NOTES - Week 1 - intro to course: Nucleic acids. DNA replication Flashcards

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1
Q

What is life? Properties of life?

No precise definition tho

A

Distinct physical form - the cell as a physical unit that can show all properties of the life

Genetic information - storage, realization

Metabolism

Homestaosis: able to regulate internal environment and also react or adapt to environment

Reproduction

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2
Q

Structural unit of living organisms - the cell

For example the humanbody

Only the features discussed in this course, examples on human body

A

The living cell has all the necessary properties

Storage and realization of genetic information - we have nucleic acids

Metabolism - ( We can synthesis different chemical substances which has ability to story energy in the chemical bounds e.g. synthesis of ATP)

Synthesis of proteins

Specific physical structure - based on cell functions (e.g erytrocytes a.k.a. red blood cells who are small, flexible and do not have nucleus because of its function. Ability to go through the smallest capillares in our body. In contrast to neurons who are bigger and have a different function & structure, are not flexible and not mobile. In conclusion- structure and function are linked.

Reproduction- cell division like mitosis and also sexual reproduction

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3
Q

General terms

Nucleus

Homeostas

Erythrocytes

Capillaries

Unicellular

Haploid

Diploid

Nucleus

Membrane

Chromosomes

Plasmids

Plasma membrane

Centrosomes

Uni and multicellular DNA

Not for ANSWERING

A

Erytrocytes - red blood cells

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4
Q

Prokaryotes vs Eukaryotes
Able to compare and name main difference in practical classes

8 things to compare

A
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5
Q

What do you see

A

Eukaryotic cell comparison

  • Protists, plants, mold, yeast etc also have nucleus
  • Compare size of bacteria and archea to the cells
  • Eukaryotic cell has mitochondria, different membrane-bounded organells, cytoskeleton etc
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6
Q

The function of the different prokaryotic files

A

Nucleoid similar to nucleus but is not membranebounded. Is just DNA bounded with some protein and RNA molecules.

Some has capsule - protects from enviroment

Has pili: important for conjugation of bacteria and can transfer genetic matetrial like plasmids to other cells.

Fimbria: important for adhesion of prokaryotic cells on the surface

Sometimes has flagellum: important for movement of bacteria

Mesosome- artifacts that we get during physical fixing in lab, does not exist in natural enviroment

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7
Q

The different types of eukaryotic cells

Who has;

mitochondria? chloroplast? Centrosomes?
+Compare appearance and mobility?
Yani what does cellwalls contain?

A

Additional info on top of image

plantcells are immobile because it has celluloses, gives the cells strength.

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8
Q

LOOK AT THE PICTURE MF AND TELL ME OUT LOUD WHAT YOU SEE

A

Now compare with the plantcells, what is similar and what is missing? Why?

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9
Q

Explain how mtDNA and cpDNA came about and why they are special?

A

Endosymbiotic Theory
The endosymbiotic theory explains the origin of mitochondria and chloroplasts as a result of a symbiotic relationship that formed between ancient eukaryotic cells and free-living prokaryotic organisms (bacteria).

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10
Q

Viruses, viroids and prions

What are they?
Are they alive?
Characteristics?

A

Viruses, viroids and prions: Agents of chaos; causes diseases for us

  • No specific cell structure
  • Cant grow
  • Cant selfproduce
  • Metabolism not present

Functions are fullfilled if they infect hostcells → grow and reproduce

Basically these mfs on their own are useless

*Classical biology - nonliving forms. Yet new research being made. *

Consist of nucleid acid molecules (either DNA or RNA)

forms; either few linear or circular molecules

Nucleid acid surrounded by protein coat called capsid. Capsid + nucleic acid = nucleocapsid

INTERLUDE

Viroids are small, circular RNA molecules without capsid, their hosts are plant cells.

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11
Q

virions and provirus

A

Extracellular form av virus which has yet to infect hostcell = virion. Infects only plantcells.

If the virus is already inside hostcell and its genetic material has integrated into hostcell DNA = provirus

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12
Q

Virus vs viroid

Not an important picture

A
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13
Q

What can you see (outloud!)

