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UNIT 3 Transcriptionand Protein Synthesis. Objectives Discuss the flow of information from DNA to RNA to Proteins Discuss the flow of information from.

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Presentation on theme: "UNIT 3 Transcriptionand Protein Synthesis. Objectives Discuss the flow of information from DNA to RNA to Proteins Discuss the flow of information from."— Presentation transcript:

1 UNIT 3 Transcriptionand Protein Synthesis

2 Objectives Discuss the flow of information from DNA to RNA to Proteins Discuss the flow of information from DNA to RNA to Proteins Explain transcription Explain transcription Differentiate introns and exons Differentiate introns and exons State functions of the noncoding regions of mRNA State functions of the noncoding regions of mRNA Describe post transcriptional modification of pre-RNA Describe post transcriptional modification of pre-RNA Distinguish between mRNA, tRNA and rRNA Distinguish between mRNA, tRNA and rRNA Distinguish the roles of ribosomes, tRNA and mRNA in protein synthesis Distinguish the roles of ribosomes, tRNA and mRNA in protein synthesis Give detailed description of the process and steps of translation Give detailed description of the process and steps of translation Describe application of SDS-Page gel electrophoresis to protein analysis Describe application of SDS-Page gel electrophoresis to protein analysis

3 DNA to RNA to Proteins DNA to RNA to Proteins

4 DNA to RNA to Proteins Eukaryotes vs. Prokaryotes DNA to RNA to Proteins Eukaryotes vs. Prokaryotes In prokaryotes, transcription and translation are coupled translation begins while the mRNA is still being synthesized. translation begins while the mRNA is still being synthesized.

5 mRNA in Prokaryotes

6 DNA to RNA to Proteins Eukaryotes vs. Prokaryotes DNA to RNA to Proteins Eukaryotes vs. Prokaryotes In Eukaryotes, transcription and translation are spatially and temporally separated In Eukaryotes, transcription and translation are spatially and temporally separated transcription occurs in the nucleus to produce a pre- mRNA molecule. transcription occurs in the nucleus to produce a pre- mRNA molecule. pre-mRNA is processed to produce the mature mRNA, which exits the nucleus and is translated in the cytoplasm. pre-mRNA is processed to produce the mature mRNA, which exits the nucleus and is translated in the cytoplasm.

7 mRNA in Eukaryotes

8 DNA to RNA to Proteins Eukaryotes vs. Prokaryotes DNA to RNA to Proteins Eukaryotes vs. Prokaryotes

9 Transcription occurs in four main stages: 1) binding of RNA polymerase to DNA at a promoter occurs in four main stages: 1) binding of RNA polymerase to DNA at a promoter 2) initiation of transcription on the template DNA strand 3) elongation of the RNA chain 4) termination of transcription along with the release of RNA polymerase and the completed RNA product from the DNA template.

10 Transcription Binding of polymerases to the initiation site at the promoter. Binding of polymerases to the initiation site at the promoter. Prokaryotic RNA polymerases can recognize the promoter and bind to it directly, but eukaryotic RNA polymerases have to rely on other proteins called transcription factors. Prokaryotic RNA polymerases can recognize the promoter and bind to it directly, but eukaryotic RNA polymerases have to rely on other proteins called transcription factors. Unwinding of the DNA double helix by helicase. Unwinding of the DNA double helix by helicase. Prokaryotic RNA polymerases have the helicase activity, but eukaryotic RNA polymerases do not. Prokaryotic RNA polymerases have the helicase activity, but eukaryotic RNA polymerases do not. Unwinding of eukaryotic DNA is carried out by a specific transcription factor. Unwinding of eukaryotic DNA is carried out by a specific transcription factor. Synthesis of RNA based on the sequence of the DNA template strand. Synthesis of RNA based on the sequence of the DNA template strand. RNA polymerases use nucleoside triphosphates (NTPs) to construct a RNA strand. RNA polymerases use nucleoside triphosphates (NTPs) to construct a RNA strand. Termination of synthesis. Termination of synthesis. Prokaryotes and eukaryotes use different signals to terminate transcription. Prokaryotes and eukaryotes use different signals to terminate transcription.

11 Promoter The DNA promoter region in prokaryotes is a stretch of about 40 base pairs adjacent to and including the transcription start point. The DNA promoter region in prokaryotes is a stretch of about 40 base pairs adjacent to and including the transcription start point. The essential features of the promoter are the start point (designated +1 and usually an A), the six- nucleotide -10 sequence, and the six-nucleotide -35 sequence. The essential features of the promoter are the start point (designated +1 and usually an A), the six- nucleotide -10 sequence, and the six-nucleotide -35 sequence. The two key sequences are located approximately 10 nucleotides and 35 nucleotides upstream from the start point. The two key sequences are located approximately 10 nucleotides and 35 nucleotides upstream from the start point.

