BIO 2 - Information flow in Biology Flashcards

1
Q

*What is the difference between genotype and phenotype?

A

Genetype: digital information stored in an organims genes (DNA)

Phenotype: the collection of an organisms characteristics i.e. the manifestation of the genotype. Shape, weight, height, smooths, wrinkled.

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2
Q

*What does the central dogma expresses?

A

It expresses that the principal direction of genetic information flow in biology is from DNA to RNA to Protein.

Exceptions include copying of information from RNA to DNA is some rare cases (viruses), but never from protein to RNA or DNA

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3
Q

What is the structure of DNA known as?

A

A double Helix, solved in 1953. H, O, N, C, P

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4
Q

*How can 2 m of human DNA be squeezed into a nucleus of 5 um diameter?

A

DNA is a charged polymer (polyelectrolyte) and would normally adopt an expanded random coil structure. It is strongly compressed and organized in a highly condensed structure called chromatin.

Histone proteins: small positively charged proteins which DNA can bind to leading to DNA being more compact.

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5
Q

What is the difference between Euchromatin and Hetereochromatin?

A

The structure DNA is condensed in is called chromatin.
Euchromatin: more lightly packed form of chromatin, in which the DNA is more easily accessible for transcription
Heterochromatin: more densely packed.

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6
Q

What happens in DNA Replication?

A

DNA replication:
Initiation: Both strands are separated by helicases and other proteins.
Elongation: new complementary strands to each of the two strands are synthesized in opposite directions. One leading strand and one lagging strand.

Termination: separation, coiling and repacking the independent double-stranded molecules

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7
Q

What is the first step of DNA replication?

A

The first step of DNA replication is initiation, during which helicases (enzyme) unwind the double helix structure of the DNA molecule at specific sites called origins of replication.

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8
Q

What enzyme is responsible for unwinding the DNA strands during DNA replication?

A

Helicases are responsible for unwinding the DNA strands during DNA replication by breaking the hydrogen bonds between the complementary base pairs.

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9
Q

What is the role of DNA polymerases in DNA replication?

A

DNA polymerases are enzymes that catalyze the synthesis of new DNA strands by adding complementary nucleotides to the template strand. They also proofread the newly synthesized DNA to ensure accuracy.

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10
Q

Describe the difference between the leading and lagging strands during DNA replication

A

The leading strand is synthesized continuously in the 5’ to 3’ direction, while the lagging strand is synthesized discontinuously in the 5’ to 3’ direction away from the replication fork, resulting in the formation of Okazaki fragments.

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11
Q

What is the function of RNA primers in DNA replication?

A

RNA primers are synthesized by primase and provide a starting point for DNA polymerases to begin synthesis. They are later removed and replaced with DNA nucleotides.

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12
Q

Explain the process of termination in DNA replication

A

Termination involves the completion of DNA synthesis and the separation of the newly synthesized DNA molecules. This includes the removal of RNA primers, synthesis of DNA in place of the RNA primers, and ligation of the DNA fragments into continuous strands.

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13
Q

How does DNA replication ensure the accuracy of the genetic information passed on to daughter cells?

A

DNA replication involves proofreading mechanisms carried out by DNA polymerases, which correct errors in base pairing. Additionally, mismatch repair mechanisms detect and repair errors that escape the proofreading process. These mechanisms collectively ensure the accuracy of the genetic information passed on to daughter cells.

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14
Q

What does DNA replication requires?

A

Replication requires:
DNA template
4 deoxyribonucleotide triphosphates (dATP, dGTP, dCTP, dTTP) building blocks
DNA polymerase (enzyme complex)
a primase to generate an RNA primer that allows the DNA polymerase to initiate DNA synthesis

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15
Q

What is Nanopore sequencing?

A

A DNA sequencing method, whereby long DNA strands are translocated through small pores and the change in ionic current when each base passes through the hole, is recorded and analysed to determine the nature of the nucleotide.

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16
Q

What happens during transcription?

