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36 Cards in this Set

  • Front
  • Back
Genophore
carrier of genetic information
Nucleotide
nitrogen-containing base + sugar pentose + phosphate
nucleoside
nitrogen-containing base + sugar pentose
bases of DNA
Adenine (A), Guanine (G) (purine)
Cytosine (C), Thymine (T) (pyrimidine)
bonds of DNA
phosphodiester bond between 3' OH and 5' phosphate
Hydrogen bonds between base pairs (AT=2, GC=3)
Chromosomes Eucaryotic
linear, 10^8 bp (human 5-25x10^7), in the nucleus containing histons (basic proteins) and acidic proteins (nonhistone proteins)
Chromosomes prokaryotic
circular, 10^6-10^7 bp. attached to plasma membrane by replication origin. contains proteins, nonhistons and histone like
Histones
H1 (linker histone), H2A, H2B, H3, H4 core is made of octamer of the last four histones, two of each, DNA is wound around the core
Acidic proteins of chromosome
Heterogenous group of proteins probably involved in 3D conformation
Structural genes
encode proteins
Genes for RNA
encode RNA which is NOT a template for translation (t and rRNA)
DNA regulatory regions (of genes)
Doesnt encode any proteins or RNA but carry information for binding specific molecules regulating gene expression
Procaryotic gene
conatins only uninterrupted DNA sequences coding for proteins, no introns/exons
Eucaryotic gene
contains Exons and Introns
Mammalian cells expressed genes represent ___ % other regions/sequences
7-10%
Regulatory regions; involved in regulation of gene expression
Repetetive sequences; DNA finger printing
Mobile elements (transposons): can copy&paste or cut&paste "jumping genes"
Pseudogenes: genes who has lost their function due to the accumulation of mutations
Genome (definition)
the complete set of DNA of the cell/organism
Genome prokaryotic
chromosome + possible plasmids
genome eucaryote
nuclear chromosome + mitochondrial chromosome (+ chloroplast chromosome + possible plasmids)
human genome (haploid) comprises approx. 30 000 genes
Human genome (haploid set) # of genes
ca 30 0000
DNA replication
REPLICON
a segment of DNA which represent a replication unit with its own replication origin
DNA replication
REPLICATION ORIGIN
a specific DNA sequence where replication starts after unwinding of the double helix, rich in T and A
DNA replication
REPLICATION FORK
two of them works in opposite directions from the replication origin.
Pro: 1000 bp/s
Eu: 100 bp/s
DNA polymerase
catalyzes the formation of phosphodiester bond between two nucleotides
Nucleotide enters the DNA polymerase reaction as
nucleoside triphosophate (ATP, GTP, CTP, TTP)
2 important limitations of DNA polymerase
Can synthesize only in 5'-3' direction
unable to start synthesis of a new strand
Several types of DNA polymerase
alfa: synthesis of lagging strand
delta: synthesis of leading strand
beta & epsilon: DNA repair
gamma: synthesis of mitochondrial DNA
DNA polymerase uses ____ as a cofactor
Magnesium ions
Replication forks, made of, does
made of helicase (motor protein, enzyme)
breaks hydrogen bonds between base pairs that keep double helix intact
DNA polymerase, proofreading activity
3'-5' direction, PREFERENTIALLY repairs mismatched base pairs of newly synthesized strand, before adding the next one
Primase
Enzyme that can start a new strand, makes a RNA primer to which the DNA polymerase then can continue to add nucleotides. Lacks proofreading skills.
repair DNA polymerase
replaces the RNA primer (synthesized by primase, removed by nuclease) with DNA
DNA ligase
joins the 5' end of one new DNA fragment with the 3' end of an other (okazaki)
Single strand binding proteins
proteins that bind to the opened DNA strand that is now exposed and would easily fold (by forming base pairs) thus making replication tricky!
Sliding clamp
protein fold that keeps DNA polymerase on DNA template. DNA polymerase can easily detach from template = good for recylcing of DNAp when synthesising Okazaki, bad for synthesis of longer strand (leading strand) Sliding clamp makes sure it stays in place
DNA mismatch repair system
recognizes distortion of the geometry of the DNA dbl helix caused by mismatched base pairs
errors in DNA replication
replication machine makes 1 per 10^7 bp, after mismatch repair system it goes down to 1 per 10^9 base pairs