12 Prokaryotic promoter

13 Elongation During elongation, RNA polymerase binds to about 30 base pairs of DNA During elongation, RNA polymerase binds to about 30 base pairs of DNA At any given time, about 18 base pairs of DNA are unwound, and the most recently synthesized RNA is still hydrogen-bonded to the DNA, forming a short RNA-DNA hybrid (12 bp long, but it may be shorter) At any given time, about 18 base pairs of DNA are unwound, and the most recently synthesized RNA is still hydrogen-bonded to the DNA, forming a short RNA-DNA hybrid (12 bp long, but it may be shorter) The total length of growing RNA bound to the enzyme and/or DNA is about 25 nucleotides. The total length of growing RNA bound to the enzyme and/or DNA is about 25 nucleotides.

14 Termination Requires a termination sequence that triggers the end of transcription. Requires a termination sequence that triggers the end of transcription. Two classes exist: Two classes exist: rho dependent rho dependent a short complementary GC-rich sequence (followed by several U residues) will form a "brake" that will help release the RNA polymerase from the template. a short complementary GC-rich sequence (followed by several U residues) will form a "brake" that will help release the RNA polymerase from the template. rho independent. rho independent. binding of rho to the mRNA releases it from the template. binding of rho to the mRNA releases it from the template.

15 Termination rho-dependent – rho-dependent – requires a protein called rho to bind to specific sequence. requires a protein called rho to bind to specific sequence.

16 Termination rho-independent - depends on a seqence in mRNA which forms a stem loop. rho-independent - depends on a seqence in mRNA which forms a stem loop.

17 Termination

18 Transcription in Eukaryotes Although transcription in eukaryotes is similar to that in prokaryotes, the process is more complex. Although transcription in eukaryotes is similar to that in prokaryotes, the process is more complex. Instead of one RNA polymerase, there are three : Instead of one RNA polymerase, there are three : RNA polymerase I (localized to the nucleolus) transcribes the rRNA precursor molecules. RNA polymerase I (localized to the nucleolus) transcribes the rRNA precursor molecules. RNA polymerase II produces most mRNAs and snRNAs. RNA polymerase II produces most mRNAs and snRNAs. RNA polymerase III is responsible for the production of pre-tRNAs, 5SrRNA and other small RNAs. RNA polymerase III is responsible for the production of pre-tRNAs, 5SrRNA and other small RNAs. The mitochondria and chloroplasts have their own RNA polymerases. The mitochondria and chloroplasts have their own RNA polymerases.

19 Transcription complex http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter18/animations.html# http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter18/animations.html# http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter18/animations.html# http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter18/animations.html#

20 Transcription in Eukaryotes Eukaryotic nuclear genes have three classes of promoters which are individual for the three types of RNA polymerases Eukaryotic nuclear genes have three classes of promoters which are individual for the three types of RNA polymerases

21 Transcription in Eukaryotes Termination signals end the transcription of RNA by RNA polymerase I and RNA polymerase III without the activity of hairpin structures as seen in prokaryotes. Termination signals end the transcription of RNA by RNA polymerase I and RNA polymerase III without the activity of hairpin structures as seen in prokaryotes. mRNA is cleaved 10 to 35 base-pairs downstream of a AAUAAA sequence (which acts as a poly-A tail addition signal). mRNA is cleaved 10 to 35 base-pairs downstream of a AAUAAA sequence (which acts as a poly-A tail addition signal).

22 RNA processing in Eukaryotes Ribosomal RNA processing Ribosomal RNA processing involves cleavage of multiple rRNAs from a common precursor, with nontranscribed spacers separate the units. involves cleavage of multiple rRNAs from a common precursor, with nontranscribed spacers separate the units. The transcription unit is transcribed by RNA polymerase I into a single long transcript (pre- rRNA) The transcription unit is transcribed by RNA polymerase I into a single long transcript (pre- rRNA)

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24 RNA processing in Eukaryotes Every tRNA gene is transcribed as a precursor that must be processed into a mature tRNA molecule by: Every tRNA gene is transcribed as a precursor that must be processed into a mature tRNA molecule by: removal of the leader sequence at the 5΄ end removal of the leader sequence at the 5΄ end replacement of two nucleotides at the 3 ΄ end by the sequence CCA (with which all mature tRNA molecules terminate) replacement of two nucleotides at the 3 ΄ end by the sequence CCA (with which all mature tRNA molecules terminate) chemical modification of certain bases chemical modification of certain bases excision of an intron. excision of an intron.

