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19.7A: Transcription

  • Page ID
    3434
  • [ "article:topic", "transcription", "authorname:kaiserg" ]

    Skills to Develop

    1. Define the following:
      1. gene
      2. transcription
    2. Briefly describethe function of the following in terms of transcription:
      1. mRNA
      2. 3' end
      3. 5' end
      4. RNA polymerase
      5. phosphodiester bond
      6. promoter
      7. leader sequence
      8. coding sequence
      9. transcription terminator
      10. codon
    3. Define the following in terms of transcription in eukaryotic cells:
      1. introns
      2. exons
      3. precurser mRNA
      4. cap
      5. poly-A tail
      6. mature mRNA

    Transcription in Prokaryotic Cells

    Description: Messenger RNA (mRNA) is synthesized by complementary base pairing of ribonucleotides with deoxyribonucleotides to match a portion of one strand of DNA called a gene. Although genes are present on both strands of DNA, only one strand is transcribed for any given gene. Following transcription, 30S and 50S ribosomal subunits attach to the mRNA and tRNA inserts the correct amino acids which are subsequently joined to form a polypeptide or a protein through a process called translation.

    The enzyme RNA polymerase transcribes DNA. This enzyme initiates transcription, joins the RNA nucleotides together, and terminates transcription. To initiate transcription in bacteria, a variety of proteins called sigma factors bind to RNA polymerases. This complex can then bind to a specific sequence of usually about 40 deoxyribonucleotide bases called the promoter located along the DNA prior to the coding region of the gene. The promotor determines what region of the DNA and which strand of DNA will be transcribed into RNA.

    Figure 1: Chemical Structure of DNA. The phosphate of one deoxyribonucleotide binding to the 3' carbon of the deoxyribose of another forms the sugar-phosphate backbone of the DNA (the sides of the "ladder"). The hydrogen bonds between the complementary nucleotide bases (adenine-thymine; guanine-cytosine) form the rungs. Note the antiparallel nature of the DNA. One strand ends in a 5' phosphate and the other ends in a 3' hydroxyl.

    Like DNA polymerase, RNA polymerase can only synthesize nucleic acid in a 5' to 3' direction while "reading" a DNA template in the 3' to 5' direction. As mentioned earlier in this unit, the 3' end of a strand of nucleic acid has a hydroxyl (OH) group on the 3' carbon of the deoxyribose or ribose and is not linked to another nucleotide. The 5' end of that strand has a phosphate group attached to the 5' carbon of the sugar and is not linked to another nucleotide (Figure 1).

    Once the RNA polymerase/sigma factor complex recognizes the correct promoter, the sigma factor dissociate from the RNA polymerase and the enzyme begins to unwind the helix of the DNA creating a region of nonpaired deoxyribonucleotides that serve as a template for RNA synthesis (Figures 2 and 3).

         

    Figures 2 and 3: Unwinding of the DNA Helix by RNA Polymerase, Step-1. Once the RNA polymerase/sigma factor complex recognizes the correct promoter, the sigma factor dissociate from the RNA polymerase and the enzyme begins to unwind the helix of the DNA creating a region of nonpaired deoxyribonucleotides that serve as a template for RNA synthesis.

    Unwinding of the DNA Helix by RNA Polymerase

    Once the RNA polymerase/sigma factor complex recognizes the correct promoter, the sigma factor dissociate from the RNA polymerase and the enzyme begins to unwind the helix of the DNA creating a region of nonpaired deoxyribonucleotides that serve as a template for RNA synthesis

    While the RNA polymerase does not transcribe the promoter itself, it does transcribe a short noncoding leader sequence just prior to the coding sequence of the gene. The leader sequence is the portion of DNA that is transcribed into the ribosome-binding site of the mRNA (below under translation.) The coding sequence contains the actual message for protein synthesis.

    Fig. 4: Transcription of mRNA Complementary to a Gene. RNA is synthesized by complementary base pairing of free ribonucleotides with the deoxyribonucleotides of a gene. The enzyme responsible for transcription is RNA polymerase. (Xs represent the ribonucleotides for the ribosome binding site prior to the Start codon AUG.)

    Once the actual transcription begins, ribonucleotides containing 3 phosphate groups hydrogen bond through the process of complementary base pairing with the exposed deoxyribonucleotides on the unwound strand that is to be transcribed (Figure 4). The ribonucleotides are then covalently bonded together by phosphodiester bonds, the energy being supplied by the cleavage of two phosphate groups from the ribonucleotide triphosphate (Figure 5). (The phosphodiester bond refers to the phosphate on the 5'C of the newly inserted nucleotide covalently bonding to the 3'C of the last ribonucleotide in the mRNA chain.) The mRNA polymerizes at a rate of about 30 nucleotides per second.

