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Relationship between Genotype and Phenotype

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Presentation on theme: "Relationship between Genotype and Phenotype"— Presentation transcript:

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

2 RNA polymerase recognizes signals for chain termination.
(1) Intrinsic: Termination site on template DNA consists of GC-rich sequences followed by A’s. Intra-molecular hydrogen bonding causes formation of hairpin loop. (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 In E. coli, this structure signals release of RNA polymerase, thus terminating transcription.

3 Colinearity of Gene and Protein
genotype DNA DNA sequence transcription RNA translation amino acid sequence protein function phenotype organism

4 Genetic Code Genetic 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). 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.

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

6 * eukaryotic RNA is monocistronic prokaryotic RNA can be polycistronic
Three RNA Polymerases RNA Polymerase I II III Synthesis of rRNA (except 5S rRNA) mRNA*, some snRNA tRNA, some snRNA, 5S rRNA * eukaryotic RNA is monocistronic prokaryotic RNA can be polycistronic

7 Eukaryotic RNA Many proteins must assemble at promoter before transcription. General transcription factors (GTF’s) bind before RNA polymerase II, while other proteins bind after RNA polymerase II binds. Primary transcript (pre-mRNA) must be processed into mature mRNA. 1. Cap at 5’ end (7-methylguanosine) 2. Addition of poly(A) tail 3. Splicing of RNA transcript Chromatin structure affects gene expression (gene transcription) in eukaryotes.

8 Prokaryotic and Eukaryotic Transcription and Translation Compared
Refer to Figure 8-11 from Introduction to Genetic Analysis, Griffiths et al., 2015.

9 Transcription Initiation in Eukaryotes
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. Refer to Figure 8-12 from Introduction to Genetic Analysis, Griffiths et al., 2015.

10 Cotranscriptional Processing of RNA
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. Refer to Figure 8-13 from Introduction to Genetic Analysis, Griffiths et al., 2015.

11 Cotranscriptional Processing
3’ 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 adenine nucleotides is added. Polyadenylation is another characteristic of transcription in eukaryotes.

12 Complex Patterns of Eukaryotic RNA Splicing
Refer to Figure 8-14 from Introduction to Genetic Analysis, Griffiths et al., 2015. Different mRNA can be produced; different a-tropomyosin can be produced. Alternative splicing is a mechanism for gene regulation. Gene product can be different in different cell types and at different stages of development.

13 Intron Splicing: Conserved Sequences
exons - coding sequences introns - noncoding sequences Small 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.

14 Spliceosome Assembly and Function
Spliceosome interacts with CTD and attaches to pre-mRNA. snRNAs in spliceosomes direct alignment of the splice sites. One end of conserved sequence attaches to conserved adenine in the intron. The “lariat” is released and adjacent exons are joined. Refer to Figure 8-16 from Introduction to Genetic Analysis, Griffiths et al., 2015.

15 Self-Splicing 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. These self-splicing introns are an example of RNA that can catalyze a reaction. Refer to Figure 8-18 from Introduction to Genetic Analysis, Griffiths et al., 2015.


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