Answer:
A) genetic influences and chemical imbalances in the brain
Explanation:
An anxiety disorder is a psychiatric disorder where the individual experiences an excessive and irrational worry in everyday situations. Generalized anxiety disorder, phobias, panic attacks, etc are examples of anxiety disorders.
<em>Anxiety does not have a specific cause, it can be the result of different factors like changes in the brain's chemistry, environmental stress or even genetics.</em>
I hope you find this information useful and interesting! Good luck!
The correct answer is: b. It is free to bind to another promoter and begin transcription
Transcription is the first step of gene expression in which DNA molecule is copied (transcribed) into RNA (mRNA) by RNA polymerase. The process of transcription is divided into three phases:
1. Initiation
• RNA polymerase with transcriptional factors bind to gene promoter
• RNA polymerase unwinds DNA double helix (transcription bubble is formed)
2. Elongation
• RNA polymerases adds nucleotides complementary to DNA
3. Termination
• RNA polymerase gets to stop codon (transcribes a sequence of DNA known as a terminator)
• Formed complementary RNA strand is released from DNA-RNA complex.
RNA polymerase is also released and can transcribe some other gene by binding to its promotor. RNA polymerase will transcribe just the genes whose products are needed at a particular moment.
Answer: percentage of mice that will be spotted is 100%, and 0% chance of being solid colored.
Explanation: First, homozygous means each parent have matching chromosomes (Like XX, instead of Xx)
Lets make a punnet square and show the data. We will use 'S' for spotted and 's' for solid
The punnet square shows that the percentage of mice that will be spotted is 100%, and 0% chance of being solid colored.
Hope this helps :)
Answer:
Since, the original DNA sequence has not been provided, the mutation can be an insertion/deletion or a frameshift mutation.
- Mutated DNA
- Frameshift mutation/ insertion or deletion
- All the amino acids changed after the point mutation
Explanation:
Frameshift Mutation:
- A frameshift mutation is the alteration in the reading frame of the DNA due to the addition/deletion of one or two nucleotides.
- This type of mutation moves the mRNA sequence one or two bases forwards or backwards which disrupts the three base codons sequence required for translation into proteins.
- The CT at the end of the sequence is indicative of a frameshift in the DNA reading frame.
- Frameshift mutation affect all amino acids in a polypeptide chain as all codons are moved one or two steps forwards or backwards.
