1.17-18 Flashcards
What can epigenetic changes lead to between identical siblings and clones?
Differences
Epigenetic changes can affect gene expression without altering the DNA sequence.
What diseases can epigenetic changes cause?
Human diseases
This includes conditions like cancer and autoimmune diseases.
How can environmental factors influence epigenetic changes?
Through diet and drug use affecting DNA methylation
Factors like malnutrition and drug use during pregnancy are particularly impactful.
What role do epigenetic factors play in autoimmune diseases?
Evidence suggests involvement in their development
This indicates a connection between epigenetics and immune system disorders.
What is cancer primarily caused by?
Unregulated cell division
This leads to the formation of tumors.
What are proto-oncogenes and tumor suppressing genes?
Important genes that regulate cell division
They are affected by DNA methylation.
What are changes in the DNA sequence called?
Mutations
Mutations can affect the nucleotide base sequence of DNA.
What can a change in a single nucleotide base affect?
The mRNA codon sequence and the primary structure of the protein
This can lead to different protein functions.
What can mutations in genes and chromosomes result from?
Errors in DNA replication or cell division, or environmental damage
Physical or chemical factors can also contribute.
What are the types of mutations?
- Deletions
- Insertions
- Substitution
- Inversion
Each type can lead to various effects on protein function.
What is a missense mutation?
A mutation that results in a different amino acid
This can alter protein function.
What is a same-sense mutation?
A mutation that causes no change due to multiple codes for the amino acid
This is often referred to as a silent mutation.
What is a non-sense mutation?
A mutation that codes for a stop codon and leads to chain termination
This has a significant effect on protein synthesis.
What is a frameshift mutation?
A mutation caused by insertions or deletions that cause big changes
This disrupts the reading frame of the genetic code.