Lecture 1 Flashcards

1
Q

The Central Dogma of molecular biology describes the directional flow of information;

A

DNA -> RNA -> Protein

  1. DNA replication
  2. DNA
  3. RNA synthesis (Transcription)
  4. RNA
  5. Protein synthesis (Translation)
  6. Protein
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2
Q

What is Genetic Material?

A

DNA (and sometimes RNA) as genetic material

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3
Q

Genetic material must have certain characteristics….

What are the Key Characteristics of genetic material? 4

A
  1. Must contain COMPLEX information
  2. Must REPLICATE faithfully
  3. Must encode the PHENOTYPE
  4. Must have the capacity to VARY
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4
Q

How do we know that DNA is the genetic material?

– the Hershey-Chase Experiment (1952)

A
  • T2 bacteriophage (DNA/protein) – infect bacteria
  • how was phage genetic material transmitted to bacteria (protein or DNA?)
  • Grew E.coli infected with T2 phage in either 32P or 35S, -> phage with radiolabelled DNA (32P) and proteins (35S).
  • Used these phage to infect unlabelled
    E.coli.
  • Then isolated the cells… only the 32P labelled phage produced progeny phage that were radiolabelled, showing DNA not protein was passed on
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5
Q

RNA can also be genetic material

– Fraenkel-Conrat & Singer (1956)

A
  • Used tobacco mosaic virus (TMV) uses RNA.
  • Mixed RNA and protein from different TMV strains
  • The viral progeny were identical to the strain of the RNA donor, not the protein donor.
  • Proved that the RNA, not the protein, is the genetic material in TMV
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6
Q

Information flow in biological systems – exceptions to the central dogma = 2

A
  1. Major information pathways
    - DNA
    - DNA REPLICATION - DNA POLYMERASE
    - Information is transferred from one DNA molecule to another
    - TRANSCRIPTION - RNA POLYMERASE
    - information is transferred from DNA to an RNA molecule
    -TRANSLATION - RIBOSOME
    - information is transferred from RNA to a protein through a code that specifies the amino acid sequence.
  2. SPECIAL INFORMATION PATHWAYS
    DNA - RNA - PROTEIN
    - RNA DEPENDENT RNA polymerase; …or to another RNA molecule
    - REVERSE TRANSCRIPTION
    in some viruses, information is transferred from RNA to DNA.
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7
Q

DNA STRUCTURE: Primary, Secondary, Tertiary

A
  1. Primary: nucleotide structure
  2. Secondary: DNA’s stable three-dimensional configuration
  3. Tertiary: packing of double-stranded DNA in chromosomes
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8
Q

DNA and RNA are composed of polynucleotide strands - what are they in a nucleotide?

A

Nucleotide:
- Deoxyribose
(DNA) or Ribose (RNA) sugar

  • Phosphate group
  • Nitrogenous base (purine: A and G, pyramidine: C and U/T)
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9
Q

DNA polynucleotide strands vs RNA polynucleotide strand

A

DNA polynucleotide strands
1. T-A have 2 HYDROGEN BONDS

  1. PHOSPHODIESTER linkage connects the 5’-phosphate group and the 3’-OH group of adjoining nucleotides.
  2. C-G pairs have 3 HYDROGEN BONDS
  3. The strands run in opposite direction; they are antiparallel
  4. DNA has deoxyribose sugar (no oxygen here).

RNA Nucleotide strand
- In RNA, uracil (U) replaces THYMINE (T)

  • RNA has ribose sugar (an OH group here)
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10
Q

The 3D shape of the double stranded DNA molecules are?

What is the most common one?

A
  • The 3- dimensional shape of the double stranded DNA molecules can vary
  • The B-DNA structure is the predominant structure in the cell
  • B-DNA helix = right-handed helix with approximately 10 BASES PER TURN.
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11
Q

Special Secondary Structures Can Form in DNA and RNA - What are they?

A
  1. Hairpin; loop + stem
    - a hairpin consisting of a region of paired bases (with form the stem) and a region of unpaired bases between the complementary sequences (which form a loop at the end of the stem)
  2. Stem = a stem with no loop
  3. Complex secondary structure; secondary structure of the RNA component of RNase P of E.coli.
    - RNA molecules often have complex secondary structures.
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12
Q

DNA molecules are very long.

