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92 Cards in this Set
- Front
- Back
Not all is transcribed. non coding (Junk) is just as important. The polymorphisms are in the noncoding regions. Non code shows where protein goes etc and can be lost in disease. |
polymorphisms |
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Why could gene A make more DNA than gene B? |
The coding regions |
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RNA helix has diff geometry and has a hole down the middle and is ______ than DNA. |
Narrower |
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The RNA backbone has ribose and the 2 prime carbon with hydroxyl group which gives it . A-U has two hydrogen bonds. |
its diff shape |
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What can cause nonconventional binding? |
RNA can form hairpin, and single stranded loop |
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Loss of function and gain of function for protein: genetically you can manipulate the protein. Manipulate genes for knock out, using _______ to silence genes. |
mRNA |
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RNA chain is displaced does not remain __________ to DNA. Only ____________ is transcribed : RNA are single stranded |
hydrogen-bonded one strand |
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complementary base pairing happens during? |
transcription |
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Many RNA copies can be made from ______ gene in short time.Average gene of ______ nucleotides ~ 50 sec |
same 1500 |
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Transcripts: fine threads (rRNA) : used as components ofRibosomes they do not?? The goal is to make? |
translate to proteins. ribosomes |
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RNA: some will make proteins and some will be _______ |
regulators |
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tRNA: |
Connects mRNA and the amino acids used to make the protein orm adaptors that select a.a. and hold them in place on ribosomes for incorporation into proteins |
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rRNA |
rRNA form ribosomes on which mRNA is translated form the core of the ribosomes structure. (Ribosome:structure used to form RNA) catalyzes protein synthesis. |
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mRNA |
codes for proteins |
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miRNA |
regulates gene expression |
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Other coding RNA's |
RNA splicing, telomere maintenance, gene regulation |
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Once transcription begins |
sigma factor is released. |
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Chain elongation continues until . |
polymeraseencounters a termination signal in DNA |
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Enzyme halts and releases bothRNA polymerase then |
DNA template andnewly made mRNA. re-associates with sigma factor |
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RNA polymerase contains called sigma factor that |
recognizes the promoter on DNA. |
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Signals in sequence of gene tells |
RNA polymerase where to start and stop transcription |
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Promoter ________________. _____________ binds and recognizes start sequence. Polymerase clamps and starts copying it, and when it senses the stop signal it stops. The process uses a______________protein. The cofactor is the sigma factor and it recognize_______________. The polymerase finds the sigma factor. When transcription starts the cofacter comes off and it will be __________________ |
regulates gene expression Polymerase integral (cofactor) s where the promoter is recycled and used for another time. |
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Promoters and terminators have specific nucleotide sequencesthat are recognized by |
RNA polymerase |
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Start site is first nucleotide transcribed |
designated +1 |
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________________ orients the polymerase and determines direction of transcription. |
Asymmetry of promotor |
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All bacterial promoters contain DNA sequences at |
-10 and -35 |
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DNA is double stranded: promoter could direct synthesis of However promoter is asymmetrical and binds |
2 different RNA transcript one left to right & other rightto left. polymerase in only one orientation. |
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Once positioned, RNA polymerase has only one choice to transcript appropriate DNA strand only in |
5’ to 3’ direction |
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bacteria have ___ RNA polymerase.Eukaryotic cells have ____ RNA polymerase |
one, three |
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RNA polymerase 1 |
most rRNA genes |
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RNA polymerase 2 |
all protein coding genes, noncoding RNA (splicesomes), miRNA genes |
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RNA polymerase 3 |
tRNA (not coding), 5s rRNA genes, genes for other small RNAs |
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TATA box is recognized by _____. The sequence promotes the binding of the next transcription factor ______. |
TFIID TFIID |
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TFIIH TFIIH also phosphorylates |
pries apart the double helix at transcription start point using energy of ATP hydrolysis exposing template strand. RNA polymerase II to allowtranscription: releases enzymes from transcription factors. |
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Site of phosphorylation is a |
long polypeptide ‘tail’ that extends from polymerase molecule. |
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Once transcription begins most general factors are released from _____ |
DNA |
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TATA-binding protein (TBP) |
binds to TATA box sequence and distorts the DNA |
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TBP Sits on top and attaches to TATA to change |
the DNA structure and then will attract other transcription factors when unwound. |
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TBP is subunit of
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TFIID that recognizes & binds TATA box sequence (letters).
