-
Asexual Reproduction
reproduce by itself
-
Asexual
Offspring that inherit genes from one parent
-
Sexual Reproduction
Offspring that inherit genes of both parents combined
-
DNA
- Neucleic Acid(macromolecule)
- Nucleotide = monomer unit
- deoxyribose sugar
- nitrogen base phosphate group
-
Double Helix
Structure of DNA
-
Chromatin
- Thing and stringy, can't see under microscope
- DNA wrapped loosly arond protein
- As a cell enters mitosis the chromatin condenses into chromosomes
-
Chromosomes
when chromatids seperate the individual strands are called chromosomes
-
Sex Chromosomes
Chromosomes that determine an individuals gender
-
Autosomes
any chromosome that is not a sex chromosome
-
Sister Chromatids
two identically joined copies of the same chromosome
-
Centromere
where the two chromatids attach at the center
-
Cell Cycle
The process that a cell goes through when doubling
-
Interphase
- NONDIVIDING stafe
- -carries out normal metabolic processes and functions
-
Go
- Normal day activities of the cell
- (g stands for gap)
-
-
S - phase
- Genetic material duplicates (DNA replication)
- (S stands for synthesis)
-
G2
- Growth phase
- cell prepares to divide
-
-
Mitosis
Nucleus and duplicated chromosomes divide into two "daughter" neclei
-
Cytokinesis
Process by which the cytoplasm is split in order to form two seperate cells
-
-
Centrosomes
- contain centrioles (only in animal cells)
- release microtubles to for the mitotic spindle
-
Phases of mitosis
- Prophase - pro = before
- Metaphase - meta - middle
- anaphase - apart
- telphase
PMAT
-
Prophase
- -Neucleolus goes away
- -Nuclear envelope breaks up
- -Spindle forming
- -Chromosome consisting of two sister cromatids
-
Metaphase
- -Spindle microtubles
- -2 chromatids
-
Anaphase
-Identical daughter chromosomes
-
Telophase
- -Chromosomes uncoiling
- -Neuclear envelope forming
- -Cell dividing into two
-
Cancer
- -Disease caused by the severe disruption of the mechanisms that normally control the cell cycle
- -Uncontrolled Cell division
-
Tumor supprressor Gene
Halts Cell Division
-
Neoplasm(Tumor)
- Abnormal new growth of tissue
- Types:
- -Benign
- -Malignant
-
Benign Tumor
- NON-cancerous
- -They CANNOT spread or invade other parts of your body
- -They CAN be dangerous i they press vital organs, such as your brain
-
Malignant TUmor
Cancer cells can migrate and form tumors elsewhere in the body
-
Metastasis
The spread of cancer beyond their original site
-
Radiation therapy
Injures or Destroys cells in the area being treated by damaging their DNA, making it impossible for more growth and divide
-
Chemotherapy
Chemicals that distrupt Cell division
-
Homologous Chromosomes
- -same chromosome structure
- -carries the same sequence of genes
-
Diploid
- 2 sets of chromosomes
- -one from mom
- -one from dad
-
Haploid
- One set of chromosomes
- -Combination of chromosomes from mom and dad
-
Karyotype
the representations of a chromosome
-
Gametes
Sex cells (germ cells)
-
Zygote
A cell formed by two gametes
-
Dizygotic Twins
- Fraternal twins
- -twins who develop from two eggs fertilized by two different sperm
-
Monozygotic Twins
- Identical twins
- -Soon after one sperm fertilized one egg to
- form the zygote, the embryo splits to form
- two identical embryos
-
Conjoined Twins
- -A form of monozygotic twins
- -Occurs when the zygote of identical twins
- fails to completely separate
-
Meiosis
- Produces 4 non-identical gametes
- -Cell Division
- Stage one
- -Chromosome reduction divison
- Stage two
- -Division
-
Non-disjunction
- The failure of the chromosomes to properly
- segregate during meiotic or mitotic anaphase,
- resulting in daughter cells with abnormal numbers of chromosomes
- -Down Syndrome
- -Turner Syndrome
- -Klinefelter Syndrome
-
Down Syndrome
