Chapter 11 Flashcards

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1
Q

What does the central dogma explain?

What about viruses?

Are they reversible?

A

Genetic information usually flows from
DNA to DNA during its transmission from generation to generation and from DNA to protein during its phenotypic expression in an organism

During the replication of RNA viruses, information is also transmitted from RNA to RNA and RNA to DNA during the conversion of the genomes of RNA tumor viruses to their DNA proviral forms.

DNA to RNA is sometimes reversible
RNA to protein is always irreversible

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1
Q

What are the two steps involved in DNA being processed into proteins?

A
  1. Transcription (DNA to RNA)
  2. Translation (RNA to Proteins)
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2
Q

Give a quick overview of what happens in transcription and translation.

A

Transcription:
-One strand of DNA in a gene is used as
a template to synthesize a complementary strand of RNA, called the gene transcript

Translation:
-The sequence of nucleotides in the RNA
transcript is converted into the sequence of amino acids in the polypeptide gene product.

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3
Q

What is the difference in the product of transcription in prokaryotes and eukaryotes?

A

Prokaryotes:
-The product of transcription, the primary
transcript, usually is equivalent to the mRNA molecule.

Eukaryotes:
-Primary transcripts often must be processed by the excision of specific sequences and the modification of both termini before they can be translated. Thus, the primary transcripts usually are precursors to mRNAs and, as such, are called pre-mRNAs.

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4
Q

What are the 5 different types of RNA molecules and what are their jobs?

A
  1. mRNA:
    -The intermediaries that carry genetic info from DNA to the ribosomes where proteins are synthesized
  2. tRNA:
    -Small RNA molecules that function as adaptors between amino acids and the codons in mRNA during translation
  3. rRNA:
    -Structural and catalytic components of the ribosomes, the machines that translate nucleotide sequences of mRNAs into amino acid sequences of polypeptides
  4. snRNA:
    -Structural components of spliceosomes, the nuclear organelles that excise introns from gene transcripts
  5. miRNA:
    -Short single-stranded RNAs that block the expression of complementary or partially complementary mRNAs by either causing their degradation or repressing their translation.
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5
Q

What RNA molecules are not translated?

A

tRNA
rRNA
snRNA
miRNA

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6
Q

How is the produced RNA molecule oriented to the DNA template strand?

A

It will be complementary and antiparallel to the DNA template strand and identical, except that
uridine replace thymidines, to the DNA nontemplate strand

mRNA molecules are coding strands of RNA and are also called sense strands of RNA because their nucleotide sequences “make sense” in that they specify sequences of amino acids in the protein gene products.

An RNA molecule that is complementary to an mRNA is referred to as antisense RNA

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7
Q

RNA synthesis occurs by a mechanism that is similar to that of DNA synthesis except for a few differences.

What are these differences?

A
  1. The precursors are ribonucleoside triphosphates rather than deoxyribonucleoside triphosphates,
  2. Only one strand of DNA is used as a template for the synthesis of a complementary RNA chain in any given region.
  3. RNA chains can be initiated de novo, without any requirement for a preexisting
    primer strand
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8
Q

How does the initiation of RNA molecules begin?

A

RNA polymerases bind to specific nucleotide
sequences called promoters, and with the help of proteins called transcription factors, initiate the synthesis of RNA molecules at transcription start sites near the promoters

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9
Q

What is a transcription unit?

A

1.A segment of DNA that is transcribed to produce one RNA molecule

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10
Q

What are the 3 stages of transcription?

A
  1. Initiation of a new RNA chain
  2. Elongation of the chain
  3. Termination of transcription and release of the nascent RNA molecule
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11
Q

What are the three steps involved in the initiation of RNA chains in prokaryotes?

A
  1. Binding of the RNA polymerase holoenzyme to a promoter region in DNA
  2. The localized unwinding of the two strands of DNA by RNA polymerase, providing a
    template strand free to base-pair with incoming ribonucleotides
  3. The formation of phosphodiester bonds between the first few ribonucleotides in the nascent (new) RNA chain
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12
Q

What makes up the complete RNA polymerase molecule in prokaryotes?

What makes up the core enzyme?

What does each do?

What is the difference in function of the complete holoenzyme and the core enzyme?

A
  1. The complete RNA polymerase molecule, the holoenzyme, has the composition α2ββ′σ.
  2. α2ββ′ (no sigma)
  3. α:
    -Involved in the assembly of the tetrameric core (α2ββ′) of RNA polymerase.

