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Mitochondria are structures within cells that convert the energy from food into a form that cells can use. Although most DNA is packaged in chromosomes within the nucleus, mitochondria also have a small amount of their own DNA. This genetic material is known as mitochondrial DNA or mtDNA. In humans, mitochondrial DNA spans about 16,500 DNA building blocks (base pairs), representing a fraction of the total DNA in cells. Mitochondrial DNA contains 37 genes, all of which are essential for normal mitochondrial function. Thirteen of these genes provide instructions for making enzymes involved in oxidative phosphorylation. Oxidative phosphorylation is a process that uses oxygen and simple sugars to create adenosine triphosphate (ATP), the cell's main energy source. The remaining genes provide instructions for making molecules called transfer RNAs (tRNAs) and ribosomal RNAs (rRNAs), which are chemical cousins of DNA. These types of RNA help assemble protein building blocks (amino acids) into functioning proteins. Mitochondrial genes are among the estimated 20,000 to 25,000 total genes in the human genome. There are genetic conditions related to mitochondrial genes. The following conditions are related to changes in mitochondrial DNA. ; cancers : Mitochondrial DNA is prone to noninherited (somatic) mutations. Somatic mutations occur in the DNA of certain cells during a person's lifetime and typically are not passed to future generations. Somatic mutations in mitochondrial DNA have been reported in some forms of cancer, including breast, colon, stomach, liver, and kidney tumors. These mutations also have been associated with cancer of blood-forming tissue (leukemia) and cancer of immune system cells (lymphoma). Somatic mutations in mitochondrial DNA may increase the production of potentially harmful molecules called reactive oxygen species. Mitochondrial DNA is particularly vulnerable to the effects of these molecules and has a limited ability to repair itself. As a result, reactive oxygen species easily damage mitochondrial DNA, causing a buildup of additional somatic mutations. Researchers continue to investigate how these mutations may lead to uncontrolled cell division and the growth of cancerous tumors. ; Leber hereditary optic neuropathy : Mutations in four mitochondrial genes, MT-ND1, MT-ND4, MT-ND4L, and MT-ND6, have been identified in people with Leber hereditary optic neuropathy. These genes provide instructions for making proteins that are part of a large enzyme complex. This group of enzymes, known as complex I, is necessary for oxidative phosphorylation. The mutations responsible for Leber hereditary optic neuropathy change single protein building blocks (amino acids) in these proteins, which may affect the generation of ATP within mitochondria. It remains unclear, however, why the effects of these mutations are often limited to the nerve that relays visual information from the eye to the brain (the optic nerve). Additional genetic and environmental factors probably contribute to the vision loss and other medical problems associated with Leber hereditary optic neuropathy. ; mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes : Mutations in at least five mitochondrial genes, MT-ND1, MT-ND5, MT-TH, MT-TL1, and MT-TV, can cause the characteristic features of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Some of these genes provide instructions for making proteins that are part of a large enzyme complex, called complex I, that is necessary for oxidative phosphorylation. The other genes provide instructions for making transfer RNA molecules, which are essential for protein production within mitochondria. Mutations in one transfer RNA gene, MT-TL1, cause more than 80 percent of all cases of MELAS. These mutations impair the ability of mitochondria to make proteins, use oxygen, and produce energy. Researchers have not determined how changes in mitochondrial DNA lead to the specific signs and symptoms of MELAS. They continue to investigate the effects of mitochondrial gene mutations in different tissues, particularly in the brain. ; neuropathy, ataxia, and retinitis pigmentosa : Mutations in one mitochondrial gene, MT-ATP6, have been found in people with neuropathy, ataxia, and retinitis pigmentosa (NARP). The MT-ATP6 gene provides instructions for making a protein that is essential for normal mitochondrial function. This protein forms one part (subunit) of an enzyme called ATP synthase. This enzyme, which is also known as complex V, is responsible for the last step of oxidative phosphorylation, in which a molecule called adenosine diphosphate (ADP) is converted to ATP. Mutations in the MT-ATP6 gene alter the structure or function of ATP synthase, reducing the ability of mitochondria to make ATP. It is unclear how this disruption in mitochondrial energy production leads to muscle weakness, vision loss, and the other specific features of NARP. ; nonsyndromic deafness : Mutations in two mitochondrial genes, MT-RNR1 and MT-TS1, are associated with nonsyndromic deafness (hearing loss without related signs and symptoms affecting other parts of the body). These genes provide instructions for making types of RNA. The MT-RNR1 gene provides instructions for a specific type of ribosomal RNA called 12S RNA. A particular form of transfer RNA, designated as tRNASer(UCN), is formed from the MT-TS1 gene. Both of these RNA molecules help assemble amino acids into full-length, functioning proteins within mitochondria. Mutations in the MT-RNR1 gene increase the risk of hearing loss, particularly in people who take antibiotic medications called aminoglycosides. These antibiotics are typically used to treat chronic bacterial infections such as tuberculosis. Aminoglycosides kill bacteria by binding to their ribosomal RNA and disrupting the bacteria's ability to make proteins. Genetic changes in the MT-RNR1 gene often make the 12S RNA in human cells look similar to bacterial ribosomal RNA. As a result, aminoglycosides can target the altered 12S RNA just as they target bacterial ribosomal RNA. The antibiotic easily binds to the abnormal 12S RNA, which impairs the ability of mitochondria to produce proteins needed for oxidative phosphorylation. Researchers believe that this unintended effect of aminoglycosides may reduce the amount of ATP produced in mitochondria, increase the production of harmful byproducts, and eventually cause the cell to self-destruct (undergo apoptosis). Nonsyndromic deafness also results from genetic changes in the MT-TS1 gene. Most of the mutations change a single building block (nucleotide) in the tRNASer(UCN) molecule. These mutations likely disrupt the normal production of the molecule or alter its structure. As a result, less tRNASer(UCN) is available to assemble proteins within mitochondria. These changes reduce the production of proteins needed for oxidative phosphorylation, which may impair the ability of mitochondria to make ATP. Researchers have not determined why the effects of mutations in the MT-RNR1 and MT-TS1 genes are usually limited to cells in the inner ear that are essential for hearing. They believe that other genetic or environmental factors must play a role in the signs and symptoms associated with these mutations. ; other disorders : Inherited changes in mitochondrial DNA can cause problems with growth, development, and function of the body's systems. These mutations disrupt the mitochondria's ability to efficiently generate energy for the cell. Conditions caused by mutations in mitochondrial DNA often involve multiple organ systems. The effects of these conditions are most pronounced in organs and tissues that require a lot of energy (such as the heart, brain, and muscles). Although the health consequences of inherited mitochondrial DNA mutations vary widely, some frequently observed features include muscle weakness and wasting, problems with movement, Diabetes, kidney failure, Heart disease, loss of intellectual functions (dementia), hearing loss, and abnormalities involving the eyes and vision. A buildup of noninherited (somatic) mutations in mitochondrial DNA has been associated with an increased risk of certain age-related disorders such as heart disease, Alzheimer disease, and Parkinson disease. Additionally, research suggests that the progressive accumulation of these mutations over a person's lifetime may play a role in the normal process of aging.

