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operator
segment of dna that controls on/off switch for genes, within the promoter
operon
entire stretch of dna including: operator, promoter, and genes
repressor
switches off operon, blocks operator from rna polymerase
regulatory gene
creates the repressor
corepressor
bonds to existing repressor to activate it
trytophan (corepressor) + trp repressor
together turns off operon
repressible operon
usually on, is wanted to turn off, repressor + operator turns off transcription, anabolic (building) pathways, repressed by high levels of final product
example of repressible operon
trp operon
inducible operon
usually off, inducer inactivates the repressor and turns on transcription, catabolic (breaking down) pathways
example of inducible operon
lac operon
lac operon
genes code for enzymes for metabolism of lactose (catabolic)
inducer
inactivates repressor to turn lac operon on
negative control of genes
operons are switched off by the active form of the repressor
cylic amp receptor protein (CRP)
activator of transcription
CRP activation
CRP + cyclic amp (cAMP)
activated CRP
attaches to promoter of lac operon and accelerates transcription
lactose
glucose alternative, must be broken down for energy, when glucose is absent → more lac operon must function
negative control in lac operon
the default mechanism that prevents transcription of the lac operon when lactose is absent and glucose present,
positive control in lac operon
enhances transcription when lactose is present, but only if glucose is scarce
differential gene expression
why the same dna in cells can express different genes
chromatin
dna wrapped around histones
histone acetylation
euchromatin, opens up chromatin and promotes transcription
dna methylation
heterochromatin, tightens chromatin, slows transcription or blocks it, can cause long term inactivated of genes in cellular differentiation
genomic imprinting
methylation regulates expression of either maternal or paternal alleles or certain genes at start
cellular differentiation
young, unspecialized cell takes on individual characteristics → reach mature form
epigenetic inheritance
ways to turn genes on or off without changing nucleotide sequence
control elements
segments of noncoding dna where transcription factors bind to regulate transcription
distal control elements
groups are called enhancers, far away from a gene, generally associated with only one gene
activator
protein that binds to an enhancer and stimulates transcription of a gene
protein mediated binding of dn
brings the bound activators into contact with mediator proteins
proximal control element
close to promoter
alternative rna splicing
same mrna can make different proteins by cutting out different exons
regulatory proteins
bind to mrna and block ribosomes from starting translation
mrna degration
getting eaten by enzymes
utr sequence
untranslated, influences life span of mrna
longer mrna lasts in cytoplasm
the more proteins made
ubiquitin
mark of degradation on proteins
proteasomes
break marked proteins into monomers
MicroRNA (miRNA)
non-coding mrna, degrades mrna or blocks translation
miRNA binds fully to target mRNA
degrades mrna
miRNA does not attach to all bases
blocks translation of the mrna
small interfering RNAs (siRNAs)
only in yeast, non-coding rna, turns chromosome centromere into heterochromatin
rna interference (RNAi)
process of siRNAs blocking gene expression by condensing the centromere
cell differentation
cells become specialized in structure and function
morphogenesis
physical processes that give organism its shape
stem cell
immature cell before determination
cytoplasmic determinants
maternal chemicals in the egg that determine the cell
induction
pathway that tells cells to tell each other what to become
determination
commits cell to become a particular cell type, precedes differentiation
differentiation
turns on genes for proteins to start the cell
myoblasts
cells determined to be muscle cells
master regulatory gene
sets up pathway of transcription facts by turning on the first factor in the chain
pattern formation
how we establish a front facing and back of an organism
positional information
tells cell its location relative to other cells and body axes
drosophilia
cytoplasmic determinants in unfertilized cell determine axes before fertilization
majority of bicoid gene
front/head
homeotic genes
edward b. lewis, hox gene, control pattern formation in late embryo, larva, and adult in drosphilia
embryonic lethals
mutations cause death
maternal effect/ egg polarity genes
bicoid gene, encode cytoplasmic determinants that make axes
no functional bicoid gene
lacks front half of its body
morphogens
establish embryos axes and other features
bicoid gene
affects front half of body, distributed front to back gradient
bicoid importance
identified specific protein required for some early steps, understanding mother’s rule in embryo development, gradient of moles can affect polarity and position
low concentration of bicoid gene
abdomen
virus
nucleic acid covered by protein
wendell stanley
discovered the existence of a virus
viral genomes can be
double or single stranded dna or rna, single linear or circular
capsid
protein coat around the viral genome
capsomeres
protein subunits that make a capsid
influenza viruses
have rna protein, rna production uses rna polymerse which doesnt have checking system so more mutations
viral envelope
protein shell of virus made from host’s membrane and viral genome, glycoprotein spike to infect hosts,
bacteriophage/phage
viruses that infect bacteria, tail attaches the virus to its host
host range
what type of cell a virus can infect, viruses can only replicate in a host cell
virus infection
replication: virus does dna replication with dna polymerase
transcription/translation: virus uses rna polymerase to make proteins
assembly: replicated viral dna and protein coat assemble and exit
lytic cycle
causes the cell to lyse (explode) open exit
virulent phage
phage (bacteria) that reproduces only by lytic cycle
lysogenic cycle
replicates phage genome by integrating into host cell’s genome, can switch to lytic cycle
temperate phage
uses lytic and lysogenic cycle
prophage
intergrated viral dna in lysogenic cycle, each time host divides it copies the phage dna and passes it down, only in bacteria
restriction enzyme
cellular enzymes identify foreign dna and cut it up
CRISPR-Cas system
CRISPR: holds dna from previous infections and transcribes it to rna that bonds with the Cas protein
Cas: protein that bonds with the RNA from CRISPR and cuts the phage dna degrading it
spacer in the CRISPR-Cas system
corresponds to dna from a phage that has infected the cell previously
membranous envelope
glycoproteins on the envelope bond to specific receptor molecules on host cell’s surface
retroviruses
infect animals, use reverse transcriptase to turn RNA genome into DNA
HIV
retrovirus that causes AIDS, the illness,
provirus
dna made by reverse transcriptase that integrated into host genome, stays permanently in the host cell, only in eukaryotic cells
vaccine for viral diseases
harmless versions of the virus which makes immune system have a defense against the actual virus
allows users to search for specific dna sequence, predicted protein sequence, common stretches of amino acids
ncbi blast
gene annotation
protein coding genes within dna sequences
transposable elements
dna that dna move from one location to another, makes repetitive dna
transposons
dna is copied and moves with a transposase enzyme
retrotransposons
copied into single stranded rna then reverse transcribed back into dna and integrated into the genome
alu elements
transcribed into rna molecules, can help regulate gene expressed
simple sequence dna
many copies of short sequences, not related to transposons, common in centromeres and telomeres
short tandem repeat
series of repeating units of 2-5 nucleotides, varies from person to person,
multigene families
two or more identical or very similar genes
alpha and beta globin
polypeptides of hemoglobin on different human chromosomes, expressed at different times in development, likely transposed from common ancestor then had mutations
psuedogenes
versions of the function genes that no longer make functional proteins
mutation
underlies much of genome evolution, earliest life forms likely only had genes necessary for survival and reproduction
rate of duplications and inversions
accelerated 100 million years ago when large dinosaurs went extinct and mammals diversified