cat has two different colored spots. The gene for spots is found on the X chromosome. In some locations on the cat's body, the X chromosome with the orange spot allele will be shut off, whereas, in other locations, the other X chromosome carrying the black spot allele would be shut off. The cat would have orange spots where the black allele is shut down, and black spots where the orange allele is shut down.





Pedigrees
A pedigree is a chart that shows the relationship within a family.  A pedigree shows the presence or absence of a trait according to the relationships between parents, siblings, and offspring.




The information gained from pedigree analysis makes it possible to determine the nature of genes and alleles associated with inherited human traits. Based on a pedigree, you can often determine if an allele for a trait is dominant or recessive, autosomal or sex-linked.


14.2
Human Genetic Disorders

Genes are expressed in the proteins they make.
Changes in a gene's DNA sequence can change proteins by altering their amino acid sequences, which may directly affect one's phenotype. 

Sickle Cell Disease
Sickle Cell Anemia is a disorder caused by a defective allele for a protein that makes up hemoglobin (Hg). The defective protein makes the Hg a bit less soluble, causing the Hg molecules to stick together when the blood's oxygen level decreases. The molecules club into long fibers, forcing cells into a distinctive sickle shape, which gives the disorder it's name.
Sickle shaped cells are more rigid than normal red blood cells and they tend to get stuck in the capillaries. If the blood stops moving through the capillaries, damage to cells, tissues, and organs can result.




Sickle cell is a recessive gene prevalent in African descendants. It shows up early in life.





Interestingly enough, people who have one or two sickle cell alleles are immune to another disease found primarily in Africa, Malaria.


Cystic Fibrosis
Another recessive disease, Cystic Fibrosis, is most common among European ancestry. CF is caused by the deletion of just three nitrogen bases in the gene for a protein which is involved in Cl- ion transport across the cell membrane. Since water follows salt, the lack of water causes the mucous membranes to secrete a very thick mucous which causes many problems including clogged ducts, gas exchange, and pneumonia.

People with one normal copy of the CF allele are unaffected by CF, because they can produce enough CFTR to allow their cells to work properly. Two copies of the defective allele are needed to produce the disorder because it is recessive. CF shows up early in life. The life expectancy is shortened.

People who carry the CF gene are resistant to Typhoid Fever caused by a bacteria.


Huntington's Disease
Huntington's is caused by a dominant allele for a protein found in brain cells. The allele for this disease contains a long string of bases in which the sequence CAG repeats itself over and over again. The more it repeats itself, the more severe the disease and the earlier the onset. However, this disease does not normally show itself until middle age. Huntington's Disease results in mental deterioration and uncontrollable movements.

Chromosomal Disorders

Most of the time, meiosis works perfectly and each human gamete gets exactly 23 chromosomes. But, every so often, an error in the separation of the chromosomes occurs. Nondisjunction which means "not coming apart" is the most common error in meiosis and occurs when the homologous chromosomes don't separate properly.
If nondisjunction occurs during meiosis, gametes with an abnormal number of chromosomes may result, leading to a disorder of chromosome numbers. 
If a gamete ends up with 3 homologous chromosomes, this is called a trisomy (three bodies).  The most common form of trisomy, involving 3 copies of chromosome 21, is Down syndrome.




Turner's Syndrome
A female with Turner's Syndrome usually inherits only one X chromosome. Women with Turner's syndrome are sterile and their sex organs do not develop properly at puberty.



Klinefelter's Syndrome
Males with this syndrome inherit an extra X chromosome which interferes with meiosis and usually prevents these individuals from reproducing. 



Down Syndrome (Trisomy 21)





***There have been no reported instances of babies being born without and X chromosome, indicating that this chromosome contains genes that are vital for the survival and development of the embryo.


Sunday, April 26, 2015

Ch 12 DNA

12.2 The Structure of DNA


There were several people who are credited with finding the structure of this most important molecule.

