The chromosomal mutation in the zygote can be traced back to "Chromosome 6 in the egg cell".
<u>Option: B</u>
<u>Explanation:</u>
In germ cells i.e. egg or sperm cells, the mutations in chromosome often happen during the meiosis phase. The number of chromosomes in egg cells or sperm cells must be haploid, so that diploid chromosomes form zygote on fertilization. Chromosome mutation in meiosis leads in an additional set of chromosomes or structural defects in the chromosome.
Chromosomal mutations are often caused by chemical agents or by mutagens.
The homologous chromosomes are segregated from sister chromatids throughout cell division, any abnormality at this point allows the chromosomes to be unequally divided or not disjuncted, same is observed in the situation seen in egg cell chromosome 6.
Answer:
They both have cell walls
Explanation:
hope it helps
Answer:
A mutation that cause changes to short stretches of nucleotides. These mutations affect the specific genes that provide instructions for various functional molecules, including protein . changes in these molecules can have impact on any number of an organism's physical characteristics
Answer:
GAR and AICAR transformylase
Explanation:
Tetrahydrofolate is essential for purine and pyrimidine synthesis, its deficiency can lead to inhibition of nucleic acid such as DNA and RNA and protein synthesis, which are important for the growth and survival of both normal cells and cancer cells. N-10-formyltetrahydrofolate acts as a donor of carbon atoms to the actively growing bases. It contribution is mediated by the action of the Glycinamide Ribonucleotide (GAR) transformylase and the N-5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) transformylase.