A

OBS smallballs around influenza are proteincode

Spikes on influenza: different proteins –> recognize and binds/infect with hostcell

Virus that infects and replicates in bacterias = bacteriophage

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14
Q

Host cells of viruses

Viruses are …. species?

What is specifity determined by?

What can viruses infect?

A

Viruses are specific species, sometimes same virus can affect different species.

Specifity is determined by - proteins on the surface of the capsid → their ability to bind to hostcell receptors.

Can infect humans, animals, fungus and bacteria

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15
Q

NOT VERY IMPORTANT!!!!!!

Example of SARS Covid-2 viral entry
Know what it consists of and how it succeeded

EDITTTTTTT

A

Has specific spike proteins on the surface → binds to human ACE2 receptor

Protease are involved: type of enzyme that can degredate or cleave proteins

→ by cleaving specific site on virus spike protein → activates its bindning with the receptor → triggers next signal transduction process → triggers fusion of viral and host membrane

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16
Q

Prions
What are they, what it does, whats special about these weirdos?

A

Prions are infectious protein particles. NO nucleic acid yet they posses protein structure.

Infect cells in the nervous system

Special because: misfolded version of a normal protein that is in nerve cells.

When it infects a nerve cell → “promotes the misfolding of the normal proteins which becomes self-propgating.” Affects its function. Causes neurodegenrative disease in animals and humans.

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17
Q

Storage of information
How it stores in prokaryotic cells

A

In prokaryotic cells most genetic info is stored in the nucleoids and a small part in plasmids.

Plasmids can leave nucleoid and be transfered to other P-cells via conjugation of bacteria (when they transfer info between each other via direct contact).
- Also important in having genes specific to toxic substances for the bacteria eg antibacterial resistance caused by genes in the plasmids.

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18
Q

How it stores in eukaryotic cells

A

3 places

Main: nucleus (nDNA)

Also in
Mitochondria (mtDNA)

In Chloroplast DNA (cpDNA)

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19
Q

Comparison between nDNA and mtDNA?
Apperance, structure, contains what information?

A
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20
Q

Human as multicellular organism
From eurkaryotes to multicellular organisms

HINT: Start of new life in embroyonic development
What is the process called

A

Via celldifferentiation

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21
Q

(Ej viktigt) Number of cells we have
Distribution of cells?

Looking at purely the count of the cells not the mass!

A

To take away from the picture: 84% red blood cells
Big number relates to size of the cells too.

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22
Q

What types of cells do eukaryotes have (humans)

A

Somatic cells: vast majority building up our organism, not involved in sexual reproduction. They have 2 copies of genetic information → diploid

Germ cells: involved in sexual reproduction. Called germcells at any stage of its development. Contain 1 copy of information →, haploid. Logical because creating new organism can be made by fusing together 2 seperate haploid genomes.

OBS image is for association
23
Q

Central dogma of molecular biology?

A

The central dogma of molecular biology deals with the detailed residue-by-residue transfer of sequential information.

It states that such information cannot be transferred
from protein to either protein or nucleic acid.

Information cannot flow back from the protein to the RNA and DNA.

24
Q

What does nucleic acids consist of?

What is a nucleoside?

What is a nucleotide?

A

3 star players

  1. Nitrogen base
  2. Pentose sugar
  3. Phosphate

Base + pentose = nucleoside

1 with that contains these 3 are called nucleotide

→ Nucleic acids = polynucleotids in linear form

25
Q

Name the 5 different nitrogenbases
That are divided into?

How can one see the difference?

A

Purines: Adenine (A) and Guanine (G)

Pyrimidines: Uracil (U), Thymine (T) and Cytosine (C)

Look at amount of rings! Purines have 2 and pyrimidines have 1.

26
Q

The sugar in nucleic acids is called… because?

Different types of this sugar? What distinguishes them? Where are they used?

A

2 types of pentose that consists of 5 carbonatoms. Ribose and Deoxyribose.
Difference is marked on the 2nd carbon atom of the pentose. Deoxyribose lacks oxygen in 2nd carbonatom.

DNA contain Deoxyribose and RNA contain Ribose as you can tell in their names!

27
Q

What is mentioned about this image?

Why is the result called “nucleotide (dAMP)” ?

