The mutated gene codes for a protein that cause a new trait
A gene that is altered or copied incorrectly is called a mutation. Mutations can occur spontaneously or be induced by external factors, and they can lead to changes in an organism's traits or characteristics.
A mutation in a gene involves a change in the sequence of DNA bases, which can occur through substitutions, insertions, or deletions. This alteration can affect the amino acid sequence of the protein encoded by the gene, potentially altering its structure and function. Depending on the nature of the mutation, it can lead to beneficial, neutral, or harmful effects on the organism. In some cases, mutations can also disrupt regulatory elements, affecting gene expression.
Yes, when a DNA base pair is mismatched during duplication, it can lead to a mutation in the DNA sequence. This can cause changes in the protein produced, potentially impacting the function of the gene and, ultimately, the organism.
A silent mutation is less harmful to an organism because it does not change the amino acid sequence of the resulting protein. This means that the protein's function is not altered by the mutation, minimizing its impact on the organism's health and survival.
A permanent heritable change in an allele that produces a different variant of the same trait is called a mutation. Mutations can lead to genetic diversity within a population and are the raw material for evolution.
The mutated gene codes for a protein that cause a new trait
The mutated gene codes for a protein that cause a new trait
The mutated gene codes for a protein that cause a new trait
The gene will code for a different protein than it should.
A point mutation, such as a substitution or insertion of a single base pair in the DNA sequence, is most likely to lead to a new trait in an organism by altering the protein structure and function. These mutations can result in new protein variants that may exhibit different characteristics or functions, leading to the emergence of a novel trait.
A gene that is altered or copied incorrectly is called a mutation. Mutations can occur spontaneously or be induced by external factors, and they can lead to changes in an organism's traits or characteristics.
A good mutation is a change in an organism's DNA that can lead to beneficial traits or improved survival. This can happen when the mutation results in a new advantageous trait, such as resistance to a disease or better adaptation to the environment. Good mutations can help organisms thrive and pass on these beneficial traits to future generations.
A mutation in a gene involves a change in the sequence of DNA bases, which can occur through substitutions, insertions, or deletions. This alteration can affect the amino acid sequence of the protein encoded by the gene, potentially altering its structure and function. Depending on the nature of the mutation, it can lead to beneficial, neutral, or harmful effects on the organism. In some cases, mutations can also disrupt regulatory elements, affecting gene expression.
When lethal genes are present in the organism's chromosomes, the organism is unable to survive. Semi Lethal genes are harmful to the organism but does not cause Death. E.g Huntington Chorea in human
The mutation in which a segment of a chromosome is repeated is known as duplication.
Polyploidy mutation is a type of mutation that results in an organism having more than two complete sets of chromosomes. This can lead to increased genetic diversity and potentially new traits in the organism.
Yes, when a DNA base pair is mismatched during duplication, it can lead to a mutation in the DNA sequence. This can cause changes in the protein produced, potentially impacting the function of the gene and, ultimately, the organism.