Nucleic Acid And Protein Synthesis Flashcards

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1
Q

What are the key features of DNA in living organisms?

A

The ability to store information - the information needed is a set of instructions for controlling the behavior of cells.
The ability to copy itself accurately-whenever a cell divides it must pass on exact copies of the “genetic material’ to each of its daughter cells so no information is lost.

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2
Q

Define a nucleotide.

A

A molecule consisting of a nitrogen containing base, pentose sugar and a phosphate group. The monomers from which DNA and RNA molecules are made up of are nucleotides.

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3
Q

Define a polynucleotide.

A

A chain of nucleotides joined together by phosphodiester bonds. DNA and RNA are examples of poly nucleotides.

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4
Q

What are nucleic acids?

A

Nucleic acids are biological organic molecules that control all processes in the cell. Together the macromolecules DNA and RNA are known as nucleic acids.

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5
Q

What are the four nitrogen containing bases found in DNA and RNA?

A

DNA-adenine, thymine, guanine, cytosine
RNA-adenine, uracil, guanine, cytosine

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6
Q

Describe the difference in the structure of nitrogenous bases.

A

Adenine and guanine are purines whereas the other three bases thymine, cytosine and uracil are pyrimidines. Purine has two rings in its structure. pyrimidine has one ring. Two purines cannot bind together as it will be larger molecules than pyramids and there is just enough room between the two sugar phosphates for one purine and one pyramidine base molecule.

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7
Q

What is a pentose sugar?

A

Five carbon atoms are called pentoses. Two pentoses are found in nucleic acids. Ribose and deoxyribose. Nucleic acid containing ribose is RNA. One containing deoxyribose is DNA. As the name suggests deoxyribose is almost the same as ribose except it has one fewer oxygen atom in its molecule. The carbon atom one is attached to a nitrogenous base.

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8
Q

What molecule gives the nucleic acids their acidic nature?

A

Phosphoric acid is the source of the phosphate group (PO4-) so it gives nucleic acids their acidic character. The phosphate group is used to link molecules of pentose sugars by condensation reactions to form the sugar phosphate backbone of nucleic acids by forming 3, 5 phosphate bonds.

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9
Q

Describe the structure of ATP.

A

ATP is not part of DNA or RNA but it is very similar to a nucleotide. (Book says it is a nucleotide). ATP is made up of three components: adenine, ribose and phosphate.

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10
Q

What is adenosine?

A

Adenine plus ribose forms a sugar base called adenosine. Adenosine can be combined with one, two or three phosphate groups to give in turn adenine monophosphate (AMP), adenosine diphosphate (ADP) or adenosine triphosphate (ATP). Do not confuse adenosine with adenine and thymine with thiamine (a vitamin).

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11
Q

What is a dinucleotide molecule?

A

The molecule formed by joining two nucleotides is called a dinucleotide. The bond formed is called a phosphodiester bond. The term diester is used because the phosphate group involved now has two extra bonds, one to each of the sugars it is connected to. The sugars and phosphates are linked by phosphodiester bonds to form a backbone from which the bases stick out sideways at right angles to the backbone.

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12
Q

What is the DNA structure held together by?

A

DNA molecules are made up of two polynucleotide strands lying side by side running in opposite directions. Each chain is a right-handed helix. The two chains coil around each other to form a double helix. The chains run in opposite directions (5’ to 3’) and (3’ to 5’).

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13
Q

Which bonds are involved in the structure of the DNA molecule and what are their functions?

A

Each polynucleotide chain has a sugar phosphate backbone made up of phosphodiester bones with bases projecting at right angles.
The bases in one chain are attracted to the bases of the other chain by hydrogen bonding between the bases. This holds the chains together.

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14
Q

What is complementary base pairing?

A

The hydrogen bonding of A with T in DNA or A and U in RNA and of C with G in both DNA and RNA. A links with T by two hydrogen bonds. C links with G by three hydrogen bonds. Because the bases are complementary the sequence of bases in one strand determines the sequence of bases in the other strand. Adenine and uracil have two hydrogen bonds between them.

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15
Q

When does a complete turn of the double helix take place?

A

A complete turn of the double helix takes place every 10 base pairs.

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16
Q

What are the three types of RNA?

A

mRNA-messenger RNA
tRNA-transfer RNA
rRNA-ribosomal RNA.
Transfer RNA and ribosomal RNA fold up into complex structures but messenger RNA remains as an unfolded strand.

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17
Q

What is meant by an antiparallel strand?

A

Antiparallel means one strand ends with 3 prime whereas the complementary strand has 5 prime.

