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144 Cards in this Set

  • Front
  • Back

Protein malnutrition

Kwashiorkor

will see in kwashiorkor patient

"MEALS":
malabsorption
edema
anemia
liver (fatty)
skin lesions
*clinical picture = small child with swollen belly

energy malnutrition

Marasmus

see in Marasmus patient

tissue/msucle wasting
loss of subcutaneous fat
variable edema

nucleosome core

H2A, H2B, H3, H4
2 each of these + charged histones

charge of dna

-

nucleosome bead

- charged DNA loops twice around nucleosome core

only histone not in nucleosome core

H1

less condensed: heterochromatin or euchromatin

euchromatin -
heterochromatin is more condensed

transciptionally active: heterochromatin or euchromatin

euchromatin -
heterochromatin is transcriptionally inactive

anti-histone ab

drug-induced sle

purines

A,G
"pure as gold"

pyrimidines

C,U,T
"cut the py"

# of rings of purines

2

# of rings of pyrimidines

1

nucleotide with a ketone

Guanine

nucleotide with a methyl group

thymine

formation of uracil

from deamination of cytosine

unique nucleotide to rna

uracil

unique nucleotide to dna

thymine

nucleotide bond

3'-5' phosphodiester bond

pairs with highest melting point

G-C
with 3 H bonds

A-T bonds

A=T, 2 H bonds

amino acids necessary for purine synthesis

Gly
Asp
Gln

nucleotide =

base pair + ribose + phosphate

subsitute a purine for a purine or pyrimidine for a pyrimidine

transition

subsitute a purine for a pyrimidine or vise versa

transversion

each codon specifies only one amino acid

unambiguous

more than one codon may code for the same amino acid

degenerate/redundant

a.a. encoded by only 1 codon

methionine

read from a fixed starting point as a continuous sequence of bases

commaless, nonoverlapping

may not be commaless or nonoverlapping

some viruses

genetic code is conserved through evolution

universal

exceptions to being UNIVERSAL (4)

mitochondria
archaebacteria
mycoplasma
some yeasts
*universal means genetic code is conserved throughout evolution

mutation results in same aa

silent

serverity of damage of mutations: silent, nonsense, missense

nonsense > missense > silent

mutation results in changed aa

missense

mutation results in changed aa that is similar in chemical structure to mutated aa

conservative

mutation results in early stop codon

nonsense

mutation results in misreading of all nucleotides downstream

frameshift
*causes early disease

what mutation often results in a truncated protein

frameshift

where replication beigins in eukaryotes

A-T rich base pairs

nascent strand

strand to be replicated

daughter strand

new strand to be made as a result of replication

multiple origins of replication: eukaryote or prokaryote

eukaryote

single origin of replication: eukaryote or prokaryote

prokaryote

continuous dna synthesis on which strand

leading

discontinuous dna synthesis on which strand

lagging (ogazaki)

creates nicks in helix to relieve supercoils in dna replication

dna topoisomerase

denatures A-T bonds at beginning of dna replication

dna-a

unwinds dna (breaks helix)

helicase

phase of mitosis where dna replication occurs

S phase

enzyme of dna replication that makes an rna primer on which dnapIII can initiate replication

primase

5'->3' synthesis with
3'->5' exonuclease
enzyme in dna replication

dnapIII

enzyme that "proofreads" in dna synthesis

exonuclease

dna synthesis enzyme that degrades RNA primer and replaces with correct dna

dnapI

dna polymerase uses this to excise primers

5'->3' exonuclease

seals dna in dna synthesis

dna ligase

which enzyme forms the replication fork

helicase

stabilizes unwound helix

SSB and DNA topoisomerase (creates nick in helix to relieve supercoils)

steps in dna replication

1. helicase unwinds
stabilized by ssb and
dna topoisomerase
2. leading strand synthesized continuously via DNAPIII
3. lagging strand synthesized discontinuously in ogasaki fragments
4. dnapI removes rna primer and replaces with correct dna
5. dna ligase seals break at ogasaki fragments to make continuous

5' end of dna

with phosphate group

3' end of dna

with hydroxyl group

dna stabilization

via H bonds and hydrophobic interactions

diseases with imparied dna repair (5)

1. ataxia-telangiectasia
2. xeroderma pigmentosa
3. fanconi anemia
4. bloom syndrome
5. hnpcc

specific endonucleases release the oligonucleotide-containing damaged bases; while dna polymerase and ligase fill and reseal the gap, respectively

nucleotide excision repair

mutated nucleotide excision repair

xeroderma pigmentosa

dry skin with melanoma and other ca's; defective dna repair

xeroderma pigmentosa

glycosylases recognize and remove damaged bases, AP endonuclease cuts dna at apyrimidinic site, empty sugar is removed, and the gap is filled and resealed

base excision repair

unmethylated, newly synthesized string is recognized, mismatched nucleotides are removed, and the gap is filled and resealed

mismatch repair

mutation in hereditary nonpolyposis colon cancer

mismatch repair

brings together 2 ends of dna fragments

nonhomologous end joining

direction of synthesis

5' to 3'

largest rna

mrna

most abundant rna

rrna

smallest rna

trna

rna polymerase I

rrna

rna polymerase II

mrna

rna polymerase III

trna

B,B,alpha

zinc fingers

opens dna at promoter site in transcription

rna polymerase II

inhibits rna polymerase

alpha-amantin

source of alpha-amantin

cap mushrooms

mRna initiation codons

AUG
GUC (rarely)

codes for methionine in eukaryotes

AUG - start codon

start codon in prokaryotes codes for....

