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Genome
The genetic material of an organism or virus; the complete complement of an organism's or virus's genes along with its noncoding nucleic acid sequences
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Chromatin
The complex of DNA and proteins that makes up eukaryotic chromosomes. When the cell is not dividing, chromatin exists in its dispersed form, as a mass of very long, thin fibers that are not visible with a light microscope.
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Chromosomes
- A cellular structure carrying genetic material, found in the nucleu of eukaryotic cells. Each chromosomes consists of one very long DNA molecule and associated proteins. (A bacterial chromosome usually consists of a single circular DNA molecule and associated proteins. It is found in the nucleoid region, which is not membrane bounded.)
- Condensed chromatin
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Chromatids
Paired chromosomes (sisters)
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Centromere
In a duplicated chromose, the region on each sister chromatid where they are most closely attached to each other by proteins that bind to specific DNA sequences; this close attachment causes a constriction in the condensed chromosome. (An uncondensed, unduplicated chromosome has a single centromere, identified by its DNA sequence.)
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Cytokinesis
The division of the cytoplasm to form two seperate daughter cells immediately after mitosis, meiosis I, or meiosis II.
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MTOC
Microtubule Organizing Center
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Prophase
The first stage of mitosis, in which the chromatin condenses into discrete chromosomes visible with a light microscope, the mitotic spindle begins to form, and the nucleolus disappears but the nucleus remains intact.
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G2 phase
The second gap, or growth phase, of the cell cycle, consisting of the portion of interphase after DNA synthesis occurs.
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Prometaphase
The second stage of mitosis, in which the nuclear envelope fragments and the spindle microtubules attach to the kinetochores of the chromosomes.
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Metaphase
The third stage of mitosis, in which the spindle is complete and the chromosomes, attached to microtubules at their kinetochores, are all aligned at the metaphase plate.
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Anaphase
The fourth stage of mitosis, in which the chromatids of each chromosome have separated and the daughter chromosomes are moving to the poles of the cell.
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Telophase
The fifth and final phase of mitosis, in which daughter nuclei are forming and cytokinesis has typically begun.
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Anchorage dependence
The requirement that a cell must be attached to a substratum in order to initiate cell division. (Example, not blood cells) Non-circulating cells need to be attached to a solid surface before they divide.
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Density-dependent inhibition
The phenomenon observed in normal animal cells that causes them to stop dividing when they come into contact with one another
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Transformed cells
Mutation of genes, defects are passed on: may make own growth factors or have a defect in a checkpoint. Many are killed by the immune system. The loss of either anchorage dependence or density-dependent inhibition which prevent uncontroleed cell growth
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Benign tumore
Localized, slow growth - easily treated, lost density dependence and may have lost G1 chechpoint
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Malignant tumour
Invasive, may change form & chromosomes. Cancer! Lost density dependence and may have lost G1 checkpoint
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Metastatic
Breakaway cells get into circulation and other tissues. Lost anchorage-dependence inhibition
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PDGF
Platelet derived growth factor - stimulates fibroblast division at wound sites
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Histone
A small protein with a high proportion of positively charged amino acids that binds to the negatively charged DNA and plays a key role in chromatin structure
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Nucleosomes
The basic, beadlike unit of DNA packing in eukaryotes, consisting of a segment of DNA wound around a protein core composed of two copies of each of four types of histone (eight histones).
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Octamer
An 8 sub-unit protein complex (the nucleosome core)
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H1
The negatively charged DNA wraps twice around the positively charged complex of 8 histone proteins. The wrapped DNA is held in place by a ninth histone called H1. This locks the DNA in place. It also allows the 10nM fibre to further coil into 30 nm fibres
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30nm fibres
The H1 histone allows the 10nm fibre to further coil into 30nm fibres. This is level two packaging.
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Looped domains
Level 3 packaging. Loops on a scaffold
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Level 4
Super coil within chromosomes (chromatid).
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Euchromatin
The less condensed form of eukaryotic chromatin that is available for transcription, consists of Level 1 and 2 packaging.
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Heterochromatin
Eukaryotic chromatin that remains highly compacted during interphase and is generally not transcribed. More condensed, 30nm fibres looped onto the nuclear lamina and a protein scoaffold called the nuclear matrix
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Nuclear lamina
A netlike array of protein filaments that lines the inner surface of the nuclear envelope and helps maintain the shape of the nucleus.
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G0 phase
A non dividing state occupied by cells that have left the cell cycle, sometimes reversibly
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G1 phase
The first gap, or growth pahse, of the cell cycle, consisting of the portion of interphase before DNA synthesis begins
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Nuclear matrix
A protein 'web' that extends through the nucleoplasm and also helps maintain the shape of the nucleus and binds and organizes the 30nm fibres as heterochromatin
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Acetylation
Acetylation of histone tails promotes loose chromatin structure that permits transcription of euchromatin. DNA accessible
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Methylation
Mythlation of histone tails effectively 'locks' up the DNA so it can't be transcribed. 30 nm fiber inaccessible
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Deoxyribose
The sugar component of DNA nucleotides, having one fewer hydroxyl group than ribose, the sugar component of RNA nucleotides
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Nitogrenous bases
- Adenine A
- Guanine G
- Cytosine C
- Uracil U
- Thymine T
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Nucleotides
- The building block of a nucleic acid, consisting of a five-carbon sugar covalently bonded to a nitrogenous base and one or more phosphate groups.
