<h3>Answer:</h3><h3>Mitochondria and chloroplasts originated from the endosymbiotic association of aerobic (more...) A critical step in the evolution of eukaryotic cells was the acquisition of membrane-enclosed subcellular organelles, allowing the development of the complexity characteristic of these cells.</h3><h3>Hope this is fine for you
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Answer:
a) DNA fragments associated with histone proteins are all multiple in length (i.e., 260 bp, 520 bp, 780 bp, etc), thereby suggesting the presence of a pattern of organization in the chromatin
b) it suggests that each unit of organization (ie, each nucleosome) consists of 260 bp associated with chromatin proteins
Explanation:
The nucleosome is considered as the basic unit of chromatin. A nucleosome consists of approximately two turns of DNA wrapped around a core of eight histone proteins (i.e., a histone octamer). The histone octamer consists of two copies of each of the histones H2A, H2B, H3, and H4. Moreover, the nucleosomes are connected together by linker DNA sequences which vary between 10 and 100 bp in length.
Answer:
Encloses specific structures.
Explanation:
The plasma membrane, also referred to as the cell membrane, has the job of keeping all the cell structures inside the cell protected and enclosed.
Answer:
Explanation:
1 Long term exposure to harmful genotoxic chemicals or ionizing radiation can cause changes in the base sequence of DNA.Chemicals might induce DNA mutations, such as polycyclic hydrocarbons (fumes found in oil stations, or smoke from a tobacco cigarette), intercalating agents such as Ethidium Bromide (carcinogen), but also radiations such as UV-radiation (C and T bases are most vulnerable and would bind to identical bases unstead of their
2 Genetic changes that are described as de novo (new) mutations can be either hereditary or somatic. In some cases, the mutation occurs in a person’s egg or sperm cell but is not present in any of the person’s other cells. In other cases, the mutation occurs in the fertilized egg shortly after the egg and sperm cells unite. (It is often impossible to tell exactly when a de novo mutation happened.) As the fertilized egg divides, each resulting cell in the growing embryo will have the mutation. De novo mutations may explain genetic disorders in which an affected child has a mutation in every cell in the body but the parents do not, and there is no family history of the disorder.
Somatic mutations that happen in a single cell early in embryonic development can lead to a situation called mosaicism. These genetic changes are not present in a parent’s egg or sperm cells, or in the fertilized egg, but happen a bit later when the embryo includes several cells. As all the cells divide during growth and development, cells that arise from the cell with the altered gene will have the mutation, while other cells will not. Depending on the mutation and how many cells are affected, mosaicism may or may not cause health problems.
The light-independents reaction
