Differences:DNA lacks one oxygen molecule DNA nitrogenous bases: ATGCRNA nitrogenous bases: AUGCDNA is double strandedRNA is single strandedSimilarities:5-carbon sugarsmade up of long chains of sub-units called nucleotidescontain a combination of 4 nucleotides each nucleotide is made up of a 5-carbon sugar, a phosphate group and one of four nitrogenous bases
- Chargaff's Rule
"thread-like molecule that is composed of two strands of nucleotide bases strung together that wrap around each other"
unwound, it looks like a ladder with the sugar-phosphate backbone (the rails of the ladder), while the nitrogenous bases from both strands face each other and form the rungs of the ladder
All of the phosphate groups for a strand have the same orientation so
each DNA strand is said to have directionality with a 5′ end and a 3′ end
The two
strands are in opposing directions to each other or said to be antiparallel.
By
convention, a strand is “read” in a 5′ to 3′ direction.
The phosphate
bridges that link the sugars together are strong, maintaining the sugar-phosphate
backbone
The hydrogen bonding between the base pairs keeps the two strands together
The hydrophilic and hydrophobic regions of the molecule keeps the sugar-phosphate backbone on the outside and the nitrogenous bases on the inside
This structure allows the DNA molecule to be extremely stable which is a necessary factor for a molecule that carries the genetic blueprint of an organism
Purines Adenine and Guanine Double-ring structurePyramidinesCytosine and Thymine Single-ring structure
A purine on one strand is always associated with a pyramidine on another strand; known as complementary base pairings
These
configurations allow for hydrogen bonding to occur between the complementary base
pairs.
A and T can form two hydrogen bonds between them while C and G can form
three.
Slide 5
DNA Replication and Repair
DNA replication is semi-conservativeProcess:
The enzyme DNA
helicase is responsible for unwinding the helix by temporarily breaking the hydrogen
bonds holding the two strands together
Specialized single-stranded binding proteins
(SSBs) then attach to the individual strands to prevent the hydrogen bonds from
reforming
Since only small areas of DNA are being unravelled at any one time, tension
can form in the twist of the helix further up the line. If the tension were to become too
great, the strands could break apart. To prevent this, DNA gyrase cuts the two DNA
strands and allows them to swivel around each other until the increased tension has
been released and then reseals the strands.3. As soon as DNA helicase opens up the helix and the SSBs stabilize it, replication
begins.4.The junction where the two strands are yet to be unravelled is called the
replication fork and replication proceeds in the direction of that fork5.It is the enzyme
DNA polymerase III that creates the new DNA strands but, certain conditions have to be
met before it can beginThe enzyme is only able to add new nucleotides to the 3′ end
of the strand. This means that the enzyme can only work in a 5′ to 3′ direction. As well, the enzyme is incapable of attaching itself to the template strand and simply stringing
the appropriate nucleotides together.6.Instead, another enzyme, RNA primase, must first
lay down a short string of temporary RNA nucleotides to provide an attachment site for
DNA polymerase III. The polymerase can then start attaching the complementary DNA
nucleotides to the temporary RNA nucleotides.
Slide 6
DNA Replication and Repair
leading strand: runs in 5' to 3' direction. DNA Polymerase III is able to do its job smoothly.lagging strand: runs in 3' to 5' direction. in order for DNA Polymerase III enzyme to work on this strand, it must move past one to two hundred
nucleotides on the template strand in a 3′ to 5′ direction without synthesizing the new
strand. It then stops, reattaches itself to a set of temporary RNA nucleotides set down
by RNA primase and then works in its normal 5′ to 3′ direction away from the replication
fork. Then, just as it does on the leading strand, it reads the order of nucleotides from the template strand and creates the complementary copy but this time, in Okazaki fragments. It continues
this action for the entire length of the strand, moving ahead, stopping, reattaching,
making a short segment, and so on.Once DNA polymerase III has commenced replication and moved forward, the
temporary RNA nucleotides can be removed and replaced by the appropriate DNA
nucleotides, this is performed by DNA Polymerase I.DNA ligase forms a phohphodiester bond
between the outer nucleotides on each Okizaki fragment to form one continuous strand.
As the replication fork continues
forward and more of the DNA strands are synthesized, the two double-stranded DNA
molecules automatically reform their helical twist and the hydrogen bonds holding the
two strands together, form. DNA replication is now complete.RepairErrors can occur during the copying process. If this were to happen regularly, the DNA of
each cell could mutate and stop functioning properly. Therefore, it
is extremely important that DNA replication be as close to error free as
possible. DNA polymerase I and III have proof-reading mechanisms for this reason. When
an error is found, both polymerases have exonuclease abilities. This allows them to cut
out an incorrect base, replace it with the correct base and then carry on with the rest of
the strand.
RNA 3 major classes:mRNA - messenger RNA; responsible for creating a copy of the genetic
information contained in the DNA and moving that information from the nucleus to the
cytoplasm where protein synthesis occurstRNA - transfer RNA; responsible for
supplying the amino acids in the correct order as the polypeptide chain is being
synthesizedrRNA - ribosomal RNA; plays a structural role and helps
form the ribosome which is the structure that synthesizes the polypeptide chain
Genetic Code
three nucleotides are required to code for each amino acid
This set of three nucleotides is referred to as a codon
The start codon tells the ribosome that this is the first codon for the amino acid chain
There are three stop codons to let the ribosome know that this is the end of the chain and to stop adding amino acids
Slide 9
Protein Synthesis
Transcription first phase of protein synthesis & involves the formation of the
mRNA moleculedivided into 4 stages:InitiationRNA polymerase binds to double helical DNA at a promoter region. DNA strand is unwound and the double helix is disrupted, exposing the template strand.ElongationmRNA is synthesized by using one strand of DNA as a template. synthesized in the 5' to 3' direction. Uracil complements adenine. As elongation proceeds, RNA polymerase moves along DNA, synthesizing mRNA. DNA that has already been transcribed rewinds into double-helical form. RNA polymerase reaches termination sequence at end of gene. TerminationRNA synthesis ceases; mRNA and RNA polymerase are released. Post-transcriptional Modification
Slide 10
Protein Synthesis
Translation
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