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144 Cards in this Set
- Front
- Back
Protein malnutrition |
Kwashiorkor |
|
will see in kwashiorkor patient |
"MEALS": |
|
energy malnutrition |
Marasmus |
|
see in Marasmus patient |
tissue/msucle wasting |
|
nucleosome core |
H2A, H2B, H3, H4 |
|
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 - |
|
transciptionally active: heterochromatin or euchromatin |
euchromatin - |
|
anti-histone ab |
drug-induced sle |
|
purines |
A,G |
|
pyrimidines |
C,U,T |
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# 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 |
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A-T bonds |
A=T, 2 H bonds |
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amino acids necessary for purine synthesis |
Gly |
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nucleotide = |
base pair + ribose + phosphate |
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subsitute a purine for a purine or pyrimidine for a pyrimidine |
transition |
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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 |
|
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 |
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mutation results in misreading of all nucleotides downstream |
frameshift |
|
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 |
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 |
|
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 |
|
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 |
|
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) |
|
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 |
|
location of rna processing |
at nucleus |
|
process after transcription |
rna processing - |
|
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 |
|
end that is capped |
5' |
|
end with poly-a tail |
3' |
|
function of poly-a tail |
protects genes from degradation |
|
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 |
|
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 |
|
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 |
|
Termination |
stop codon enters a site. complete protein is released from ribosome. protein is dislocated. empty trna occupies E site |
|
posttranslational modifications (3) |
trimming |
|
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 |