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genetic information directs the synthesis
of proteins
DNA is the genetic material within
the nucleus
replication creates new copies of
DNA
transcription creates an RNA using
DNA information
translation creates a protein using
RNA information
The RNA intermediate allows organism to
amplify the gene expression and regulate gene expression
RNA chemical structure contains what ribose
sugar
deoxyribose is a sugar used in
DNA by the presence of an additional -OH group
RNA contains the base uracil, which differs from thymine, by the absence of a
-CH3 group
The chemical linkage between nucleotides in RNA—a phosphodiester bond—is the same as that in
DNA
RNA molecules can fold into specific structures that are held together by what bond?
hydrogen bonds between different bases
RNA is largely single-stranded, but it often contains
short stretches of nucleotides that can base-pair with complementary sequences found elsewhere on the same molecule
base pair interactions allow an RNA molecule to fold into a
3D structure that is determined by its sequence of nucleotide
Transcription of a gene produces an
RNA complementary to one strand of DNA
the bottom strand of DNA is called the
template strand because it is used to guide the synthesis of the RNA molecule
the non template strand is sometimes called the
coding strand because its sequence is equivalent to the RNA product
An RNA molecule is usually depicted by
the 5’ end and moving to the left
type of RNA produced in cells
messenger RNA, ribsosomal RNA, MicroRNAs, Transfer RNA, Small interfering RNA’s, long non coding RNAs
what does messenger RNA do
Code for proteins
what does Ribosomal RNA do?
form the core of the ribosome’s structure and catalyze protein synthesis
what does mircoRNA do?
regulate gene expression
what does Transfer RNAs do?
serve as adaptors between mRNA and amino acids during protein synthesis
what does small interfering RNA do?
provide protection from viruses and proliferating transposable elements
what does long noncoding RNAs do?
acts as scaffolds and serve other diverse functions
what does other noncoding RNA do?
Used in RNA splicing, gene regulation, telomere maintenance, and other processes
The complimentary messenger RNA strand that would be synthesized from the DNA base sequence of CTGAC would be...?
GACUG
What are the 3 polymerases in eukaryotic cells
DNA polymerase 1, DNA polymerase 2, DNA polymerse 3
what genes do DNA polymerase 1 transcribe
Most rRNA genes
what genes do DNA polymerase 2 transcribe
all protein coding genes, miRNA genes, plus genes for other noncoding RNA
what genes do DNA polymerase 3 transcribe
tRNA genes, 5S rRNA gene, genes for many other small RNAs
A transcription unit is defined as
that region of DNA that includes the signals for transcription initiation, elongation, and termination
DNA-dependent RNA polymerase is the enzyme responsible for the
polymerization of ribonucleotides into a sequence complementary to the template strand of the gene
The enzyme; polymerase attaches at a specific site
the promoter on the template strand
enzyme attaching to the promoter site is then followed by
initiation of RNA synthesis at the starting point, and the process continues until a termination sequence is reached.
Signals in the DNA Tell RNA Polymerase
where to start and stop transcription
promoter in transcription sites where RNA polymerase
binds and start transcription
terminator is the
site where transcription ends
sigma factor in bacteria recruits
RNA polymerase
bacterial RNA polymerase contains a subunit called
sigma factor
sigma factor recognizes
the promoter of the gene
Once transcription has begun, sigma factor is
released, and the polymerase moves forward and continues synthesizing the RNA
. Elongation continues until the polymerase encounters a sequence in the gene called the
terminator
After transcribing this sequence into RNA, the enzyme
halts and releases both the DNA template and the newly made RNA transcript
The polymerase then reassociates with a free sigma factor and searches for another promoter to
begin the process again
All bacterial promoters contain DNA sequences at positions
-10 and -35
. The numbers above the DNA indicate the positions of nucleotides counting from the first nucleotide transcribed, which is designated
+1
transcription begins at the _ , proceeds through the _ and ends at the _
promoter, coding regions, and terminator
In eukaryotes, the core promoter of a transcription unit generally includes:
TATA box, initiator
On an individual chromosome, some genes are transcribed using
one DNA strand as a template and others are transcribed from the other DNA strand
RNA polymerase always moves in the
3’-5’ direction with respect to the template DNA strand
the strand that will serve as the template is determined by the
polarity of the promoter sequences at the beginning of each gene
To begin transcription, eukaryotic RNA polymerase II requires
a set of general transcription factors.
