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HU protein
prokaryotic
binds to the DNA and each other for bending of DNA and the formation of loops (similar to histones in eukaryotes)
Supercoiling
the spinning of the circular DNA after breaking it, to create bends, making the DNA shorter and further compacted (carried out by DNA Gyrase)
Positive supercoiling
turning the DNA in the same direction as the DNA
Negative supercoiling
turning the DNA in the different direction as the DNA (“unwinding” makes opening and transcription easier)
Chromatin
eukaryotic
complex of DNA and proteins
chromosomes are made of condensed chromatin
Proteins involved in chromatin structure
eukaryotic
histones
non-histone chromosomal proteins
Histones
eurkaryotic
positively charged
DNA wrapped around 8 histone proteins to form a nucleosome
H1 histone helps pull the nucleosomes together to further compact (one H1 per core nucleosome)
H2a H2b H3 H4 (2 of each forms a nucleosome)
Condensin
eukaryotic
binds same DNA to form loops
when chromosomes decondense, they fall into territories rather than a mixture of random places
Euchromatin
eukaryotic
chromatin packing
less packed
undergoes process of normal condensation and decondensation (decondenses during interphase into territories)
light in a scan
easier for transcription
Heterochromatin
eukaryotic
chromatin packing
more packed
stays condensed throughout the cycle
dark in a scan
compacted during interphase
Histone acetylation
eukaryotic
adds acetyl group, making histones LESS positive —> DNA binds less tightly
open chromatin structure
Histone deacetylation
eukaryotic
removes acetyl group, making histones more positive —> DNA binds more tightly
compacted chromatin structure
Eukaryotic Origin of replication
part of eukaryotic chromosome
allows replication of a DNA in S phase
specific sequence where DNA synthesis starts
multiple ones on each chromosome
Centromere
part of eukaryotic chromosome
allows segregation in meiosis and mitosis
site of kinetochore - spindle microtubule attachment
holds sister chromatids together
constricted due to satellite DNA packed as heterochromatin
lower eukaryote: specific centromere sequence
higher eukaryote: more complex sequence -satellite repeats, no genes
instead of H3, has CENP-A histone
pinched structure for rmicrotubule attachment
Telomere
part of eukaryotic chromosome
protects ends of linear DNA
repeats at ends needed for DNA replication problem of 5’ ends (shorter 5’ ends of newly replicated strands — on the lagging strand)
telomerase protein expands repeats to solve the problem^
shelterin protein and folding over of DNA protects ends from degradation & triggering repair enzymes
unique DNA
~50%
includes genes and introns
highly repetitive DNA
short sequenes tandemly repeated many times
satellite
minisatellite
microsatellite
moderately repetitive DNA
functional genes needed in large numbers- rRNA, tRNA, often tandem arrays in places around genome
transposable elements
satellite DNA
5-150bp
forms chunks found around CENTROMERES
minisatellites
10-60bp
scattered in smaller chunks over GENOME
microsatellites
1-6bp repeated 10-100 times
scattered over GENOME
variable number of repeats due to mistake sin replication or repair
useful for CODIS- Forensic DNA fingerprint 13 STR
if in genes- variable # of aa: Huntington’s & Fragile X
DNA transposons
cuts & pastes
transposable element
transposase- enzyme that cuts and pastes
bacteria IS (insertion sequences) elements and transposable elements (captured gene)
corn (maize) - Ac element hops in and out
Drosophila P element
Retroelements
copies & pastes
uses RNA intermediate
related to retrovirus
reverse transcriptase (RT) copies RNA virus to DNA, which inserts in DNA
Transcription forms RNA copy
Types of retroelements
Endogenous retroviruses (ERV)
LINE
SINE
ERV
defective retroviruses 8-9 Kbp
has RT that allows to make RNA transcript into a DNA that gets inserted elsewhere in genome
LINE
has no terminal repeat, 6-8 Kbp
has RT that allows to make RNA transcript into a DNA that gets inserted elsewhere in genome
SINE
example: Alu element (short 80-630 bp) related to 7S signal particle
NO RT gene, relies on LINE or ERV’s RT to move
Genetic effects of tranposons
can disrupt a gene when hops into/near it
changing regulation of gene
^can reverse potentially when it hops out
creates sites for recombination of nonhomologous chromosomes or different parts in the same chromosome