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Unique DNA bending caused by TBP |
two kinks in double helix separated by unwound DNA helps attract other transcription factors. |
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TBP is a |
single polypeptide chain folded into 2 similar domains (blue & green). Sits on top of DNA helix like saddle |
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The initiation of transcription is the most common way organisms |
control gene expression. |
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Eukaryotic mRNA is processed in the |
nucleus |
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Eukaryotic RNAs must be processed in the _________ and exported to ________ |
nucleus, cytoplasm |
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Transcription occurs in ________, translation occurs in _________. This export of RNA occurs via ________________. |
nucleus, cytoplasm, pores in the nuclear envelope |
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Prior to nuclear export, _________________. |
RNA processing occurs Occurs as RNA is being made. Synthesizing RNA and proofreads at same time. (not in bacteria) |
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RNA processing occurs as _______________, it is processed. The tail is phosphorylated.Machinery sits on the “tail” of the eukaryotic _________________. There are variations, it is not conservedDifferent types of processing occurs depending of what type of RNA is being made. |
RNA is being made RNA polymerase |
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Eukaryotic mRNA processing |
Involves adding 5’-caps and 3’-polyadenylation tails (poly-A tails) and splicing. |
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5’-caps and poly-A tails do? |
Increase stability of RNA.Identifies the molecule as mRNA.Marks the mRNA as being complete. |
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Usually gets trimmed back first before few hundred “a” added. |
Poly A tail |
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Phosphorylation of RNA polymerase II allows |
RNA processing proteins to assemble on its tail |
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Polymerase transcribes |
DNA into RNA. |
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Polymerase also carries |
RNA-processing proteins that act on newly formed RNA. |
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Proteins bind to RNA polymerase tail when |
it is phosphorylated late in the process oftranscription initiation. |
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Capping, polyadenylation, and splicingare |
modification made to RNA during thisprocess. |
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mRNA are modified by _________. Once it is methylated_____________. |
capping and polyadenylation It is viewed as processed RNA |
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Ends modified by addition of cap at _________ & cleavageof _______________ & addition of _________________.The unusual 5’ to 5’ linkage of 7-methyl G to remainderof RNA.In eukaryotes cap contain additional modification2’-hydroxyl group on 2nd ribose sugar is methylated. |
5’ end, primary transcript, poly-A tail at 3’ end |
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In Eukaryotes, Protein-Coding Genes Are Interrupted by |
Noncoding Sequences Called Introns |
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Eukaryotic mRNA processing also involves |
RNA splicing |
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Eukaryotic genes are often interrupted by _____________ |
noncoding sequences (introns). So they are spliced out |
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Exons-Introns- |
(coding) expressed sequences (noncoding) intervening/nonexpressed sequences |
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Bacterial gene consists of Eukaryotic genes (Exons) are |
single stretch of uninterrupted nucleotide sequence that encodes the a.a. sequence of a protein. are interrupted by noncoding sequences (Introns).Exons are shorter; Introns are longer : can be up to 10,000 nucleotides.Some no introns, others few, most have many. |
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β-globin gene encodes Factor VIII gene encodes |
one of the subunits of oxygen carrying protein hemoglobin : contains 3 exons. a protein Factor VIII that functions in clotting pathway : contains 26 exons. |
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Introns Are Removed From _____________ by RNA Splicing |
pre-mRNAs |
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Only nucleotides shown are required to remove an intron. These sequences are recognized by ___________________________ which cleave RNA intron-exon borders and covalently link exon sequence together. |
small nuclear ribonucleoproteins (snRNPs) |
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A lariat structure forms and the hydroxyl group |
will bind to 5 prime side |
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An intron forms a |
branched structure during splicing |
