A group of mutations, known as MT-ND1, have been identified in mitochondrial DNA. These mutations are associated with a number of debilitating diseases stemming from the production of nonfunctional proteins in the mitochondria.

Which of the following cellular deficiencies would most likely be related to these MT-ND1 mutations?
a. The cell is unable to synthesize most proteins required for normal cell functions.
b. The cell is unable to break down toxic materials and would accumulate large volumes of these materials.
c. The cell is able to synthesize proteins, but the proteins would not fold properly and would not contain the correct molecular tags for export from the cell.
d. The cell is unable to complete reactions related to electron transport and ATP production.



Answer :

The cell is unable to complete reactions related to electron transport and ATP production would most likely be related to these MT-ND1 mutations. So the correct option is (d).

Rare mutations in the MT-ND1 gene are responsible for stroke-like episodes, lactic acidosis, and mitochondrial encephalomyopathy (MELAS). A small number of MELAS cases originating from mutations in the MT-ND1 gene have been described, while the majority of MELAS cases are caused by mutations in other mitochondrial genes.

The proteins in the mitochondrion's inner membrane are involved in the electron transport chain and the generation of ATP. Reduced ATP generation in the mitochondrion is probably caused by dysfunctional proteins.

Therefore, senescent dysfunction of long-lived post-mitotic cells, such as neurons, cardiac myocytes, skeletal muscle fibers, and RPE, is primarily triggered by decreased ATP generation and increased oxidative stress. The cell is unable to complete reactions related to electron transport and ATP production would most likely be related to these MT-ND1 mutations. So the correct option is (d).

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