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Summary Exam 2 Review - Genetics; Dr. Seth Blair $7.99
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Summary Exam 2 Review - Genetics; Dr. Seth Blair

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Complete review and summary of all exam 2 - Genetics - lecture materials given by Dr. Seth Blair in intro biology 151 at the university of Wisconsin-Madison. Each main subject outlined in a different color with molded key terms and supporting diagrams.

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  • December 21, 2024
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O
portation #
RNA polymerase
topoisomerase cuts strands,allowingeeem
CHAGRAFF : base pairing rules & species specific ratios helicase :
UnzipS DNA
RNAcleotides




-
GRIFFITHS AVERY :
S(smooth) strains R(rough) strain.

genetic info can be transferred between bacterial strains

hensteve Chaser actrophage Made

new phages produced had same protein and DNA as original PNA
1



ue
amplifies
① denaturation

② annealing :
:




cooling
to
heating


template
to
to


61 ° C

DNA
so
quoc to separate


PNA primers can
apart
DNA strands


attach (anneal)
origin of 'replication

*
reads 3- 5'
③ extension temperature raised to eukaryotes have longer linear chroms s need many origins
:
72 C
resistant
builds 5'-3'
: , neat




i
builds new strand of PNA by
taq polymerase
TELOMERASE

iiiiiiiiintemplate
·
* adds telomeres start


end
bases to




&
lend of strand) or else telomerase DNA of gene
DNA would shorten with
each replication




ispermoeggli
I
* made in :
DNA to RNA a
transcription
template
·
germ cells promoter terminator
DD ·
·
stem cells reasons for MRNA :




momNA
& PNA-RNA binding is tempora se
cancer cells shifts over
lamplification many
·
· :




nokarotenements
one mRNA



· can attach to s'end of mRNAS start translation
conta
productions
:
can regulae a
now it is translatedA
* only parts of Put used as

only single strand made
templates
toftranscripta
proteins =
genes
transcription factor proteins promote or inhibit transcription (binds recruit RNA poly)




Eukaryotes -
5




Kamaldamagemin
Il bad replication

Se
exon1 intron exo n




,
① ends of pre-mRNA modified




stabilizes
3) selfish DNA
TRIPLETCODONO MRA NA -special uncleation t cap
mRNAs attaches to ribosome




·
poly A tail added to 3'end which
binds smallribosomalsubuiit is
·




bindstoproteinsthathelpstile
one


attaches etA Stop won

recrits large subunit binds release factor
which releases
protein
polypeptide
②removalofnoncodingintosremain
~
by splisosomes (proteinsS SURNA) FRAMESHIFT MUTATIONS : Amino end normal ,




spicesosom mineO
·




StemtasSe
carboxyl end abnormal or truncated
A alternative splicing to get diff
inversion :
adding deletion : removing
same DNA
id/trNA mRNAs from the
in single base
POINT MUTATIONS :
change or loss a

exon 2


synonymous (silent) : codes for same amino acid



I
tRNA synthesase uses




mmm
* specific aminoacyl acid
to specific tRNAS missense :
wrong amino nonsense :
Stop codon
ATP to attach specific amino acds




&
-
* UNTRANSLATED REGIONS (UTRS) :
ON PLEOTROPIC :
single mutant effects many tissues o processes


regions where no translation occurs
MELOSIS n
haploid

GAMETES
naploid, i
71
:

FERTILIZATION :
Combines nucleus of eggs Sperm n = 23
homologous pair


H OMOLOGOUS CHROMOSOMES : same genes in same




&
locationsdifferent alleles,separatechromos

until
is REPLICATION (Sphase) homologouschromosome
a




turned centromere to make one chromosome -sperm In diploig
genes
yredi
which are chromatids
regulate
= Sister


on/off GREGOR MENDEL / ↳tradione chromad

aneyecel doesn'tneed
> to a a
* LAW OF SEGREG AMON gametes have one
:
MELOSIS FERTILIZATION MELOSIS I homologs separated