    Fig. 5: Transcription of mRNA Complementary to DNA. RNA is synthesized by complementary base pairing of free ribonucleotides with the deoxyribonucleotides of a gene. The ribonucleotides are then covalently bonded together by phosphodiester bonds, the energy being supplied by the cleavage of two phosphate groups from the ribonucleotide triphosphate.The enzyme responsible for transcription is RNA polymerase (not shown here)

    As the RNA polymerase moves down the DNA, the previous stretch of DNA again pairs with its complementary strand. This process continues until the RNA polymerase encounters a "stop" signal or transcription terminator at the end of the gene. This causes the completed mRNA to drop off the gene.

    Transcription of mRNA Complementary to DNA

    Once the RNA polymerase/sigma factor complex recognizes the correct promoter, the sigma factor dissociate from the RNA polymerase and the enzyme begins to unwind the helix of the DNA creating a region of nonpaired deoxyribonucleotides that serve as a template for RNA synthesis. Transcription is under control of the enzyme RNA polymerase which is not shown here.

    Once the RNA polymerase moves beyond the promotor region, a new molecule of RNA polymerase can bind to the promotor and start a new round of transcription. In this way, a single gene can be transcribed multiple times.

    Transcription is summarized in Figs. 6 and 7.

    There are 22 amino acids that can be encoded by the genetic information carried on mRNA. The mRNA molecule is divided up into codons. A codon is a series of three consecutive mRNA bases coding for one specific amino acid. The various codons and the amino acids for which they code are shown in Table 16.8.1. There are 64 codons. One codon, AUG, also serves as a start codon to initiate translation, and three codons, UAG, UAA, and UGA, function as stop or nonsense codons to terminate translation. (Alternative start codons are different from the standard AUG codon and are found occasionally in both prokaryotes and eukaryotes.)

    Table 16.8.1: The Genetic Code - Codons
     
    U
    C
    A
    G
     
    U
    UUU = Phe
    UUC = Phe
    UUA = Leu
    UUG = Leu
    UCU = Ser
    UCC = Ser
    UCA = Ser
    UCG = Ser
    UAU = Tyr
    UAC = Tyr
    UAA = Stop
    UAG = Stop
    UGU = Cys
    UGC = Cys
    UGA = Stop
    UGG = Trp
    U
    C
    A
    G
    C
    CUU = Leu
    CUC = Leu
    CUA = Leu
    CUG = Leu
    CCU = Pro
    CCC = Pro
    CCA = Pro
    CCG = Pro
    CAU = His
    CAC = His
    CAA = Gln
    CAG = Gln
    CGU = Arg
    CGC = Arg
    CGA = Arg
    CGG = Arg
    U
    C
    A
    G
    A
    AUU = Ile
    AUC = Ile
    AUA = Ile
    AUG = Met
    ACU = Thr
    ACC = Thr
    ACA = Thr
    ACG = Thr
    AAU = Asn
    AAC = Asn
    AAA = Lys
    AAG = Lys
    AGU = Ser
    AGC = Ser
    AGA = Arg
    AGG = Arg
    U
    C
    A
    G
    G
    GUU = Val
    CUC = Val
    GUA = Val
    GUG = Val
    GCU = Ala
    GCC = Ala
    GCA = Ala
    GCG = Ala
    GAU = Asp
    GAC = Asp
    GAA = Glu
    GAG = Glu
    GGU = Gly
    GGC = Gly
    GGA = Gly
    GGG = Gly
    U
    C
    A
    G
      Phe = phenylalanine
    Leu = leucine
    Ile = isoleucine
    Met = methionine
    Val = valine
    Ser = serine
    Pro = proline
    Thr = threonine
    Ala = alanine
    Tyr = tyrosine
    His = histidine
    Gln = glutamine
    Asn = asparagine
    Lys = lysine
    Asp = aspartic acid
    Glu = glutamic acid
    Cys = cysteine
    Trp = tryptophan
    Arg = arginine
    Gly = glycine
     
    AUG = start codon, UAA, UAG, and UGA = stop (nonsense) codons

    In bacteria, a mRNA can be monocistronic or polycistronic. A monocistronic mRNA is a transcript of a single gene. A polycistronic mRNA carries a transcript of multiple genes, often involved in a single biochemical pathway. Groups of related genes that are transcribed together to form a polycistronic mRNA are known as operons. There are also specific genes along the DNA from which each of the different transfer RNAs (tRNAs) and the ribosomal RNAs (rRNAs) are transcribed.