Remember the 4 organic molecules (molecules that make up living things)? 
carbohydrates
lipids
proteins
nucleic acids

DNA is a nucleic acid made up of nucleotides joined into long strands or chains by covalent bonds.

Nucleic Acids are long, slightly acidic (hence, the name) molecules usually found in the cells nucleus (if there is one). They are polymers made up of smaller units (monomers) called Nucleotides.

A nucleotide contains 3 smaller molecules:
a phosphate group
a 5 carbon sugar (carb) called deoxyribose
a nitrogen base

There are 4 different types of nucleotides. The nitrogen bases can change but the sugar and phosphate stay the same.

The four nitrogen bases are:
Guanine
Cytosine
Thymine
Note: G and A are larger, 2 ring structures while C and T are smaller, single ring structures. Each single ring structure always pairs with a 2 ring structure in a double helix. An easy way to remember which are double ringed is that they are G and A, like GA (Georgia) which is a larger state than CT (Connecticut), C and T.

Nucleotides are held together to build nucleic acids by covalent bonding between the sugars and the phosphate groups along the outside of the "ladder".

The nucleotides can be joined in any order, meaning any sequence of bases is possible. 

It just so happens that this chemical structure is especially good at absorbing UV Light. This isn't necessarily a good thing because this can cause mutations in the order of nucleotides.



Chargaff's Rule

Edwin Chargaff, an Austrian-American biochemist, had discovered that the percentages of adenine (A) and thymine (T) bases are almost always equal in any sample of DNA. The same rings true for guanine (G) and cytosine (C). This observation known as "Chargaff's rule" led us to the knowledge that  T always pairs with A and G always pairs with C.



Rosalind Franklin

In the 1950's, British scientist Rosalind Franklin began to study DNA. Using x-ray diffraction, she was able to record the scattering pattern of DNA shows that the strands in DNA are twisted around each other like the coils of a spring, a shape known as a helix.

Watson and Crick
American biologist, James Watson, and British physicist, Francis Crick, had built 3D models of the molecule... but not until in 1953, when they saw Franklin's remarkable X-ray pattern, did they figure out the correct double helical structure for DNA.





Watson and Crick's model of DNA was a double helix, in which two strands of nucleotide sequences were wound around each other. This explains Chargaff's rule of base pairing and how the two strands of DNA are held together.


Antiparallel Strands
The two strands of connected DNA run in opposite directions, and are "anti-parallel".
The two strands are joined at the nitrogen bases and are held together by Hydrogen Bonds. H bonds are weaker bonds than covalent. This is helpful when the strands have to separate for DNA replication in cell division.
Note that C and G are always held by 3 H bonds, while A and T are always held by 2 H bonds.
This nearly perfect fit between A-T and G-C nucleotides is known as base pairing.




Watch Hank's great description here about the structure and replication of DNA!
                                        

For 12.2 Powerpoint click here:


12.3 DNA Replication



Base pairing in the double helix explains how DNA can be copied!

Each strand of the double helix has all the info needed to reconstruct the other half by using base pairing. The strands are said to be complementary.

Before a cell divides, it duplicates its DNA in a copying process called replication, which occurs during the S phase of interphase. During replication, the DNA molecule separates into two strands and then produces two new complementary strands. Each original strand serves as a template, or model, for the new strand.

During replication, the two original strands of the double helix "unzip", allowing two replication forks to form. Each strand now becomes a template for its complimentary new strand to form on. Each of the two new double strands are made up of one original strand and one new strand. 

Enzymes

DNA replication is carried out by a series of enzymes. 

1. Enzymes "unzip" a molecule of DNA by breaking the H bonds between the base pairs and unwinding the two strands of the molecule.

2. DNA polymerase joins individual nucleotides to produce a new strand of DNA. Then, DNA polymerase adds the sugar-phosphate bonds that hold the nucleotides together. Finally, DNA polymerase also "proofreads" each new strand to check for mistakes.