- Adenosine-monophosphate (AMP)
- Guanosine-monophosphate (GMP)
- Cytidine-monophosphate (CMP)
- Uridine-monophosphate (UMP)
- Deoxythymidine-monophosphate (dTMP)
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Bacterial Transformation
Bacteria can take up and incorporate genetic material from dead bacteria and use it to make a pathogenic capsule coat.
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Bacteria
One of two prokaryotic domains, the other being Archaea
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Fred Griffith
1928 accidently discovers that bacteria can take up and incorporate genetic material from dead bacteria and use it to make a pathogenic capsule coat.
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Avery, McLeod & McCarthy
follow up on Griffiths work and isolate or enzymatically destroy each of the classes of macrmolecules and test in bacterial transformation experiments. Only intact nucleic acid transforms the bacteria.
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Hershey and Chase
In 1952 made either DNA or protein radioactive. Tracked to see which compound passed on to new viruses/phage
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Chargaff's rule
Porportionally # of A = # of T & # of G = # of C
Knew that there were nucleotide polymers with defferent nitrogenous bases, determined that different organisms had different ratio's of each base: Adenine, Thymine, Guanine & Cytosine - therefore some diversity
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Linus Pauling
California, predicted a triple helix (wrong)
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Maurice Wilkins & Rosalind Franklin
London, created the data but didn't fully resolve the structure
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James Watson and Francis Crick
Collaborated and made a model to fit the x-ray diffraction data, a probable helix, consistently 2 nm in diameter. Eventually put together that nitrogenous bases face each other, and figured out that they are held together by hydrogen bonds. Only A with T and G with C. This had consistent width and met Chargaff's rule
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Potential diversity
Ability within the structure to have random order within a DNA helix
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Strand Complementarity
In DNA, the two strands that complement each other always go together.
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Anit-parallel
Referring to the arrangement of the sugar-phosphate backbones in a DNA double helix (they run in opposite 5` to 3` directions).
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Double Helix
has two strands that complement each other, therefore you can use one strand to reproduce or replicate the other as T always pairs with A & G always pairs with C
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Polymerase
Adds nucleotides to the chain in the 5` to 3` direction.
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Origins of replication
Site where the replication of a DNA molecule beings, consisting of a specific sequence of nucleotides
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Helicases
An enzyme that untwists the double helix of DNA at replication forks, seperating the two strands and making them available as template strands
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DNA polymerase
An enzyme that catalyzed the elongation of new DNA (for example, at a replication fork) by the addition of nucleotides to the 3` end of an existing chain. There are several different DNA polymerases; DNA polmerase III and DNA polymerase I play major roles in DNA replication of E. coli
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Single strand binding protiens
A protein that binds to the unpaired DNA strand during DNA replication, stabilizing them and holding them apart while they serve as templates for the synthesis of complementary strands of DNA
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Primase
An enzyme that joins RNA nucleotides to make a primer during DNA replication, using the parental DNA strand as a template
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Topoisomerase
A protein that breaks, swivels, and rejoins DNA strands. During DNA replication, topoisomerase helps to relieve strain in the double helix ahead of the replication fork
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Okazaki Fragments
A short segment of DNA synthesized away from the replication fork on a templacte strand durin DNA replication. Many such segments are joined together to make up the lagging strand of newly synthesized DNA.
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Pol I
A distinct DNA Polymerase replaces the RNA primer with DNA and then Ligase joins the Okazaki fragments together
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Ligase
Ligates/joins the all- DNA Okazaki fragments
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Gyrase
Has similar function to topoisomerase in preventing DNA 'knots'
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Frederick Sanger
In 1953, he showed that core the core element of a protein is a sequence of amino acids, therefor DNA sequence is the blueprint for amino acid sequence.
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genes
Contain both instructional information and design information
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Transcription
The synthesis of RNA using a DNA template
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Translation
The synthesis of a polypeptide using the genetic information encoded in an mRNA molecule. There is a change of "language" from nucleotides to amino acids.
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Codon
A three-nucleotide sequence of DNA or mRNA that specifies a particular amino acid or termination signal; the basic unit of the genetic code.
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AUG
Methionine, start codon
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Silent mutation
No change to AA encoded
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Mis-sense
Codon change causes AA change
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Non-sense
Codon changes to stop codon
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Frame shift
Can occur when a nucleotide is deleted or added, as the sequence is read in 3 reading frames
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Inter-genic DNA
In eukaryotes the genes are seperated from one another with these non-coding DNA
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Pre-RNA
The step that eukaryotes take before RNA, prokaryotes skip this step.
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Eukaryotic Transcription Initiation
Sequence 'motifs' in the promoter are recognized by transcription factors
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Promoter
A specific nucleotide sequence in the DNA of a gene that bonds RNA polymerase, positioning it to start transcribing RNA at the appropriate place.
