The spontaneous mutation rate in E.coli was determined to be 1 mistake for every 109 nucleotides copied.This was determined by measuring the frequency of a particular AT-to-GC change.This was accomplished using a strain of E.coli that started out unable to produce histidine (His-) because of an inserted UGA stop codon that disrupted the region coding for an enzyme required to produce histidine.When a spontaneous mutation arose that enabled the UGA stop codon to code for tryptophan, the E.coli cells were then able to produce the enzyme required for histidine production.
You discover that if the stop codon were to change to code for cysteine (instead of tryptophan), this change would also allow the bacteria to produce histidine.How would the previously calculated spontaneous mutation rate of 1 mistake every 109 nucleotides copied change, given this new information? Explain.(The codon table is shown in Figure 9-48 to help you answer this question.) The Genetic Code
U C A G U UUU Phe (F) UUC - UUA Leu (L) UUG - CUU Leu (L) CUC - CUA - CUG − AUU Ile (I) AUC - AUA - AUG Met (M) GUU Val (V) GUC - GUA - GUG - C UCU Ser (S) UCC - UCA – UCG - CCU Pro (P) CCC - CCA - CCG − ACU Thr (T) ACC - ACA - ACG - GCU Ala (A) GCC - GCA - GCG - A UAU Tyr (Y) UAC - UAA Stop UAG Stop CAU His (H) CAC - CAA Gin (Q) CAG − AAU Asn (N) AAC - AAA Lys (K) AAG - GAU Asp (D) GAC - GAA Glu (E) GAG - G UGU Cys (C) UGC - UGA Stop UGG Trp (W) CGU Arg (R) CGC - CGA - CGG − AGU Ser (S) AGC - AGA Arg (R) AGG - GGU Gly (G) GGC - GGA - GGG -
Figure 9-48
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Heterozygous Dihybrid
An individual possessing two different alleles for two traits, resulting from the cross of parents differing in two specific traits.
Genotype
The genetic constitution of an organism, determining specific characteristics by encoding instructions for proteins.
AaMm
Represents a genotype consisting of two different alleles, Aa, for one trait and two different alleles, Mm, for another trait, indicating a hybrid individual.
Dominant Allele
An allele that expresses its phenotype even in the presence of a different (recessive) allele at the same genetic locus in a heterozygote.