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Microbrial DNA Structure and Function
DNA, Nucleotides, histones, chromosomes
Central Dogma of Moelcular biology
DNA→ mRNA→Protein→ Function
Transcription
DNA→mRNA
RNA polymerase is during what
Transcription
What is RNA polymerase function?
During transcription, RNA polymerase binds to the DNA template strand and builds a complementary mRNA molecule.
This converts the cell’s genetic blueprint into an RNA copy that can be used for protein synthesis
DNA replication is semiconservation
Which means each new DNA has one orignal strand
Helicase function
unwinds DNA
DNA polymerase function
adds nucleotides to the strand
translation transition
mRNA→ protein
In trasnaltion what is a tRNA
It contaisn anticodon that recognizes the codon and carries the maino acid specific for that sequence
polypeptide
ribosome links amino acids
translation ends at ____ codon
stop
Genotype
genetic code
phenotype
expression (proteins, traits) result of genotype
Mutation definition
permanent change in DNA
Kinds of mutations (mechnanisms)
small-scale (point mutations) or Large-scale mutations (chromosomal) mutations
small-scale mutations (point mutations)
insertion, deletion, or subsititon
insertion point mutations
extra bases added
deletion point mutations
baes removed
subsition point mutations
one base replaced with another
large-scale mutations (chromosomal mutations) include
duplication, inversion, translocation
duplication chromosomal mutation
a segment of DNA is compied and inserted
translocation chromosomal mutations
a segment of DNA moves to a new loation, often between chomosomes
inversion chomosomal mutations
a segment of DNA is flipped in orientation
types of outcomes for mutations
silent, missense, nonsense
Silent mutation outcome
Base changes, but amino acid stays the same
missense
(DNA base change → different amino acid is substitutied ex sickle cell, anemia:Glu-Val)
Nonsense mutation outcome
DNa base change creates a stop codon
Causes of mutations
spontaneous (replication errors, base shifts), induced (UV, chemicals, viruses)
Efffects of mutations
can be neutral, harmful (disease), or beneficial (antiobiotic resistance).
Viruses are
Infectious genetic material (DNA or RNA, never both)
Viruses are not
living organisms
Parts of animal virus
spikes, envelope, capside, nucleic acid (DNA or RNA)
enclosed in a protein coat (capsid)
some have a lipid envelope with spikes (glycoproteins)
inside in the nucleic acid (DNA or RNA)
Virus are what kind of parasites
Obligate intracellular parasites; require a host to replicate
Spikes function
Help virus attach to receptors on host cells
Viral life cycle
Attachment
penetration/entry
uncoating
biosynthesis
assembly/maturation
release
Attachment
binds to specific repceptors on the host cell
lock and key mechanism
penetration/entry
the virus or its genome enters the host cell
uncoating
viral nucleic acid is released
biosynthesis
viral nucleic acid is replicated and viral proteins rae produced
assembly/maturation
new viral particles are sasembled
release
new viruses leave the host cell where replication occurs depends on hte virus
possible outcomes virus
lytic infection, latent infection
lytic infection
virus replicates and kills the cell
latent infection
viral DNA integrates into host genome and remains dormant
how are viruses release
by budding
How does HIV convert RNA to DNA
enzyme reverse trasncriptase
note trasncription: DNA to mRNA so makes sense that its reverse trascriptase
HIV DNA cant be inserted into host DNA through an ezyme called
integrase
HIV destroys certain immune cells aka
CD4+ helper T cells and leaves patients vulnerable to many infections that can quickly become deadly
When HIV is reactivated can lead to
lysis of T cells
Two major surface proteins in Influenca Virus
Hemagglutinin (H), Neuraminidase (N)
Hemagglutinin (H) Hemagglutinin
binds host receptors (Sialic Acid)
Neuraminidase (N) Neuraminidase Neuraminidase Neuraminidase
Helps release new viruses
Antigenic drift
small mutation produces slihglt ydifferent virus strains → yearly vaccine updates
antigenic shift
gene reassortment, creates anentirely new subtype → pandemics
bacteriophages
viruses that infect bacteria
bacteriophage
virus that that infect bacteria
structure for bacteriphage
capsid head, dna in the capsid head, sheath, contracts to inject dna. baseplate and pins, tail fibers. pin is how they inject their dna from.
how bacteriophage infects bacteria
landing, pining, tailing contraction, dna injection
lysogenic conversion
when a phage incorprorates genes into a bacterial genome that then leads to production of some product so some phages will incorprorate traits in a bacterial cell
pathology
study of diease
Etiology
cause of diase
pathogenesis
how a disease developes
infection
invasion or colonzation of the body by microorganisms, infection does not always lead to disease,
disease
abonormal condition that disrupts normal body function
classification of diseases
communicable disease
contagious disease: easily spread
Noncommunicable:not spread, transmitted person-to-person
infectious: caused by pathogens
Duration of diseases
acute: rapid onset, short duration (flu)
Chronic: long-lasting
Latent: inactive, may reactivate (herpes, shingles)
stages of disease
incubation period: interval between initial infectiona nd first signs and symtpoms
prodromal period: short period after incubation, early, mild symptoms
period of illnessL disease is most seere transmission can occur
period of decline: signs and symptoms subside
period of conalescence: body recoer and return back to norma
1.ncubation
prodromal
illness the most seere and transmission cna occure
decline: symptoms and signs subside
convalescence: recovery incubation prodromal illness decline convalescnece incuation prodromal illness decline convalescence
types of infection
local, systemic, sepsis
local: confined area
systemic: spreads through body
Sepsis: microbes/toxins spread in blood
bacteremia: bacteria in blood
toxemia: toxins in blood
viremia: viruses in blood
pimary infection
initial illness, acute infection
secondary infection
after the primary infection weakens body’s defenses, secondary infections can be caused by opportunitistic pathogens
subclinical infection
infections that don’t cause any noticeable illness
reservoir
source where pathogen lives (humans, animals, enironemnt,
zoonoses / zoonotic
diseaes transmitted from animals to humans
human reservoirs (carriers)
may have inapparent infections or latent diseaeses
transmission routes
contact, vehicle, vector
contact trasnmisison
direct (person to person)
indirect (formites)
droplet (sneeze, cough)
congenital (mother to fetus)
vehicle
airborne
waterborne
foodborne
vector transmission
mechanical: passive (flies)
biological: via bite or fluid (mosquitoes, ticks