- Mental Retardation
- - Characteristic Facial Appearance
- - Increased risk for heart defects (~50% have a heart defect), digestive problems,
- leukemia, Alzheimer disease, hearing problems, hypothyroidism
- - Life Expectancy - 55 years
-
Turner Syndrome
-presence of only one complete X chromosome and no Y chromosome
-
Klinefelter Syndrome
An abnormal condition in a male characterized by two X chromosomes and one Y chromosome
-
Chorionic villus sampling
- -used for women 35 or
- older
- -earlier Test: 10-12 wks
- -increased risk for
- miscarriage: about 2%
-
Amniocentesis
- Used for women 35 or
- older
- -Test: 16-18 wks
- -Increased risk for
- miscarriage: less than 1%
-
Crossing Over
- exchange of genetic material between
- homologous chromosomes (tetrad)
-
Tetrad
group of 4 chromosomes
-
Double Helix
The structure of DNA in a shape of a spiral that consists of paired polynucleotides
-
Nucleotide
something that makes up DNA
-
Nitrogen Base
- Purines-double ring
- -Adenine
- -Guanine
- Pyrimidines
- -Cytosine
- -Thymine
-
Phosphodiester bonds
In RNA or DNA that holds a polynucleotide chain together
-
Antiparallel
Not parallel
-
DNA replication
Replication of DNA
-
Gene
A short segment of DNA that contains the instructions for building a protein
-
Locus
- Location of a gene on a chromosome
- - the genes address
-
Allele
Variation of a gene
-
Genotype
Genetic make up seq. Of DNA
-
Phenotype
The organisms physical traits
-
mRNA
Messenger ribonucleic acid
-
-
-
Genome
The collection of All of the genes in an organism
-
Ribosome
Forms peptide bonds between amino acids in order to for polypeptides
-
Transcription
- Step 1- DNA unzips
- Step 2- form the mRNA strand
-
Translation
The process that uses the codons in the mRNA molecules to specify the sequence of amino acid in a polypeptide chain
-
DNA polymerase
Addition of nucleotides to form the complementary DNA strand
-
RNA polymerase
Adds RNA nucleotides that are complementary with the DNA bases of the gene sequence
-
-
Codon
Three consecutive nucleotides on mRNA that code for a specific amino acid
-
Anitcodon
the complimentary sequence of the codon sequence
-
Genetic Code
The set of bases and the amino acids they code for
-
-
Stop Codon
- Termination
- -UAG, UAA, or UGA
-
Mutation
A permanent change in the DNA sequence of a gene
-
Point Mutation
- Mutations that effect one nucleotide
- Types
- -Substitution
- -Insertion
- -Deletion
-
Substitution Mutation
Taking one nucleotide out of the original DNA and replacing it with a different nucleotide
-
Insertion Mutation
Adding a single nucleotide
-
Deletion Mutation
Taking one nucleotide out of the DNA seq.
-
Silent Mutation
A mutation that codes for the same amino acid
-
Frameshift Mutation
- A mutation that shifts the "reading" frame of the genetic message by inserting or deleting a nucleotide
- Types:
- -Insertion
- -Deletion
-
Chromosomal Mutations
- Involve changes in many nucleotides
- Types:
- -Deletion
- -Duplication
- -Inversion
- -Translocation
-
Epigenetics
- Refers to all ptovesses that act on DNA and modify the expression of genes
- Two main processes
- -Chromatin Remodeling
- -DNA Methylation
-
Allele
Alternate forms of a gene
-
Homozygous
- Both alleles for a trait are the same
- eg. TT or tt
-
Heterozygous
- Both alleles are different
- e.g. Tt
-
Dominant
- When only one of the two different alleles in a heterozygous individual appears to affect the trait
- e.g. T
-
Recessive
- The allele that seems to be suppressed by the dominant allele in the heterozygous state
- e.g. t
-
Genotype
- Genetic Makeup of a gene
- e.g. TT or Tt or tt
-
Phenotype
- Observable Trait (gene product)
- e.g. Tall or Short
-
True - Breeding
If allowed to self-pollinate, they would produce offspring identical to themselves.
