DNA
STRUCTURE OF NUCLEIC ACIDS
● 2 types of nucleic acids in humans:
1. DNA (deoxyribonucleic acid)
2. RNA (ribonucleic acid)
● consists of monomers called nucleotides
● each nucleic acid consists of a phosphate (P), sugar molecule (S) & a nitrogenous base
(NB)
BRIEF HISTORY OF THE DISCOVERY OF DNA
● 1952 - Rosalind Franklin & assistant Maurice Wilkins researched the structure of DNA
using x-ray diffraction images
● 1953 - Watson & Crick did independent research on DNA & upon seeing Franklin’s
images, they proposed a 3-D double helix model for DNA
● 1962 - Watson & Crick received a nobel prize for discovering DNA’s structure, Wilkins
received an award for his x-ray photography & Franklin died of cancer
LOCATION OF DNA
● DNA is found in a cell in 2 locations:
1. in the nucleus
2. outside the nucleus
1. in the nucleus:
○ referred to as nuclear DNA
2. outside the nucleus:
○ referred to as extra-nuclear DNA
○ 2 types of extra-nuclear DNA
- chloroplastic DNA, which is found in the chloroplasts of plant cells
- mitochondrial DNA, which is found in the mitochondria & is useful for tracing
ancestory
THE STRUCTURE OF DNA
● has a double helix structure that consists of monomers called nucleotides
● the nucleotides link to form long chains called polymers
● sugar is called deoxyribose sugar & is attached to a nitrogenous base
● phosphate & sugar molecules are attached by strong bonds to form polymers
● 4 types of nitrogenous bases:
1. adenine (A)
2. thymine (T)
3. cytosine (C)
4. guanine (G)
● nitrogenous bases are complementary & join speci cally:
- adenine & thymine
- cytosine & guanine
● pairing of bases means that 2 strands of DNA are joined together, which forms a long
ladder-like structure
● nitrogenous bases are held together by weak hydrogen bonds
● the ladder-like structure becomes coiled & is known as a double helix structure
● DNA strands wind around proteins called histones
double helix struxture
fi
simple structure of DNA
ROLE OF DNA
● carries hereditary information in the form of genes
● genes are short sections of DNA which code for a speci c trait & determine the physical
characteristics & behaviour of an organism
● most DNA strands don’t code for anything & are known as non-coding DNA
● the importance of non-coding DNA is still being researched
● 3 main functions of DNA:
1. controls the functioning of cells
2. regulates the functioning of genes
3. passes on hereditary characteristics
RNA
● 3 types of RNA:
1. messenger RNA (mRNA)
2. ribosomal RNA (rRNA)
3. transfer RNA (tRNA)
● the 3 types of RNA are formed in the nucleus by DNA
● they perform different functions in different places in a cell
LOCATION OF RNA
● messenger RNA (mRNA) is formed in the nucleus & then enters the cytoplasm where it
attaches to ribosomes
● ribosomal RNA (rRNA) is found in ribosomes in the cytoplasm of the cell
● transfer RNA (tRNA) is found freely in the cytoplasm of the cell
THE STRUCTURE OF RNA
● RNA also consists of monomers (nucleotides), which link to form long chains (polymers)
● RNA is a single-stranded structure
● it’s not coiled
● sugar is called ribose sugar & is attached to a nitrogenous base
● phosphate & sugar molecules are attached to each other to form the long chains
(polymers)
● 4 types of nitrogenous bases:
adenine & uracil join
1. adenine (A) together
cytosine & guanine join
2. uracil (U) together
3. cytosine (C) they join together when
DNA is transcribed into
RNA
4. guanine (G)
simple structure of RNA
ROLE OF RNA
● the 3 types of RNA play an important role to protein synthesis
● each type plays a unique role to protein synthesis
COMPARISON BETWEEN DNA & RNA
● similarities:
1. contains sugar with a phosphate
2. contains adenine, cytosine & guanine
3. plays a role in protein synthesis
● differences:
DNA RNA
1. deoxyribose sugar 1. ribose sugar
2. double helix structure 2. single-stranded structure
3. nitrogenous base - thymine (T) 3. nitrogenous base - uracil (U)
4. only found in nucleus 4. found in nucleus, ribosomes &
cytoplasm
DNA REPLICATION
● DNA double helix structure unwinds
● the weak hydrogen bonds between nitrogenous bases are broken
● DNA strands unzip (separate)
● each original DNA strand serves as a template on which its complement is built
● free oating nucleotides build a DNA strand onto each of the original DNA strands by