Micrograph showing a pair of replication forks in human DNA

Telomeres
Telemeres are the white (stained) part of the blue human chromosome
DNA at the tips of chromosomes are known as telomeres. These telomeres sometimes like to break off. This DNA is particularly difficult to replicate. Cells use a special enzyme, telomerase, to solve the problem by adding short, repeated DNA sequences to the telomeres.

Prokaryotic DNA Replication

Remember that in prokaryotes, there is no nucleus to contain the DNA. Prokaryotes have a single, circular DNA molecule in the cytoplasm, containing nearly all the cell's genetic info. 

DNA replication begins when a regulatory protein binds to a single starting point on the chromosome. These proteins trigger the beginning of the S phase, and DNA replication begins.


Replication in most prokaryotic cells starts from a single point and proceeds in two directions until the entire chromosome is copied. The two chromosomes produced by replication are attached to different points inside the cell membrane and are separated when the cell splits.

Eukaryotic DNA replication

Eukaryotic chromosomes are generally much bigger than those of prokaryotes. In eukaryotic cells, replication may begin at dozens or even hundreds of places on the DNA molecule, proceeding in both directions until each chromosome is completely copied.


The system is not foolproof even though a number of proteins check DNA for chemical damage or base pair mismatches prior to replication. 

The two copies of DNA produced by replication in each chromosome him remain closely associated until the cell enters prophase of mitosis. At that point, the chromosomes condense, and the two chromatids in each chromosome become visible.


What this video to help understand DNA replication!

Ba
For 12.3 Powerpoint click here:














Sunday, March 15, 2015

Ch 11 Intro to Genetics

Chapter 11 Genetics


11.1 The Work of Gregor Mendel


What's your inheritance?
The modern science of genetics was founded by an Austrian monk named Gregor Mendel. Mendel spent several years studying science and started genetics experiments in the monastery gardens on pea plants. 


He used ordinary garden peas because they are small and easy to grow. Also, they produces hundreds of offspring in a short life cycle. Today, his research with pea plants is called a model system.

Fertilization
During sexual reproduction, male and female reproductive cells join in a process known as fertilization to produce a new cell (organism). The new cell develops into a tiny embryo encased within a seed. 
Flowers are the reproductive organs on plants. Pea flowers are normally self-pollinating, which means that sperm cells fertilize egg cells from within the sam flower. A plant grown from a seed produced by self-pollination inherits all of its characteristics from the single plant that bore it; It has a single parent. Therefore, the traits of each successive generation would be the same. Traits are specific characteristics of an individual. 
Cross-Pollination
Mendel decided to cross-pollinate the pea flowers by removing the male reproductive organs from one plants flower and fertilizing the female reproductive organ on another plant. In this way, the new organism will have two parents with different DNA. By crossing two plants with different traits, he was able to study how genes are passed and expressed over generations. Crossing two organisms with different traits creates a hybrid

Mendel studied seven different traits of pea plants. 
When doing genetic crosses, the original pair of plants is called the P or parental generation. Their offspring are called the F1 or first filial generation. The grandchildren of the P generation are the F2 generation.

Much to his surprise, when Mendel crossed two plants with different traits, only one of the traits showed up in the offspring. Where did the other one go?

Mendel drew two conclusions:

1. An individual's characteristics are determined by factors that are passed from one parental generation to the next. Today we call these factors genes. Different forms of a gene are called alleles. For example, everyone has a gene for eye color. The different alleles for eye color might be blue, brown, green, and hazel.

2. Principle of Dominance: states that some alleles are dominant and others are recessive. An organism with a least one dominant allele for a particular form of a trait will exhibit that form of the trait. The recessive allele for a particular form of a trait will exhibit that form only when the dominant allele for the trait is not present.




Mendel discovered that the round seed shape, yellow seed color, gray seed coat, smooth pod shape, green pod color, axial flower position, and tall plant height were the dominant alleles for pea plants.