S
T St
allele or the other , not both . equal chance

TRANSCRIPTION FACTOR PROTEINS bind to specific DNA and




porment
increase or decrease expression of
nearby genes
*
OFINDEPENDANTASSORTMENT T
LAN
> directly indirectly safrect activity of but . 4 equally probable gametes ovary
Sisterchromatis
a



estis
Most
or Separate ~
diploid
zotE
:

> increases genetic variation multicellular 2n = 46

regulationas
fancywayof
LAC OPERON
I possiblegametsa
in ecoli bacteria adults
operon
determines
on
irs




empmupmptndividual
S
* genetic regulatory mechanism




· prompta tes deptrmness
·inbridcrossinetrogous
:




recruits
9 : 3 : 3 : 1 ratio
not genetic
SEX CHROMOSOMES :
genetic choice between Sperm or egg (1 pair)
wrapping up the e a
geneexpressionby


·
·
· vani,
ega
9) nolactoserepressorproteinbopmesnotahcripinSt
high glucose : no transcription (high glucose - low CAMP)
modifyhistonestomake
<
e
a


· one inactive X E
(DNA methylation)

MoMbipwichbinds topromote
low glucose :
> or modify DNA

SEX-LINKED GENES :
Only on X or Y chromosome

BARR BODIES : Inactive , very condensed (by histones) X chroms in XX cells

VARIATION WIOUT CELL DIVISION random choice of which to inactivate creates epigenic mosaic
Abtween homologous chromosome
>




·
test cross:x apart
A
TRANSFORMATION Specialized channels nemizygous for one other X
:
) act as or
*
take up DNA from outside then get
,
INCOMPLETE (CO) DOMINANCE :
Heterozygote has phenotype that is intermediate between that of homozygotes
incorporated into chromosome
2 / ratio (See both traits in hetero blood type
> neither is dominant <1 : : Tex :

transcents
CONJUGATION : pili pass plasmids -




POLYGENIC TRAIT :
one trait influenced by multiple genes leads to complex outcomes
fragments from chromosomes
.




(quantitative traits caused by polygenic inheritance (eX : skin color) TWIN TEST : is concordance higher in identical (same genes )
or fraternal (different genes) twins ?




u
EPISTASIS :
complex interactions between genes straits
&moreunidenticalgenetica both twins
7 A epistatic/dominates over BgC (example)


GENE DOSAGE


NEW MUTATIONS
GERM line mutations : inherited ; from the cells that make gametes

SOMATIC mutations : not passed to offspring ; only affect adult



EXPANDING MUTATIONS :
get worse in successive mutations

trinucleotide repeat


NONDISJUNCTION :the failure of chromosomes to separate during meiosis

disjunction = chromosome separation




dosageproblemwrongnumberofchromosome ingametea chromatics


< trisomy : 3 of one chromosome (monosomy : 1 of one chromosome




I I I
· 13 ,
18 , 21 (autism) Survive after birth · none survive after birth

function ? they function in cells ?
X chromosome trisomy & monosomy don't really effect the cell
types of RNA Where do they How do
bodies
> no matter how many XS a cell has , only one is active and the others form Barr


a
1 NHERITANCE BY ORGANELLES
mitochondria s chloroplasts have their own circular DNA
mRNA
(messenger) prokamocytoplasmarregemeinffompranc MRNA is processed before leaving


-pinbinamssonmaternallyonlynotfrom e is
+ RNA
cytoplasm bringaminacidstoribosome duringaanticodon
eugenics : "improvement" of humans through selective reproduction (dark history (transfer)
forms structural s catalytical core of ribosomes ,
URNA
atlyzespeptidebondformation
facilitation
cribosomal) ribosomes



SURNA
nucleus /removeintronmmRNA parto
Splice xns

(small nuclear)
-

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