A

One of the two DNA strands of a double helix is copied into RNA. Both strands can in principle act as templates.

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17
Q

What does transcription requires?

A

DNA template
4 ribonucleotide triphosphates (ATP, GTP, CTP, UTP) building blocks
RNA polymerase (enzyme)

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18
Q

What are the 3 phases of transcription?

A

Transcription process has 3 phases:
Initiation, RNA polymerase starts RNA synthesis
Elongation, RNA chain lengthening
Termination, RNA polymerase stops RNA synthesis, dissociates from DNA

19
Q

What are the differences between the structure of DNA and RNA?

A

DNA and RNA are very similar except:

RNA: has OH group on the carbon atom number 2 in the ribose ring
DNA: Has not

Base pairs
RNA: Uracil
DNA: Thymine

20
Q

What are the differences between the properties of DNA and RNA?

A

DNA: long term information storage
RNA: Short term messaging to make sure a given protein is produced at a given point in time.

Their stabilities are very different due to intrinsic thermodynamic stability differences but also because enzymes that can degrade RNA are everywhere.

21
Q

What happens in translation?

A

RNA is translated to polypeptide or protein. The genetic information stored in RNA (originally from DNA) is converted into an amino acid sequence. This happens in the ribosome.

22
Q

Which 4 letters does the RNA alphabet contains?

A

A , C , G , U

23
Q

How can translation displays a significantly higher level of specificity than one would expect

A

Due to the introduction of a high energy intermediate. It leads to two points alonge the reaction where wrong building blocks can deteach which can gives us a higher specificity. It costs energy.

24
Q

*What is the principle of the PCR reaction and what is it used for?

A

The Polymerase chain reaction is used to demonstrate the presence of a particular DNA sequence in a given sample.

Its principle is based on the use of DNA polymerase which is an in vitro replication of specific DNA sequences. This method can generate tens of billions of copies of a particular DNA fragment (the sequence of interest, DNA of interest, or target DNA) from a DNA extract (DNA template).

applications including biomedical research and forensic science.

25
Q

*What are the overall ideas behind DNA sequencing by synthesis and nanopore DNA sequencing?

A

Nanopore sequencing: Long DNA strands are translocated through small pores and the change in ionic current when each base passes through the hole is recorded and analysed to determine the nature of the nucleotide.

Sequencing by synthesis: where a complementary strand is sequenced and the individual nucleotides are read off through different fluorescent colors

26
Q

*Does the entire genome of an organism consist only of genes, i.e. encodes proteins?

A

In humans, only 5% of the DNA of the genome actually encodes proteins. The rest serves either as regulatory sequences that specify the conditions under which a gene will be transcribed, as introns (sequences that are transcribed but not translated), or as spacer DNA of yet unknown function.

27
Q

*What are the requirements and sequential steps of DNA transcription into RNA?

A

Transcription requires:
DNA template
4 ribonucleotide triphosphates (ATP, GTP, CTP, UTP) building blocks
RNA polymerase (enzyme)

Transcription process has 3 phases:
Initiation, RNA polymerase starts RNA synthesis
Elongation, RNA chain lengthening
Termination, RNA polymerase stops RNA synthesis, dissociates from DNA

28
Q

*What is the chemical difference between DNA and RNA?

A

DNA and RNA are very similar, except for the absence of the OH group on the carbon atom number 2 in the ribose ring of DNA, and the substitution of thymine by uracil in RNA.

DNA is double-stranded, forming a double helix, while RNA is usually single-stranded. The sugar in DNA is deoxyribose, whereas RNA contains ribose.

Furthermore, DNA uses the bases adenine, THYMINE, cytosine, and guanine
while RNA uses adenine, URACIL, cytosine, and guanine.

29
Q

*What are the different roles of DNA and RNA in an organism?

A

DNA: Long term information storage
RNA: short term messaging to make sure a given protein is produced at a given point in time.

30
Q

What different types of RNA are there?

