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Biology Chapter 13	 RNA and Protein Synthesis Biology Chapter 13	 RNA and Protein Synthesis

Biology Chapter 13 RNA and Protein Synthesis - PowerPoint Presentation

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Biology Chapter 13 RNA and Protein Synthesis - PPT Presentation

I RNA 131 A Describe RNA Ribonucleic Acid B Differences between DNA and RNA DNA RNA Deoxyribose Ribose Doublestranded Singlestranded G C A Thymine G C A Uracil C Types of RNA ID: 930590

rna amino acid base amino rna base acid sequence dna gene mrna mutation change protein codes mutations single transcription

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Slide1

Biology Chapter 13

RNA and Protein Synthesis

Slide2

I. RNA [13.1]

A. Describe RNA –

Ribonucleic AcidB. Differences between DNA and RNA

DNARNA

DeoxyriboseRibose

Double-strandedSingle-stranded

G, C, A, Thymine

G, C, A, Uracil

Slide3

C. Types of RNA

1. mRNA - (messenger RNA) carries protein synthesis instructions from nucleus to ribosomes 2. tRNA -

(transfer RNA) carries amino acids toribosomes, matches A. A. to mRNA 3. rRNA - (ribosomal RNA) forms portion of ribosomes (rest is protein)

Slide4

II. Gene Expression (starting with RNA synthesis) [13.1]

A. TRANSCRIPTION (just a short description)-

Changing DNA codes into RNA codes B. GENE –

Portion of DNA which codes for a particular protein C. Enzyme involved – RNA Polymerase D. PROMOTOR REGION – Region of DNA which is recognized by RNA polymerase (often multiple TACTACTAC triplets)

Slide5

E. Sequence (of RNA Transcription)

1. Unwind section of DNA 2. “Sense” strand of DNA is rewritten into a complementary

strand of mRNA 3. Transcription proceeds from promoter region toward termination sequence 4. In Eukaryotes, mRNA moves out of the nucleus to ribosomes

Slide6

5. In Eukaryotes… there may be RNA editing (pieces removed)

a. INTRONS – discarded portions of mRNA

b. EXONS – remaining pieces of mRNA which are expressedhttp://www.stolaf.edu/people/giannini/flashanimat/molgenetics/transcription.swf

Slide7

III. Reading the Genetic Code [13.2]

A. GENETIC CODE – Sequence of nitrogenous bases  B. There are 20 common amino acids; what led to the concept of the triplet code?

1. DNA has four nitrogenous bases: A, G, T, C  a. If the match was 1 base: 1 amino acid, there would be __4___ possible amino acids  b. If the match was 2 bases: 1 amino acid, there would be __16___ possible amino acids  c. If the match was 3 bases: 1 amino acid, there would be __64___ possible amino acids

Slide8

2

. With that many possibilities, what happens to all the extra triplets? There are duplications and 3 stop codons

C. CODON – 3-letter sequence of bases in mRNA 1. Start Codon – AUG (methionine) 2. Stop Codons – UGA, UAA, UAG

Slide9

IV. Translation

A. TRANSLATION – Converting an mRNA sequence into an amino acid sequence 

B. tRNA is the amino acid carrier. 1. ANTICODON: 3-base sequence on the end of a tRNA molecule It is complementary to a codon!

Slide10

C

. Translation Sequence: (at the ribosomes) 1. 6-base section of mRNA is held in place; 2 tRNA molecules match to codons;

dehydration synthesis forms bonds between amino acids 2. after peptide bond forms, 1st tRNA is released ribosome moves 3 bases 3. another tRNA/amino acid moves into place new peptide bond forms process repeats until “stop” codon is reachedhttp://vcell.ndsu.edu/animations/translation/movie.htm

Slide11

D

. Central Dogma of Molecular Biology – Information is transferred from DNA to RNA to protein 

  E. GENE EXPRESSION – Process by which DNA, RNA, and proteins are involved in putting a gene to work

Slide12

V. Mutations [13.3]

A. GENE MUTATIONS – Inheritable changes at the level of nucleotides (changes in base sequence) 

1. POINT MUTATIONS –  Changes in one or a few nucleotides 2. SUBSTITUTIONS –  One base is exchanged for another a. How will a base substitution affect the protein for which the affected gene codes?1 amino acid is affected (or not –depending on change)