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18
Q

What are the similarities between RNA and DNA?

A
  1. Both are polynucleotides and macromolecules
  2. Both can be found in the nucleus
  3. Both contain sugar phosphate backbone
  4. Both contain nitrogenous bases (cytosine, guanine and adenine ).
  5. The sugars are linked to phosphate groups at one end and nitrogen base at the other end.
  6. Both have phosphodiester bones.
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19
Q

What are the differences between RNA and DNA?

A

DNA has two polynucleotides strands whereas RNA has a single polynucleotide strand.
DNA is a double helix structure whereas RNA is not a helix structure and is just as straight chain.
DNA is a deoxyribose and the carbon number two attaches to a hydrogen whereas in ribose sugar the carbon at the number two attaches to OH.
In DNA there is a thymine base and no uracil whereas in RNA there is uracil and no thymine.
In DNA there was hydrogen bonding between all bases whereas in RNA there is either none or some hydrogen bonding between some bases.
In DNA the ratio between A and G and C to T is equal to 1 whereas in RNA the ratio between A to G and c to u varies.
DNA is a longer molecule than RNA.
RNA is of three types whereas DNA is only of one type.

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20
Q

During which phase of the cell cycle does the DNA replicate?

A

DNA replicates during the s phase of the cell cycle.

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21
Q

What is replication controlled by?

A

Replication is controlled by enzymes.

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22
Q

What is DNA replication?

A

Every time a cell undergoes cell division all of its DNA is copied. This process is called DNA replication.

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23
Q

What is the first stage in DNA replication?

A

In the first stage the enzyme DNA helicase attaches to the DNA molecule. DNA helicase causes the hydrogen bonds between complementary bases to break. This causes the two polynucleotide strands to separate from each other. (This is the unzipping).

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24
Q

What is the second stage in DNA replication?

A

In the second stage free nucleotides(from the cytoplasm) line up there were complimentary bases on the DNA strands. At this stage the free nucleotides are only held together by hydrogen bonds between the complementary bases. They are not bonded to each other by phosphodiester bonds. At this stage a second enzyme now attaches. This enzyme is called DNA polymerase. DNA polymerase moves down the molecule and

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25
Q

What is semi-conservative replication?

A

Each of the single polynucleotide DNA strands acts as a template for the formation of a new strand - the original strand and the new strand then join together to form a new DNA molecule. This method of replicating DNA is called semi-conservative replication because half of the original DNA molecule is kept (conserved) in each of the two new DNA molecules.

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26
Q

What is the role of DNA polymerase?

A
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27
Q

What are activated nucleotides or nucleoside triphosphates?

A

In the nucleus there are free nucleotides to which two extra phosphates have been added. These free nucleotides with three phosphate groups are known as nucleoside triphosphates or activated nucleotides. The extra phosphate activates the nucleotides enabling them to take part in DNA replication.

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28
Q

What is the role of DNA polymerase?

A

A molecule of DNA polymerase attaches to each of the single template strands. It adds one new nucleotide at a time which is held by hydrogen bonding to the strand being copied. DNA polymerase can only copy in the 5 to 3 direction along each strand. DNA polymerase simply follows the unwinding process, copying the DNA as it is unwound.

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29
Q

What are okazaki fragments?

A

The series of short fragments of copied DNA in the lagging strand are called okazaki fragments.

30
Q

What is the lagging strand?

A

During DNA replication, the parent strand that runs in the 5 to 3 direction is copied to produce the lagging strand.

31
Q

What is the lagging strand?

A

During DNA replication the parents strand that runs in the 5 to 3 direction is copied to produce the lagging strand.

32
Q

What is the role of DNA ligase?

A

Another enzyme called DNA ligase finishes the process. The enzyme catalyzes the joining together of two nucleotides with covalent phosphodiester bonds during DNA replication. Before this they are connected only with hydrogen bones between complementary bases.

33
Q

What is semi-conservative replication?

A

The method by which a DNA molecule is copied to form two identical molecules, each containing one strand from the original molecule and one newly synthesized strand.

34
Q

What is conservative replication

A

In conservative replication a DNA double helix is formed containing two new strands and the parent DNA molecule would remain at the end of the process.

35
Q

Why must the daughter cells produced by cell division be identical to the parent cells?

A

To avoid mutation
To avoid formation of genetic diseases for example sickle cell anemia or cancer
To avoid formation of an altered protein
To avoid tissue rejection by the immune system

36
Q

What is a gene?