A

Phosphoric acid residue attached to 5th carbonatom of pentose. 1 residue in the nucleic acid. C1 links between pentose and nitrogenbase.

dAMP: deoxyadenosine monophosphate
d= the sugar deoxyribose
A= nitrogenbase adenine
M= mono meaning 1
P= phosphate group

28
Q

How does number of residues affect nomenclature
What sugargroup?

A

Adding 1 phosphate changes the name e.g. adenosine mono/di/tri-phosphate

29
Q

Explain what you see

A

Nucleotids in a chain- polynucleotides.

Bounded between with Phosphodiester bond

Meaning of the 5’ (prime) end and the 3’ end

5 prime end” has a free hydroxyl (or phosphate) on a 5’ carbon and the “3 prime end” has a free hydroxyl (or phosphate) on a 3’ carbon. Video for understanding this linked below

For elongation (extend) polynucleotide - only attach to 3’ end!

https://www.google.com/search?q=5%27+end+vs+3%27+end+dna&rlz=1C5CHFA_enSE960SE960&oq=5%27+end+&gs_lcrp=EgZjaHJvbWUqBwgBEAAYgAQyBggAEEUYOTIHCAEQABiABDIICAIQABgWGB4yCAgDEAAYFhgeMggIBBAAGBYYHjIICAUQABgWGB4yCAgGEAAYFhgeMggIBxAAGBYYHjIICAgQABgWGB4yCAgJEAAYFhge0gEINTE0NWowajeoAgCwAgA&sourceid=chrome&ie=UTF-8#fpstate=ive&vld=cid:9ff776cd,vid:qWZYpHSXvJo,st:0

30
Q

Difference between DNA and RNA

A
31
Q

Explain the structure of DNA
also explain complementarity

A

Double helix, double stranded molecule.

DNA structure

  • consists of two complementary strands wound around each other to form a double helix
  • The double helix is stabilized by weak hydrogen bonds between A and T bases and stronger bonds between C and G bases. (Relate to number of bonds between them)
  • The backbone is made by the sugar-phosphate alternating bond
32
Q

What is incompatibility

Amount of nucleotide base relative to each other? Explain the numbers also.

A

Incompatibility in the chemical level of bases:
Adenine and Cytosine

Acceptor and donor which forms the bounds will not be compatible + molecular strucure puts it into distance = no hydrogen bonds.

Amount of A = T and C=G

Instead of T in RNA we will se U = difference between A and T in %

DNA is majority of nucleic acids in body, by a massive amount.

33
Q

How is the double-helix formed?

A

Double-Helix
* Is stabilized by hydrogen bonds between bases and by stacking of the aromatic rings of the
bases in the center of the helix
* Aromatic rings on the one strand are building on top of each other and are slightly shifted by
forming approx. 36° angle twist from previous base pair
* Double-helix strands are antiparallel – one strand 5’ - 3’ direction, second strand 3’ - 5’ direction

34
Q

The different parts of the double helix?
Is there any reason for having a double-helix form? Reason for grooves?

A

Its structure is serving its purpose and functionality

35
Q

Bounds between A, T, C and G

A

A - T (2 hydrogen bonds)
G - C (3 hydrogen bonds)

36
Q

2 sort of DNA molecules? Where they are found, contains, arranged?

A
37
Q

RNA structure

A

Primary: Single stranded RNA

Secondary: Base level, includes single stranded, double stranded and loop structure.

Tertiary: Similar to proteins
Structure depends on function, RNA is usually more varied than DNA

38
Q

Biological function of
DNA,
RNA,
mRNA and
tRNA?

A

ADDITIONAL
DNA always locked and protected in the nucleus (except when cell divides and nuclear envelope is disintegrated → located free in the cytoplasm)

39
Q

Biological function of rRNA

And regulatory RNA and its different types:

A

ribosomal complex consists of ribosomal RNA and many proteins.

40
Q

DNA replication

What is it? Why do cells need this process?

A

Duplication of DNA based on the principle of complementarity.

To ensure cell division (sexual replication of cells) - we need duplicate genetic material to be distributed equally to the new daughter cells. Altho we have 2 copies of genteic material in somatic cells it still needs to be transferred to daughter cells as the 2 copies.