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26 RNA processing in Eukaryotes Transcription of eukaryotic pre-mRNAs often proceeds beyond the 3΄ end of the mature mRNA. Transcription of eukaryotic pre-mRNAs often proceeds beyond the 3΄ end of the mature mRNA. An AAUAAA sequence located slightly upstream from the proper 3΄ end then signals that the RNA chain should be cleaved about 10- 35 nucleotides downstream from the signal site, followed by addition of a poly-A tail catalyzed by poly(A) polymerase. An AAUAAA sequence located slightly upstream from the proper 3΄ end then signals that the RNA chain should be cleaved about 10- 35 nucleotides downstream from the signal site, followed by addition of a poly-A tail catalyzed by poly(A) polymerase.

27 RNA processing in Eukaryotes Messenger RNA in eukaryotes Messenger RNA in eukaryotes is first made as heterogeneous nuclear mRNA / pre-mRNA then processed into mature mRNA through: is first made as heterogeneous nuclear mRNA / pre-mRNA then processed into mature mRNA through: the addition of a 5 prime cap - a guanosine nucleotide methylated at the 7th position the addition of a 5 prime cap - a guanosine nucleotide methylated at the 7th position addition of poly-A tails addition of poly-A tails the splicing out of introns. the splicing out of introns.

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30 Introns and Exons Eukaryotic genes have interrupted coding sequences. Eukaryotic genes have interrupted coding sequences. There are long sequences of bases within the protein- coding sequences of the gene that do not code for amino acids in the final protein product. There are long sequences of bases within the protein- coding sequences of the gene that do not code for amino acids in the final protein product. The nocoding regions within the gene are called introns (intervening sequences). The nocoding regions within the gene are called introns (intervening sequences). The exons (expressed sequences) are part of the protein-coding sequence. The exons (expressed sequences) are part of the protein-coding sequence.

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34 How introns are removed

35 The intron loops out as snRNPs (small nuclear ribonucleoprotein particles, complexes of snRNAs and proteins) bind to form the spliceosome. The intron loops out as snRNPs (small nuclear ribonucleoprotein particles, complexes of snRNAs and proteins) bind to form the spliceosome. The intron is excised, and the exons are then spliced together. The intron is excised, and the exons are then spliced together. The resulting mature mRNA may then exit the nucleus and be translated in the cytoplasm. The resulting mature mRNA may then exit the nucleus and be translated in the cytoplasm.

36 Animation – How introns are removed http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter15/animations.html# http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter15/animations.html# http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter15/animations.html# http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter15/animations.html#

37 Introns and Exons A typical eukaryotic gene may have multiple exons and introns and the numbers are quite variable. A typical eukaryotic gene may have multiple exons and introns and the numbers are quite variable. In many cases the lengths of the introns are much greater than those of the exon sequences. In many cases the lengths of the introns are much greater than those of the exon sequences. For instance the ovalbumin gene contains about 7700 base pairs, 1859 of them in exons. For instance the ovalbumin gene contains about 7700 base pairs, 1859 of them in exons.

38 Ovalbumin gene

39 Functions of Introns Evidence now exists that introns have many functions, including for regulation and structural purposes, and that many of the roles now hypothesized for introns are plausible but need further elucidation. Evidence now exists that introns have many functions, including for regulation and structural purposes, and that many of the roles now hypothesized for introns are plausible but need further elucidation.

40 Please read at least three of the following articles for tutorial http://www.sciencedaily.com/releases/2009/05/090528203730.htm http://www.sciencedaily.com/releases/2007/07/070712143308.htm http://www.sciencedaily.com/releases/2006/11/061113180029.htm http://www.sciencedaily.com/releases/2009/06/090606105203.htm http://www.sciencedaily.com/releases/2006/04/060404090831.htm http://www.sciencedaily.com/releases/2005/10/051020090946.htm http://www.sciencedaily.com/releases/2009/05/090520140408.htm http://www.sciencedaily.com/releases/2008/11/081104180928.htm http://www.sciencedaily.com/releases/2008/10/081017080145.htm

41 Roles of ribosomes, mRNA and tRNA in Protein Synthesis

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43 Protein Synthesis http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter15/animations.html# http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter15/animations.html# http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter15/animations.html# http://highered.mcgraw- hill.com/sites/0072437316/student_view0/chap ter15/animations.html#

