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Nucleic Acids: structure and function

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Topics Nucleic Acids: structure and function DNA RNA Organization of the genome Protein Synthesis (genetic expression) Transcription Translation Mutations – PowerPoint PPT presentation

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Title: Nucleic Acids: structure and function


1
Topics
  • Nucleic Acids structure and function
  • DNA
  • RNA
  • Organization of the genome
  • Protein Synthesis (genetic expression)
  • Transcription
  • Translation
  • Mutations
  • Post-transcriptional modification
  • epigenetics

2
  • DNA Structure and Function

3
DNA Function
  • genetic information
  • how to build, operate, and repair cell
  • Specifically how and when to make proteins
  • passed from one cell generation to the next
  • from parent to child (gametes/sex cells)
  • From one cell to the next within an individual

4
DNA Structure
  • long chains of nucleotides
  • Nucleotide sugar phosphate nitrogenous base
  • Sugar deoxyribose (5C)
  • 4 Different Bases A, T, G, C
  • Bases pyrimidines (1 ring) or purines (2 rings)

5
DNA Structure Cont.Double Helix
hydrogen bond
  • double stranded
  • sugar-phosphate backbonecovalent
  • base-basehydrogen
  • Twistedhelix

covalent bond
f-five f phosphate 5 end
6
DNA Structure Cont.Complementary Base Pairing
  • 4 different bases
  • Complementary pairing
  • CG
  • AT

7
Functional Characteristics of DNA IMPORTANT!!
  • Information order of the bases/base sequence
  • ATTGCGCA
  • ATTGCGGA
  • Complementary base pairing
  • Allows DNA to be copied over and over and the
    information stays the same.

Different sequences?different meaning/info
(proteins)
8
Importance of base-pairing
9
Importance of base-pairing continued
10
DNA Organization
  • DNA molecule genes regulatory DNA other
  • gene protein instructions
  • 20-25k estimated genes (but gt100,000 estimated
    proteins.problem..)
  • regulatory when to activate gene/make a protein
  • e.g., transcription factors such as hormones can
    bind regulatory DNA and signal a gene to be used

chromosome
3 of DNA
non-coding 97 of DNA
Regulates when protein is made (gene activated)
Protein building instructions (gene)
11
DNA Organization
  • DNA is wrapped around histone (a protein)
  • DNA Histone Chromatin

Chromatin
histone
3-31
12
DNA Organization Histone and access to genes
  • Histone is important in making genes accessible
    (usable) or inaccesible (non-usable)
  • If DNA cant be accesses?gene cant be used (no
    protein)
  • If DNA can be accessed?gene can be used when
    needed
  • Histone can control which/if genes can be
    usedEpigenetics
  • acetylation allows access
  • deacetylation shuts off/prevents access
  • methylation prevents access/shuts off
  • demethylation allows access/shuts off
  • and others.

13
Chromatin continued
Condensed chromatin transcription factors cant
get to regulatory DNA to activate gene use
acetylation and demethylation
Open/loose structure allows transcription factors
to access DNA and initiate gene use
and methylation
deacetylation and methylation
Condensed chromatin inaccessible
3-33
14
REPLICATION duplication of DNA as part of cell
division
15
DNA Replication
  • Happens as part of cell cycle
  • In preparation for cell division
  • Duplicates all the DNA 1 copy ? 2 copies
  • One copy for each cell
  • Semiconservative
  • Errors in replication ? mutations (i.e. a change
    in genetic information/DNA sequence)

16
1 copy of DNA
1 copy of all DNA
2 copy of All DNA
1 copy of DNA
Replication of DNA
  • Mitosis divides/separate the two copies of
    identical chromosomes
  • Cytokinesis divides up the cytoplasm contents

Parent/mother cell
daughter cells each one identical copy of all
the DNA genetically identical to the mother cell
17
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18
DNA Replication
  • DNA helicase unzips the DNA
  • New nucleotides are added/paired with the
    existing strands
  • DNA polymerase binds the new nucleotides together
    creating the P-S backbone
  • Result is two identical DNA molecules (i.e., the
    base sequence is the same)

19
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20
Genetic ExpressionProteins Synthesishow dna
is used to make functional proteins
21
Genetic Expression from DNA to cell
function/structure
  • DNA ? mRNA ? Proteins ? cell function/structure
  • structure
  • transport
  • contraction
  • receptors
  • cell ID
  • hormones/signaling

22
Protein Synthesis making proteins from DNA
  1. Transcription DNA ? mRNA (in nucleus)
  2. Translation mRNA ? Protein (in cytoplasm _at_
    ribosome)

