Protein Synthesis & Mutations...Protein Synthesis & Mutations. RNA 1. Contains the sugar ribose...
Transcript of Protein Synthesis & Mutations...Protein Synthesis & Mutations. RNA 1. Contains the sugar ribose...
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Protein Synthesis & Mutations
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RNA
1. Contains the sugar ribose instead of deoxyribose.
2. Single-strandedinstead of double stranded.
3. Contains uracil in place of thymine.
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RNA Contains:1. Adenine2. Cytosine3. Guanine4. Uracil (not
Thymine)
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Three Main Types of RNA1. Messenger RNA (mRNA) - Carries copies of
instructions, for the assembly of amino acids into proteins, from DNA to the ribosome (serve as “messenger”)
* Made in the nucleus
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Three Main Types of RNA
2.Ribosomal RNA (rRNA) – Makes up the major part of ribosomes, which is where proteins are made.• Made in the nucleolus
Ribosomal RNA
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Three Main Types of RNA3. Transfer RNA (tRNA) – Transfers (carries)
amino acids to ribosomes as specified by codons in the mRNA
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Proteins• Proteins are made up of a chain of amino
acids.• Proteins are enzymes, which catalyze and
regulate chemical reactions.
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2 Steps to Make a Protein1. Transcription
• DNA → RNA2. Translation
• RNA → Protein (Chain of amino acids)
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Step 1: Transcription• Transcription - Process in
which part of the nucleotide sequence of DNA is copied into a complementary sequence in RNA.• RNA polymerase separates
the DNA strands. • One strand of DNA is used as
a template from which nucleotides are assembled into a strand of RNA.
• Occurs in the nucleus.
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Transcription: DNA → RNA
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After Transcription
• The mRNA leaves the nucleus and travels to the ribosomes in the cytoplasm.
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Codons• Codon - Three-nucleotide sequence on
messenger RNA that codes for a single amino acid.
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The Genetic Code• The “language” of mRNA instructions is
called the genetic code. • The genetic code is read three letters at a
time, so that each “word” of the coded message is three bases long.
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1.How the code is read:a. Every 3 bases on mRNA is
called a codon.b. Every codon codes for an amino
acid (building block of protein)c. Amino acids are abbreviated
most times by using the first 3 letters of the amino acid’s name.• Met = methonine• Leu = leucine
mRNA, Codons
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Start and Stop Codons• Start Codons: Found at the beginning of a protein;
Only one - AUG (methionine)• Stop Codons: Found at the end of a protein; three
exist, which make the production of the protein stop: UAA, UAG,UGA
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Reading the Codon Chart
Third Position
First Position
Examples:
AUG = Methionine
CAU = Histidine
UAG = Stop
Try these:
GCU:
UAC:
CUG:
UUA:
Answers:
Alanine
Tyrosine
Leucine
LeucineThis chart only works for mRNA codons!
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Step 2: Translation• Translation - Decoding of a mRNA message into a
protein (amino acid chain)• Takes place on the ribosomes• Each tRNA contains:
1. An amino acid2. Three unpaired bases.
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Anticodon• Each tRNA molecule has three unpaired
bases called the anticodon, which are complementary to one mRNA codon.
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Steps of Translation1. Begins when an mRNA molecule in the cytoplasm
attaches to a ribosome.2. As each codon of the mRNA molecule moves
through the ribosome, the proper amino acid is brought into the ribosome by tRNA.
3. The ribosome forms a peptide bond between the first and second amino acids.
4. The polypeptide chain continues to grow until the ribosome reaches a stop codon on the mRNA molecule and a protein has been made.
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mRNA↓
t RNA
mRNA →
Start codon
Ribosome
Methionine
PhenylalanineLysine
Nucleus
Translation
Go to Section:
← Anticodon
Jan
2006
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The Polypeptide “Assembly Line”
mRNARibosome
Translation direction
Lysine tRNA
tRNA
Ribosome
Growing polypeptide chain
mRNA
Completing the Polypeptide
Translation
Go to Section:
Jan
2006
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Mutations• Mutation - Change in a DNA sequence that
affects genetic information; error or mistake in copying DNA.
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Types of Mutations• Chromosomal Mutations
- Involve changes in the number or structure of chromosomes.Ex. Downs Syndrome
• Gene Mutations -Mutations that produce changes in a single gene.