44 References/ sources of images http://evolution.berkeley.edu/evolibrary/article/0_0_0/mutations_03 http://evolution.berkeley.edu/evolibrary/article/0_0_0/mutations_03 http://evolution.berkeley.edu/evolibrary/article/0_0_0/mutations_03 usmlemd.wordpress.com/2007/07/14/dna-replication/ usmlemd.wordpress.com/2007/07/14/dna-replication/ usmlemd.wordpress.com/2007/07/14/dna-replication/ http://employees.csbsju.edu/hjakubowski/classes/ch331/dna/centraldogma.jpg http://employees.csbsju.edu/hjakubowski/classes/ch331/dna/centraldogma.jpg http://employees.csbsju.edu/hjakubowski/classes/ch331/dna/centraldogma.jpg http://www.usask.ca/biology/rank/demo/replication/cons.rep.gif http://www.usask.ca/biology/rank/demo/replication/cons.rep.gif http://www.usask.ca/biology/rank/demo/replication/cons.rep.gif http://click4biology.info/c4b/3/images/3.4/SEMICON.gif http://click4biology.info/c4b/3/images/3.4/SEMICON.gif http://click4biology.info/c4b/3/images/3.4/SEMICON.gif http://www.bio.miami.edu/~cmallery/150/gene/sf12x16.jpg http://www.bio.miami.edu/~cmallery/150/gene/sf12x16.jpg http://www.bio.miami.edu/~cmallery/150/gene/sf12x16.jpg http://publications.nigms.nih.gov/findings/sept08/images/hunt_gene_big.jpg http://publications.nigms.nih.gov/findings/sept08/images/hunt_gene_big.jpg http://publications.nigms.nih.gov/findings/sept08/images/hunt_gene_big.jpg http://ghr.nlm.nih.gov/handbook/illustrations/duplication.jpg http://ghr.nlm.nih.gov/handbook/illustrations/duplication.jpg http://ghr.nlm.nih.gov/handbook/illustrations/duplication.jpg http://images.google.com.jm/imgres?imgurl=http://ghr.nlm.nih.gov/handbook/illustrations/duplication.jpg &imgrefurl=http://ghr.nlm.nih.gov/handbook/illustrations/duplication&usg=__BgKRLXXos- xRaUqN5EyP7qchszc=&h=400&w=370&sz=38&hl=en&start=2&tbnid=ZfARmmvAKG02xM:&tbnh=124 &tbnw=115&prev=/images%3Fq%3Dduplication%2Bmutation%26gbv%3D2%26hl%3Den%26client%3Dfir efox-a%26rls%3Dorg.mozilla:en-US:official%26sa%3DG http://images.google.com.jm/imgres?imgurl=http://ghr.nlm.nih.gov/handbook/illustrations/duplication.jpg &imgrefurl=http://ghr.nlm.nih.gov/handbook/illustrations/duplication&usg=__BgKRLXXos- xRaUqN5EyP7qchszc=&h=400&w=370&sz=38&hl=en&start=2&tbnid=ZfARmmvAKG02xM:&tbnh=124 &tbnw=115&prev=/images%3Fq%3Dduplication%2Bmutation%26gbv%3D2%26hl%3Den%26client%3Dfir efox-a%26rls%3Dorg.mozilla:en-US:official%26sa%3DG http://images.google.com.jm/imgres?imgurl=http://www.phschool.com/science/biology_place/biocoach/im ages/transcription/euovrvw.gif&imgrefurl=http://www.phschool.com/science/biology_place/biocoach/trans cription/tctlpreu.html&usg=__- hoX0ehn3x9zc2nUeciZ8gLYLqQ=&h=288&w=261&sz=20&hl=en&start=10&um=1&tbnid=X11pPXboE KhRIM:&tbnh=115&tbnw=104&prev=/images%3Fq%3Dtranscription%26ndsp%3D18%26hl%3Den%26sa %3DG%26um%3D1 http://images.google.com.jm/imgres?imgurl=http://www.phschool.com/science/biology_place/biocoach/im ages/transcription/euovrvw.gif&imgrefurl=http://www.phschool.com/science/biology_place/biocoach/trans cription/tctlpreu.html&usg=__- hoX0ehn3x9zc2nUeciZ8gLYLqQ=&h=288&w=261&sz=20&hl=en&start=10&um=1&tbnid=X11pPXboE KhRIM:&tbnh=115&tbnw=104&prev=/images%3Fq%3Dtranscription%26ndsp%3D18%26hl%3Den%26sa %3DG%26um%3D1 www.asa3.org/ASA/PSCF/2001/PSCF9-01Bergman.html www.asa3.org/ASA/PSCF/2001/PSCF9-01Bergman.html www.asa3.org/ASA/PSCF/2001/PSCF9-01Bergman.html http://www.mun.ca/biology/desmid/brian/BIOL2060/BIOL2060-21/CB21.html http://www.mun.ca/biology/desmid/brian/BIOL2060/BIOL2060-21/CB21.html http://www.mun.ca/biology/desmid/brian/BIOL2060/BIOL2060-21/CB21.html http://www.mun.ca/biology/desmid/brian/BIOL2060/BIOL2060-21/2101.jpg http://www.mun.ca/biology/desmid/brian/BIOL2060/BIOL2060-21/2101.jpg


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