formyl-methionine (f-met)

mrna stop codons

UGA, UAA, UAG

binds promoter sequence of dna in transcription

rnapII

intial steps of transcription (3)

1. ranpII binds promoter sequence of dna (tata and caat box)
2. dna unwinds and forms "transcription bubble"
3. rnapII moves along "sense" strand, adding ribonucleotides to growing strand of mrna

site where rna polymerase and other transcription factors bind to DNA upstream from gene locus

promoter

site of promoter

A-T rich upstream sequence with TATA and CAAT box

mutation resulting in dramatic decline in amount of gene transcribed

promoter mutation

stretch of dna that alters gene expression by binding transcription factors

enhancer

operator

site where negative regulators (repressors) bind

contain the actual genetic information coding for a protein

exons

intervening noncoding segments of dna

introns

different exons can be combined to make unique proteins in different tissues

alternative splicing

primary transcript combines with snRNP's to form.....

spliceosome

intermediate formed to spliceosome

lariat-shaped intermediate that is released to remove introns and join 2 exons

steps in splicing (3)

1. primary transcript combines with snRNPs to form spliceosome
2. lariat-shaped intermediate is generated
3. lariat is released to remove introns and join 2 exons

location of rna processing

at nucleus

process after transcription

rna processing -
1. capping at 5' end
2. poly a tail at 3' end
3. splice out introns

capped and tailed transcript

mRNA

initial transcript before rna processing is called....

hnRNA (heterogeneous nuclear RNA)

only step of rna processing that does not occur at the nucleus (instead at the cytoplasm)

capping on 5' end

added during capping

7-methyl-G
add methyl group on c7
and add guanesine

end that is capped

5'

end with poly-a tail

3'

function of poly-a tail

protects genes from degradation
guides rna to 30s to read 3' end

how many A's in the poly-A tail

~200 A's added to 3' end

# of nucleotides in trna

75 - 90

cloverleaf shaped rna

trna

sequence at 3' end of trna

CCA

location of anticodon

in middle loop - opposite 3' end

end of amino acid covalent bond in trna

3' end of trna

attaches aa to 3' end of trna

aminoacyl-trna synthetase

scrutinizes aa before and after it binds to trna

aa-trna synthetase

if aa bound to trna is incorrect, bond is hydrolyzed by

synthetase (aa-trna synthetase)

aa-trna bond has this for formation of peptide bond

energy

mischarged trna

reads usual codon
interts wrong amino acid

ACC at 3' end of trna codes for......

Met

"wobble" position

3rd nucleotide of an mrna codon

says that accurate base pairing is required only in the first 2 nucleotide positions of an mRNA codon

"wobble" theory

3 main steps of protein synthesis

1. initiation
2. elongation
3. termination

location of protein synthesis

ribosome

occupies A site

trna of next aa to be added to the growing polypeptide

occupies P site

trna containing growing peptide chain

helps assemble the 30s ribosomeal subunit with the initiator tRNA

IF initiation factor

released when mrna and ribosomal subunit assemble with the complex

IF initiation factor

codon recognized by initiator trna

AUG

occurs during Initiation of protein synthesis

IF's help assemble the 30s ribosomal subunit with the initiator tRNA. then if's are released when mRNA and ribosomal subunit assemble with the complex

during elongation, aminoacyl trna binds to.....

A site

during elongation, catalyzes peptide bond formation, transfering growing polypeptide to amino acid in A site

peptidyl transferase

energy needed for tRNA activation

ATP (charging)

energy needed for tRNA translocation

GTP

ribosome advances 3 nucleotides toward 3' end of rna

during elongation, to move peptidyl RNA to p site

completed protein is released from ribosome when stop codon enters a site

TERMINATION step of protein synthesis

holds Empty tRNA as protein exits

E site

3 steps of elongation

1. aminoacyl tRNA binds A site
2. peptidyltransferase catalyzes peptide bond formation, transfers growing popypeptide to amino acid in A site
3. ribosome advances 3 nucleotides toward 3' end of RNA, moving peptidyl RNA to P site

Termination

stop codon enters a site. complete protein is released from ribosome. protein is dislocated. empty trna occupies E site

posttranslational modifications (3)

trimming
covalent alteration
proteasomal degradation

removal of N- or C- terminal pro-peptides from zymogens to generate mature proteins

trimming

phosphoylation, glycosylation, and hydroxylation

covalent alterations

attachment of ubiquitin to defective proteins to tag them for breakdown

proteosomal degradation