23
Nucleic Acids - RNA
  • Single stranded chains of nucleotides
  • Sugar ribose
  • Bases and Pairing
  • G, C, A, U replaces T
  • G-C
  • T-A or A (dna) U (rna)
  • types of RNA (made from DNA)
  • Messenger RNA mRNA
  • Transfer RNA tRNA
  • Ribosomal RNA rRNA
  • others (siRNA, miRNA, RNA based enzymes, etc)

2-59
24
Transcriptionfrom DNA ? mRNA
  • Transcription Begins
  • When Transcription factors (e.g., hormones) bind
    DNA transcripition starts/is initiated
  • RNA polymerase binds to a start sequence/codon
    unzips DNA
  • promoter how much transcription
  • RNA Polymerase moves down template strand
  • complimentary RNA bases bind DNA
  • RNA nucleotides bind together (via RNA poly)
  • at end of gene mRNA detaches and RNA poly
    detaches
  • DNA zips up when transcription is done
  • Post-transcriptional modification

3-35
25
Transcription
Template strand
Coding strand
3-36
26
Transcription
27
mRNA a copy of the information on a gene
  • Created by transcription
  • Single strand of nucleotides
  • Phosphate, ribose sugar, bases
  • U instead of T
  • Codons 3-base groups
  • One codon is a start codon
  • Three codons are stop codons
  • Each of the remaining 60 codons corresponds to an
    amino acid

28
tRNA
  • Single stranded piece of RNA
  • tRNA carries and delivers amino acids to
    mRNA/ribosome
  • tRNA anticodon binds to mRNA codon
  • complementary
  • Each tRNA carries a specific amino acid that
    corresponds to its anticodon

3-44
29
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30
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31
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32
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33
Protein Synthesis and the Genetic Code
DNA template strand
3-43
34
Mutations, DNA, and Protiens
  • Mutation change in DNA base sequence
  • change in protien ? change in structure and/or
    function

35
Basic Types of Mutations
  • Point mutations
  • substitution
  • insertion
  • deletion

frame-shift mutations
36
Point Mutations
  • Substitution
  • ATT GCG AGT TAT CCG
  • ATT GCG AGT TAG CCG
  • Insertion
  • ATT GCG AGT TAT CCG
  • ATT GCG TAG TTA TCC G
  • Deletion
  • ATT GCG AGT TAT CCG
  • ATT GCG GTT ATC CG
  • A

frameshifts
37
Base Sequences and Human Variation
  • SNPs (single nucleotide polymorphisms)
  • single nucleotide differences in the DNA between
    different individuals
  • responsible for most differences in appearance
    and physiology
  • ATT GCG ATC CGA TAT TTT AAC CCC ATA CGG TAT TTT
    TCG
  • ATT GCG TTC CGA TAT TTT AAC CCC ATA CGG TAT TTT
    TCG
  • ATT GCG ATC CGA TAT TTG AAC CCC ATA CGG TAT TTT
    TCG
  • ATT GCC ATC CGA TAT TTT AAC CCC ATA CGG TAA TTT
    TCG
  • ATT GCC ATC CGA TAT TTT CAC CCC ATA CGG TAT TTT
    TCG
  • ATT GCG ATC CGA TAT TTT CAC CCC ATA CGG TAA TTT
    TCG

38
RNA Synthesis Post-transciptional Modification
  • Human genome has lt25,000 genes
  • Yet produces gt100,000 different proteins
  • 1 gene codes for an average of 3 different
    proteins
  • Accomplished by alternative splicing of exons
  • This allows a given gene to produce several
    different mRNAs

3-39
39
  • Post-transcriptional Modifcation
  • non-coding introns removed from mRNA
  • Coding exons spliced together to make the mRNA
    that will be used in translation
  • multiple splicing patterns for each pre-mRNA
  • 1 gene ? multiple mRNA/proteins

3-38
40
  • Alternative Splicing of mRNA
  • one gene ? two proteins

introns
From one gene
exons
Two types of protein
41
Alternative Splicing of mRNAone gene ? 3
proteins
From one gene
Three types of protein
42
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43
Epigenetics
  • Changes in genetic expression that do not involve
    changes in base sequences (gene and regulatory
    DNA has not been altered)
  • Changes in expression are due to changes in
    histone.
  • Genes can be turned off or allowed to be
    accessed
  • Gene silencing (i.e., preventing gene use by
    making them inaccessible) can be cause by (but is
    not limited to)
  • Acetylation/deacetylation
  • Methylation/demethylation
  • These changes can be copied and
    transferred/inherited from generation to
    generation
  • Can contribute to diseases such as cancer,
    fragile X syndrome, and lupus
  • Identical twins can have differences in gene
    expression
  • --because of epigenetic changes in response to
    differences in their environments

3-74
44
acetyl, methyl, ubiquitin, phosphate, S.U.M.O
45
DNA (genetics) ? characteristics/physiology
  • DNA environment phenotype (characteristics)
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