Question
Meditation as a process that creates genetic variation mutation creates variations in protein coating portions of genes that can affect the protein itself. Or often it creates variations in the switches that control when and where protein is active and how much protein is made. For example, of black tastes and eggs on the helps. You and spray down lactose a sugar and milk. Normally the team that votes for lack taste is active in babies and then turned off at about age 4. When people who do not make lactates consumed. No, thanks for the experience discovered. But some people have a variation and a genetic switch that keeps a lot taste. Keen active and people eat out of computer and their diet see Vanessa does. Tatians are a source of genetic vmutations that occur in sex cells or gamings can be passed from one generation to the next limitations that occur in psychopathy. Self recommendation, causing skin cancer will not be passed on. Rotations can be classified as harmful, as is the case of the sickle cell team beneficial or having no impact on the organism at all neutral. Most of the mutations in our dna are naturally occurring. For example, when a cell device, it makes a copy of its dna and sometimes the. Obviously not perfect. That's not different from the original DNA sequences immutation mutations can also be caused by exposure to specific chemicals or radiation news agency. There are many different ways that DNA can be changed, resulting in different types of mutation substitution. The substitution is a mutation that exchanges one base or another. A substitution could change a code on to one that encodes a different Domino acid and cause a small change in the protein produced. For example, sickle cell vanilla is caused by a substitution in the data heat of a gene which all. Colombino acid and a protein produced chain to code on to one that encodes the same amino. Acid and causes no change in a protein produced. These are called silent mutations. Changing amino acid code on to a single stop code out and coordinate complete protein. This could have serious effects since the incomplete protein. Probably won't function insertion. Insertions or mutations in which extra-base pairs are inserted into a new place in the dna deletion deletions and mutations in which a section of dna is lost or deleted.
Partake when DNA replication occurs before.Myanmar says t t a tag is competent to complimentary strand g t c a c h e c a t c what type of mutation has occurred
Insertion
Substitution
Part b when DNA replication occurs before myou're horrified.Since the original DNA strange TCA g GC ATC.Yes, yes, CAG CG test.What type of mutation has occurred
Delete them answer insertion in version
Translocation
Partake when DNA replication occurs before.Myanmar says t t a tag is competent to complimentary strand g t c a c h e c a t c what type of mutation has occurred
Insertion
Substitution
Part b when DNA replication occurs before myou're horrified.Since the original DNA strange TCA g GC ATC.Yes, yes, CAG CG test.What type of mutation has occurred
Delete them answer insertion in version
Translocation
Answers
GPT-4o mini
It seems that you're discussing various aspects of genetic mutations, their types, and how they can arise. To clarify your questions about specific mutations occurring during DNA replication:
1. **In the first part of your query**, you mentioned:
- Original DNA: `TTA GTC ACG`
- New strand after replication: `TTA GTC ACG`
Since there is no change in the sequence, this does not indicate an insertion, deletion, or substitution; therefore, it is not classified as any type of mutation. If the new strand was the same as the original strand, it suggests there has been no mutation.
2. **In the second part**:
- Original DNA: `TCA GGC ATC`
- New strand after replication: `CAG CGT`
If the original sequence is `TCA GGC ATC` and has changed to `CAG CGT`, there seems to be both a **deletion** (where parts of the sequence are missing) and potentially a **substitution** (where some base pairs have been replaced).
To identify the specific types of mutations:
- **Deletion**: If any segment of the DNA was completely removed.
- **Substitution**: If any of the bases were exchanged for another base.
Given the sequences you've shared, if `TCA` from the original is missing in `CAG`, this indicates a deletion. Additionally, if other bases differ (like reading `GGC` as being replaced in the new strand), that would indicate substitutions.
However, the precise classification would depend on the details of the new sequence and what has specifically changed from the original.
If you need further clarification or have additional questions, feel free to ask!
1. **In the first part of your query**, you mentioned:
- Original DNA: `TTA GTC ACG`
- New strand after replication: `TTA GTC ACG`
Since there is no change in the sequence, this does not indicate an insertion, deletion, or substitution; therefore, it is not classified as any type of mutation. If the new strand was the same as the original strand, it suggests there has been no mutation.
2. **In the second part**:
- Original DNA: `TCA GGC ATC`
- New strand after replication: `CAG CGT`
If the original sequence is `TCA GGC ATC` and has changed to `CAG CGT`, there seems to be both a **deletion** (where parts of the sequence are missing) and potentially a **substitution** (where some base pairs have been replaced).
To identify the specific types of mutations:
- **Deletion**: If any segment of the DNA was completely removed.
- **Substitution**: If any of the bases were exchanged for another base.
Given the sequences you've shared, if `TCA` from the original is missing in `CAG`, this indicates a deletion. Additionally, if other bases differ (like reading `GGC` as being replaced in the new strand), that would indicate substitutions.
However, the precise classification would depend on the details of the new sequence and what has specifically changed from the original.
If you need further clarification or have additional questions, feel free to ask!