A meta phase it’s a bit spread out and that’s the second step in the phases
Explanation:
C. A cut in skin heals
This process involves wound healing and tissue regeneration of somatic cells via mitosis.
Further Explanation:
All the genetic information within the eukaryotic cell is stored within the nucleus as helical DNA. This DNA is tightly wound around histones as chromosomes. To produce daughter cells during cell division, the chromosomes (total number of chromosomes (2n)) are copied before the cell splits into two daughter cells.
This process is known as mitosis, and occurs in cell division and growth processes. Two new nuclei are formed, along with identical cells. These are the same as the parent cell and the chromosome number (2n) is maintained. This process occurs regularly in somatic cells for growth, or to repair damaged tissue.
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Answer/Explanation:
DNA replication doubles each chromosome, meaning the cell can pass on DNA to daughter cells - the duplicated DNA is divided equally between the two new cells formed from the parent.
The laws of inheritance are:
1) The Law of Dominance: An organism with alternate forms of a gene, called alleles, will always display the form that is dominant, masking the recessive trait.
2) The Law of Segregation: In a diploid genome, like most eukaryotes, each trait is defined by a pair of genes (alleles). Each allele is randomly passed on to the gametes so that each gamete only contains one allele. The offspring inherits one allele from each parent during the process of fertilization.
2) The Law of Independent Assortment: Genes for different traits are sorted independently from one another That is, the inheritance of one trait does not depend on the inheritance of another trait. so that the inheritance of one trait is not dependent on the inheritance of another.
Answer:
Lysosomes.
Explanation:
HEXA (Hexosaminidase A) is the functional enzyme and encoded by the HEXA gene. The main function of this enzyme is the hydroxylation of the gangliosides.
The mutation in this gene leads to the lysosomal storage disease. The GM2 starts accumulating in the lysosomes and causes Tay Sach's disease. This is a genetic disorder that leads to the breakdown of the cells of the spinal cord and the brain.
Thus, the answer is lysosomes.
