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transmission genetics
passing of traits from parents to offspring
molecular genetics
DNA leading to RNA leading to protein
population genetics
studying traits in an entire population
model organism
organisms with characteristics that make them useful for genetic analysis. If you want a model organism similar to humans, you have to go up in complexity like mice
short generation time
production of numerous progeny
ability to be raised in a lab
gregor mendel
father of genetics
principles of heredity
1850s, same time as Darwin
schleiden and schwann
came up with cell theory
viruses are not living organisms
disproved that life could spring out of nothing
cell theory
all organisms are made of cells and all cells come from pre-existing cells
darwin
discovered evolution and natural selection
natural selection
varying traits and fitness. some traits are more favorable than others
sutton
discovered that genes are located on chromosomes
watson and crick
structure of DNA
roselyn franklin
used x-ray crystallography to help watson and crick
hershey and chase
DNA is the genetic material
bacteriaphage in blenders
messholson and stall
figured out how DNA replication works
semiconservative replication
genome
complete set of genetic instruction for an organism
only viruses have RNA for a genome
gene
section of DNA that encodes a protein
central dogma of molecular biology
DNA is the genetic material, then it’s transcribed to make RNA template, then RNA leaves nucleus where it is translated into a protein
replication - in the nucleus
transcription - makes RNA copy of DNA. moves to the ribosomes
translation - proteins are made in the ribosomes
4 features of genetic material
complex information
accurate replication
ability to vary/ mutations
encode a phenotype
Griffith
pneumonia in mice, rough strain and smooth strain
discovered transformation
avery, mccleod, mccarty
DNase
Protease
RNase
R and s strain
DNA is the genetic material
Hershey and Chase
bacteriaphage in blenders
DNA is the genetic material
Chargroff
complimentary base pairing
A=T and C=G
number of purines = number of pyrimidines
nucleotide
made of sugar, phosphate group, nitrogenous base
ATCG
purines
adenine and guanine
2 ring structures
pyrimidines
cytosine and thymine
single ring structures
DNA structure
backbone made of sugars linked by phosphates
double stranded antiparallel
sugar: deoxyribose
RNA structure
single stranded
sugar: ribose
phosphodiester bond
bonds that form the sugar and phosphate backbone of DNA
hydrogen bond
holds the 2 strands of DNA together
T + A = 2 hydrogen bonds
C + G = 3 hydrogen bonds
B form
most common form of DNA found in cells
right handed helix
follows Watson and Crick model
A form
found in dehydrated cells
right handed helix
twisted more tightly than B form
Z form
not really certain this exists irl
left handed helix
exists because scientists manipulated it
bacterial DNA
single circular chromosome
more euchromatin than humans but less heterochromatin
euchromatin
many genes
chromatin is less condensed
transcription is often
heterochromatin
very few genes
chromatin is more condensed
transcription is infrequent
junk DNA - non-coding B form
nucleosome
DNA wrapped around histones
chromatin
the form of DNA in interphase of the cell cycle
looser form
chromosomes
DNA and proteins more compact during mitosis
tightest form of DNA
conservative model of replication
results in one original DNA molecule and one all new DNA molecule
dispersive model of replication
part new and part old alternating like a puzzle
like a hybrid
semiconservative model of replication
one strand of original DNA and one strand of new DNA twisted
replication origin
where replication begins
theta replication
circular replication
helicase
unzips the DNA and breaks the hydrogen bonds
gyrase
puts nicks in the sugar phosphate backbone to prevent supercoiling
primase
adds a short primer so DNA POL III can attach
DNA POL III
attaches to primer during replication to add bases
only works 5’ to 3’
single stranded binding proteins
keeps the helix open
prevents hydrogen bonds from forming back together
DNA POL I
removes the RNA primers and adds appropriate DNA bases
ligase
seals the gap where the primer was
proof reading
DNA POL can back up one base to fix a mistake
during replication
mismatch repair
DNA POL corrects the errors after replication is complete
telomere
the ends of our linear chromosomes
telomerase
adds junk DNA to the end of chromosomes so when telomeres are shortened after rounds of replication, only not important DNA is lost
primary RNA structure
single stranded RNA
ACGU
secondary RNA structure
RNA folds in on itself
EX: cloverleaf, hairpin
internal base pairing
when RNA folds in on itself, hydrogen bonds between bases form
rRNA
ribosomal RNA
physical part of the ribosome
mRNA
messenger RNA
carries information for a gene, used to form a protein
tRNA
transfer RNA
brings amino acids to the ribosomes
snRNA
small nuclear RNA
splices pre- mRNA
SnRNP
used for RNA processing
cut out the intons and fuse the exons
siRNA
small interfering RNA
gene expression
if protein is not needed but DNA is already transcribed, this degrades the mRNA to prevent translation
promoter
a specific DNA sequence that tells RNA POL where to start. RNA POL binds here to open up the double helix. sigma factor binds here as well
RNA coding sequence
RNA POL adds on the complimentary bases for RNA
terminator
transcription ends here
RNA POL
builds the RNA 5’ to 3’
sigma factor
binds to the promoter when transcription starts
Rho
protein that attaches to mRNA during transcription once RNA POL gets to the terminator.
uses helicase to separate mRNA from DNA template
5’ cap
pre mRNA modification
backwards guanine directs mRNA to the ribosomes
poly A tail
pre mRNA modification
many adenines added on the end of RNA to prevent degradation in the cytoplasm
splicing
post mRNA modification
introns are removed and exons are fused together
exon
expressed sequences
intron
intervening sequence
amino acid
essential carbon bound with an amino group, carboxyl group, hydrogen, and R group
R group is what differs between amino acids
peptide bond
bond between 2 amino acids
codon
3 sequential bases that will translate into one amino acid
sense codon
encode for any amino acid
start codon
codon that codes for MET
termination codon
say stop coding
reading frame
part of the genetic sequence that’s encoding for RNA or making proteins
wobble hypothesis
james watson
It states that the third base of a codon (in mRNA) can sometimes pair with multiple bases in the first position of the anticodon (in tRNA)
tRNA charging
attaches the amino acid to the correct tRNA
aminoacyl tRNA synthase
enzyme responsible for tRNA charging
initiation of translation
in cytoplasm
ribosome breaks into small and large subunit
mRNA joins to the small subunit
tRNA attaches to start codon
large subunit smooshes everything together
elongation of translation
everything slides down one codon at a time to grow the polypeptide
A - aminoacyl site - tRNA arrives here
P - peptidyl site - peptide bond forms between MET and incoming amino acid.
E - exit site - tRNA leaves charged with MET
termination of translation
termination codons are read
release factors enter A site and everything comes apart
diploid
chromosomes come in pairs
2n=46
haploid
one of each chromosome
gametes
1n=23
allele
different forms of a gene
sister chromatid
when a single chromosome replicates and joins to its replicate, the two chromosomes are sister chromatids
identical
G1
part of interphase
cellular function, metabolism, actively dividing
G0
offshoot of G1
cell is not actively dividing
S stage
section of interphase
DNA is replicating
G2
section of interphase
cell prepares for division
G1 checkpoint
makes sure the DNA is healthy before it starts duplicating
kinases
enzymes that pause the cell cycle
mutations in kinases lead to cancer
G2 checkpoint
cell cycle checkpoint that ensures DNA replicated properly
spindle assembly checkpoint
during mitosis, ensures spindle fibers attach to centromeres properly
genotype
set of alleles possessed by an individual organism