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1. Branch point adenine in intron 2. The cut 5’ end of intron becomes covalently linked 2. The cut 5’ end of intron becomes covalently linked 3. 3’-OH end of exon sequence then 4. Forms continuous coding sequence & releases introns in form of |
1. attacks the 5’ splice site and cuts sugar-phosphate backbone of RNA. 2: to 2’-OH group of ribose of A to form branched structure. 3. reacts with start of next exon sequence, joining the two exons together. 4.lariat structure which is degraded. |
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snRNPs come together and assemble to the site that shows THe 5 core snRNPs are _____________ |
the beginning and end of splicing. U1, U2, U4, U5 and U6. |
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Alternative splicing leads to RNA splicing enables |
greater protein diversity from single gene.Can produce distinct proteins. increases coding potential of their genomes. |
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Alternative splicing, so ________________ The alternative splicing comes from ______________________ allowing more diversity of proteins for survivability. Creates different functions. ex: |
not every RNA is spliced the same way. alpha tropomyosin gene Coiled-coil Muscle contraction |
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The Nuclear Pore Complex |
recognizes and exports only completed mRNAs |
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Nuclear Pore Complex: Transport out of nucleus is _________Nuclear pore complex recognizes _______________ only.Must be bound to appropriate proteins: signal correct.Includes ______________________________ |
highly selective. completed mRNAs polyA binding proteins, cap-binding complex, completed RNA splice protein (EJC: exon junction complex). |
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(Nuclear Pore complex) Waste mRNAs digested by _________ and then reused for transcription.Sequences in the __________ help determine how much protein synthesized. Stability of mRNA:________mRNA with long lifetimes (3’UTR) high levels of proteins:________. |
RNAse, 3’-UTR, 3’-UTR, β-globin |
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NPC: mRNA binds to proteins __________ to leave the nucleus |
Poly A tail |
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Eventually all mRNA molecules are degraded into nucleotides via ________ in the ________. Sequences in the _________ help determine stability.
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RNases, cytosol, 3’-UTR |
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The Earliest Cells May Have Had ________ in Their Genes |
Introns |
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RNA linear polymer of 4 different nucleotides: so how many possibilities? combinations of three nucleotides: ex ex |
64, AAA, AUA, AUG etc. |
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tRNA molecules are adaptors that link _________ _________ |
a.a. to codons |
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Anticodon recognizes __________________ to start ______________ |
complementary strand, replication |
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More than________ for many AAs.Some tRNAs recognize > 1 codon, this is called theUnpaired nucleotides: ____________Anticodon bind complementary codon in __________ |
1 tRNA, wobble phenomenon, anticodon, mRNA |
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Genetic code is translated by means |
of 2 adaptors that act on one another |
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Aminoacyl-tRNA synthetase |
couples a particular a.a. to its corresponding tRNA : Charging. |
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Anticodon of tRNA forms |
base pair with codon on mRNA: Charging. |
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There are 20 synthetases that |
catalyze amino acid to tRNA |
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Synthtase catalyzed reactions attach _________ uses ATP later used to link _______________ |
a.a. to tRNA , a.a. to polypeptide chain. |
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the mRNA message is decoded by |
ribosomes |
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RNA message is decoded on |
Ribosomes |
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Protein is synthesized in the |
ER |
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80 ribosomal proteins; several RNA molecules (ribosomal RNA) form ribosome.Eukaryotic and prokaryotic ribosome are very different.___________________ form ribosome.Two subunits come together on ____________, near ________ to begin protein synthesis.As mRNA moves through it, ribosome translates nucleotide sequence into a.a. sequence one codon at a time using _________ |
One large and one small subunit: together form ribosome. mRNA molecule, 5’end, tRNAs as adaptors. |
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A ribosome is a large complex of _______ and more than ______ proteins |
4 RNAs, 80 |
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Each ribosome has __ binding site for mRNA and ______ binding sites for tRNA
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one, three (EPA) |