Answer:
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Explanation:
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<span> Harmful, because there will not be enough space for both of them</span><span> </span>
Answer:
Many scientists use dichotomous keys to identify plants, animals, and other organisms. They may also use dichotomous keys to identify species, or to determine whether a particular organism has been identified and described before. However, dichotomous keys are not used only to identify organisms.
Explanation:
The DNA contains many regulatory sequences that are very important, even though they do not code for proteins.
For example, the expression of every gene is regulated by a region called the Promoter. The promoter sequence, located close by the coding region of the gene, usually binds the RNA polymerase (the enzyme that transcribes genes into mRNA) as well as other proteins necessary for transcription,
The promoter sequence, thus, does not itself code for proteins, but is essential for transcription and must be highly conserved so that the RNA polymerase can find it.
None: Only those mutations that occur in the germ line and result in gametes will have a chance of being passed on to progeny. An alteration in DNA that occurs after conception.
Somatic mutations can occur in any of the body's cells except germ cells (sperm and egg) and are therefore not passed on to children. These alterations can (but not always) cause cancer or other diseases. Mutations in somatic cells are called somatic mutations. Because they do not occur in the cells that give rise to gametes, the mutation is not transmitted to the next generation sexually. Human somatic cells have 46 chromosomes: 22 pairs and 2 sex chromosomes that may or may not form a pair. This is the 2n or diploid condition. Human gametes have 23 chromosomes, each of 23 unique chromosomes, one of which is a sex chromosome. Somatic cells are the cells in the body other than sperm and eggs (called germ cells). In humans, somatic cells are diploid, meaning they contain two sets of chromosomes, one inherited from each parent. Mutations in a somatic cell occur in somatic cells and are transmitted by mitosis, resulting in cancer. However, mutations in a gamete are passed on by meiosis, resulting in mutated offspring. A genetic mutation occurs during DNA replication, and chromosomal mutations occur during meiosis.
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