How are they packed into a tiny cell? 3.

Overrotated, Underrotated, Topoisomerases

A

Supercoiling results from strain produced when rotations are added to a relaxed DNA molecule or removed from it.

    • Overrotated: positive supercoiling;
      underrotated: negative supercoiling
  1. *Topoisomerases ADD/REMOVE ROTATIONS by BREAKING the NUCLEOTIDE STRANDS
    • Most DNA FOUND in cells is NEGATIVELY SUPERCOILED
  • SEPARATION of the TWO STRANDS of DNA easier during REPLICATION and TRANSCRIPTION
  • SUPERCOILED DNA can be PACKED INTO a SMALLER SPACE THAN RELAXED DNA
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13
Q

Positive Supercoil vs Negative supercoil DNA process

A
  1. Relaxed circular DNA
    ***Supercoild DNA is overwound or underwound, causing it to twist on itself.

a.) Add two turns (OVERROTATE)
a.) Positive supercoil -
a.) Positive supercoiling occurs when DNA is overrotated; the helix twists on itself

b.) Remove tow turns (UNDERROTATE)
b.)Negative supercoil
b.)negative supercoiling occurs when DNA is underrotated; the helix twists on itself in the opposite direction

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14
Q

Within a cell, DNA is associated with specialised proteins that organise it and give it structure

A

PROKARYOTIC CELL
- DNA, Wrapped around histone protein, chromosome,

nucleotide: (irregularly-shaped region within the cell of a prokaryote that contains all or most of the genetic material.)

  • plasmid:( is a small, circular, double-stranded DNA molecule that is distinct from a cell’s chromosomal DNA.)

EUKARYOTIC CELL
- Chloroplast DNA

  • Nuclear DNA
  • Mitochondrial DNA
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15
Q

Chromatin is a highly complex structure with several levels of organisation - WHAT ARE THEY?

7.

A
  1. At the simplest level, chromatin is a DOUBLE-STRANDED HELICAL STRUCTURE OF DNA
  2. DNA is complexed with HISTONES to form NUCLEOSOMES
  3. Each nucleosome consists of 8 HISTONE proteins around which the DNA wraps 1.65 times
  4. The nucleosomes fold TO PRODUCE A 30-NM FIBER…
  5. ..that FORMS LOOPS averaging 300 nm in LENGTH
  6. The 300-nm LOOPS are COMPRESSED and FOLDED to PRODUCE a 250-nm-wide fibre.
  7. TIGHT COILING of the 250-nm fibre produces the CHROMATID of a CHROMOSOME.
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16
Q

Eukaryotic DNA packaging is dynamic & changes throughout the cell cycle

What is it usually? When does it change and what does it change to?

A
  • Mostly, CHROMATIN IS RELATIVELY UNCONDENSED.
    the DNA can be ACCESSED relatively EASILY by cellular machinery.
  • CONDENSATION TAKES PLACE WHEN THE CELL IS ABOUT TO DIVIDE. Chromosomes progress from a HIGHLY PACKAGED STATE to a state of EXTREME CONDENSATION, which is necessary for chromosome MOVEMENT IN MITOSIS AND MEIOSIS.
  • DNA packing also changes locally DURING TRANSCRIPTION AND TRANSLATION, when the TWO NUCLEOTIDE STRANDS must UNWIND so that PARTICULAR BASE SEQUENCES ARE EXPOSED.
17
Q

What are the 2 basic types of Chromatin?

A

The two basic types of chromatin are:

euchromatin (most of the chromosome, active)
- legs of the chromsomes

and heterochromatin (densely packed)
- middle, centromere and telomeres

LOOK AT DIAGRAM - LECTURE 1 SLIDE 19

18
Q

What is the Characteristic of EUCHROMATIN? (3)

Found on Legs of the chromosome.