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Types of Gene Mutations1. Point Mutations - affect a single nucleotide,
or point in the DNA sequence, usually by substituting one nucleotide for another.
Original: AUGUAC → Met – TyrMutated: AUGUAG → Met – Stop(causes the amino acid chain to stop protein production early)
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Types of Gene Mutations• Frameshift Mutations - Mutation that shifts the
“reading” frame of the genetic message by inserting or deleting a nucleotide.
– Insertions – A base is inserted into the DNA sequence.
– Deletions - A base is removed from the DNA sequence.
Original: The fat cat ate the wee rat.Frame Shift: The fat caa tet hew eer at.
(Frame shift mutations affect all subsequent amino acids!)
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Meiosis & Genetics (Chromosomes & Punnett Squares)
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Chromosomes & Genes
• Chromosome - Very long, continuous single piece of DNA, contains many genes
• Gene - Sequence of DNA that codes for a protein and thus determines a trait
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• Homologous Chromosomes - Term used to refer to chromosomes that each have a corresponding chromosome from the opposite-sex parent.• Both chromosomes have all the same
genes in the same location, but different ‘versions’ of those genes.
Homologous Chromosomes
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Haploid vs. Diploid• Haploid - Term used to refer
to a cell that contains only a single set of chromosomes and therefore only a single set of genes; “one set”; represented by N.
• Diploid - Term used to refer to a cell that contains both sets of homologous chromosomes; “two sets”; represented by 2N.
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Gamete vs. Zygote• Gamete - A mature sexual reproductive cell
that has a haploid numbers that unites with another cell to form a new organism. • Example: Sperm or egg cell
• Zygote - The cell formed by the union of two gametes.
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Sexual Reproduction - Process by which two cells from different parents unite to produce the first cell of a new organism.
Diploid zygote
2n+ =1n
Haploid sperm
(gamete)
Haploid egg
(gamete)
1n
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Meiosis• Meiosis - Process by which the number of
chromosomes per cell is cut in half through the separation of homologous chromosomes in a diploid cell; Haploid (N) gamete cells are produced from diploid (2N) cells.
Produce Haploid (N) Cells
Begin with Diploid (2N) Cells
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Four gametes are made during cell division by meiosis. The gamete cells have half the number of chromosomes as the original cell.
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Meiosis• Meiosis usually involves two distinct
divisions:1. Meiosis 12. Meiosis 2
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Meiosis 1• Prior to meiosis I, each
chromosome is replicated.• The cells then begin to divide
in a way that looks similar to mitosis.
• One big difference:• Each chromosome pairs with its
corresponding homologous chromosome to form a structure called a tetrad and exchange portions of their chromatids in a process called crossing-over.
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Crossing Over• Produces new combinations
of alleles.• Meiosis 1 is similar to mitosis
except:• The two cells produced by meiosis I have sets
of chromosomes and alleles that are differentfrom each other and from the diploid cell that entered meiosis I.
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Meiosis 2• Two cells produced by meiosis I now enter
a second meiotic division. • Unlike the first division, neither cell goes
through a round of chromosome replication before entering meiosis II.
• Those four daughter cells now contain the haploid number (N)—just 2 chromosomes each.
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Nondisjunction• The most common error
in meiosis occurs when homologous chromosomes fail to separate.• This is known as nondisjunction.• Results in abnormal numbers of chromosomes in
gametes.• Example - Down syndrome,
which results when an individual has three copies of chromosome 21.
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Mitosis vs. Meiosis• Mitosis
• Allows an organism's body to grow and replace cells. • Used in asexual reproduction to produce a new
organism. • New (daughter) cell is identical to the parent cell and
to each other.• Produces two diploid (2N) daughter cells.
• Meiosis• Used in sexual reproduction to produce gametes.• New (daughter) cells are genetically different from the
parent cells and from one another. • Produces four haploid (N) cells.• Is responsible for the genetic variation among species.
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Inheritance & Cell Type• You can only inherit a trait from
gametes, not other somatic (body) cells!
• Mutations within somatic (body) cells do not affect future offspring genes. Whereas, mutations within gametes do alter offspring genes.• For example, if your mother has skin cancer, you will
not inherit this mutation because the mutation is on her somatic (body) cells and these are not inherited.