If recessive alleles disappear in the 2nd generation, where did they go?

Mendel continued to breed the 2nd generation with itself by self-pollination and found that the recessive traits showed up again in the 3rd generation. 

Mendel assumed that a dominant allele had masked the corresponding recessive allele in the F1 generation. However, because the recessive trait showed up in the F2 generation. This showed that the F1 plants carried the recessive allele.

Segregation
During the production of gametes (sex cells), eggs and sperm, reproductive organs undergo meiosis. Meiosis produces cells with half the normal number of chromosomes. Therefore, the sperm and egg cells only carry one allele for  each genes. This is a product of meiosis, or segregation:

After each parent cell segregates and forms gametes, the offspring could inherit either of the two parent's alleles, strictly by chance of which gamete it formed from. 


For 11.1 powerpoint please click link below:

https://docs.google.com/presentation/d/1z57BO3TQKotC62yP5b8kgyRSz6jg_8j7aBisEnEA1Ts/edit?usp=sharing

11.2 Applying Mendel's Principles

Probability

Probability is the chance that an event or outcome will occur. Mendel uses probability to describe the different probable outcomes of offspring after cross-pollinating.

In a coin flip, there are two sides to a coin so there are two possible outcomes. The probability that the coin will land on one of the two sides is 1/2, or 50%.

In segregation, each of the two parent alleles separate to form gametes or sex cells. The gametes then only carry one of the parents alleles. The parent has a 50-50% chance of passing on either allele to their offspring. This happens purely by chance. The offspring could inherit either allele from the parent. The new offspring will inherit only one allele from one parent and only one allele from the other parent so that the new offspring now has two of its own alleles.


Homozygous and Heterozygous

Homozygous - organisms that have two identical alleles for the same gene

Heterozygous - organisms that have two different alleles for the same gene

Eye color

Homozygous

BB (homozygous dominent)
or
bb (homozygous recessive)

Heterozygous

Bb (the dominant allele will show up)

Probabilities Predict Averages

Probabilities can predict the average outcome of a large number of events. If you flip a coin twice, you could get one heads and one tails. Or, you could get two heads or two tails. 

The larger the number of coin flips, or offspring, the closer the results will be to the predicted values.

Genotype and Phenotype

Every organism has a genetic makeup as well as a set of observable traits.

The genotype is the genetic makeup of an organism for any given gene. It contains two alleles for that gene. For instance, a persons genotype for eye color could be Bb. (Geno means "race, kind")

The phenotype is the observable characteristic of the trait. For instance, the phenotype for eye color for a person with Bb would be Brown (even though they also carry a blue gene). (Pheno means "to show")

The genotype can be homozygous dominant, homozygous recessive, or heterozygous.

The phenotype will be only the dominant allele or the recessive allele.

Two organisms can have the same phenotypes but different genotypes.

PUNNETT SQUARES

Punnett Squares use mathematical probability to help predict the genotype combinations in genetic crosses. This diagram is one of the best ways to predict the outcome of a genetic cross.



Using the Punnett Square you can deduce that the offspring will have one of the four above genotypes, BB, Bb, bB, or bb. There are actually only three possibilities because Bb and bB are the same genotype. From these genotypes you can deduce that the phenotypes may be dominant or recessive. In this case the probabilities of having a dominant phenotype is 3/4 or 75% and a recessive phenotype is 1/4 or 25%.


It is possible to determine the probability when two or more factors are involved as well.

 In this example, the color of the squares represents pod color. Alleles in black indicate short plants, while alleles in red indicate tall plants


Mendel crossed plants that were homozygous dominant for round yellow peas with plants that were homozygous recessive for wrinkled green peas below.

All of the F1 offspring were heterozygous dominant for round yellow peas.

Below, when Mendel crossed F1 plants that were heterozygous dominant for round yellow peas...
He found that the alleles segregated independently to produce the F2 generation.