    Most mRNAs in prokaryotes have a half-life on the order of a few minutes. Molecules of rRNA and tRNA, on the other hand, are much more stabile. Because rRNA and tRNA are highly folded molecules, unlike mRNA, they are much more resistant to degradation by ribonucleases. Once transcribed, the mRNA can be translated into protein.

    Transcription in Eukaryotic Cells

    Transcription is more complex in eukaryotic cells than in those that are prokaryotic. Activator proteins bind to genes known as enhancers which help determine which genes are switched on and speed up transcription. Repressor proteins bind to genes called silencers which interfere with activator proteins and slow down transcription. Coactivators, adapter molecules which coordinate signals from activator and repressor proteins, relay this information to basal factors which then position RNA polymerase at the start of the coding region of the gene to begin transcription.

    Once the actual transcription begins, ribonucleotides containing 3 phosphate groups form hydrogen bonds through the process of complementary base pairing with the exposed deoxyribonucleotides on the unwound strand that is to be transcribed. The ribonucleotides are then covalently bonded together by phosphodiester bonds, the energy being supplied by the cleavage of two phosphate groups from the ribonucleotide triphosphate (Figure 16.8B.5). (The phosphodiester bond refers to the phosphate on the 5'C of the newly inserted nucleotide covalently bonding to the 3'C of the last ribonucleotide in the mRNA chain.)

    Figure 18.6B.5: Transcription of mRNA Complementary to DNA. RNA is synthesized by complementary base pairing of free ribonucleotides with the deoxyribonucleotides of a gene. The ribonucleotides are then covalently bonded together by phosphodiester bonds, the energy being supplied by the cleavage of two phosphate groups from the ribonucleotide triphosphate.The enzyme responsible for transcription is RNA polymerase (not shown here)

    Unlike prokaryotes, most genes in higher eukaryotic cells contain large amounts - as much as 98% in the human genome - of regionscalled introns that are not part of the code for the final protein. These are interspersed among the coding regions or exons that actually code for the final protein.

    RNA polymerase copies both the exons and the introns to form what is called precursor mRNA or pre-mRNA. Early in transcription, a cap in the form of an unusual nucleotide, 7-methylguanylate, is added to the 5' end of the pre-mRNA. This cap helps ribosomes attach for translation. As transcription is nearly completed, a series of 100-250 adenine ribonucleotides called a poly-A tail is added to the 3' end of the pre-mRNA. This poly-A tail is thought to help transport the mRNA out of the nucleus and may stabilize the mRNA against degradation in the cytoplasm. After transcription of the precursor mRNA, non-protein coding regions (introns) are excised and coding regions (exons) are joined together by complexes of ribonucleoproteins called spliceosomes to produce what is termed mature mRNA as shown in Figure 9. This process is called RNA processing.

    Fig. 9: mRNA Processing in Eukaryotic Cells (Excision of Interons and Joining of Exons). During processing of the precursor mRNA, interons are excised and exons are joined together to produce a mature mRNA that can be translated into protein.

     

     

    The mature mRNA then passes through the pores in the nuclear membrane to be translated into protein by tRNA on eukaryotic 80S ribosomes (composed of 60S and 40S subunits) in a manner similar to prokaryotes.

    The mRNA molecule is divided up into codons. A codon is a series of three consecutive mRNA bases coding for one specific amino acid. The various codons and the amino acids for which they code are shown in Figure 8. There are 64 codons. One codon, AUG, also serves as a start codon to initiate translation, and three codons, UAG, UAA, and UGA, function as stop or nonsense codons to terminate translation. (Alternative start codons are different from the standard AUG codon and are found occasionally in both prokaryotes and eukaryotes.)

    In addition to the genes that are transcribed into mRNA to be translated into polypeptides and proteins, there are also specific genes in the DNA from which each of the different transfer RNAs (tRNAs) and the ribosomal RNAs (rRNAs) are transcribed.

    Once transcribed, the mRNA can be translated into protein.

    As mentioned above, introns make up the majority of DNA in higher eukaryotic cells and for decades was considered to be "junk DNA" accumulated over millions of years of evolution. Over recent years however, it has been discovered that much of this intergenic DNA, although it does not code for protein synthesis, is transcribed into functional molecules of RNA with names such as antisense RNA microRNA, and riboswitch RNA that play important roles in whether or not a protein is actually made.