A

mRNA = messenger RNA, tRNA = transfer RNA, rRNA= ribosomal RNA, snRNA = small nuclear RNA

31
Q

What happens in translation? What is the ribosome?

A

Ribosomes: large RNA-protein complexes convert mRNA to proteins
The genetic code (determined by tRNA’s and aminoacyl-tRNA synthetases)

32
Q

*How many different amino acids are used to make proteins? How are they encoded by nucleotides in RNA?

A

The RNA alphabet is of 4 letters A, C, G, U referring to the four nucleotides in RNA.
They are in a sequence coding for specific amino acids.
In the ribosome this sequence is read. Start by the start codon in the sequence AUG. Every CODON consists of 3 RNA letters. These can be placed in 64 different combinations. All 61 referring to a specific amino acid the 3 remaining are stop CODONS.

33
Q

Start og stop codon

A

START: AUG
STOP: UAA, UAG, UGA

34
Q

Number og possible codons for each amino acid

A

Leucine: 6 codons
Cysteine: 2 codons
Serine: 6
Valine: 4
Stop codons: 3

35
Q

You need to be able to compare the combinatorial diversity of DNA/RNA and protein sequences of different lengths

A

Combinatorial diversity: total number of unique combinations possible within a given system.

DNA sequence of length 10 the diversity would be 4^10
RNA sequence of length 15 the diversity would be 4?15.

36
Q

*What is kinetic proof reading and why does it exist?

A

In cells, kinetic proofreading helps to reduce errors in processes like DNA replication and protein synthesis, ensuring that the final product—whether it’s a new DNA strand or a protein—is as accurate as possible.

enhance the accuracy of molecular processes such as DNA replication, transcription, and translation

37
Q

*What is an (open) reading frame? You need to be able to determine/estimate how many reading frames there are in a given piece of dsDNA or in a piece of DNA of given length (see exercises).

A

ORF: A stretch of DNA or RNA that potentially encodes a protein. It starts with a start codon and ends with a stop codon with a length that is a multiple of three nucleotides.

38
Q

*Why does gene expression need to be regulated?

A

Gene regulation is how a cell controls which genes, out of the many genes in its genome, are “turned on” (expressed). Thanks to gene regulation, each cell type in your body has a different set of active genes – despite the fact that almost all the cells of your body contain the exact same DNA. These different patterns of gene expression cause your various cell types to have different sets of proteins, making each cell type uniquely specialized to do its job.
For example, one of the jobs of the liver is to remove toxic substances like alcohol from the bloodstream. To do this, liver cells express genes encoding subunits (pieces) of an enzyme called alcohol dehydrogenase. This enzyme breaks alcohol down into a non-toxic molecule. The neurons in a person’s brain don’t remove toxins from the body, so they keep these genes unexpressed, or “turned off.” Similarly, the cells of the liver don’t send signals using neurotransmitters, so they keep neurotransmitter genes turned off

39
Q

*What is an operon? How does the lac operon work (schematically)?

A

An operon controls the expression of genes. The lac operon allow bacteria to use lactose as an energy source.

For bacteria to use lactose as energy source the bacteria must express the lac operon genes which encodes key enzymes for lactose uptake and metabolism.

When: Lactose is available and glucose is not available.

40
Q

What are epigenetic modifications?

A

Epigenetics: refers to changes in gene expression controlled by factors other than changes in DNA sequence.

covalent modifications of DNA bases (cytosine) by methylation and covalent modifications (acetylations, methylations) of histone proteins.

41
Q

What are advantages and disadvantages of DNA as a data storage medium?

A

It is slow to read and write, but very energy efficient, stable and represents a universal modality.

42
Q

What is CRISPR-Cas and what is it used for?

A

Scientists uses this technique to remove or replace genes. Inspired from bacteria that uses CRISPR as a tool to protect them from viruses hijacking them. Like a immunsystem. Very precise technique to take out some bad genes.

43
Q

DNA sequencing methods:

A
  1. Chain termination methods
    2) Sequencing by synthesis
    3) Nanopore sequencing