Most eukaryotic promoters contain a DNA sequence called the
TATA box
The TATA box is recognized by a subunit of the
the general transcription factor TFIID, called the TATA-binding protein (TBP)
The binding of TFIID, which distorts the DNA, enables
the adjacent binding of TFIIB.
the rest of the genreal transcription factors then assemble at the
promoter, using energy provided by ATP hydrolysis
TFIIH opens the
double helix at the transcription start point, exposing the template strand of the gene
TFIIH also phosphorylates RNA polymerase II, releasing its
attachment to the general transcription factors and allowing it to begin transcription
The site of phosphorylation is a long polypeptide “tail” that extends from the
polymerase
Once the polymerase moves away from the promoter, most of the general transcription factors are released
form the DNA; the exception is TFIID
A set of elongation factors assemble on the actively transcribing
RNA polymerase to facilitase access to the DNA
Which transcription factor is responsible for recognizing the TATA box during PIC assembly?
TBP (part of TFIID)
In Eukaryotes, Protein-coding Genes Are Interrupted by
noncoding sequences called introns
A bacterial gene consists of a single stretch of
uninterrupted nucleotide sequence that encodes the amino acid sequence of a protein
the protein-coding sequences of most eukaryotic genes (exons) are interrupted by
noncoding sequences
pre m-RNA is modified in 3 ways before exiting nucleus in eukaryotes
5’ capping: adding 7- methylguanosine
polyadenylation: adding AAAAAAAAA
splicing: intron removal
processing of messenger RNA 5’ cap
a methylguanosine “cap: is added to the 5’ end of the transcript (5’-5’ triphosphate bridge)
significance: prevent digestion, aids in export from nucleus, aids in initiation of translation
eukaryotic mRNA molecules are modified by
capping and polyadenylation
A eukaryotic mRNA has a cap at the
5’ end
A eukaryotic mRNA has a tail at the
3’ end
The noncoding portion at the 5′ end is called the
5′ untranslated region, or 5′ UTR, and that at the 3′ end is called the 3′ UTR.
Which of the following proteins is deposited near exon–exon junctions after splicing and is important for nonsense-mediated decay (NMD)?
Exon Junction Complex (EJC)
if you wanted to extract all mRNAs from the total pool of RNA, which characteristic of mRNA can be used?
mRNA poly-A-tail
introns
non coding regions, need to be removed before mRNA exist the nucleus
Exons
coding regions
The special sequences are recognized primarily by
small nuclear ribonucleoproteins (snRNPs), which direct the cleavage of the RNA at the intron–exon borders and catalyze the covalent linkage of the exon sequences.
Special nucleotide sequences in a pre-mRNA transcript signal the
beginning and the end of an intron
Splicing is carried out by a collection of RNA–protein complexes called
snRNPs
In the first steps of splicing, U1 recognizes the
5’ splice site
U2 recognizes the
lariat branch-point site through complementary base-pairing
U6 snRNPs will
then “double-checks” the 5′ splice site by displacing U1 and base-pairing with the same intron sequence itself. This “rereading” step improves the accuracy of splicing by confirming the 5′ splice site before carrying out the splicing reaction
conformational changes in U2 and U6—triggered by the
hydrolysis of ATP by spliceosomal proteins
Once the splicing reactions have occurred
the spliceosome deposits a group of RNA-binding proteins, known as the exon junction complex, on the mRNA to mark the splice site as successfully completed
During the catalytic activation of the spliceosome, which rearrangement is essential?
U1 is displaced from the 5′ splice site by U6
RNAi is a natural biological process that regulates gene expression by
“interfering” with messenger RNA (mRNA), which carries DNA's instructions for making new proteins.
Medicines use RNA interference (RNAi) to
“silence” or turn off the production of specific genes that cause disease or that contribute to disease such as cardiovascular diseases, viral infections, and cancer.