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2 reasons why eukaryotic genomes are large
number of genes (complex organisms) & amount of non-coding dna (around 97%)
promoter
part of gene that controls transcription
2 types of repetitive sequences
interspersed repetitive dna & tandemly repetitve satellite dna
interspersed repetitive dna
repeated units scattered throughout genome, single unit - 100-10,000 bp, makes up 25-40% of mammalian genomes
tandemly repetitive dna
classified according to length of repetitive region, a lot is located at telomeres and centromeres, cause of some genetic diseases
regular satellite dna length
100,000 - 10 million bp per site
minisatellite dna length
100 - 100,000 bp per site
microsatellite dna length
10 -100 bp per site
centromeres are important for
chromosome organisation
telomeres are involved in
protecting ends of chromosomes
chromatin structure
intricate form of packaging for dna - 10,000 fold compaction
heterochromatin
highly condensed during interphase, not actively transcribed, occurs during interphase in some regions of chromosome
euchromatin
less condensed during interphase, able to be transcribed - more of the chromosome is in this form during interphase
nucleosome
basic unit of chromatin
histones
proteins with positively charged amino acids that bind to the negatively charged dna, plays key role in chromatin structure
2 ways of chemical modification of chromatin
dna methylation for gene silencing, histone acetylation for gene activation
dna methylation
attachment of CH3 groups to bases, triggers formation of compact chromatin structure, associated with inactive dna
histone acetylation
attachment of COCH3 to histones, acetylated histones grip dna less tightly, involved in switching genes on and off
closed chromatin
DNA methylated, histones not acetylated
open chromatin
dna unmethylated, histones acetylated
rna pol 1
ribosomal rna
rna pol 2
mRNA
rna pol 3
small rna eg. tRNA
promoter determines ..
where transcription starts, rate of transcription
TATA box
part of promoter, provides site of initial binding of the transcription initiation machinery
preinitiation complex
forms before transcription - TF2D binds to TATA box to form initial committed complex, addition of other TFs, binding of TF2F and RNA pol2, then TF2E and TF2H
how do TFs affect rate of transcription
TFs bind to proximal/distal control elements - dna folding brings distal sequences into proximity with the promoter so they can work
post transcriptional regulation
capping of 5' end, polyadenylation of 3' end, splicing to remove introns