Explanation:
During meiosis, sister chromosomes of a homologous pair separate into different cells during gamete formation . This mainly occurs in Metaphase I of meiosis where the homologous chromosomes line up the metaphase plate in their sets. Each chromosomes of a pair are then pulled to different poles of the cells separating them. Each of these chromosomes carries a set of alleles of a gene. Each cell/gamete, therefore, carried half the set of alleles of all genes compared to autosomal cells. There many combinations of these sets that can occur depending on the number of chromosomes the organism has.
These cells when combined with that of another parent during fertilization, form a zygote that grows and develops into a mature organism. The offspring will bear the characteristics of both parents because it inherits half a set of chromosomes from both parents.
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Stomata is present at epidermis of the leaves lenticels are present at bark
Answer:
The number of protons in the nucleus of an atom determines an element's atomic number
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The question is incomplete as it does not have the options which are:
photoreactivation
reactivation repair pathway
nucleotide excision repair pathway
UV repair pathway
p53 repair pathway
Answer:
p53 repair pathway
Explanation:
ATM gene or ataxia telangiectasia-mutated is a gene which codes for the protein kinase involved in the DNA double-stranded break.
The DNA double-stranded break is repaired easily as the protein kinase is recruited to the site of the break where it allows the DNA repair machinery to repair the DNA.
The gene also controls the cell growth therefore this gene is important to study cancer. Since the p53 protein is a suppressor protein which if mutated is repaired by the ATM gene and if the gene becomes mutated then the p53 repair pathway is affected.
Thus, p53 repair pathway is the correct answer.