A

A gene is a part of a DNA molecule where nucleotide sequence codes for just one polypeptide.

37
Q

How does DNA control all activities of the cell?

A

As all activities of the cell are controlled by chemical reactions, all chemical reactions are controlled by enzymes. Enzymes are proteins and DNA carry genes that code for proteins and regulate protein synthesis. Control protein structure by determining the exact order of amino acids that join together during a protein synthesis thus controlling all activities of the cell.

38
Q

What are the two stages of protein synthesis?

A

The process by which DNA makes mRNA is transcription. The process by which the message carried by mRNA is decoded to make protein is called translation.

39
Q

Define transcription

A

Transcription is copying of the genetic information in a molecule of DNA into a complementary strand of mRNA. A single strand of DNA is used as a template (this is called the template or transcribe strand ) - the enzyme responsible is RNA polymerase.

40
Q

Where does transcription occur

A

Transcription occurs in the nucleus.

41
Q

Explain the process of transcription

A
  1. Dna unwinds at the area of the required gene
  2. One strand of DNA is used as a template strand called the sense strand for making RNA
  3. RNA polymerase enzyme binds to a controlled region called promoter on the sense strand of the DNA.
  4. Transcription continues until the RNA polymerase enzyme reaches the region of DNA called a terminator sequence that codes for the end.
    The last triplet transcribed on MRNA is one of the DNA triplet codes for stop called a stop codon. The hydrogen bones holding the DNA and RNA together are broken and double bones of DNA reforms.
42
Q

What is a primary transcript?

A

In eukaryotes, the mRNA is modified (partly changed) before it leaves the nucleus. The original molecule before it is modified is called the primary transcript.

43
Q

What is RNA processing?

A

In eukaryotes the mRNA is modified before it leaves the nucleus. The process of modification is called RNA processing. One step in this process is RNA splicing. Splicing is the removal of sections of the primary transcript. The sections that are removed are called introns (as are the sections of DNA that code for them). The nucleotide sequences that remain after the introns are removed are called exons.They have to be joined together after removal of introns.

44
Q

Which direction does DNA polymerase copy from?

A

DNA polymerase can only copy in the 5 to 3 direction along each strand.

45
Q

What is the role of the enzyme ligase in transcription?

A

DNA ligase finishes the transcription process. It’s job is to connect all the new nucleotides with covalent bonds. Before this they are only holding on to the parent’s strand with hydrogen bonds between complementary bases. DNA ligase connects neighbor nucleotides with phosphodiester bones to form the sugar phosphate backbone of the new DNA molecule.

46
Q

Where does translation take place?

A

Translation takes place at the ribosomes.

47
Q

Define translation.

A

Translation is a stage in protein synthesis during which a sequence of nucleotides in a molecule of messenger RNA is converted into a corresponding sequence of amino acids in a polypeptide chain.

48
Q

How can a gene code for different proteins?

A

In some cases a given primary transcript molecule can be sliced in different ways this results in different mRNAs being made from the original primary transcript. These different MRNAs will produce different proteins when translated. This means that one gene can code for several different proteins or different forms of the same protein.

49
Q

How is DNA read?

A

The DNA code is read three bases at a time. In DNA a set of three bases coding for the amino acid is called a triplet.

50
Q

What is a codon?

A

A sequence of three bases on an mRNA molecule that codes for a specific amino acid or for a stop signal is called a codon. The codon is complementary to the triplet code on the DNA. The codon codes for same amino acid as the triplet code.

51
Q

What is ribosome made up of?

A

Translation is such a complex process that is special organelle the ribosome is used to bring all the molecules involved together. Ribosomes have a small and a large subunit and they are made up of rRNA and protein.

52
Q

What is tRNA?

A

Translation involves the third type of RNA called transfer RNA. The job of tRNA is to transfer amino acids from the cytoplasm to the ribosome. Transfer RNA is where the actual translation from a base sequence to an amino acid takes place. Each amino acid has a different tRNA molecule to carry it. Yamato acid is attached at one end of the TRNA molecule at the other end of the molecule three projecting bases form an anticodon. This is complementary to the codon for the amino acid carried by that tRNA.

53
Q

What holds responsibility for making sure that each tRNA carries the correct amino acid?

A

Enzymes

54
Q

Describe the structure of tRNA.

A

tRNA is a single stranded molecule that is folded back on itself forming a clover-leaf shape. An amino acid attaches at one end of the molecule. At the other end is the anticodon that will recognize the codon for the amino acid carried by the tRNA.

55
Q

Where does an MRNA molecule arrive at a ribosome?

