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Molecular Basis for Relationship between Genotype and Phenotype DNA RNA protein genotype functio n organism phenotype DNA sequence amino acid sequence transcription translation

Molecular Basis for Relationship between Genotype and Phenotype

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Molecular Basis for Relationship between Genotype and Phenotype. genotype. DNA. DNA sequence. transcription. RNA. translation. amino acid sequence. protein. function. phenotype. organism. Complementarity and Asymmetry in RNA Synthesis. - PowerPoint PPT Presentation

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  • Molecular Basis forRelationship between Genotype and PhenotypeDNARNAproteingenotypefunctionorganismphenotypeDNA sequenceamino acidsequencetranscriptiontranslation

  • Complementarity and Asymmetry in RNA Synthesis Only one strand of DNA is used as template for RNA synthesis. Template strand is antiparallel to RNA transcript. RNA bases are complementary to bases of template DNA.

  • RNA Polymerase RNA polymerase adds ribonucleotides in 5 to 3 direction. RNA polymerase in E. coli consists of 4 different subunits (see model below).A single type of RNA polymerase transcribes RNA in prokaryotes. s recognizes the promoter. Holoenzyme is needed for correct initiation of transcription.

  • Promoters signal transcription in prokaryotes.Promoter Sequences in E. coli

  • s subunit positions RNA polymerase for correct initiation.Upon initiation of transcription, s subunit dissociates.Transcription Initiation in Prokaryotes

  • ElongationRNA polymerase adds ribonucleotides in 5 to 3 direction.RNA polymerase catalyzes the following reaction:NTP + (NMP)n(NMP)n+1 + PPiDNA

    Mg++RNA polymerase

  • TerminationTermination of transcription occurs beyond the coding sequence of a gene. This region is 3 untranslated region (3 UTR), which is recognized by RNA polymerase.

  • TerminationRNA polymerase recognizes signals for chain termination.(1) Intrinsic: Termination site on template DNA consists of GC-rich sequences followed by As. Intra-molecular hydrogen bonding causes formation of hairpin loop. In E. coli, this structure signals release of RNA polymerase, thus terminating transcription.(2) rho factor (hexameric protein) dependent: These termination signals do not produce hairpin loops. rho binds to RNA at rut site. rho pulls RNA away from RNA polymerase.rut site

  • Colinearity of Gene and ProteinDNARNAproteingenotypefunctionorganismphenotypeDNA sequenceamino acidsequencetranscriptiontranslation

  • There are three stop (termination) codons. They are often called nonsense codons.

    Genetic Code is degenerate. Some amino acids are encoded by more than one codon. Genetic CodeGenetic Code is nonoverlapping.

    A codon (three bases or triplet) encodes an amino acid.

    Genetic Code is read continuously from a fixed starting point.

    There is a start codon (AUG).

  • Molecular Basis forRelationship between Genotype and PhenotypeDNARNAproteingenotypefunctionorganismphenotypeDNA sequenceamino acidsequencetranscriptiontranslation

  • Eukaryotic RNAThree RNA PolymerasesRNA Polymerase

    IIIIIISynthesis of

    rRNA (except 5S rRNA)mRNA*, some snRNAtRNA, some snRNA, 5S rRNA* eukaryotic RNA is monocistronic prokaryotic RNA can be polycistronic

  • Eukaryotic RNAPrimary transcript (pre-mRNA) must be processed into mature mRNA.

    1. Cap at 5 end (7-methylguanosine)2. Addition of poly(A) tail3. Splicing of RNA transcriptMany proteins must assemble at promoter before transcription.

    General transcription factors (GTFs) bind before RNA polymerase II, while other proteins bind after RNA polymerase II binds.Chromatin structure affects gene expression (gene transcription) in eukaryotes.

  • Prokaryotic and Eukaryotic Transcription and Translation Compared

  • TATA binding protein (TBP), part of TFIID complex, must bind to promoter before other GTFs and RNA polymerase II can form preinitiation complex (PIC).

    Phosphorylation of carboxyl tail domain (CTD), the protein tail of b subunit of RNA polymerase II, allows separation of RNA polymerase II from GTFs to start transcription.Transcription Initiation in Eukaryotes

  • State of phosphorylation of CTD determines the type of proteins that can associate with the CTD (thus defining cotranscriptional process).

    5 end of pre-mRNA is capped with 7-methylguanosine. This protects the transcript from degradation; capping is also necessary for translation of mature mRNA.Cotranscriptional Processing of RNA

  • Cotranscriptional Processing3 end of the transcript typically contains AAUAAA or AUUAAA.

    This sequence is recognized by an enzyme that cleaves the newly synthesized transcript ~20 nucleotides downstream.

    At the 3 end, a poly(A) tail consisting of 150 - 200 adenine nucleotides is added.

    Polyadenylation is another characteristic of transcription in eukaryotes.

  • Different mRNA can be produced; different a-tropomyosin can be produced.Alternative splicing is a mechanism for gene regulation. Gene product can be differentin different cell types and at different stages of development.Complex Patterns of Eukaryotic RNA Splicing

  • Intron Splicing: Conserved Sequencesexons - coding sequences introns - noncoding sequencesSmall nuclear ribonucleoprotein particles (snRNPs) recognize consensus splice junction sequence of GU/AG.

    snRNPs are complexes of protein and small nuclear RNA (snRNA). Several snRNPs comprise a spliceosome.

    Spliceosome directs the removal of introns and joining of exons.

  • One end of conserved sequence attaches to conserved adenine in the intron.

    The lariat is released and adjacent exons are joined.Spliceosome interacts with CTD and attaches to pre-mRNA.

    snRNAs in spliceosomes direct alignment of the splice sites.

    Spliceosome Assembly and Function

  • Reactions in Exon Splicing

  • These self-splicing introns are an example of RNA that can catalyze a reaction. RNA molecules can act somewhat like enzymes (ribozymes).

    In the protozoan Tetrahymena, the primary transcript of an rRNA can excise a 413-nucleotide intron from itself.Self-Splicing Reaction

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