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Dominant vs. Recessive
• Dominant - Masks the other trait; the trait that shows if present• Represented by a capital letter
• Recessive – An organism with a recessive allele for a particular trait will only exhibit that trait when the dominant allele is not present; Will only show if both alleles are present• Represented by a lower case letter
R
r
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Dominant & Recessive Practice
TT - Represent offspring with straight hairTt - Represent offspring with straight hairtt - Represents offspring with curly hair
T – straight hairt - curly hair
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Homozygous vs. Heterozygous
• Homozygous – Term used to refer to an organism that has two identical alleles for a particular trait (TT or tt)• Sometimes called purebred
• Heterozygous - Term used to refer to an organism that has two different alleles for the same trait (Tt)• Sometimes called hybrid
RR
Rr
rr
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Genotype vs. Phenotype• Genotype – The genetic makeup of an organism;
The gene (or allele) combination an organism has. • Example: Tt, ss, GG, Ww
• Phenotype – The physical characteristics of an organism; The way an organism looks• Example: Curly hair,
straight hair, blue eyes, tall, green
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Punnett Squares• Punnett Square – Diagram showing the gene
combinations that might result from a genetic cross
• Used to calculate the probability of inheriting a particular trait• Probability – The chance
that a given event will occur
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Punnett Square
Parent
Parent Offspring
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How to Complete a Punnett Square
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Y-Yellowy-white
Genotype:1:2:1
(YY:Yy:yy)25%, 50%, 25%
Phenotype:3 Yellow, 75%1 White, 25%
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You Try It Now!
• Give the genotype and phenotype for the following cross: TT x tt (T = Tall and t = Short)
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TT x ttStep One: Set Up Punnett Square (put one parent on the top
and the other along the side)
T Tt
t
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TT x ttStep Two: Complete the Punnett Square
T Tt
t
Tt Tt
Tt Tt
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TT x tt
Step Three: Write the genotype and phenotype
T Tt
t
Tt Tt
Tt Tt
Genotype: 4 – Tt or 100%
Phenotype:100% Tall
Remember: Each box is 25%
![Page 57: Protein Synthesis & Mutations...Protein Synthesis & Mutations. RNA 1. Contains the sugar ribose instead of deoxyribose. 2. Single-stranded instead of double stranded. 3. Contains uracil](https://reader034.fdocuments.us/reader034/viewer/2022051805/5ff5fdc4d17f47334e52cdf8/html5/thumbnails/57.jpg)
You Try It Now!• Give the genotype and phenotype for the
following cross: Tt x tt
![Page 58: Protein Synthesis & Mutations...Protein Synthesis & Mutations. RNA 1. Contains the sugar ribose instead of deoxyribose. 2. Single-stranded instead of double stranded. 3. Contains uracil](https://reader034.fdocuments.us/reader034/viewer/2022051805/5ff5fdc4d17f47334e52cdf8/html5/thumbnails/58.jpg)
Tt x ttStep One: Set Up Punnett Square (put one
parent on the top and the other along the side)
T tt
t
![Page 59: Protein Synthesis & Mutations...Protein Synthesis & Mutations. RNA 1. Contains the sugar ribose instead of deoxyribose. 2. Single-stranded instead of double stranded. 3. Contains uracil](https://reader034.fdocuments.us/reader034/viewer/2022051805/5ff5fdc4d17f47334e52cdf8/html5/thumbnails/59.jpg)
Tt x ttStep Two: Complete the Punnett Square
T tt
t
Tt tt
Tt tt
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Tt x ttStep Three: Write the genotype and phenotype
T tt
t
Tt tt
Tt tt
Genotype:Tt - 2 (50%)tt - 2 (50%)
Phenotype:50% Tall50% Short
Remember: Each box is 25%
![Page 61: Protein Synthesis & Mutations...Protein Synthesis & Mutations. RNA 1. Contains the sugar ribose instead of deoxyribose. 2. Single-stranded instead of double stranded. 3. Contains uracil](https://reader034.fdocuments.us/reader034/viewer/2022051805/5ff5fdc4d17f47334e52cdf8/html5/thumbnails/61.jpg)
Four Types of Chromosomal Mutations
1. Deletion – A chromosome segment is deleted or removed.
2. Duplication – A chromosome segment is duplicated or repeated
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Four Types of Chromosomal Mutations
3. Inversion – A segment of a chromosome breaks off, turns around, and reattaches in the reverse order; reverses a segment within a chromosome
4. Translocation – A segment of a chromosome is moved to another chromosome.