Slide13

b

. Example i. The genetic cause of sickle-cell anemia is 

a single nucleotide substitution (1 base in over 1000)  ii. The effect of sickle-cell anemia is hemoglobin molecules form fibers – change the shape of red blood cellshttp://www.rcsb.org/pdb/explore/jmol.do?structureId=4HHB&opt=3&bionumber=1

Slide14

3

. FRAMESHIFT MUTATION – Mutations which cause reading frame (3 letters or triplet) to move forward or backward 

a. INSERTION – Adding a base, shifts reading frame 1 base to the right  i. How will an INSERTION affect the protein for which the affected gene codes?All amino acids downstream will be affected and changed

Slide15

b

. DELETION –  Removal of a base from a sequence i

. How will a DELETION affect the protein for which the affected gene codes? All the amino acids downstream from the mutation will changeTHE CAT ATE THE RATTHE ICA TAT ETH ERA T INSERTION THE ATA TET HER AT

DELETION

Slide16

c. MISSENSE MUTATION

Single base change which alters one amino acid in a chain

as opposed to frameshift that alters all the downstream amino acidsd. NONSENSE MUTATION - Single base change which causes a stop codon to be transcribed, bringing transcription to an early halt

Slide17

e. SILENT MUTATION -

Single base change which alters a triplet, but translation produces the same amino acid (due to duplicate triplet codes)

Slide18

B. CHROMOSOMAL MUTATION –

change in structure of a chromosome 1. Quickly describe the effects of the following mutations:

a. DELETION – removal (loss) of a section or a whole chromosome b. DUPLICATION – extra copy of a section or a whole chromosome example: Trisomy 21, Trisomy 13

Slide19

c. INVERSION –

reversal of direction of a section of chromosome d. TRANSLOCATION –

part of one chromosome gets moved from one to another

Slide20

C

. Causes of Mutations and Cancer– 1. MUTAGEN – agent which can cause a mutation

a. Examples – UV light, Pesticides, X-rays, 2. CARCINOGEN mutagen which can specifically cause cancer

Slide21

D. How can mutations be harmful to organisms?

Cell Death Cancer

E. How can mutations be helpful to organisms? New genetic combinations – may improve on previous condition

Slide22

VI. Gene Regulation [13.4]

A. A Prokaryotic Example – The Lac Operon B. Vocabulary 1. OPERON –

Group of genes that are regulated together  2. OPERATOR – Portion of DNA which can prevent access to structural genes

Slide23

3

. REPRESSOR –

 Molecule which binds to operator – prevents transcription  4. INDUCER –

Molecule which changes shape of repressor; this allows RNA polymerase access to structural genes C. The lac operon produces – Galactosidase

Slide24

D. Sequence of events

1.

In order to produce beta

galactosidase, RNA polymerase must (first) bind to – promoter region 2

. In the “off” mode, a ___repressor___ __protein____ is bound to the ___operator__ ____region

__ of the lac operon.

Slide25

D. Sequence of events

3. When the operon turns “on”, lactose binds to the __repressor__.

4. The _shape__ _of_ _the_ _repressor_ is changed and it can no longer bind to the ____operator_____.

5. Without the repressor in place – transcription can take placehttp://highered.mcgraw-hill.com/olc/dl/120080/bio27.swfhttp://bcs.whfreeman.com/thelifewire/content/chp13/1302001.html

Slide26

E. Repressing the production of an enzyme has an advantage for the organism –

no energy is spent for an enzyme which is unneeded

(lactose is the substrate and the inducer in this system) F. Gene regulation in eukaryotes is much more complicated.

Slide27

Additional notes (due to my mistakes)

Mutation Vocabulary

Missense – Single base change which alters one amino acid in a chain As opposed to frameshift that alters all the downstream amino acidsNonsense – Single base change which causes a stop codon to be transcribed, bringing transcription to an early halt

Silent mutation – Single base change which alters a triplet, but translation produces the same amino acid (due to duplicate triplet codes)

Slide28