Given our understanding of genetics, we can confirm that the gene in question is of the homeotic type.
<h3>What is a gene? </h3>
- In biology, we refer to a gene as the most basic unit of genetic information.
- It is a segment of DNA that encodes for a certain trait that <u>may or may not be expressed.</u>
- A gene carries the information for a specific trait, for example:
1) Eye color
2) Body organization
3) Height
<h3 /><h3 /><h3>What does it mean for a gene to be homeotic?</h3>
- In the case of this question, the gene in question is a homeotic gene.
- Homeotic genes are those that are in charge of the organization of the organism's body.
- These genes control the <u>general pattern of the body</u>, such as where the arms and legs will be, and so on.
<h3 /><h3 />
Therefore, given the definition of a homeotic gene, we can confirm that this is the type that best fits the description of the mutation in the question since it affected the formation and normal organization of the body.
To learn more about homeotic genes visit:
brainly.com/question/7991651?referrer=searchResults
Answer;
-Scaffolding
Explanation;
Scaffolding as a metaphor in teaching and learning describes the adaptive and temporary support provided by a more competent person (e.g., teacher or adult) to a less competent person (e.g., student or child). For example; mother–child interaction during the game of peekaboo.
Scaffolding is one of the several aspects of effective instruction that can be applied in the context of language learning. Although teachers might be enthusiastic about the idea of scaffolding, it must be borne in mind that scaffolding is not simply synonymous with teacher support.
Vestigial traits are adaptations to environmental pressures which are no longer present.
homologous structures are similar structures found in different species that were present in a common ancestor.
analogous traits are similar traits found in different species that were developed independently (this process is known as convergent evolution)
Answer:
Answered below.
Explanation:
A karyotype is defined as the size, shape, and number of chromosomes present in an organism.
An analysis is usually done on a karyotype to see if individuals have abnormal numbers or sizes of chromosomes. Such abnormalities may arise from;
Deletion: which implies that a chromosomal part is missing.
Duplication: where parts of a chromosome are repeated.
Translocation: which occurs when a chromosomal part breaks off and gets attached to another chromosome.
Nondisjunction: in which chromosomes do not separate from the parent cells.
Common chromosomal disorders arising from these abnormalities include;
Down's syndrome
Edwards syndrome
Turner's syndrome
Klinefelter syndrome
Prada-willi syndrome
Cri-du-chat syndrome
Patau's syndrome