β:
-Contains the ribonucleoside triphosphate binding site

β′:
-Harbors the DNA template-binding region.

σ:
-Involved only in the initiation of transcription; it plays no role in chain elongation

-To recognize and bind RNA polymerase to
the transcription initiation or promoter sites in DNA

4.The core enzyme (with no σ) will catalyze RNA synthesis from DNA templates in vitro (in dish), but, in so doing, it will initiate RNA chains at random sites on both strands of DNA.

In contrast, the holoenzyme (σ present)
initiates RNA chains in vitro (in dish) only at sites used in vivo (living subject).

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13
Q

By convention, the nucleotide pairs are numbered relative to the transcript initiation site (designated +1).

What do each indicate?

A

Base pairs preceding (before) the initiation site are given minus (−) prefixes (upstream)

Those following (after) the initiation site are given plus (+) prefixes. (downstream)

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14
Q

Within prokaryotes, what are the midpoints of the two conserved sequences and where do they occur?

A

The midpoints of the two conserved sequences occur at about 10 and 35 nucleotide pairs before the transcription-initiation site.

Thus they are called the −10 sequence and the −35 sequence, respectively.

They are consensus sequences

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15
Q

What are consensus sequences?

A

The nucleotide sequence that is present in
the majority of genetic signals or elements that perform a specific function

16
Q

How is the elongation of RNA chains carried out in a prokaryote?

A
  1. Elongation of RNA chains is catalyzed by the RNA polymerase core enzyme, after the release of the σ subunit.
  2. The covalent extension of RNA chains takes place within the transcription bubble,
    a locally unwound segment of DNA.
  3. The RNA polymerase molecule contains both DNA unwinding and DNA rewinding activities.
  4. RNA polymerase continuously unwinds the DNA double helix ahead of the polymerization site and rewinds the complementary DNA strands behind the polymerization site as it moves along the double helix.

5.The nascent RNA chain is displaced from the DNA template strand as RNA polymerase moves along the DNA molecule.

17
Q

How is the stability of the transcription complex maintained in prokaryotes?

A

The stability of the transcription complex is maintained primarily by the binding of the DNA and the growing RNA chain to RNA pol, rather than by the basepairing between the template strand of DNA and the nascent RNA.

18
Q

How is the termination of RNA chains initiated?

What are the two types of transcription terminators in E. coli?

Explain the difference between the two?

A
  1. When RNA polymerase encounters a termination signal
  2. Rho Dependent:
    -Results in termination only in the presence of a protein called rho (ρ).

Rho Independent
-Results in the termination of transcription without the involvement of rho

19
Q

Explain the difference between Rho Independent and Rho Dependent.

A

Rho Dependent:
-Similar to that of rho-independent termination in that both involve the formation of a hydrogen-bonded hairpin structure upstream from the site of termination. In both cases, these hairpins impede the movement of RNA polymerase, causing it to pause. However, rho-dependent terminators contain two additional sequences: a 50–90 nucleotide-pair sequence upstream from the inverted repeat sequences that produces an RNA strand with many C’s but few G’s, which therefore forms no hairpins or other secondary structures, and a sequence specifying a rho protein binding site called rut (for rho utilization) near the 3′ end of the transcript. Rho protein binds to the rut sequence in the transcript and moves 5′ to 3′ following RNA polymerase. When polymerase encounters the hairpin, it pauses, allowing rho to catch up, pass through the hairpin, and use its helicase activity to unwind the DNA/RNA base-pairing at the terminus and release the RNA transcript.

Rho Independent
-Contains a GC-rich region followed by six or more AT base pairs, with the A’s present in the
template strand.

-The nucleotide sequence of the GC-rich region contains inverted repeats—sequences of nucleotides in each DNA strand that are inverted and complementary.

-When transcribed, these inverted repeat regions produce single-stranded RNA sequences that can base-pair and form hairpin structures.

-The RNA hairpin structures form immediately after the synthesis of the participating regions of the RNA chain and retard the movement of
RNA polymerase molecules along the DNA, causing pauses in chain extension.

-Since AU base-pairing is weak, requiring less energy to separate the bases than any
of the other standard base pairs, the run of U’s after the hairpin region facilitates the release of the newly synthesized RNA chains from the DNA template when the hairpin structure causes RNA polymerase to pause at this site