41
Q

Explain what DNA replication essentially means

A

A-T and C-G are complimentary.

42
Q

Where and why does DNA replication start?

(Initiated)

A

For prokaryots its simple in the same place.

Eukaryots have specific nucleotide sequence - recognised by specific initiation proteins. Repeated in many places. DNA replication can start in a few places in the long strand of DNA.

43
Q

DNA replication
Initiation

A

To start initiaton of the DNA replication:
Initiator proteins need to recognise these specific sequences on the DNA.

Grooves of DNA molecules are able to bind with proteins → DNA can be bended and also unwinded

Initator protein task is to recognise where in DNA replication will start and bind with DNA to initate opening of the 2 strands of DNA.
Opening done by enzyme helicase: cuts hydrogen bonds between complementary nucleotids → opens strands of DNA → Y-shaped replication fork is formed.

To keep DNA molecules undamaged = we need enzyme topoisomerase. Prevents DNA from supercoiling. Can damage becuase creating an opening between 2 strands creates tension on the rest. Topoisomerase cleaves another strand further away to release tension - ensures DNA strand is not damaged.

Singlestrand binding proteins ensures holding the position of the replication fork. Binds to the opened single strand of DNA to prevent reforming of the doublestranded, essentially preventing complimentary bases to reform hydrogenbonds. Keeps it opened.

44
Q

1 origin of replication
Explain the 2 types of of synthesis of new DNA strand

Look at video again
7.35

https://panopto.rsu.lv/Panopto/Pages/Viewer.aspx?id=1db06386-56c0-4b77-8684-b1db0064bf81

A
  • The reason why it is a difference in leading and lagging strand is because the DNA
    polymerase always synthesis the DNA
    from 5´ to 3´. The strands are antiparallel,

meaning the leading strand will synthesis new DNA continuously while lagging strand will synthesis new DNA discontinosly creating okazaki fragments. This difference means that the leading starnd will only need one primer to synthesis the DNA while the lagging strand needs a primer for each okazaki fragment.

45
Q

Initiation of DNA synthesis

A

To start we need small fragments called primers, built from RNA molecule.

Needed= new forming nucleotide can be added to the new synthesized strand only if hydroxygroup on C3 on pentose is available.

46
Q

What does rNTP and dNTP do?

What is RPA

A
47
Q

Synthesis of DNA

A
48
Q

Elongation in DNA replication
Polymerases;
Leading strand is syntheized by… ?
Lagging strand is syntheized by…?
What do they have in common and what does it mean?

What does RNase H do?

What does DNA polymerase β (beta)

What does DNA ligase do?

A

They both have repair activity: DNA polymerase can detect if the wrong nucleotide is added into the newly syntheized strand and can remove it.

When you have lagging strand = have number of RNA primers joined together with newly syntheized okazaki fragments. BUT we dont RNA primers in the new DNA strand only DNA sequence. Here comes RNase H to recognise and degrades the primers

→ Now gap between okazaki fragments, needs to be filled in by DNA fragments, fills in by DNA polymerase β (beta)

Still unjoined ends of the DNA fragments, here comes DNA ligase to make sure it is uninterruted newly syntheized DNA strand.

49
Q

Proteins involed in eukaryotic DNA replication and their function.

A
50
Q

The ends of linear DNA is known as?
What do they consist of and how often are they repeated?
What problem are they associated with?
Solution to this problem?

A
51
Q

Natural reasons for the telomeres shortening

End replication problem

A

The end-replication problem eukaryotes

The ends of linear DNA are known as telomeres, are made up of a 100-1000 timesrepeated TTAGGG sequence in humans.
At the 3’ end these are single stranded and form a cap.

After replication of the lagging strand, a problem arises since there are no free 3’ OH groups.

The enzyme telomerase consists of several sub-units and contain an integral RNA components that acts as a template for single stranded telomere cap synthesis.

Telomere length is lost through normal DNA replication, replication errors and oxidative DNA damage.

52
Q

Replication in prokaryotes
Where does it start?

A
53
Q

Explain this image

A

Similar idea to eukaryotes but a bit different.

54
Q

Compare replication in prokaryotes vs eukaryotes

nt = nucleotides?

A