Mitochondrial DNA (mtDNA) is the DNA located in organelles called mitochondria. Most other DNA present in eukaryotic organisms is found in the cell nucleus. Mitochondrial DNA was discovered by Margit M. K. Nass and Sylvan Nass by electron microscopy as DNAase-sensitive thread inside mitochondria, and by Ellen Haslbrunner, Hans Tuppy and Gottfried Schatz by biochemical assays on highly purified mitochondrial fractions. Nuclear and mitochondrial DNA are thought to be of separate evolutionary origin, with the mtDNA being derived from the circular genomes of the bacteria that were engulfed by the early ancestors of today's eukaryotic cells. Each mitochondrion is estimated to contain 2-10 mtDNA copies. In the cells of extant organisms, the vast majority of the proteins present in the mitochondria (numbering approximately 1500 different types in mammals) are coded for by nuclear DNA, but the genes for some of them, if not most, are thought to have originally been of bacterial origin, having since been transferred to the eukaryotic nucleus during evolution. In most multicellular organisms, mtDNA is inherited from the mother (maternally inherited). Mechanisms for this include simple dilution (an egg contains 100,000 to 1,000,000 mtDNA molecules, whereas a sperm contains only 100 to 1000), degradation of sperm mtDNA in the fertilized egg, and, at least in a few organisms, failure of sperm mtDNA to enter the egg. Whatever the mechanism, this single parent (uniparental) pattern of mtDNA inheritance is found in most animals, most plants and in fungi as well. mtDNA is particularly susceptible to reactive oxygen species generated by the respiratory chain due to its close proximity. Though mtDNA is packaged by proteins and harbors significant DNA repair capacity, these protective functions are less robust than those operating on nuclear DNA and therefore thought to contribute to enhanced susceptibility of mtDNA to oxidative damage. Mutations in mtDNA can in some cases cause maternally inherited diseases and some evidence suggests that they might be major contributors to the aging process and age-associated pathologies.[citation needed] In humans (and probably in metazoans in general), 100-10,000 separate copies of mtDNA are usually present per cell (egg and sperm cells are exceptions). In mammals, each circular mtDNA molecule consists of 15,000-17,000 base pairs, which encode the same 37 genes: 13 for proteins (polypeptides), 22 for transfer RNA (tRNA) and one each for the small and large subunits of ribosomal RNA (rRNA). This pattern is also seen among most metazoans, although in some cases one or more of the 37 genes is absent and the mtDNA size range is greater. Even greater variation in mtDNA gene content and size exists among fungi and plants, although there appears to be a core subset of genes that are present in all eukaryotes (except for the few that have no mitochondria at all). Some plant species have enormous mtDNAs (as many as 2,500,000 base pairs per mtDNA molecule) but, surprisingly, even those huge mtDNAs contain the same number and kinds of genes as related plants with much smaller mtDNAs.