    Antisense RNA is RNA transcribed off of the strand of DNA complementary to the one being transcribed into mRNA. In other words, it is an RNA molecule complementary to a mRNA and as such may complementary base pair with the mRNA and prevents it from being translated into protein.

    MicroRNA, often transcribed from intron DNA, folds over upon itself to resemble double-stranded RNA, a form of RNA produced by many viruses during their life cycle. Viral double-stranded RNA activates a host defense mechanism that degrades that viral RNA. The MicroRNA frequently binds to mRNA and tricks this defense mechanism into degrading that mRNA so it can not be translated into protein.

    Riboswitch RNA, often transcribed from introns, exists in an inactive form until a specific target chemical binds. The binding of the target chemical turns the riboswitch RNA to an active form that can be translated into a specific protein.

    Summary

    1. During protein synthesis, the order of nucleotide bases along a gene gets transcribed into a complementary strand of mRNA which is then translated by tRNA into the correct order of amino acids for that polypeptide or protein.
    2. The order of deoxyribonucleotide bases along the DNA determines the order of amino acids in the proteins, that is, its primary structure.
    3. Because certain amino acids can interact with other amino acids, the order of amino acids for each protein determines its final three-dimensional shape, which in turn determines the function of that protein.
    4. Messenger RNA (mRNA) is synthesized by complementary base pairing of ribonucleotides with deoxyribonucleotides to match a portion of one strand of DNA called a gene.
    5. Although genes are present on both strands of DNA, only one strand is transcribed for any given gene.
    6. The enzyme RNA polymerase transcribes DNA.
    7. To initiate transcription in bacteria, a variety of proteins called sigma factors bind to RNA polymerases. This complex can then bind to a specific DNA sequence called the promoter located along the DNA prior to the coding region of the gene. The promotor determines what region of the DNA and which strand of DNA will be transcribed into RNA.
    8. Like DNA polymerase, RNA polymerase can only synthesize nucleic acid in a 5' to 3' direction while "reading" a DNA template in the 3' to 5' direction.
    9. Once the RNA polymerase/sigma factor complex recognizes the correct promoter, the sigma factor dissociate from the RNA polymerase and the enzyme begins to unwind the helix of the DNA creating a region of nonpaired deoxyribonucleotides that serve as a template for RNA synthesis.
    10. During transcription, ribonucleotides hydrogen bond through the process of complementary base pairing with the exposed deoxyribonucleotides on the unwound strand that is to be transcribed. The ribonucleotides are then covalently bonded together by phosphodiester bonds.
    11. This process continues until the RNA polymerase encounters a "stop" signal or transcription terminator at the end of the gene.
    12. A single gene can be transcribed multiple times.
    13. The mRNA molecule is divided up into codons. A codon is a series of three consecutive mRNA bases coding for one specific amino acid.
    14. Three codons, UAG, UAA, and UGA, function as stop or nonsense codons to terminate translation.
    15. In bacteria, a mRNA can be monocistronic or polycistronic. A monocistronic mRNA is a transcript of a single gene; a polycistronic mRNA carries a transcript of multiple genes, often involved in a single biochemical pathway. Once transcribed, the mRNA can be translated into protein by tRNA on 70S ribosomes (composed of 50S and 30S subunits).
    16. Transcription is more complex in eukaryotic cells than in those that are prokaryotic. Activator proteins bind to genes known as enhancers which help determine which genes are switched on and speed up transcription. Repressor proteins bind to genes called silencers which interfere with activator proteins and slow down transcription. Coactivators, adapter molecules which coordinate signals from activator and repressor proteins, relay this information to basal factors which then position RNA polymerase at the start of the coding region of the gene to begin transcription.
    17. Most genes in higher eukaryotic cells contain regions called introns that are not part of the code for the final protein. These are interspersed among the coding regions or exons that actually code for the final protein.
    18. After transcription of the precursor mRNA, non-protein coding regions (introns) are excised and coding regions (exons) are joined together by complexes of ribonucleoproteins called spliceosomes to produce what is termed mature mRNA.
    19. The mature mRNA then passes through the pores in the nuclear membrane to be translated into protein by tRNA on 80S ribosomes (composed of 60S and 40S subunits) in a manner similar to prokaryotes.

    Contributors

    • Dr. Gary Kaiser (COMMUNITY COLLEGE OF BALTIMORE COUNTY, CATONSVILLE CAMPUS)