A
  • Most of the chromosome
  • CONDENSATION and
    DECONDENSATION with the cell cycle
  • TRANSCRIPTIONALLY ACTIVE
19
Q

What are the Characteristics of Heterochromatin? (4)

Found in Middle, centromere and tips and tops of the chromosome legs, TELOMERES

A
  • Remains in a HIGHLY CONDENSED state throughout the cell cycle, even during interphase
  • Constitutive (PERMANENT) heterochromatin at the telomeres and centromeres
  • FACULTATIVE heterochromatin at certain DEVELOPMENTAL STAGED
  • Repeated sequences, few genes
20
Q

Sensitivity to DNase I shows that chromatin structure changes with gene activity…

EXPLAIN HOW

A
  • DNase I = enzyme that digests DNA
  • Its ability to digest DNA depends on chromatin structure (histone-bound DNA is less sensitive)
  • GLOBIN genes ENCODE HEMOGLOBIN & are expressed in the ERYTHROBLASTS of chicks at different stages of development
  • Experiments on globin genes in chick embryos show that DNase SENSITIVITY is CORRELATED with GENE ACTIVITY

DNase I = enzyme that digests DNA
- ability to digest DNA depends on chromatin structure
- DNA sensitivity is CORRELATED WITH GENE ACTIVITY

21
Q

EXPERIMENT:
QUESTION: is chromatin structure altered in transcription?

METHOD? RESULTS? CONCLUSION?

A

METHOD: DNA’S Sensitivity to DNase I was tested on different tissues and at different times in development.

RESULTS:
1. Before Haemoglobin synthesis, none of the globin genes are sensitive to DNase I.

  1. After Globin synthesis has begun, all genes are sensitive to DNase I, But the embryonic globin gene U is the most sensitive.
  2. In the 14-day-old embryo, when only adult haemoglobin is expressed, adult genes are most sensitive and the embryonic gene is insensitive.
  3. Globin genes in the brain-which does not produce globin - remain insensitive throughout development.

CONCLUSION:
Sensitivity of DNA to digest by DNAse I is correlated with gene expression, suggesting that chromatin structure changes in the course of transcription.

DNase I sensitivity is correlated with the transcription of globin genes in chick embryos.

22
Q

What are Epigenetic changes?

A

STABLE CHANGES IN GENE ACTIVITY

NOT CAUSED BY CHANGED IN DNA SEQUENCE ITSELF BUT IT I ENVIRONMENTAL

23
Q

Epigenetic changes are stable changes in gene activity which are not caused by changes in the DNA sequence itself
….WHY? (2)

A
  • DNA METHYLATION is a common type of epigenetic modification in eukaryotes – the CYTOSINE BASED in DNA are METHYLATED
  • CHEMICAL MODIFICATION of the HISTONE PROTEINS leads to changes in CHROMATIN STRUCTURE
24
Q

All the Genetic Information Must Be Accurately Copied Every Time a Cell Divides.

WHY?

A
  • ensures that each DAUGHTER CELL gets a copy of the genome, and therefore, SUCCESSFUL INHERITANCE of GENETIC TRAITS
  • essential for INHERITANCE of TRAITS that DEFINE the PHENOTYPE of CELLS and the ORGANISM
25
Q

What is DNA replication?
Process?

4 CHARACTERISTICS:

A

DNA replication is:
* RAPID
* ACCURATE
* HIGHLY REGULATED in eukaryotes
* SEMICONSERVATIVE

PROCESS: (DNA helix unwinds and separates into 2 single strands which form the templates for the new strands to be synthesised, complementary to the existing ones).

26
Q

What is a Replicon?

A

A replicon is a REGION of an organism’s GENOME that is INDEPENDENTLY REPLICATED from a SINGLE ORIGIN of REPLICATION.

27
Q

A segment of DNA that undergoes replication is called a replicon.. EXPLAIN (2)

A
  • Each replicon contains an ORIGIN of REPLICATION
  • Different organisms use different MODES of REPLICATION
  • Theta, Rolling circle, Linear eukaryotic
28
Q

What are the different modes of replication Organisms use?

List and Define/Explain them:

A
  1. Theta replication: the two nucleotide strands of a circular DNA molecule unwind at the origin, creating a replication bubble (circular DNA – bacteria)
  2. Rolling circle replication: initiated by a break in one strand of circular DNA, which produces a 3 ′ -OH group to which new nucleotides are added (some viruses & F factor)
  3. Linear eukaryotic replication: Linear eukaryotic DNA contains many origins of replication. Unwinding and replication take place on both templates at both ends of the replication bubble until adjacent replicons meet
29
Q

Explain the process of each different modes of replication Organisms use?

A

Lectures 1-4 page 25.