A

When an mRNA molecule arrives at a ribosome, it enters a groove between the two subunits at the ribosome where it is held ready to receive the first tRNA molecule.

56
Q

Describe what happens after a mRNA enters the ribosome.

A

The tRNA with the anticodon complementary to the first codon on the mRNA enters the ribosome and attaches to the codon by hydrogen bonding. Two TRNA molecules can fit into the ribosome at one time, so the second tRNA enters the ribosome. This has the anticodon which matches the second codon in the mRNA. The amino acids carried by the two tRNAs are now side by side and a peptide bond is formed between them. The first tRNA now leaves, The ribosome clicks forward one codon and the third TRNA enters, carrying the next amino acid. This process is repeated until a stop codon is reached.

57
Q

What is the first codon on a mRNA molecule?

A

AUG, so the first amino acid is methionine.

58
Q

What happens after translation?

A

The completed polypeptide leaves the ribosome and folds up into its secondary and tertiary structures. The folding may be assisted and controlled by special proteins. The polypeptide may enter the endoplasmic reticulum for transport to another part of the cell.

59
Q

Where is rRNA made?

A

rRNA is made inside the nucleolus, attached to proteins.

60
Q

Which part of the cell cycle does transcription occur?

A

Transcription occurs throughout interphase.

61
Q

What is a gene mutation?

A

A change in the base sequence in part of a DNA molecule.

62
Q

What is chromosome mutation?

A

A random and unpredictable change in the structure or number of chromosomes in a cell.

63
Q

What can cause a mutation to occur?

A

Mutation occurs when a wrong nucleotide is inserted. This may be because of errors during DNA replication (copying errors) or because damage is done to the DNA by factors such as radiation or carcinogens. The change in the base sequence of the DNA may cause a change in the amino acid sequence of the polypeptide coded for by the mutated DNA. Something that can cause mutations is called a mutagen. X-ray radiation is an example of a mutagen.

64
Q

Are gene mutations harmful?

A

Gene mutations are random events and are likely to be harmful. This is because making a random change in the amino acid sequence (primary structure) of a polypeptide is likely to be harmful. Such a change may affect the way the polypeptide folds up and in turn change the tertiary structure of a protein. This could affect the functioning of a polypeptide. Mutations in certain genes can even cause cancer.

65
Q

What are the types of gene mutations

A

Three of the most common types of gene mutations are:
Substitution - a base is replaced by a different base
Deletion - a base is lost and not replaced
Insertion - a base is added

66
Q

Does substitution always change the amino acid

A

Substitution does not necessarily affect the sequence of a minor acids coded for. Some amino acids are coded for by more than one triplet code which is an example of the fact that the genetic code is degenerate.

67
Q

Give an example of a substitution mutation

A

An example of how significant a substitution can be is the genetic disorder sickle cell anemia which affects the protein hemoglobin.

68
Q

What is a frame shift mutation frame?

A

Frame shift mutation is a type of gene mutation caused by insertion or deletion of one or more nucleotides, resulting in incorrect reading of the sequences of triplets in the genetic code due to a shift in the reading frame.

69
Q

What is the significance of a frameshift mutation as compared to substitution mutation?

A

Deletion and insertions are more likely to be serious than substitutions because they cause frame-shift mutations. All the triplets from the mutations onwards are affected and therefore all the amino acids coded for will probably be incorrect so the polypeptide or protein made as a result is likely to be non-functioning.

70
Q

What are the features of the genetic code?

A

It has a three letter code, known as a triplet code. This means that three bases make the code for one amino acid.
The code is universal. This means that each triplet codes for the same amino acid in all living things.
The code has punctuations. Three of the DNA triplets acts as full stops in the message. During protein synthesis, these stop triplets mark the end of the gene. Some triplets can act as start signals where the process of copying a gene starts.
The code is described as redundant or degenerate. This means that some amino acids are coded for by more than one triplet.

71
Q

Where does semiconservative replication of DNA in eukaryotes occur?

A

The process will take place in the nucleus.

72
Q

Describe the process of DNA replication? Past paper question.

A

DNA double helix unwinds. Hydrogen bonds break between base pairs. Both of the strands are used as templates. The process is catalysed by DNA free activated nucleotides are added to the complementary nucleotides on the template strands step by step. The process continues along the whole DNA molecule. As the DNA polymerase can only copy in the five prime to three prime direction, the DNA strand in the three prime to 5 prime direction is replicated in short strands called the okazaki fragments. DNA replication is semiconservative which means that from the two strands only one is newly synthesized.