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Transcription factors (TFs)
A regulatory protien that binds to DNA and affects transcription of specific genes
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Transcription initiation start point
TFs bind both DNA and the RNA polymerase and direct the latter to this
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Transcription Initiation Complex
The complete assembly of transcription factors and RNA polymerase bound to a promoter
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TATA box
A DNA sequence in eukaryotic promoters crucial in forming the transcription initiation complex.
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Coding strand
The RNA Transcript has same sequence as the coding strand
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Template strand
The DNA strand that provides the pattern, or template, for ordering, by complementary base pairing, the sequence of nucleotides in an RNA transcript (with uracil substituted for thymine)
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Elongation
The transcription continues and the RNA strand gets longer
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Termination
When the transcription is complete, the transcription is ended.
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Termination Sequence
AAUAAA tells the Polymerase to stop transcribing
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Poly (A) tail
A sequence of 50-250 adenine nucleotides added onto the 3` end of a pre-mRNA molecule
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Non-templated addition
The Poly A tails are not on the template strand
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AAUAAA
frequently referred to as the Poly (A) signal
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Introns
A noncoding, intervening sequence within a primary transcript during RNA processing; also refers to the region of DNA from which this sequence was transcribed. Introns space out the exons
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Exons
A sequence within a primary transcript that remains in the RNA after RNA processing; also refers to the region of DNA from which this sequence was transcribed. These are spaced out by non-coding introns
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Spliceosome
A large complex made up of proteins and RNA molecules that splices RNA by interacting with the ends of an RNA intron, releasing the intron and joinging two adjacent exons.
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snRNP
Make up the spiceosome, they are small nuclear ribonucleo-proteins
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snRNA
Small nuclear RNA approx 150 nt in length (between 100-200 nt)
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UTR
Untranslated regions, these are flanking RNA sequences for the coding segment that provide a bit of flexibility (slack at both ends) and can regulate translation rates.
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Promoter
Defines transcription start site for RNA Poylmerase (Pol)
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Enhancer
Regulates the role of the promoter - transcription factors bound to the enhancer can either block or speed up the loading of RNA Pol at the promoter. They can be upstream of downstream of the gene, or in introns
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Sigma Factor
In bacteria, instead of transcription factors, the sigma factors bind first to the RNA Polymerase and this complex binds to the promoter sequence
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Polyeistronic
In bacteria, one mRNA can encode multiple different polypeptides (this is unique to bacteria).
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Consensus motif
An optimal sequence motif for binding
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Operon
A unit of genetic function found in bacteria and phages, consisting of a promoter, an operator, and a coordinately regulated cluster of genes whose products function in a common pathway.
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Operator
A key element of an operon, which is a DNA nucleotide motif that controls whether RNA Pol can pass by
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Repressor
A protein that inhibits gene transcription. In prokaryotes, repressors bind to the DNA in or near the promoter. In eukaryotes, repressors may bind to control elements within enhancers, to activators, to activators, or to other proteins in a way that blocks activators from binding to DNA
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Post-translational modifications
Polypeptides are often modified in preparation for their final function
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Obligates
Pathogens that are obligated to have a host to reproduce
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Facultative
Pathogens that do not require a host.
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Viruses
- Not living things, they lack: ability to take up energy & make use of it, ability to transport themselves, ability to reproduce themselves, and lack any metabolic abilities or function.
- They are just genetic material and usually a protective casing.
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Capsid
The protein shell that encloses a viral genome. It may be rod-shaped, polyhedral, or more complex in shape.
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Virion
An infectious virus particle
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Reverse Transcriptase
An enzyme encoded by certain viruses (retroviruses) that uses RNA as a template for DNA synthesis.
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Provirus
A viral genome that is permanently inserted into a host genome
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Apoptosis
A type of programmed cell death, which is brought about by activation of enzymes that break down many chemical components in the cell. If the virus can disturb this, there is a potential for cancer.
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Provirus
A viral genome that is permanently inserted into a host genome.
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Lytic
A type of phage replicative cycle resulting in the release of new phages by lysis (and death) of the host cell.
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Lysogenic
A type of phage replicative cycle in which the viral genome becomes incorporated into the bacterial host chromosome as a prophage, is replicated along with the chromosome, and does not kill the host.
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Transduction
A proces in which phages (viruses) carry bacterial DNA from one bacterial cell to another. When these two cells are members of different species, transduction results in horizontal gene transfer.
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Four mechanisms that bacteria use to become antibiotic resistant
- Pump the antibiotics out the cells via efflux pumps
- Develop enzymes that degrade the antibiotic
- Develop enzymes that alter the antibiotic to inactivate it
- Alter the chemistry of the antibiotics target, so that antibiotic can't bind to it's target
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Virulence factors
- Allow the pathogen to:
- Invade the host or a specific site in the host
- Enter or leave a host cell (intracellular pathogens)
- Evade the host immune response (e.g. bacterial capsule)
- Obtain nutrients from the host (catabolize the host)
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Prions
An infectious agent that is a misfolded version of a normal cellular protein. Prions appear to increase in number by converting correctly folded versions of the protein to more prions
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