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Published byΠαλλάς Δημαράς Modified over 6 years ago
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Synthetic lethal- A screening method used to uncover mutations in a second gene that will require the cell to maintain a wild-type copy of the gene being studied in order to survive st mutation + 2nd mutation = lethality This screen is commonly used in yeast genetics, but can be used in other model organisms as well.
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Dead yeast don’t talk
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a a b a A A a b a b X B
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a b a b B A A a b a b B X
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Mutation The process that produces a gene or a chromosome set that is differing than that of the wild type. The gene or a chromosome set that results from such a process.
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Gene product DNA Protein mRNA RNA Structural Enzyme Structural
Functional & Regulatory RNAs
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a+ --> a- mutation (forward mutation)
a > a+ reverse mutation (reversion)
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Forward Reverse
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Presence of pink pigment + / -
Four-o’clock plants Incomplete dominance the term used to describe the general case in which the phenotype of a heterozygote is intermediate between those of the two homozygotes, on some quantitative scale of measurement
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Point mutations at the molecular level
Purine replaced by a different purine; pyrimidine replaced by a different pyrimidine: TRANSITIONS Purine replaced by a pyrimidine; pyrimidine replaced by a purin: TRANSVERSIONS
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Transition and transversion
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Now, insertions and deletions of base pairs:
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Selection of auxotrophs by filter enrichment
Forward mutation-A mutation that converts a wild-type allele into a mutant allele
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Reverse mutation-The production of a wild-type gene from a mutant gene
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Intragenic suppressor
Equivalent reversion UCC (Ser) forward UGC (Cys) reverse AGC (Ser) Wild type Mutant Wild type CGC (Arg, basic) forward CCC (Proline) reverse CAC (His, basic) Wild type Mutant Pseudo-wild type
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Intragenic suppressor
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Intergenic suppressor
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Intergenic suppressor
Nonsense suppressor
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ADE2
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ade2
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The Sup11 case WT ade2-101 ade2-101 sup11
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The Sup11 case
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Chromosome transmission fidelity (Ctf) assay
non-essential Chromosome Fragment M SUP11 ade2-101 WT ade2-101 kar3D sic1D rad50D xrs2D CIN mutant ade1-101 ade2-101
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Regulatory Coding
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A situation in which the third nucleotide
WOBBLE A situation in which the third nucleotide of an anticodon (at the 5’ end) can form two alignments. This third nucleotide can form hydrogen bonds not only with its normal complementary nucleotide in the third position but also with different nucleotide in the position.
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I stands for inosine, one of the rare bases found in tRNA, often in anticodon
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The genetic code is said to be degenerate because in many cases
MESSAGE The genetic code is said to be degenerate because in many cases more then one codon is assigned to a single amino acid, and, in addition, several codons can pair with more then on anticodon (wobble)
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