Independent Assortment
The principle of independent assortment states that genes for different traits can segregate independently during the formation of gametes. Independent assortment helps account for the many genetic variations observed in plants, animals, and other organisms--- even when they have the same parents!


Summary of Mendel's Principles

Mendel's principles of heredity, observed through patterns of inheritance, form the basis of modern genetics.

1. The inheritance of biological characteristics is determined by individual units called genes, which are passed from parents to offspring.
2. Where two or more forms (alleles) of the gene for a single trait exist, some alleles may be dominant and others may be recessive.
3. In most sexually reproducing organisms, each adult has two copies of each gene---one from each parent. These genes segregate from each other when gametes are formed.

4. Alleles for different genes usually segregate independently of each other.

Mendel's principles apply to all organisms that reproduce sexually. In the early 1900s, Thomas Hunt Morgan used the insect known as the fruit fly, Drosophila melanogaster, to reproduce the same results that Mendel gave. A single pair of fruit flies can produce hundreds of offspring.




For 11.2 Powerpoint click below


11.3 Other Patterns of Inheritance

Exceptions to Mendel's Rules

Sometimes, some alleles are neither dominant nor recessive.

Incomplete dominance - the heterozygous phenotype lies somewhere between the two homozygous phenotypes. Example: if a chicken has incompletely dominant alleles for black and white feathers, the feather may turn out grey. 

In four o'clock plants, the alleles for red and white flowers show incomplete dominance. Heterozygous (RW) plants have pink flowers - a mix of red and white coloring.

Codominance: the phenotypes produced by both alleles are clearly expressed. Example: in the case of chickens with a black and a white allele, rather than "mixing" the two colors, there will be areas of black and areas of white making the chicken appear speckled instead of grey (incomplete dominance).


Red blood cells carry antigens, molecules that can trigger an immune reaction, on their surfaces. Human blood type A carries an A antigen, type B has a B antigen, type AB has both antigens, and type O carries neither antigen. The gene for these antigens has three alleles; A, B, and O.
Multiple alleles: Many genes exist in several different forms and are therefore said to have multiple alleles. When there are more than two alleles for a gene, there is said to be multiple alleles.
A and B are dominant alleles. O is a recessive allele.
Therefore, a person whose phenotype for blood is A can have AA or AO genotype.
A person whose phenotype for blood is B can have BB or BO phenotype.
A person whose phenotype for blood is O has a genotype of OO, because it is recessive.
And, because A and B are codominant, a person who has a genotype of AB has a phenotype of AB.
O is the universal donor. AB is the universal recipient.


Polygenic Traits - traits that are produced by the interaction of several genes. For example, at least three genes are involved in making the reddish-brown pigment in the eyes of fruit flies. And, human skin color comes from a combination of four different genes.

Genes and the Environment
Environmental conditions can affect gene expression and influence genetically determined traits.

Temperature and Wing Color
Western white butterflies that hatch in the spring have darker wing patterns than those that hatch in summer. The dark wing color helps increase their body heat. This trait is important because the butterflies need to reach a certain temperature in order to fly. The buckeye butterflies shown below also have different wing patterns at different times of year. These butterflies are darker in the autumn than they are in the summer 
This is an example of how the environment affects the phenotype of an organism.



For 11.3 Powerpoint click below

https://docs.google.com/presentation/d/1w9s1NFW64ePkqRzUwV1LDfs8PEr9mSOw4mooyafr2kE/edit?usp=sharing

11.4 Meiosis

An organism with two parents must inherit a single copy of every gene from each parent.  Matching chromosomes from each parent are called Homologous chromosomes. This means that, in fruit flies, each of the four chromosomes from the male parent has a corresponding chromosome from the female parent. A cell that contains both sets of homologous chromosomes is said to be diploid. When an organism produces gametes, those two sets of genes must be separated so that each gamete contains just one set of genes.