attaching their complementary nitrogenous bases
fl
● this results in 2 identical DNA molecules
● each molecule consists of 1 original strand & 1 new strand
IMPORTANCE OF DNA REPLICATION
● it’s important for cell division (mitosis)
● it allows each chromosome to be copied, so that each new identical daughter cell
produced, contains the same no. & type of chromosomes
ERRORS THAT OCCUR DURING DNA
REPLICATION
● errors that occur during DNA replication may lead to mutations, such as a change in the
nitrogenous base sequence
● if the incorrect nitrogenous base attaches to the original strand & a nitrogenous base is
added or deleted, then the sequence of the nitrogenous bases changes on the new DNA
molecule, which results in a change in the gene structure
DNA PROFILING
● a pattern produced on x-ray lm
● consists of lines that are different lengths, thicknesses & are in different positions
● all individuals, except identical twins, have a unique DNA pro le
● DNA pro les are used to:
- identify crime suspects in forensic investigations
- prove paternity (father) & maternity (mother)
- determine the causes of genetic defects
- establish the compatibility of tissue types for organ transplants
● DNA pro ling is generally extremely reliable
● the interpretation & comparison of pro les should be done with caution bc:
- humans interpret the results, which means mistakes could be made
- the method of pro ling may be different in different labs, which produces inconsistencies
- only a small piece of DNA is used, so the pro le may not be 100% unique to a particular
individual
- it’s expensive & not easily accessible to those who can’t afford it
- it may reveal information about a person, which could be used against them in a
prejudicial way
a DNA profile for 3 different
individuals
fi
fi
fi
fi
fi
fi
PROTEIN SYNTHESIS
● the process in which proteins are made is called protein synthesis
● proteins are made by linking different amino acids that are present in the cytoplasm of
cells
● there are 20 different amino acids & they combine in a large variety of combinations
● the no. & sequence of amino acids determines the type of protein formed
● the bond between amino acids is called a peptide bond
● the genes found in DNA contain the code which determines which type of protein will be
formed
● the smallest protein contains 50 amino acids linked together
● proteins generally contain 300+ amino acids
● 3 consecutive nitrogenous bases on the DNA strand is called the base triplet
● base triplets determine which amino acid will be placed into the protein & the sequence in
which the amino acids will be joined
● protein synthesis occurs in 2 stages:
1. transcription (stage 1)
2. translation (stage 2)
1. transcription:
○ occurs in the nucleus
○ DNA double helix unwinds
○ weak hydrogen bonds between the nitrogenous bases of DNA break
○ the DNA strand unzips
○ 1 strand acts as a template
○ this DNA template forms a complementary strand of messenger RNA (mRNA) by
using free RNA nucleotides in the nucleoplasm
○ the mRNA now contains the code for the protein that will be formed
○ 3 adjacent nitrogenous bases on mRNA are called codons
○ codons code for a speci c amino acid
○ mRNA moves out of the nucleus through a nuclear pore & into the cytoplasm, where
is attaches onto a ribosome
fi
2. translation:
○ occurs in the cytoplasm
○ transfer RNA (tRNA) in the cytoplasm has 3 adjacent nitrogenous bases called an
anti-codon
○ a mRNA’s codon is complementary to a tRNA’s anti-codon
○ each tRNA will carry a speci c amino acid
○ according to the codons on mRNA, tRNA will bring the required amino acid to the
ribosome
○ the amino acids are linked by a peptide bond to form the required protein
DNA = base triplets
mRNA = codons
tRNA = anti-codons
fi
● the diagram below shows the process protein synthesis in a cell:
THE EFFECT OF MUTATION ON DNA
SEQUENCE
● a mutation is a change in the nitrogenous base sequence of a DNA molecule or gene
● mRNA is copied from the DNA molecule during transcription, which results in a change in
fhe codons
● this means that different tRNA molecules carrying different amino acids are required
● the sequence of amino acids changed & forms a different protein
● if the same amino acid is coded for, then there will be no change in the protein structure