Chapter 19 - Genetics of Living Systems Flashcards
In lac operon, what happens when there is no lactose present?
- The repressor protein binds to the operator
- This means that RNA polymerase cannot bind to the promoter, so no transcription of the enzymes occurs
In lac operon, what does the lac Z gene code for?
B-galactosidase
In lac operon, what does the lac Y gene code for?
Lactose permease
What does B-galactosidase do to lactose?
It breaks it down into more easily metabolisable sugars (glucose and galactose)
What does lactose permease do in lac operon?
It helps to transfer lactose into the cell
In what organisms are lac operons found?
Prokaryotes- common example is E. coli
What is an operon?
An operon is a group of genes under the control of the same regulatory mechanism and are expressed at the same time
In lac operon, what is the role of allolactose?
Allolactose will also be present when lactose is present, and will bind to the repressor protein. This will prevent the repressor protein from binding to the operator
In lac operon, what happens when the repressor protein is no longer bound to the operator?
It allows RNA polymerase to bind to the promoter and so allows for the transcription of the genes which code for the enzymes necessary to metabolise lactose
What is the role of cAMP in lac operon?
If cAMP is present, it will bind to the CAP. The CAP will then bind to the CAP site, which increases the rate of transcription, allowing the required quantity of enzymes needed to efficiency metabolise lactose to be produced.
What is the relationship between cAMP and glucose and what does this mean in a regulatory sense?
Glucose inhibits the creation of cAMP, therefore when glucose is present, cAMP will not be (and visa versa)
This means that when there are high levels of glucose, the rate of transcription will be much lower (even if lactose is present), as there is no need to metabolise lactose when the preferred sugar (glucose) is present.
What are the 3 structural genes in lac operon and what is their role?
LacZ, lacY and lacA. They code for three different enzymes, that are involved in the metabolism of lactose
What is the role of the regulator gene (lacI), which is found near the lac operon?
It codes for the repressor protein that inhibits transcription from occurring when lactose is not present
What is it called when only one nucleotide is affected by mutation?
Point mutation
What does insertion or deletion of a nucleotide lead to?
A frameshift mutation, which will shift the reading frame of the sequences of bases, hence changing every successive codon from the point of mutation
What is the effect of damaging mutations?
The phenotype of an organism is affected in a negative way, as proteins are no longer synthesised, or the proteins synthesised are non-functional
How are some mutations beneficial (with an example)?
Very rarely, a protein is synthesised that results in a new and useful characteristic in the phenotype.
For example a mutation in a protein in cell surface membranes of human cells can give HIV immunity
Where do mutations often spontaneously occur?
During DNA replication
What is a mutagen?
An agent that increases the rate/likelihood of mutations
What are the 3 types of mutagens?
Physical, chemical and biological
Give an example of a physical mutagen
Ionising radiation such as x-rays
Give an example of a chemical mutagen
Deaminating agents
How do deaminating agents work?
Chemically alter bases in DNA, changing the base sequence
Give an example of a biological mutagen
A virus
How are viruses biological mutagens?
Viral DNA may insert itself into a genome, changing the base sequence
What does it mean for a mutation to be silent?
The mutations do not change any proteins, or the activity of any proteins synthesised. Therefore they have no effect on the phenotype
Why are most mutations silent?
- They can occur in the non-coding regions of DNA
- Due to the degenerate nature of genetic code, mutated codons can code for the same amino acid
What are nonsense mutations?
Nonsense mutations result in a codon becoming a stop codon instead of coding for an amino acid. This creates a shortened often non-functional protein
What are missense mutations?
Result in the incorporation of an incorrect amino acid into the primary structure during protein synthesis. The missense mutation can be conservative or non-conservative
What is a conservative missense mutation?
When the amino acid change leads to an amino acid that has similar properties to the original being added to the primary structure, meaning the mutation is less severe
What is a non-conservative missense mutation?
When the amino acid change leads to an amino acid that has different properties to the original being added to the primary structure, meaning the mutation is more severe