Diploid Cells: Having two complete sets of inherited chromosomes, one set from each parent (two complete sets of genes). This is the number of chromosomes that are in all body cells except the ones made in reproductive organs, the sex cells (eggs and sperm). Diploid number (twice haploid) is represented by the letter "2N".

Haploid Cells: Cells that contain only a single set of chromosomes (a single set of genes). The gametes of sexually reproducing organisms are haploid. Gametes are the sex cells (cells meant for reproduction which will combine with another sex cell to make a new organism). Haploid cells are created as a product of two cell divisions (Meiosis). Haploid number is represented by the letter "N".

In fruit flies, the diploid number (2N) of chromosomes is 8. The haploid number is 4.
 Meiosis: first stage in sexual reproduction. This is the process of making gametes for reproduction. The parent cell goes through two cell divisions to produce 4 daughter cells with half the number of chromosomes as the parent cell. Each new gamete is genetically different from each other and from the parent cell it came from.
Meiosis, like Mitosis, is preceded in the cell cycle by Interphase. During Interphase, in preparation for cell division, the DNA is duplicated.




Prophase I: After interphase I, the cell begins to divide, and the chromosomes pair up. Each replicated chromosome pairs with its corresponding homologous chromosome.

This pairing forms a structure called a tetrad, which contains four chromatids. As the homologous chromosomes form tetrads, they undergo a process called crossing-over. 

First, the chromatids of the homologous chromosomes cross over one another. Then, the crossed sections of the chromatids - which contain alleles - are exchanged. Crossing-over therefore produces new combinations of alleles in the cell. 

Metaphase I: paired homologous chromosomes line up across the center of the cell. 


Anaphase I: spindle fibers pull each homologous chromosome pair toward opposite ends of the cell.



Telophase I and Cytokinesis: a nuclear membrane forms around each cluster of chromosomes. Cytokinesis follows telophase I, forming two new cells. 

Because of crossing over, the two cells formed from Meiosis I do not have the same exact genetic make up of each other, or the parent cell, since they "traded" some DNA in crossing-over. 

Following Meiosis I, the two new cells (2N) now enter immediately into Prophase II. Unlike before the first division, neither new daughter cell goes through a round of chromosome replication before entering meiosis II.




Prophase II: their chromosomes (each consisting of two chromatids) become visible. There are no tetrads, because the homologous pairs were already separated during meiosis I.




Metaphase II: chromosomes line up in the center of each cell.






Anaphase II: the paired chromatids separate.





Telophase II and Cytokinesis: nuclear membranes start to reform around the now haploid nuclei. Cells pinch off resulting in four haploid (N) cells (gametes). In the example (left), each of the four daughter cells produced in meiosis II received two chromosomes.




Gametes - haploid cells produced by meiosis II are gametes that are so important to heredity. In male animals, these are called sperm and all 4 sperm can go on to fertilize and egg. In female animals, these haploid cells are called eggs. Only one of the 4 female gametes will mature into an egg for reproductive purposes. 
Zygote - When a sperm fertilizes an egg, these two haploid cells will fuse to form a new diploid cell, the first cell of a new organism. The zygote will then undergo mitosis forming a new organism.

Comparing Mitosis and Meiosis

Mitosis - asexual reproduction, used for growing and repairing in multicellular organisms
Meiosis - sexual reproduction, used to produce gametes for producing new organisms






In mitosis, when the two sets of genetic material separate, each daughter cell receives one complete set of chromosomes. In meiosis, homologous chromosomes line up and then move to separate daughter cells. As a result, the two alleles for each gene are segregated, and end up in different cells. This sorting and recombination of genes in meiosis result in a greater variety of possible gene combinations than could result from mitosis.

Also, mitosis does not normally change the chromosome number of the original cell. This is not the case for meiosis, which reduces the chromosome number by half.

And finally, mitosis is a single cell division, resulting in the production of two identical daughter cells. On the other hand, meiosis requires two rounds of cell division, and in most organisms, produces a total of four daughter cells.




For 11.4 Powerpoint click below