-
Hybrid
The offspring of two different true - breeding varieties
-
Mendel's Law of Segregation
The two alleles for a character separate during the formatino of gametes
-
Monohybrid Cross
- -A mating event between two individuals involving one gene
- -Determines the genotypes and phenotypes of the offspring based upon the genotypes of the parents
-
Test-Cross
Breeds an individual of unkown genotype, but dominant phenotype with a homozygous reccessive individual in order to figure out whethere the parent is homozygous dominant or heterozygous god a given trait
-
P - generation
parental generation
-
F1
Offspring of the P generation
-
F2
The offspring of a cross between two individuals from the F1 generation
-
Menel's Law of Independent Assortment
-Genes located on different chromosomes will be inherited indipenditly of each other
-
Dihybrid Crosses
- Cross between two individuals that includes two completely different traits
- -Each type of gene should have a unique leteter symbol
-
Incomplete Dominance
Both Alleles are dominant and the heterozygote shows an intermediate phenotype
-
Codominance
When heterozygous for two dominant traits, the individual expresses both traits
-
Multiple Alleles
There are more than two alleles available in the gene pool out of which only two will be inherited.
-
Anitigen
A substance taht can trigger an immune response causing the production of antibodies as part of the body's defence against infection and disease.
-
Rh-factor
A protein that is found on red blood cells. If the Rh factor protein is present on the cells, a person is Rh-positive. If there is no Rh factor protein, the person is Rh-negative.
-
Autosomes
All chromosomes except the sex chromosomes
-
Sex Chromosomes
Chromosomes that deterime the gender of an organism
-
Sex Linkage
The location of a gene on a sex chromosome, typically on the X chromosome. (X-linkage)
-
Polygenic Inheritance
Traits controlled by multiple genes
-
Dominant Disorder
- Only one defective gene is necessary for the person to have the disorder
- -Every affected individual has at lease one affected parent.
-
Recessive Disorder
Both copies of the gene need to be defective in order to have the disorder
-
Carrier
Tt(carries a defective gene but does not have the disorder)
-
Pedigree
- A diagram that shows the pattern of inheritance of a gene in a family
- -An individual who exhibits the trait in question is represented by a filled in symbol
-
ATP
- Main engery carrier
- -Verry good at energy transfer
- -Engergy Currency
- -Not good at storing engergy
-
Chemical Work
- Building or breaking-down a large molecule
- Energy is required to for bonds within a molecule.
- Energy is released when bonds are broken in a molecule.
-
Mechanical Work
Moving a muscle protein
-
Transport Work
Pumping solutes across a membrane
-
Photosynthesis
- Process by which plants convert light energy into chemical energy (carbohydrates).
- 6CO2 + 6H2O --> C6H12O6+ 6 O2
-
Mesophyll
The area of the leaf where chloroplasts are concentrated
-
Stomata
Pores in the leaf in which carbon dioxide enters and oxygen leaves
-
Veins
- Xylem
- -Transports water form the roots to the leaves
- Phloem
- -Transports sugar from the leaves to the roots
-
Chloroplast
A structure that makes photosynthesis happen
-
Stroma
where the calvin cycle takes place in the chloroplasts
-
Thylakoid
The thylakoid is in the chloroplast
-
Granum/a
are in the chloroplasts and store energy
-
Pigment
A pigment is something that changes a plants color
-
Chlorophyll
Turns the chloroplasts green
-
Why are cells small?
The smaller the cells the more cells in your body.
-
How is Cytokinesis different in animal cells than in plant cell?
When the plant cells are dividing they form a cell plate.
-
Explain the process of metastasis.
- Forming Secondary Tumors
- -The spread of cancer beyond their original site.
-
If an organism has 42 chromosomes in the diploid state how many chromosomes will it have in a halpoid state?
21
-
What is the difference between mitosis and meiosis?
- Meiosis produces 4 non-identical gametes
- Mitosis forms two identical somatic cells
-
Who determined the structure of DNA
- James Watson and Francis Crick
- - Were trying to build a three-dimensional model of DNA
- -They used Rosalind Franklin's x-ray diffraction picture
- -Determind the structure of DNA was a double helix
-
Structure of DNA
- Nucleic Acid
- -Deoxyribose Sugare
- -Phosphate group
- -Nitrogen base
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