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Q: What do you think researchers discovered in the mitochondrial DNA taken from the heart of cells of older adults?
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What do you think researchers discovered in the mitochondrial DNA taken from the heart cells of older adults?

There are more mitochondria in cells that need a lot of energy, such as heart muscle cells. Some researchers are studying mitochondrial DNA in the heart cells of different age groups.

What cellular structures are found in plant cells but NOT in animal cells?


What cellular structures are found in plant cells but not animal cells?

Cell wall

Where is the most ATP generated for eukaryotic cells?

in the mitochondrial matrix

Which organelles are responsible for making most of the cells ATP?

the Mitochondrial.

How does the inheritance of mitochondrial dna differ from the inheritance of dna found in the nucleus of cells?

Mitochondrial dna is inherited solely from the mother.

Mutations in mitochondrial genes often cause disorders that affect cells?

the mitochondrial mutations effect to those cells which have maternal inherritance character and the mutation is called poky mutation

What is the obesity gene that is expressed in fat cells and codes for a hormone-like protein that researchers have identified known as?

The obesity gene that researchers have identified is known as leptin-E100. This was the first fat cell protein to be discovered.

What has the author Roberto Scatena written?

Roberto Scatena has written: 'Advances in mitochondrial medicine' -- subject(s): Mitochondrial pathology, Mitochondrial Diseases, Effect of drugs on, Cells, Mitochondria, Physiology

Where in cells are the enzymes of the citric acid cycle located?

mitochondrial matrix

Where does the electron transport occur in eukaryotes cells?

Inner mitochondrial membrane

What are the two types of DNA in the in the eukaryotic cells nuclear and mitochondrial?


What is the function of the sperm cells mitochondrial spiral?

Producing energy APEX

What do researchers do with embryonic stem cells?

Researchers use embryonic stem cells to study diseases such as Parkinson's. They can be used to develop cures.

Name some associated genes of human mitochondrial genome?

Some associated genes of human mitochondrial genome are the Eukaryotic cells and the cell nucleus. Mitochondrial DNA is inherited only from the mother's ovum.

Where are the enzymes located during the Krebs cycle in eukaryotic cells?

in the mitochondrial matrix

What takes place within the mitochondrial membrane?

ATP is produced for use by cells

What invention enabled researchers to see cells?

the microscope

Is there a cell in humans that don't have DNA?

No. Not all cells have a nucleus, which contains nuclear DNA; but all cells have mitochondria, which have their own DNA, called mitochondrial DNA, or mDNA. In humans, the cells that lack a nucleus and therefore nuclear DNA, are mature red blood cells, but they do have mitochondria and mitochondrial DNA.

When were cells discovered?

Cells were first discovered by Robert Hooke in 1663.

What are the three types of stem cells in adults?

Three types of stem cells in adults are hematopoietic stem cells, mesenchymal stem cells, and neural stem cells.

How does the inheritance of mitochondrial DNA different found in the nucleus of cells?

mitochondrial dna is not changed when passed to offspring. dna in the nucleus can be changed due to dominant and recessive traits.

How does mitochondrial disease affect a person's life?

Mitochondria are seat of energy generation in the body cells. Mitochondrial disease will adversely affect metabolic activities in that person.

Can adults grow new brain cells?

No one can grow new brain cells. Kids or adults.

What is the purpose of the inner mitochondrial membranes being five times the area of the outer mitochondrial membranes and 17 times that of the cells plasma membrane?

It increases the surface for oxidative phosphorylation